Familial hematuria (Q36958957)

17 August 2017

2 references

3 July 2020

Familial hematuria (English)

1 reference

17 August 2017

1 reference

3 July 2020

Clifford E Kashtan

1

1 reference

17 August 2017

2 October 2007

1 reference

PMCID

2731159

17 August 2017

1 October 2009

1 reference

3 July 2020

2 references

17 August 2017

3 July 2020

24

1 reference

17 August 2017

1951-1958

1 reference

17 August 2017

10

1 reference

Creative Commons Attribution

17 August 2017

1 reference

3 July 2020

0 references

https://scigraph.springernature.com/pub.10.1007/s00467-007-0622-z

0 references

cites work

Choosing a mouse model to study the molecular pathobiology of Alport glomerulonephritis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731159

Renal transplantation in patients with Alport syndrome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731159

Distribution of type IV collagen in the cochlea in Alport syndrome.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731159

Retransplantation in Alport post-transplant anti-GBM disease.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731159

Epidermal basement membrane alpha 5(IV) expression in females with Alport syndrome and severity of renal disease

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731159

X-linked Alport syndrome: natural history and genotype-phenotype correlations in girls and women belonging to 195 families: a "European Community Alport Syndrome Concerted Action" study

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731159

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731159

Determination of the genomic structure of the COL4A4 gene and of novel mutations causing autosomal recessive Alport syndrome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731159

Targets of alloantibodies in Alport anti-glomerular basement membrane disease after renal transplantation.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731159

Treatment of X-linked hereditary nephritis in Samoyed dogs with angiotensin converting enzyme (ACE) inhibitor

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731159

Mutations in Alport syndrome associated with diffuse esophageal leiomyomatosis.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731159

Deletion of the paired alpha 5(IV) and alpha 6(IV) collagen genes in inherited smooth muscle tumors

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731159

Hereditary nephropathy (Alport syndrome): correlation of clinical data with glomerular basement membrane alterations.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731159

Ophthalmologic assessment of young patients with Alport syndrome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731159

The effect of aldosterone blockade in patients with Alport syndrome.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731159

Cyclosporin therapy in patients with Alport syndrome.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731159

Preemptive ramipril therapy delays renal failure and reduces renal fibrosis in COL4A3-knockout mice with Alport syndrome

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731159

Structure of the human type IV collagen gene COL4A3 and mutations in autosomal Alport syndrome.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731159

X-linked Alport syndrome: natural history in 195 families and genotype- phenotype correlations in males.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731159

High mutation detection rate in the COL4A5 collagen gene in suspected Alport syndrome using PCR and direct DNA sequencing.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731159

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2731159

Alport syndrome and the X chromosome: implications of a diagnosis of Alport syndrome in females

20 October 2018

1 reference

12 December 2020

Isolated hematuria in children: indications for a renal biopsy

1 reference

12 December 2020

Thin basement membrane nephropathy as a cause of recurrent haematuria in childhood

1 reference

12 December 2020

Renal biopsy and family studies in 65 children with isolated hematuria

1 reference

12 December 2020

Distribution of the alpha 1 and alpha 2 chains of collagen IV and of collagens V and VI in Alport syndrome

1 reference

12 December 2020

Immunohistologic studies of type IV collagen in anterior lens capsules of patients with Alport syndrome

1 reference

12 December 2020

Immunohistochemical study of alpha 1-5 chains of type IV collagen in hereditary nephritis

1 reference

12 December 2020

Autosomal recessive Alport syndrome: Immunohistochemical study of type IV collagen chain distribution

1 reference

12 December 2020

Renal allograft survival according to primary diagnosis: a report of the North American Pediatric Renal Transplant Cooperative Study

1 reference

12 December 2020

Recurrent corneal erosion associated with Alport's syndrome. Rapid communication

1 reference

12 December 2020

Ocular manifestations of autosomal recessive Alport syndrome

1 reference

12 December 2020

X-linked Alport syndrome in females

1 reference

12 December 2020

Renal biopsy diagnosis in children presenting with haematuria

1 reference

12 December 2020

Long-term effects of cyclosporine A in Alport's syndrome

1 reference

12 December 2020

Identification of COL4A5 defects in Alport's syndrome by immunohistochemistry of skin

1 reference

12 December 2020

Familial hematurias: what we know and what we don't

1 reference

12 December 2020

Nephroprotection by antifibrotic and anti-inflammatory effects of the vasopeptidase inhibitor AVE7688

1 reference

12 December 2020

10.1007/S00467-007-0622-Z

Identifiers

DOI

1 reference

17 August 2017

1 reference

17 August 2017

1 reference

PMCID

2731159