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Literature DB >> 7211891

Alport's syndrome. A report of 58 cases and a review of the literature.

M Gubler, M Levy, M Broyer, C Naizot, G Gonzales, D Perrin, R Habib.

Abstract

Entities: Disease

Mesh：

Year: 1981 PMID： 7211891 DOI： 10.1016/0002-9343(81)90571-4

Source DB: PubMed Journal: Am J Med ISSN： 0002-9343 Impact factor: 4.965

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68 in total

1. Genotype-phenotype correlation in X-linked Alport syndrome.

Authors: Mir Reza Bekheirnia; Berenice Reed; Martin C Gregory; Kim McFann; Alireza Abdollah Shamshirsaz; Amirali Masoumi; Robert W Schrier
Journal: J Am Soc Nephrol Date: 2010-04-08 Impact factor: 10.121

2. Effect of cyclosporin A on proteinuria in patients with Alport's syndrome.

Authors: L Callís; A Vila; J Nieto; G Fortuny
Journal: Pediatr Nephrol Date: 1992-03 Impact factor: 3.714

3. 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

Review 4. Alport's syndrome.

Authors: F Flinter
Journal: J Med Genet Date: 1997-04 Impact factor: 6.318

5. Alport syndrome: deducing the mode of inheritance from the presence of haematuria in family members.

Authors: Judy Savige
Journal: Pediatr Nephrol Date: 2018-11-30 Impact factor: 3.714

6. Familial spastic paraplegia, bilateral sensorineural deafness, and intellectual retardation associated with a progressive nephropathy.

Authors: J S Fitzsimmons; A R Watson; D Mellor; P R Guilbert
Journal: J Med Genet Date: 1988-03 Impact factor: 6.318

Alport's syndrome. A report of 58 cases and a review of the literature.

1. Genotype-phenotype correlation in X-linked Alport syndrome.

2. Effect of cyclosporin A on proteinuria in patients with Alport's syndrome.

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

Review 4. Alport's syndrome.

5. Alport syndrome: deducing the mode of inheritance from the presence of haematuria in family members.

6. Familial spastic paraplegia, bilateral sensorineural deafness, and intellectual retardation associated with a progressive nephropathy.

7. Samoyed hereditary glomerulopathy (SHG). Evolution of splitting of glomerular capillary basement membranes.

8. Alport retinopathy results from "severe" COL4A5 mutations and predicts early renal failure.

9. The use of ocular abnormalities to diagnose X-linked Alport syndrome in children.

10. Ocular manifestations of Alport's syndrome: a hereditary disorder of basement membranes?