L-2-Hydroxyglutaric Aciduria is a Diagnostic Indicator of Leukodystrophy: A Case Report

by ASHRAFI, Mahmoud Reza, NIKKHAH, Ali, HOUSHMAND, Massoud, ARYANI, Omid
Published 2011

A Novel Mutation in Aspartoacylase Gene; Canavan Disease

by ASHRAFI, Mahmoodreza, TAVASOLI, Alireza, KATIBEH, Pegah, ARYANI, Omid, VAFAEE-SHAHI, Mohammad
Published 2015

Molecular Investigation of Glutaric Aciduria Type1 in Iran

by HOUSHMAND, Massoud, ARYANI, Omid, PIRZADEH, Zahra, GHASEMI, Fereshteh, SALEHPOUR, Shadab, TEHRANI, Freshteh
Published 2012

A Novel Mutation of GDAP1 Associated with Charcot-Marie-Tooth Disease in An Iranian Family

by MOHAMMADI PARGOO, Esmaeel, ARYANI, Omid, TONEKABONI, Seyyed Hassan, KAMALIDEHGHAN, Behnam, HOUSHMAND, Massoud
Published 2012

Measuring Serum Level of Ionized Magnesium in Patients with Migraine

by ASSARZADEGAN, Farhad, ASADOLLAHI, Mostafa, DERAKHSHANFAR, Hojjat, KASHEFIZADEH, Azam, ARYANI, Omid, KHORSHIDI, Mona
Published 2015

Clinical feature and Genetics in Rett syndrome; A report on Iranian patients

by Karimzadeh, Parvaneh, Kheirollahi, Majid, Houshmand, Seyed Massoud, Dadgar, Sepideh, Aryani, Omid, Yaghini, Omid
Published 2019

Glutaric aciduria type 1: clinical, biochemical, neuroimaging and molecular findings in Iranian patients

by Pirzadeh, Zahra, Tonekaboni, Seyed Hassan, Houshmand, Massoud, Nasiri, Jafar, Mollamohammadi, Mohsen, Sedighi, Mostafa, Aryani, Omid
Published 2017

A Report of Two Cases of TGM1 Mutations in Iranian Patients with Lamelar Ichthyosis

by FARAJI, Abolfazl, MOBARAKI, Maryam, YAZDI, AmirReza, SEYYED HASSANI, Seyyed Mohammad, ARYANI, Omid, HOUSHMAND, Massoud
Published 2011

Effect of growth hormone on muscle strength, tone and mobility of children with Prader-Willi syndrome

by SALEHPOUR, Shadab, Rohani, Farzaneh, ARYANI, Omid, HOUSHMAND, Massoud, HASHEMINEZHAD, Farhad, REZVANI KASHANI, Morteza, MAHVELATI SHAMSABADI, Farhad, POURNASIRI, Zahra
Published 2011

Clinical and Molecular Study of NPC in Iran: Report of 5 Novel Mutations

by TONEKABONI, Seyed Hassan, ARYANI, Omid, KARIMZADEH, Parvaneh, ZAMAN, Talieh, ASHRAFI, Mahmoud Reza, SALEHPOUR, Shadab, DEHGHAN MANSHADI, Masoumeh, KHALILI E, Elham, HOUSHMAND, Masoud
Published 2015

Lysosomal Storage Disease in Iran (Report of Molecular Study)

by HOUSHMAND, Massoud, TONEKABONI, Seyed Hassan, KARIMZADEH, Parvaneh, ARYANi, Omid, ASHRAFI, Mahmoudreza, SALEHPOUR, Shadab, BADV, Shervin, SHAKIBA, Marjan, ALAEE, Mohammad Reza, FARSHIDI, Shahla
Published 2012

Genetic Analysis of MECP2 Gene in Iranian Patients with Rett Syndrome

by Nasiri, Jafar, Salehi, Mansoor, Hosseinzadeh, Majid, Zamani, Mahdi, Fattahpour, Shirin, Aryani, Omid, Fazel-Najafabadi, Esmat, Jabarzareh, Maryam, Asadi, Sara, Gholamrezapour, Tahereh, Sedghi, Maryam, Ghorbani, Fatemeh
Published 2019