Childhood thin GBM disease: review of 22 children with family studies and long-term follow-up (Q36154359)

12 August 2017

Childhood thin GBM disease: review of 22 children with family studies and long-term follow-up (English)

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12 August 2017

3

Lesley Rees

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12 August 2017

Carla Carasi

1

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12 August 2017

William G Van't Hoff

2

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12 August 2017

R Anthony Risdon

4

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12 August 2017

Richard S Trompeter

5

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12 August 2017

Michael J Dillon

6

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12 August 2017

7 June 2005

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12 August 2017

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12 August 2017

20

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12 August 2017

8

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12 August 2017

1098-1105

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https://scigraph.springernature.com/pub.10.1007/s00467-005-1879-8

12 August 2017

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cites work

Thin-basement-membrane nephropathy in adults with persistent hematuria

1 reference

12 December 2020

Benign primary hematuria. Clinicopathologic study of 65 patients

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12 December 2020

Thin basement membranes in minimally abnormal glomeruli

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12 December 2020

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

1 reference

12 December 2020

Abnormally thin glomerular basement membranes associated with hematuria, proteinuria or renal failure in adults

1 reference

12 December 2020

1 reference

12 December 2020

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

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12 December 2020

Thin basement membrane syndrome in adults

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12 December 2020

Alport's syndrome: experience at Hôpital Necker

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12 December 2020

BENIGN RECURRENT HEMATURIA

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12 December 2020

Renal biopsy diagnosis in children presenting with haematuria

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12 December 2020

Benign familial hematuria due to mutation of the type IV collagen alpha4 gene

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12 December 2020

Isolated hematuria in children: indications for a renal biopsy

1 reference

12 December 2020

Benign familial hematuria associated with a novel COL4A4 mutation

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12 December 2020

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

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12 December 2020

Glomerular basement membrane attenuation in familial nephritis and "benign" hematuria

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12 December 2020

Thin GBM nephropathy: premature glomerular obsolescence is associated with hypertension and late onset renal failure

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12 December 2020

Mutations in theCOL4A4 and COL4A3 genes cause familial benign hematuria

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12 December 2020

Symptomless haematuria in childhood

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12 December 2020

Recurrent haematuria in childhood

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12 December 2020

Glomerular basement membrane thinning in adults: Clinicopathological correlations of a new diagnostic approach

1 reference

12 December 2020

Mutations in the COL4A4 gene in thin basement membrane disease

1 reference

12 December 2020

Idiopathic persistent microscopic hematuria in children. Prognostic features

1 reference

12 December 2020

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

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12 December 2020

Autosomal dominant Alport syndrome caused by a COL4A3 splice site mutation

1 reference

12 December 2020

Aberrant splicing of the COL4A5 gene in patients with Alport syndrome

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12 December 2020

Genetic, clinical, and morphologic heterogeneity in Alport's syndrome

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12 December 2020

Familial benign essential hematuria

1 reference

12 December 2020

Mutations in the type IV collagen alpha 3 (COL4A3) gene in autosomal recessive Alport syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Thin membrane nephropathy: a clinico-pathological study

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12 December 2020

Red cell traverse through thin glomerular basement membranes

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12 December 2020

Glomerular basement membrane. Identification of a novel disulfide-cross-linked network of alpha3, alpha4, and alpha5 chains of type IV collagen and its implications for the pathogenesis of Alport syndrome

1 reference

12 December 2020

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

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12 December 2020

Alport syndrome--is there a genotype-phenotype relationship?

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12 December 2020

Familial hematuria; clinico-pathological correlations

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12 December 2020

Renal biopsy and family studies in 65 children with isolated hematuria

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12 December 2020

Alport syndrome and thin glomerular basement membrane disease

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12 December 2020

Recurrent haematuria in 17 children.

1 reference

12 December 2020

COL4A3 mutations and their clinical consequences in thin basement membrane nephropathy (TBMN).

1 reference

12 December 2020

Split and extremely thin glomerular basement membranes in hereditary nephropathy (Alport's syndrome).

1 reference

12 December 2020

Pediatric hematuria and thin basement membrane nephropathy: what is it and what does it mean?

1 reference

12 December 2020

Identification of mutations in the alpha 3(IV) and alpha 4(IV) collagen genes in autosomal recessive Alport syndrome

1 reference

12 December 2020

10.1007/S00467-005-1879-8

Identifiers

DOI

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12 August 2017

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