Items where Author is "HOUSHMAND, Massoud"

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Medhi HEIDARI, Mohammad and KHATAMI, Mehri and HOUSHMAND, Massoud and MAHMOUDI, Eisa and NAFISSI, Shahriar (2011) Increased Prevalence 12308 A > G mutation in Mitochondrial tRNALeu (CUN) Gene Associated with earlier Age of Onset in Friedreich Ataxia. Iranian Journal of Child Neurology, 5 (4). pp. 25-31.

Reza ASHRAFI, Mahmoud and NIKKHAH, Ali and HOUSHMAND, Massoud and ARYANI, Omid (2011) L-2-Hydroxyglutaric Aciduria is a Diagnostic Indicator of Leukodystrophy: A Case Report. Iranian Journal of Child Neurology, 5 (4). pp. 37-38.

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