Family Social Status and Dietary Adherence of Patients with Phenylketonuria

Por Alaei, Mohammadreza, Asadzadeh-Totonchi, Gelareh, Gachkar, Latif, Farivar, Shirin
Publicado em 2011

Are There Neurological Symptoms in Type 1 of Gaucher Disease?

Por ALAEI, Mohammadreza, JAFARI, Narjes, ROHANI, Farzaneh, AHMADABADI, Farzad, AZADI, Rezvan
Publicado no Iran J Child Neurol (2018)

Four Years of Diagnostic Challenges with Tetrahydrobiopterin Deficiencies in Iranian Patients

Por Khatami, Shohreh, Dehnabeh, Soghra Rouhi, Zeinali, Sirous, Thöny, Beat, Alaei, Mohammadreza, Salehpour, Shadab, Setoodeh, Aria, Rohani, Farzaneh, Hajivalizadeh, Fatemeh, Samavat, Ashraf
Publicado no JIMD Rep (2016)

Genome-Wide Homozygosity Analysis Reveals HADH Mutations as a Common Cause of Diazoxide-Responsive Hyperinsulinemic-Hypoglycemia in Consanguineous Pedigrees

Por Flanagan, Sarah E., Patch, Ann-Marie, Locke, Jonathan M., Akcay, Teoman, Simsek, Enver, Alaei, Mohammadreza, Yekta, Zeinab, Desai, Meena, Kapoor, Ritika R., Hussain, Khalid, Ellard, Sian
Publicado em 2011