Prospects of genetic testing for steroid-resistant nephrotic syndrome in Nigerian children: a narrative review of challenges and opportunities. (Q64929779)

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scientific article published on 8 May 2019

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English	Prospects of genetic testing for steroid-resistant nephrotic syndrome in Nigerian children: a narrative review of challenges and opportunities.	scientific article published on 8 May 2019

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scholarly article

1 reference

Europe PubMed Central

1 July 2019

http://europepmc.org/abstract/PMC/6512787

1 reference

Europe PubMed Central

Prospects of genetic testing for steroid-resistant nephrotic syndrome in Nigerian children: a narrative review of challenges and opportunities. (English)

1 reference

Europe PubMed Central

1 July 2019

http://europepmc.org/abstract/PMC/6512787

nephrotic syndrome

1 reference

based on heuristic

inferred from title

author name string

Emmanuel Ademola Anigilaje

1

1 reference

Europe PubMed Central

1 July 2019

http://europepmc.org/abstract/PMC/6512787

Ayodotun Olutola

2

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Europe PubMed Central

1 July 2019

http://europepmc.org/abstract/PMC/6512787

language of work or name

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publication date

8 May 2019

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Europe PubMed Central

1 July 2019

http://europepmc.org/abstract/PMC/6512787

International Journal of Nephrology and Renovascular Disease

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Europe PubMed Central

1 July 2019

http://europepmc.org/abstract/PMC/6512787

12

1 reference

Europe PubMed Central

1 July 2019

http://europepmc.org/abstract/PMC/6512787

119-136

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Europe PubMed Central

1 July 2019

http://europepmc.org/abstract/PMC/6512787

copyright license

Creative Commons Attribution-NonCommercial 3.0 Unported

1 May 2019

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April 2022 Public Data File from Crossref

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0 references

Abnormal haemoglobins in the Sudan savanna of Nigeria. I. Prevalence of haemoglobins and relationships between sickle cell trait, malaria and survival

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nephrotic syndrome in children: prediction of histopathology from clinical and laboratory characteristics at time of diagnosis. A report of the International Study of Kidney Disease in Children

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Herediatary anhidrotic ectodermal dysplasia. Studies in a Nigerian famil

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinicopathological features of childhood nephrotic syndrome in northern Nigeria.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A profile of sickle cell disease in Nigeria

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Importance of Sample Size in the Interpretation of the Renal Biopsy

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Quartan malarial nephrotic syndrome. Collaborative clinicopathological study in Nigerian children

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Selectivity of proteinuria and response to prednisolone or immunosuppressive drugs in children with malarial nephrosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dystrophia myotonica in a Nigerian family

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The incidence of Down's syndrome in Nigeria

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The incidence of Turner's syndrome in Ibadan, Nigeria

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal trisomy 18 and 13 syndromes in Ibadan, Nigeria

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Primary nephrotic syndrome in Arab children

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence and pattern of renal disease in eastern Libya

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spectrum of bone dysplasias in African children: Ibadan Nigerian experience.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The primary nephrotic syndrome in children. Identification of patients with minimal change nephrotic syndrome from initial response to prednisone. A report of the International Study of Kidney Disease in Children

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The genetics of omphalocele

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Beckwith-Wiedemann syndrome in Nigerian infants (exomphalos, macroglossia and gigantism).

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alternative treatment to corticosteroids in steroid sensitive idiopathic nephrotic syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glomerular dynamics and morphology of aged spontaneously hypertensive rats. Effects of angiotensin-converting enzyme inhibition.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Renal disorders in children: a Nigerian study.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Angiotensinogen gene in human hypertension. Lack of an association of the 235T allele among African Americans

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Distribution of anthropometric variables and the prevalence of obesity in populations of west African origin: the International Collaborative Study on Hypertension in Blacks (ICSHIB).

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphisms of renin-angiotensin genes among Nigerians, Jamaicans, and African Americans.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Obesity and hypertension prevalence in populations of African origin. The Investigators of the International Collaborative Study on Hypertension in Blacks

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypertension, serum angiotensinogen, and molecular variants of the angiotensinogen gene among Nigerians.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nephrotic syndrome in South African children: changing perspectives over 20 years.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Relationship of two apolipoprotein B polymorphisms with serum lipoprotein and lipid levels in African blacks

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nephrotic syndrome in Nigerian children with homozygous sickle cell disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Positionally cloned gene for a novel glomerular protein--nephrin--is mutated in congenital nephrotic syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Routine screening for sickle cell haemoglobinopathy by electrophoresis in an infant welfare clinic.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Epidemiology and clinicopathologic characteristics of childhood nephrotic syndrome in Benin-City, Nigeria

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High incidence of focal segmental glomerulosclerosis in nephrotic syndrome of childhood

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Changing patterns in the histopathology of idiopathic nephrotic syndrome in children

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Changing trends of histopathology in childhood nephrotic syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spectrum of disease in familial focal and segmental glomerulosclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The predominance of membranoproliferative glomerulonephritis in childhood nephrotic syndrome in Ibadan, Nigeria

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

In search of susceptibility genes for type 2 diabetes in west africa: The design and results of the first phase of the AADM study

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Collapsing focal segmental glomerulosclerosis following treatment with high-dose pamidronate.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Changing trends of histopathology in childhood nephrotic syndrome in western Saudi Arabia.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lithium-induced nephrotic syndrome in a young pediatric patient

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Replication and compartmentalization of HIV-1 in kidney epithelium of patients with HIV-associated nephropathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Do current recommendations for kidney biopsy in nephrotic syndrome need modifications?

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cell biology of the glomerular podocyte

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nephrotic syndrome in childhood.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Possible aetiological role of Plasmodium malariae in "nephrotic syndrome" in Nigerian children

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nephrosis in Nigerian children. Role of Plasmodium malariae, and effect of antimalarial treatment.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The nephrotic syndrome and other renal diseases in children in Western Nigeria.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Is there really an increase in non-minimal change nephrotic syndrome in children?

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pathologic classification of focal segmental glomerulosclerosis: a working proposal

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The sickle-cell trait in western Nigeria; a survey of 1,881 cases in the Yoruba.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Patients with mutations in NPHS2 (podocin) do not respond to standard steroid treatment of nephrotic syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Genome-Wide Search for Type 2 Diabetes Susceptibility Genes in West Africans: The Africa America Diabetes Mellitus (AADM) Study

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

SNP haplotypes in the angiotensin I-converting enzyme (ACE) gene: analysis of Nigerian family data using gamete competition models.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Increased steroid responsiveness of young children with nephrotic syndrome in Nigeria

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Computational simulation of renal biopsy accuracy in focal segmental glomerulosclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pattern of paediatric renal disease in inpatients in Calabar, Nigeria

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Childhood nephrotic syndrome: change in pattern and response to steroids.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The normal kidney filters nephrotic levels of albumin retrieved by proximal tubule cells: retrieval is disrupted in nephrotic states

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sirolimus Therapy of Focal Segmental Glomerulosclerosis Is Associated With Nephrotoxicity

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A familial childhood-onset relapsing nephrotic syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Idiopathic nephrotic syndrome in New Zealand children, demographic, clinical features, initial management and outcome after twelve-month follow-up: results of a three-year national surveillance study

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pattern of renal diseases in children in midwestern zone of Nigeria.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High sirolimus levels may induce focal segmental glomerulosclerosis de novo

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Specific podocin mutations correlate with age of onset in steroid-resistant nephrotic syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Synaptopodin immunoexpression in steroid-responsive and steroid-resistant minimal change disease and focal segmental glomerulosclerosis]

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Properties of the glomerular barrier and mechanisms of proteinuria

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

African genetic diversity: implications for human demographic history, modern human origins, and complex disease mapping

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Podocyte foot process effacement as a diagnostic tool in focal segmental glomerulosclerosis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial forms of nephrotic syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Disease recurrence in paediatric renal transplantation

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Specific podocin mutations determine age of onset of nephrotic syndrome all the way into adult life

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Kidney transplantation for primary focal segmental glomerulosclerosis: outcomes and response to therapy for recurrence.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cellular origins of type IV collagen networks in developing glomeruli.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Management of childhood onset nephrotic syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dystroglycan in the diagnosis of FSGS.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Quartan malaria-associated childhood nephrotic syndrome: now a rare clinical entity in malaria endemic Nigeria

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Development of focal segmental glomerulosclerosis after anabolic steroid abuse

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pediatric nephrology in developing countries

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genome-wide association of anthropometric traits in African- and African-derived populations

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of trypanolytic ApoL1 variants with kidney disease in African Americans

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Exome sequencing: the sweet spot before whole genomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Childhood idiopathic steroid resistant nephrotic syndrome in Southwestern Nigeria.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary kidney diseases: highlighting the importance of classical Mendelian phenotypes

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Podocyte-secreted angiopoietin-like-4 mediates proteinuria in glucocorticoid-sensitive nephrotic syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Screening for NPHS2 mutations may help predict FSGS recurrence after transplantation

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical utility of genetic testing in children and adults with steroid-resistant nephrotic syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glomerular hyperfiltration and albuminuria in children with sickle cell anemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variation in genome-wide mutation rates within and between human families

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Circulating urokinase receptor as a cause of focal segmental glomerulosclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Focal segmental glomerulosclerosis and chronic kidney disease in pediatric patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Arhgap24 inactivates Rac1 in mouse podocytes, and a mutant form is associated with familial focal segmental glomerulosclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

APOL1 genetic variants in focal segmental glomerulosclerosis and HIV-associated nephropathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

NGAL distinguishes steroid sensitivity in idiopathic nephrotic syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Educational paper: the podocytopathies

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chronic kidney disease in sub-Saharan Africa: hypothesis for research demand

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of the sickle cell trait and the ABO blood group with clinical severity of malaria in southwest Nigeria.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Soluble urokinase receptor and focal segmental glomerulosclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Adrenergic alpha-1 pathway is associated with hypertension among Nigerians in a pathway-focused analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Kidney disease in hospitalised HIV positive children in Ibadan, south west Nigeria.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High-throughput mutation analysis in patients with a nephronophthisis-associated ciliopathy applying multiplexed barcoded array-based PCR amplification and next-generation sequencing

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A form of apolipoprotein a-I is found specifically in relapses of focal segmental glomerulosclerosis following transplantation

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Collapsing glomerulopathy following anthracycline therapy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

New TRPC6 gain-of-function mutation in a non-consanguineous Dutch family with late-onset focal segmental glomerulosclerosis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic testing in nephrotic syndrome--challenges and opportunities

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Design of the Nephrotic Syndrome Study Network (NEPTUNE) to evaluate primary glomerular nephropathy by a multidisciplinary approach

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Retention of fetuin-A in renal tubular lumen protects the kidney from nephrocalcinosis in rats

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The rationale and design of Insight into Nephrotic Syndrome: Investigating Genes, Health and Therapeutics (INSIGHT): a prospective cohort study of childhood nephrotic syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Viruses and collapsing glomerulopathy: a brief critical review

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Obesity and kidney disease: potential mechanisms

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial focal segmental glomerulosclerosis (FSGS) in a Nigerian family and exclusion of mutations in NPHS2,WT1 and APOL1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetics of steroid-resistant nephrotic syndrome: a review of mutation spectrum and suggested approach for genetic testing

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Low birthweight and premature birth are risk factors for podocytopenia and focal segmental glomerulosclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Increasing frequency of acute kidney injury amongst children hospitalized with nephrotic syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation-dependent recessive inheritance of NPHS2-associated steroid-resistant nephrotic syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Initial steroid sensitivity in children with steroid-resistant nephrotic syndrome predicts post-transplant recurrence

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Why we are not all multiregionalists now.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Killer-cell immunoglobulin-like receptors and falciparum malaria in southwest Nigeria

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel IRF6 mutations in families with Van Der Woude syndrome and popliteal pterygium syndrome from sub-Saharan Africa

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Research capacity. Enabling the genomic revolution in Africa

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High Steroid Sensitivity among Children with Nephrotic Syndrome in Southwestern Nigeria

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rare hereditary COL4A3/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A circulating antibody panel for pretransplant prediction of FSGS recurrence after kidney transplantation

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sleep apnea and the kidney: is sleep apnea a risk factor for chronic kidney disease?

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fourteen monogenic genes account for 15% of nephrolithiasis/nephrocalcinosis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Defects of CRB2 cause steroid-resistant nephrotic syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spectrum of steroid-resistant and congenital nephrotic syndrome in children: the PodoNet registry cohort

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genes and podocytes - new insights into mechanisms of podocytopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

APOL1 Risk Variants Are Strongly Associated with HIV-Associated Nephropathy in Black South Africans

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Translating genetic findings in hereditary nephrotic syndrome: the missing loops

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Response to cyclosporine in steroid-resistant nephrotic syndrome: discontinuation is possible

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel domain-specific POU3F4 mutations are associated with X-linked deafness: examples from different populations

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Canadian Childhood Nephrotic Syndrome (CHILDNEPH) Project: overview of design and methods.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

KANK deficiency leads to podocyte dysfunction and nephrotic syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human Heredity and Health (H3) in Africa Kidney Disease Research Network: A Focus on Methods in Sub-Saharan Africa

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Renal and Hematological Effects of CLCF-1, a B-Cell-Stimulating Cytokine of the IL-6 Family.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Indications and results of renal biopsy in children: A single-center experience from Morocco

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chronic kidney disease in congenital heart disease patients: a narrative review of evidence

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biallelic Mutations in Nuclear Pore Complex Subunit NUP107 Cause Early-Childhood-Onset Steroid-Resistant Nephrotic Syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic testing in steroid-resistant nephrotic syndrome: when and how?

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evaluation of genome wide association study associated type 2 diabetes susceptibility loci in sub Saharan Africans

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Trends in the histopathology of childhood nephrotic syndrome in Ibadan Nigeria: preponderance of idiopathic focal segmental glomerulosclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ethical and legal issues in renal transplantation in Nigeria

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The global nephrology workforce: emerging threats and potential solutions!

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in nuclear pore genes NUP93, NUP205 and XPO5 cause steroid-resistant nephrotic syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An electronic atlas of human malformation syndromes in diverse populations.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Towards a more representative morphology: clinical and ethical considerations for including diverse populations in diagnostic genetic atlases

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ethnic Differences in Childhood Nephrotic Syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tumour necrosis factor alpha promoter polymorphism, TNF-238 is associated with severe clinical outcome of falciparum malaria in Ibadan southwest Nigeria

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Steroid Resistant Nephrotic Syndrome-Genetic Consideration

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Genetics of Nephrotic Syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Exome and genome sequencing for inborn errors of immunity

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Interventions for idiopathic steroid-resistant nephrotic syndrome in children.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nigeria's National Health Act: An assessment of health professionals' knowledge and perception

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recent advances in our understanding of recurrent primary glomerulonephritis after kidney transplantation

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterisation of the opposing effects of G6PD deficiency on cerebral malaria and severe malarial anaemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomic and clinical profiling of a national nephrotic syndrome cohort advocates a precision medicine approach to disease management.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rare coding variants associated with blood pressure variation in 15 914 individuals of African ancestry

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Focal Segmental Glomerulosclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genome-wide analysis identifies an african-specific variant in SEMA4D associated with body mass index.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetics of hereditary nephrotic syndrome: a clinical review

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Novel Biomarker Panel to Identify Steroid Resistance in Childhood Idiopathic Nephrotic Syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Palaeoanthropology: On the origin of our species

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The role of novel biomarkers in childhood idiopathic nephrotic syndrome: a narrative review of published evidence.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loss-of-Function GRHL3 Variants Detected in African Patients with Isolated Cleft Palate.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nephrotic syndrome in infants and children: pathophysiology and management

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Childhood nephrotic syndrome in tropical Africa: then and now.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic testing in steroid-resistant nephrotic syndrome: why, who, when and how?

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Steroid-resistant nephrotic syndrome: past and current perspectives.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel GREM1 Variations in Sub-Saharan African Patients With Cleft Lip and/or Cleft Palate.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical and pathological phenotype of genetic causes of focal segmental glomerulosclerosis in adults.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

National survey found that managing childhood nephrotic syndrome in Nigeria varied widely and did not comply with the best evidence

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Medical genetics and genomic medicine in Nigeria.

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recurrence of nephrotic syndrome following kidney transplantation is associated with initial native kidney biopsy findings

1 reference

https://pubmed.ncbi.nlm.nih.gov/31190951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.2147/IJNRD.S193874

1 reference

Europe PubMed Central

1 July 2019

http://europepmc.org/abstract/PMC/6512787

1 reference

Europe PubMed Central

1 July 2019

http://europepmc.org/abstract/PMC/6512787

1 reference

Europe PubMed Central

1 July 2019

http://europepmc.org/abstract/PMC/6512787

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