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Literature DB >> 4219460

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

H J Rumpelt, K H Langer, K Schärer, E Straub, W Thoenes.

Abstract

Entities: Disease

Mesh：

Year: 1974 PMID： 4219460 DOI： 10.1007/bf00433075

Source DB: PubMed Journal: Virchows Arch A Pathol Anat Histol ISSN： 0340-1227

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16 in total

1. Anatomy of the glomerulus as observed in biopsy material from young and healthy human subjects.

Authors: A BERGSTRAND; H BUCHT
Journal: Z Zellforsch Mikrosk Anat Date: 1958

2. [Alport's syndrome--light and electron microscopic investigations on the kidney in the early stage (author's transl)].

Authors: K H Langer; W Thoenes
Journal: Verh Dtsch Ges Pathol Date: 1971

3. Diffuse familial nephropathy: a clinicopathological study.

Authors: D B Kaufman; R M McIntosh; F G Smith; R L Vernier
Journal: J Pediatr Date: 1970-07 Impact factor: 4.406

4. Pathologic characteristics of hereditary nephritis.

Authors: J Churg; R L Sherman
Journal: Arch Pathol Date: 1973-06

5. Progressive and nonprogressive hereditary chronic nephritis.

Authors: J P Grünfeld; E P Bois; N Hinglais
Journal: Kidney Int Date: 1973-09 Impact factor: 10.612

6. Editorial: Alport's syndrome: a consideration of pathogenesis.

Authors: G S Spear
Journal: Clin Nephrol Date: 1973 Nov-Dec Impact factor: 0.975

7. [Electron microscopical findings in the kidneys in Alport's syndrome].

Authors: H David; P Grossmann; I Marx; R Natusch
Journal: Frankf Z Pathol Date: 1966

8. The ultastructure of the normal human glomerulus. Thickness of glomerular basement membrane.

Authors: F Jorgensen; M W Bentzon
Journal: Lab Invest Date: 1968-01 Impact factor: 5.662

9. Characteristic ultrastructural lesion of the glomerular basement membrane in progressive hereditary nephritis (Alport's syndrome).

Authors: N Hinglais; J P Grünfeld; E Bois
Journal: Lab Invest Date: 1972-11 Impact factor: 5.662

10. An electron microscope study of the glomerulus in nephrosis, glomerulonephritis, and lupus erythematosus.

Authors: M G FARQUHAR; R L VERNIER; R A GOOD
Journal: J Exp Med Date: 1957-11-01 Impact factor: 14.307

13 in total

1. Clinical and genetic features in autosomal recessive and X-linked Alport syndrome.

Authors: Yanyan Wang; Vanessa Sivakumar; Mardhiah Mohammad; Deb Colville; Helen Storey; Frances Flinter; Hayat Dagher; Judy Savige
Journal: Pediatr Nephrol Date: 2013-11-02 Impact factor: 3.714

2. Nephritogenic antigen determinants in epidermal and renal basement membranes of kindreds with Alport-type familial nephritis.

Authors: C Kashtan; A J Fish; M Kleppel; K Yoshioka; A F Michael
Journal: J Clin Invest Date: 1986-10 Impact factor: 14.808

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

1. Anatomy of the glomerulus as observed in biopsy material from young and healthy human subjects.

2. [Alport's syndrome--light and electron microscopic investigations on the kidney in the early stage (author's transl)].

3. Diffuse familial nephropathy: a clinicopathological study.

4. Pathologic characteristics of hereditary nephritis.

5. Progressive and nonprogressive hereditary chronic nephritis.

6. Editorial: Alport's syndrome: a consideration of pathogenesis.

7. [Electron microscopical findings in the kidneys in Alport's syndrome].

8. The ultastructure of the normal human glomerulus. Thickness of glomerular basement membrane.

9. Characteristic ultrastructural lesion of the glomerular basement membrane in progressive hereditary nephritis (Alport's syndrome).

10. An electron microscope study of the glomerulus in nephrosis, glomerulonephritis, and lupus erythematosus.

1. Clinical and genetic features in autosomal recessive and X-linked Alport syndrome.

2. Nephritogenic antigen determinants in epidermal and renal basement membranes of kindreds with Alport-type familial nephritis.

3. Do mutations in COL4A1 or COL4A2 cause thin basement membrane nephropathy (TBMN)?

Review 4. Alport's syndrome: specificity and pathogenesis of glomerular basement membrane alterations.

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

6. The Alport nephropathy: clinicopathological correlations.

7. Childhood thin GBM disease: review of 22 children with family studies and long-term follow-up.

8. Retinal basement membrane abnormalities and the retinopathy of Alport syndrome.

Review 9. Opinion: Ocular features aid the diagnosis of Alport syndrome.

10. Temporal macular thinning associated with X-linked Alport syndrome.