Literature DB >> 20773074

HEREDITARY FAMILIAL CONGENITAL HAEMORRHAGIC NEPHRITIS.

A C Alport.   

Abstract

Entities:  

Year:  1927        PMID： 20773074      PMCID： PMC2454341          DOI： 10.1136/bmj.1.3454.504

Source DB:  PubMed          Journal:  Br Med J        ISSN： 0007-1447


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  92 in total

1.  A locus for posterior polymorphous corneal dystrophy (PPCD3) maps to chromosome 10.

Authors:  Satoko Shimizu; Charles Krafchak; Nobuo Fuse; Michael P Epstein; Miriam T Schteingart; Alan Sugar; Maya Eibschitz-Tsimhoni; Catherine A Downs; Frank Rozsa; Edward H Trager; David M Reed; Michael Boehnke; Sayoko E Moroi; Julia E Richards
Journal:  Am J Med Genet A       Date:  2004-11-01       Impact factor: 2.802

Review 2.  Alport syndrome, basement membranes and collagen.

Authors:  C E Kashtan; M M Kleppel; R J Butkowski; A F Michael; A J Fish
Journal:  Pediatr Nephrol       Date:  1990-09       Impact factor: 3.714

3.  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

Review 4.  Glomerular diseases: genetic causes and future therapeutics.

Authors:  Chih-Kang Chiang; Reiko Inagi
Journal:  Nat Rev Nephrol       Date:  2010-07-20       Impact factor: 28.314

5.  Hereditary nephritis and the heart.

Authors:  L Gofman; J Tarján
Journal:  Int Urol Nephrol       Date:  1977       Impact factor: 2.370

6.  Ocular manifestations of Alport syndrome.

Authors:  Jian-Min Xu; Shi-Sheng Zhang; Qiong Zhang; Ying-Ming Zhou; Cai-Hong Zhu; Jian Ge; Ling Wang
Journal:  Int J Ophthalmol       Date:  2010-06-18       Impact factor: 1.779

7.  Inner ear defect similar to Alport's syndrome in the glomerulosclerosis mouse model Mpv17.

Authors:  A M Meyer zum Gottesberge; A Reuter; H Weiher
Journal:  Eur Arch Otorhinolaryngol       Date:  1996       Impact factor: 2.503

8.  Otologic symptoms in chronic renal failure. The possible role of aminoglycoside-furosemide interaction.

Authors:  J Thomsen; P Bech; W Szpirt
Journal:  Arch Otorhinolaryngol       Date:  1976-08-31

9.  Alport syndrome: a rare cause of uraemia.

Authors:  Soumik Ghosh; Manavdeep Singh; Ratnakar Sahoo; Sachin Rao
Journal:  BMJ Case Rep       Date:  2014-02-13

10.  Array-CGH in unclear syndromic nephropathies identifies a microdeletion in Xq22.3-q23.

Authors:  Alexander Hoischen; Christina Landwehr; Sarah Kabisch; Xiao-Qi Ding; Detlef Trost; Gerhard Stropahl; Marianne Wigger; Bernhard Radlwimmer; Ruthild G Weber; Dieter Haffner
Journal:  Pediatr Nephrol       Date:  2009-05-15       Impact factor: 3.714
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