Neveen Soliman
Professor of Pediatrics
99 El Manial St, Cairo 11451
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Letter and Reply
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Citation:
Letter and Reply, neveen soliman , Nephrol Dial Transplant, Volume 1, p.2, (2009)
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http://www.nature.com/ki/journal/vaop/ncurrent/full/ki2013508a.html
Globally novel genetic mutations in nephronophthisis-related ciliopathy
New gene linked to heritable kidney disease nephronophthisis
Professor Soliman Nature Genetics Publication featured on Cairo University website
The 17th IPNA Congress
Recent Publications
COVID-19 infection and the kidneys: Learning the lesson.
Refining genotype-phenotype correlations in 304 patients with autosomal recessive polycystic kidney disease and PKHD1 gene variants.
Multisystem inflammation and susceptibility to viral infections in human ZNFX1 deficiency.
Mutations in Are a Novel Cause of Galloway-Mowat Syndrome.
Recessive variants impair actin remodeling and cause glomerulopathy in humans and mice.
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