Genetic investigation of Leukodystrophy in Iran

由 HOUSHMAND, Massoud
出版 2014

Mitochondrial Genetics, Disease and Inheritance

由 HOUSHMAND, Massoud
出版 2013

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

由 Hajizadeh, Ali;, Houshmand, Massoud;, Hosseini, Mojgan;
出版 2017

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

由 ASHRAFI, Mahmoud Reza, NIKKHAH, Ali, HOUSHMAND, Massoud, ARYANI, Omid
出版 2011

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

由 HEIDARI, Mohammad Medhi, KHATAMI, Mehri, HOUSHMAND, Massoud, MAHMOUDI, Eisa, NAFISSI, Shahriar
出版 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

由 Parvizi Omran, Sima, Houshmand, Massoud, Donkor, Dominic, Farjami, Zahra, Karimzadeh, Parvaneh
出版 2019

Molecular Investigation of Glutaric Aciduria Type1 in Iran

由 HOUSHMAND, Massoud, ARYANI, Omid, PIRZADEH, Zahra, GHASEMI, Fereshteh, SALEHPOUR, Shadab, TEHRANI, Freshteh
出版 2012

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

由 MOHAMMADI PARGOO, Esmaeel, ARYANI, Omid, TONEKABONI, Seyyed Hassan, KAMALIDEHGHAN, Behnam, HOUSHMAND, Massoud
出版 2012

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

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

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

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

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

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

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

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

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

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

Lysosomal Storage Disease in Iran (Report of Molecular Study)

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