A Case Series: Congenital Hyperinsulinism

por Alaei, Mohammad Reza, Akbaroghli, Susan, Keramatipour, Mohammad, Alaei, Ali
Publicado 2016

Gaucher Disease: New Expanded Classification Emphasizing Neurological Features

por ALAEI, Mohammad Reza, TABRIZI, Aydin, JAFARI, Narjes, MOZAFARI, Hadi
Publicado 2019

Whole Exome Sequencing Reveals a BSCL2 Mutation Causing Progressive Encephalopathy with Lipodystrophy (PELD) in an Iranian Pediatric Patient

por Alaei, Mohammad Reza, Talebi, Saeed, Ghofrani, Mohammad, Taghizadeh, Mohsen, Keramatipour, Mohammad
Publicado 2016

Once in a Blue Moon, a Very Rare Coexistence of Glutaric Acidemia Type I and Mucopolysaccharidosis Type IIIB in a Patient

por Alaei, Mohammad Reza, Kheirkhahan, Meghdad, Talebi, Saeed, Davoudi-Dehaghani, Elham, Keramatipour, Mohammad
Publicado 2020

Relationship Between Obesity and Liver Enzymes Levels in Turner’s Syndrome

por Rohani, Farzaneh, Golgiri, Fatemeh, Alaei, Mohammad Reza, Karimi, Mojgan, Nikraftar, Parham, Bozorgmehr, Ramin
Publicado 2017

Chitotriosidase Activity and Gene Polymorphism in Iranian Patients with Gaucher Disease and Sibling Carriers

por MOZAFARI, Hadi, TAGHIKHANI, Mohammad, KHATAMI, Shohreh, ALAEI, Mohammad Reza, VAISI-RAYGANI, Asad, RAHIMI, Zohreh
Publicado 2016

Mutation analysis and clinical characterization of Iranian patients with mucopolysaccharidosis type I

por Taghikhani, Mohammad, Khatami, Shohreh, Abdi, Mohammad, Hakhamaneshi, Mohammad Said, Alaei, Mohammad Reza, Zamanfar, Daniel, Vakili, Rahim
Publicado 2019

Clinical and Paraclinical Characteristics of Non-Classic Phenylketonuria

por SHAKIBA, Marjan, SANEIFARD, Hedyeh, ALAEI, Mohammad Reza, MOSALLANEJAD, Asieh, LOTFI, Mojtaba, YASAEI, Mehrdad, ALIZADE NADERI, Elahe
Publicado 2021

ELISA Cut-off Point for the Diagnosis of Human Brucellosis; a Comparison with Serum Agglutination Test

por Sanaei Dashti, Anahita, Karimi, Abdollah, Javad, Vadood, Shiva, Farideh, Fallah, Fatemeh, Alaei, Mohammad Reza, Angoti, Goli, Pournasiri, Zahra
Publicado 2012

Analysis of glucocerebrosidase (GBA) gene mutations in Iranian patients with Gaucher disease

por MOZAFARI, Hadi, TGHIKHANI, Mohammad, RAHIMI, Zohreh, VAISI RAYGANI, Asad, ANSARI, Shahla, KHATAMI, Shohreh, ALAEI, Mohammad Reza, SAGHIRI, Reza
Publicado 2021

Study protocol of a randomized controlled clinical trial investigating the effects of omega-3 supplementation on endothelial function, vascular structure, and metabolic parameters...

por Khorshidi, Masoud, Sayyari, Aliakbar, Olang, Beheshteh, Alaei, Mohammad Reza, Shab-Bidar, Sakineh, Khalili, Mitra, Salehi, Masoud, Aryaeian, Naheed
Publicado 2021

Validation of Urinary Glycosaminoglycans in Iranian patients with Mucopolysaccharidase type I: The effect of urine sedimentation characteristics

por ABDI, Mohammad, HAKHAMANESHI, Mohammad Said, ALAEI, Mohammad Reza, AZADI, Namam-Ali, VAKILI, Rahim, ZAMANFAR, Daniel, TAGHIKHANI, Mohammad, KHATAMI, Shohreh
Publicado 2014

Next-generation sequencing identified novel truncating mutations in BBS9 causing Bardet Biedl syndrome in two Iranian consanguineous families

por AKBAROGHLI, Susan, KOOSHAVAR, Daniz, GOLCHEHRE, Zahra, KARAMZADE, Arezou, SABERI, Mohammad, ALAEI, Mohammad Reza, ABBASI SADEGH, Masoud, ASADOLLAHI, Mostafa, KERAMATIPOUR, Mohammad
Publicado 2022

Mutational Analysis and Genotype Investigation of Less Known Gaucher Mutations through Haplotype Analysis in Iranian Gaucher Patients

por Sardarpour, Negar, Bagherian, Hamideh, Zafarghandi Motlagh, Fatemeh, Shirzadeh, Tina, Asnavandi, Sadaf, Younesikhah, Shahrzad, Salehpour, Shadab, Setoodeh, Aria, Alaei, Mohammad Reza, Zeinali, Sirous
Publicado 2023