Genetic investigation of Leukodystrophy in Iran

by HOUSHMAND, Massoud
Published 2014

Mitochondrial Genetics, Disease and Inheritance

by HOUSHMAND, Massoud
Published 2013

TNP1 NON-GENE REGION AND INFLUENCES TUMOR CHARACTERISTICS BY LOW-RISK ALLELES IN BREAST CANCER

by Hajizadeh, Ali;, Houshmand, Massoud;, Hosseini, Mojgan;
Published 2017

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

Increased Prevalence 12308 A > G mutation in Mitochondrial tRNALeu (CUN) Gene Associated with earlier Age of Onset in Friedreich Ataxia

by HEIDARI, Mohammad Medhi, KHATAMI, Mehri, HOUSHMAND, Massoud, MAHMOUDI, Eisa, NAFISSI, Shahriar
Published 2011

No Hot Spot Mutations CHRNE c.1327 delG, CHAT c.914T>C, and RAPSN c.264C>A in Iranian Patients with Congenital Myasthenic Syndrome

by Parvizi Omran, Sima, Houshmand, Massoud, Donkor, Dominic, Farjami, Zahra, Karimzadeh, Parvaneh
Published 2019

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

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

Mutations in Corneal Carbohydrate Sulfotransferase 6 Gene (Chst6) in Iranian Macular Corneal Dystrophy (MCD) Patients: A Report of 7 Patients from Iran

by ATAEI, Mitra, ZARE MEHRJERDI, Mohammad Ali, YAZDI, Amir Reza, ZAMANI, Akram, FARAJE ILANJEGH, Abolfazl, HOUSHMAND, Massoud
Published 2010

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

Sodium Channel Gene Mutations in Children with GEFS+ and Dravet Syndrome: A Cross Sectional Study

by TONEKABONI, Seyed Hassan, EBRAHIMI, Ahmad, BAKHSHANDEH BALI, MohammadKazem, HOUSHMAND, Massoud, MOGHADDASI, Mehdi, TAGHDIRI, Mohammad Mahdi, NASEHI, Mohammad Mahdi
Published 2013

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