Mostafa Asadollahi

发表

Dysfunction of the ciliary ARMC9/TOGARAM1 protein module causes Joubert syndrome.

Caitlin V. Miller, D. Nickerson, M. Bamshad, 2020, The Journal of clinical investigation.

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

M. Alaei, M. Keramatipour, Daniz Kooshavar, 2022, Iranian journal of child neurology.

Measuring Serum Level of Ionized Magnesium in Patients with Migraine

H. Derakhshanfar, F. Assarzadegan, O. Aryani, 2015, Iranian journal of child neurology.

Protective properties of the aqueous extract of saffron (Crocus sativus L.) in ischemic stroke, randomized clinical trial.

H. Sahraei, B. Hatef, G. Pirzad Jahromi, 2019, Journal of ethnopharmacology.

Evaluation of modulatory effects of saffron (Crocus sativus L.) aqueous extract on oxidative stress in ischemic stroke patients: a randomized clinical trial

M. Jafari, G. Pirzad Jahromi, S. Gudarzi, 2020, Nutritional neuroscience.

Secondary headaches attributed to arterial hypertension

Omid Aryani, Nahid Beladi moghadam, O. Hesami, 2013, Iranian journal of neurology.

Comparison of Peripapillary Retinal Nerve Fiber Layer Thickness in Patients with MS and Normal Population

M. Yaseri, M. Entezari, M. Nazari, 2017 .

A Novel Mutation in the OXCT1 Gene Causing Succinyl-CoA:3-Ketoacid CoA Transferase (SCOT) Deficiency Starting with Neurologic Manifestations

M. Keramatipour, S. Talebi, R. Hosseini, 2023, Iranian journal of child neurology.

A novel missense variant in EIF2B5 identified in a consanguineous Iranian family with vanishing white matter disease and a brief review of the literature

M. Keramatipour, Y. Eshaghkhani, Arezou Karamzade, 2023, Journal of Genetics.