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Literature DB >> 3054112

Alport's syndrome.

M A Crawfurd¹.

Abstract

Entities: Disease

Mesh：

Year: 1988 PMID： 3054112 PMCID： PMC1051541 DOI： 10.1136/jmg.25.9.623

Source DB: PubMed Journal: J Med Genet ISSN： 0022-2593 Impact factor: 6.318

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53 in total

1. Hereditary chronic kidney disease: an alternative to partial sex-linkage in the Utah kindred.

Authors: J B GRAHAM
Journal: Am J Hum Genet Date: 1959-12 Impact factor: 11.025

2. Partially sex-linked cominant inheritance of interstitial pyelonephritis.

Authors: F E STEPHENS; G T PERKOFF; D A DOLOWITZ; F H TYLER
Journal: Am J Hum Genet Date: 1951-12 Impact factor: 11.025

3. Alport familial nephritis. Absence of 28 kilodalton non-collagenous monomers of type IV collagen in glomerular basement membrane.

Authors: M M Kleppel; C E Kashtan; R J Butkowski; A J Fish; A F Michael
Journal: J Clin Invest Date: 1987-07 Impact factor: 14.808

4. Striped nails and kidney transplantation.

Authors: I M Braverman
Journal: Ann Intern Med Date: 1978-08 Impact factor: 25.391

5. Pathologic characteristics of hereditary nephritis.

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

6. Goodpasture antigen of the glomerular basement membrane: localization to noncollagenous regions of type IV collagen.

Authors: J Wieslander; J F Barr; R J Butkowski; S J Edwards; P Bygren; D Heinegård; B G Hudson
Journal: Proc Natl Acad Sci U S A Date: 1984-06 Impact factor: 11.205

7. Alport's syndrome: experience at Hôpital Necker.

Authors: R Habib; M C Gubler; N Hinglais; L H Noël; D Droz; M Levy; P Mahieu; J M Foidart; D Perrin; E Bois; J P Grünfeld
Journal: Kidney Int Suppl Date: 1982-05 Impact factor: 10.545

8. 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

Alport's syndrome.

1. Hereditary chronic kidney disease: an alternative to partial sex-linkage in the Utah kindred.

2. Partially sex-linked cominant inheritance of interstitial pyelonephritis.

3. Alport familial nephritis. Absence of 28 kilodalton non-collagenous monomers of type IV collagen in glomerular basement membrane.

4. Striped nails and kidney transplantation.

5. Pathologic characteristics of hereditary nephritis.

6. Goodpasture antigen of the glomerular basement membrane: localization to noncollagenous regions of type IV collagen.

7. Alport's syndrome: experience at Hôpital Necker.

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

9. Hereditary nephritis: a re-examination of its clinical and genetic features.

10. Use of a monoclonal antibody in differential diagnosis of children with haematuria and hereditary nephritis.

Review 1. Thrombocytopenias: a clinical point of view.

2. Exclusion of epidermal growth factor and high-resolution physical mapping across the Rieger syndrome locus.