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Hussain S, Akhtar N, Qamar R, Khan N, Naeem M. Molecular study of nephronophthisis in 7 unrelated Pakistani families. Iranian Journal of Kidney Diseases 12 (2018) 240-242.
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Murtaza G, Siddiq S, Khan S, Hussain S, Naeem M. Molecular study of X-linked ichthyosis: Report of a novel 2-bp insertion mutation in the STS and a very rare case of homozygous female patient. Journal of Dermatological Science 74 (2014) 159-182.
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Parrock S, Hussain S, Issler N, Differ AM, Lench N, Guarino S, Oosterveld MJ, Keijzer-Veen M, Brilstra E, van Wieringen H, Konijnenberg AY, Amin-Rasip S, Dumitriu S, Klootwijk E, Knoers N, Bockenhauer D, Kleta R, Zdebik AA. Mutations display differential sensitivity to heteromerisation with KCNJ16. Nephron Physiology 123 (2013) 7-14.
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Mustafa M, Hussain S, Qureshi S, Malik SA, Kazmi AR, Naeem M. Study of the effect of antiviral therapy on homocysteinemia in hepatitis C virus- infected patients. BMC Gastroenterology 12 (2012) 117
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Naeem M, Hussain S, Akhtar N. Mutation in the tight-junction gene Claudin19 (CLDN19) and familial hypomagnesaemia, hypercalciuria, nephrocalcinosis (FHHNC) and severe ocular disease. American Journal of Nephrology 34 (2011) 241-248.
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