Identification of a novel mutation in ARSA gene in three patients of an Iranian family with metachromatic leukodystrophy disorder

por Golchin, Neda, Hajjari, Mohammadreza, Malamiri, Reza Azizi, Aminzadeh, Majid, Mohammadi-asl, Javad
Publicado 2017

Coexistence of p190 BCR/ABL Transcript and CALR 52-bp Deletion in Chronic Myeloid Leukemia Blast Crisis: A Case Report

por Seghatoleslami, Mohammad, Ketabchi, Neda, Ordo, Alireza, Asl, Javad Mohammadi, Golchin, Neda, Saki, Najmaldin
Publicado 2016

Whole exome sequencing revealed a novel dystrophin-related protein-2 (DRP2) deletion in an Iranian family with symptoms of polyneuropathy

por Tahmasebi-Birgani, Maryam, Hajjari, Mohammadreza, Golchin, Neda, Shalbafan, Bita, Mohammadi-Asl, Javad, Sadeghian, Forouzan
Publicado 2019

Lipid Profile Improvement after Four Group Psychological Interventions in Combination to Nutritional and Physical Activity Instructing Among Overweight and Obese Individuals

por AGAH HERIS, Mojgan, ALIPOUR, Ahmad, JANBOZORGI, Masoud, HAJIHOSSEINI, Reza, SHAGHAGHI, Farhad, GOLCHIN, Neda, NOUHI, Shahnaz
Publicado 2013

Identification of A Novel Compound Heterozygous Mutation in BBS12 in An Iranian Family with Bardet-Biedl Syndrome Using Targeted Next Generation Sequencing

por Nikkhah, Emad, Safaralizadeh, Reza, Mohammadiasl, Javad, Tahmasebi Birgani, Maryam, Hosseinpour Feizi, Mohammad Ali, Golchin, Neda
Publicado 2018

Rare Cytogenetic Abnormalities and Alteration of microRNAs in Acute Myeloid Leukemia and Response to Therapy

por Shahjahani, Mohammad, Khodadi, Elahe, Seghatoleslami, Mohammad, Asl, Javad Mohammadi, Golchin, Neda, Zaieri, Zeynab Deris, Saki, Najmaldin
Publicado 2015