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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jun 8, 2023. (Total: 217765Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Edema and NPHS2[original query]
NPHS2 gene, nephrotic syndrome and focal segmental glomerulosclerosis: a HuGE review.
Genetics in medicine : official journal of the American College of Medical Genetics 2006 Feb 8 (2): 63-75.
Franceschini Nora, North Kari E, Kopp Jeffrey B, McKenzie Louise, Winkler Cher
NPHS2 p.V290M mutation in late-onset steroid-resistant nephrotic syndrome.
Pediatric nephrology (Berlin, Germany) 2013 May 28 (5): 751-7.
Kerti Andrea, Csohány Rózsa, Szabó Attila, Arkossy Ottó, Sallay Péter, Moriniére Vincent, Vega-Warner Virginia, Nyír? Gábor, Lakatos Orsolya, Szabó Tamás, Lipska Beata S, Schaefer Franz, Antignac Corinne, Reusz George, Tulassay Tivadar, Tory Kálm
Gene mutation analysis in 12 Chinese children with congenital nephrotic syndrome.
BMC nephrology 2018 12 19 (1): 382.
Li Guo-Min, Cao Qi, Shen Qian, Sun Li, Zhai Yi-Hui, Liu Hai-Mei, An Yu, Xu Ho
Analysis of the association of NPHS2 and ACTN4 genes polymorphism with nephrotic syndrome in Egyptian children.
Molecular biology reports 2023 4 .
Al-Azzawy Mohammed F, Al-Haggar Mohammad, ElSaid Afaf M, El-Khawaga Omali
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