Genetic investigation of Leukodystrophy in Iran

por HOUSHMAND, Massoud
Publicado 2014

Mitochondrial Genetics, Disease and Inheritance

por HOUSHMAND, Massoud
Publicado 2013

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

por Hajizadeh, Ali;, Houshmand, Massoud;, Hosseini, Mojgan;
Publicado 2017

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

por ASHRAFI, Mahmoud Reza, NIKKHAH, Ali, HOUSHMAND, Massoud, ARYANI, Omid
Publicado 2011

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

por HEIDARI, Mohammad Medhi, KHATAMI, Mehri, HOUSHMAND, Massoud, MAHMOUDI, Eisa, NAFISSI, Shahriar
Publicado 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

por Parvizi Omran, Sima, Houshmand, Massoud, Donkor, Dominic, Farjami, Zahra, Karimzadeh, Parvaneh
Publicado 2019

Molecular Investigation of Glutaric Aciduria Type1 in Iran

por HOUSHMAND, Massoud, ARYANI, Omid, PIRZADEH, Zahra, GHASEMI, Fereshteh, SALEHPOUR, Shadab, TEHRANI, Freshteh
Publicado 2012

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

por MOHAMMADI PARGOO, Esmaeel, ARYANI, Omid, TONEKABONI, Seyyed Hassan, KAMALIDEHGHAN, Behnam, HOUSHMAND, Massoud
Publicado 2012

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

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

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

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

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

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

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

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

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

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

Lysosomal Storage Disease in Iran (Report of Molecular Study)

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