Literature DB >> 8918631

Evolution of glomerular basement membrane lesions in a male patient with Alport syndrome: ultrastructural and morphometric study.

A M Cangiotti1, A Sessa, M Meroni, R Montironi, M Ragaiolo, V Mambelli, S Cinti.   

Abstract

Entities:  

Mesh：

Year:  1996        PMID： 8918631

Source DB:  PubMed          Journal:  Nephrol Dial Transplant        ISSN： 0931-0509            Impact factor:   5.992


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  6 in total

1.  Novel heterozygous COL4A3 mutation in a family with late-onset ESRD.

Authors:  Julia Hoefele; Bärbel Lange-Sperandio; Despina Ruessmann; Judith Glöckner-Pagel; Martin Alberer; Marcus R Benz; Mato Nagel; Lutz T Weber
Journal:  Pediatr Nephrol       Date:  2010-02-23       Impact factor: 3.714

2.  Outcomes of male patients with Alport syndrome undergoing renal replacement therapy.

Authors:  Johanna Temme; Anneke Kramer; Kitty J Jager; Katharina Lange; Frederick Peters; Gerhard-Anton Müller; Reinhard Kramar; James G Heaf; Patrik Finne; Runolfur Palsson; Anna V Reisæter; Andries J Hoitsma; Wendy Metcalfe; Maurizio Postorino; Oscar Zurriaga; Julio P Santos; Pietro Ravani; Faical Jarraya; Enrico Verrina; Friedo W Dekker; Oliver Gross
Journal:  Clin J Am Soc Nephrol       Date:  2012-09-20       Impact factor: 8.237

3.  The Alport nephropathy: clinicopathological correlations.

Authors:  Richard H R White; Faro Raafat; David V Milford; Filadelfia Komianou; Nadeem E Moghal
Journal:  Pediatr Nephrol       Date:  2005-04-26       Impact factor: 3.714

4.  Identification of 47 novel mutations in patients with Alport syndrome and thin basement membrane nephropathy.

Authors:  Stefanie Weber; Katja Strasser; Sabine Rath; Achim Kittke; Sonja Beicht; Martin Alberer; Bärbel Lange-Sperandio; Peter F Hoyer; Marcus R Benz; Sabine Ponsel; Lutz T Weber; Hanns-Georg Klein; Julia Hoefele
Journal:  Pediatr Nephrol       Date:  2016-01-25       Impact factor: 3.714

Review 5.  The role of molecular genetics in diagnosing familial hematuria(s).

Authors:  Constantinos Deltas; Alkis Pierides; Konstantinos Voskarides
Journal:  Pediatr Nephrol       Date:  2011-06-19       Impact factor: 3.714

6.  The multifaceted phenotypic and genotypic spectrum of type-IV-collagen-related nephropathy-A human genetics department experience.

Authors:  Jasmina Ćomić; Korbinian M Riedhammer; Roman Günthner; Christian W Schaaf; Patrick Richthammer; Hannes Simmendinger; Donald Kieffer; Riccardo Berutti; Velibor Tasic; Nora Abazi-Emini; Valbona Nushi-Stavileci; Jovana Putnik; Nataša Stajic; Adrian Lungu; Oliver Gross; Lutz Renders; Uwe Heemann; Matthias C Braunisch; Thomas Meitinger; Julia Hoefele
Journal:  Front Med (Lausanne)       Date:  2022-08-31
  6 in total

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