Literature DB >> 35352193

Gross hematuria, edema, and hypocomplementemia in a 9-year-old boy: Answers.

Juanjuan Ding1, Panli Liao1, Gaohong Zhu1, Chang Qi1, Lili Liu2, Peiwei Zhao3, Xiaowen Wang4.   

Abstract

Entities:  

Keywords:  Alport syndrome; C3 glomerulonephritis; COL4A5 mutation; Child; Hematuria; Hypocomplementemia; Proteinuria

Mesh：

Substances：

Year:  2022        PMID： 35352193     DOI： 10.1007/s00467-022-05539-9

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN： 0931-041X            Impact factor:   3.651


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  23 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.  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

3.  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

4.  Genetic heterogeneity of Alport syndrome.

Authors:  J Feingold; E Bois; A Chompret; M Broyer; M C Gubler; J P Grünfeld
Journal:  Kidney Int       Date:  1985-04       Impact factor: 10.612

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

Authors:  H J Rumpelt; K H Langer; K Schärer; E Straub; W Thoenes
Journal:  Virchows Arch A Pathol Anat Histol       Date:  1974

6.  X-linked Alport syndrome: natural history in 195 families and genotype- phenotype correlations in males.

Authors:  Jean Philippe Jais; Bertrand Knebelmann; Iannis Giatras; Mario DE Marchi; Gianfranco Rizzoni; Alessandra Renieri; Manfred Weber; Oliver Gross; Kai-Olaf Netzer; Frances Flinter; Yves Pirson; Christine Verellen; Jörgen Wieslander; Ulf Persson; Karl Tryggvason; Paula Martin; Jens Michael Hertz; Cornelis Schröder; Marek Sanak; Sarka Krejcova; Maria Fernanda Carvalho; Juan Saus; Corinne Antignac; Hubert Smeets; Marie Claire Gubler
Journal:  J Am Soc Nephrol       Date:  2000-04       Impact factor: 10.121

Review 7.  Collagen IV diseases: A focus on the glomerular basement membrane in Alport syndrome.

Authors:  Dominic Cosgrove; Shiguang Liu
Journal:  Matrix Biol       Date:  2016-08-27       Impact factor: 11.583

8.  Next generation sequencing as a useful tool in the diagnostics of mosaicism in Alport syndrome.

Authors:  Sonja Beicht; Gertrud Strobl-Wildemann; Sabine Rath; Oliver Wachter; Martin Alberer; Elke Kaminsky; Lutz T Weber; Tanja Hinrichsen; Hanns-Georg Klein; Julia Hoefele
Journal:  Gene       Date:  2013-05-31       Impact factor: 3.688

Review 9.  A review of clinical characteristics and genetic backgrounds in Alport syndrome.

Authors:  Kandai Nozu; Koichi Nakanishi; Yoshifusa Abe; Tomohiro Udagawa; Shinichi Okada; Takayuki Okamoto; Hiroshi Kaito; Katsuyoshi Kanemoto; Anna Kobayashi; Eriko Tanaka; Kazuki Tanaka; Taketsugu Hama; Rika Fujimaru; Saori Miwa; Tomohiko Yamamura; Natsusmi Yamamura; Tomoko Horinouchi; Shogo Minamikawa; Michio Nagata; Kazumoto Iijima
Journal:  Clin Exp Nephrol       Date:  2018-08-20       Impact factor: 2.801

10.  Co-existence of Alport syndrome and C3 glomerulonephritis in a proband with family history.

Authors:  Yin Ding; Xuanli Tang; Yuanyuan Du; Hongyu Chen; Dongrong Yu; Bin Zhu; Bohan Yuan
Journal:  Eur J Med Res       Date:  2021-07-08       Impact factor: 2.175
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