Literature DB >> 15458479

Heterozygous NPHS1 or NPHS2 mutations in responsive nephrotic syndrome and the multifactorial origin of proteinuria.

Gianluca Caridi, Roberta Bertelli, Francesco Perfumo, Gian Marco Ghiggeri.   

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Year:  2004        PMID： 15458479     DOI： 10.1111/j.1523-1755.2004.938_9.x

Source DB:  PubMed          Journal:  Kidney Int        ISSN： 0085-2538            Impact factor:   10.612


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  4 in total

1.  Clinical features and outcome of childhood minimal change nephrotic syndrome: is genetics involved?

Authors:  Anne-Tiina Lahdenkari; Maija Suvanto; Eero Kajantie; Olli Koskimies; Marjo Kestilä; Hannu Jalanko
Journal:  Pediatr Nephrol       Date:  2005-06-21       Impact factor: 3.714

2.  Post-transplant recurrence of steroid resistant nephrotic syndrome in children: the Italian experience.

Authors:  William Morello; Sairaj Puvinathan; Giuseppe Puccio; Gian Marco Ghiggeri; Luca Dello Strologo; Licia Peruzzi; Luisa Murer; Michela Cioni; Isabella Guzzo; Enrico Cocchi; Elisa Benetti; Sara Testa; Luciana Ghio; Gianluca Caridi; Massimo Cardillo; Rosanna Torelli; Giovanni Montini
Journal:  J Nephrol       Date:  2019-10-15       Impact factor: 3.902

Review 3.  Molecular stratification of idiopathic nephrotic syndrome.

Authors:  Moin A Saleem
Journal:  Nat Rev Nephrol       Date:  2019-10-25       Impact factor: 28.314

Review 4.  Deriving and understanding the risk of post-transplant recurrence of nephrotic syndrome in the light of current molecular and genetic advances.

Authors:  Agnieszka Bierzynska; Moin A Saleem
Journal:  Pediatr Nephrol       Date:  2017-10-11       Impact factor: 3.714
  4 in total

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