A boy with blistering of sun-exposed skin and finger shortening: the first case of Variegate Porphyria with a novel mutation in protoporphyrinogen oxidase (PPOX) gene in Iran: a ca...

por Vafaee-Shahi, Mohammad, Ghasemi, Saeide, Riahi, Aina, Sadr, Zahra
Publicado 2022

Intracranial angiomatoid fibrous histiocytoma: report of a rare case

por TABIBKHOOEI, Alireza, ASGARZADEH, Leila, SADEGHIPOUR, Alireza, VAFAEE SHAHI, Mohammad
Publicado 2022

A rare presentation of Carnitine palmitoyltransferase II (CPT-2) deficiency with normal acylcarnitine profile in a 10-year-old boy with muscle weakness and bilateral hearing loss;...

por VAFAEE SHAHI, Mohammad, GHASEMI, Saeide, TAHERNIA, Leila, RIAHI, Aina
Publicado 2022

A Novel Mutation in Aspartoacylase Gene; Canavan Disease

por ASHRAFI, Mahmoudreza, TAVASOLI, Alireza, KATIBEH, Pegah, ARYANI, Omid, VAFAEE-SHAHI, Mohammad
Publicado 2015

The first febrile seizure; predisposing factors and recurrence rate

por KAZEMI, Alinaghi, Shervin BADV, Reza, FALLAH, Ramazan, PIRI, Ali, TAHERNIA, Leila, VAFAEE SHAHI, Mohammad
Publicado 2021

Giant axonal neuropathy: The first Iranian case with a variation in the gigaxonin gene and a glance to the other cases

por Vafaee-Shahi, Mohammad, Ghasemi, Saeideh, Ghahvechi-Akbar, Masood, Tahernia, Leila, Davarzani, Atefeh, Hajati, Reza, Zare-Abdollahi, Davood, Alavi, Afagh
Publicado 2020

Bilateral horizontal gaze palsy in an 8‐year‐old girl: A rare case with NDUFS4 gene mutation

por Vafaee‐Shahi, Mohammad, Ghasemi, Saeide, Beiraghi Toosi, Mehran, Ashrafi, Mahmoud Reza, Badv, Reza Shervin, Tavasoli, Ali Reza, Tahernia, Leila
Publicado 2021

The effect of Rosa canina L. and a polyherbal formulation syrup in patients with attention-deficit/hyperactivity disorder: a study protocol for a multicenter randomized controlled...

por Golsorkhi, Haide, Qorbani, Mostafa, Kamalinejad, Mohammad, Sabbaghzadegan, Saeideh, Bahrami, Mohsen, Vafaee-Shahi, Mohammad, Montazerlotfelahi, Hadi, Abniki, Elham, Dadmehr, Majid
Publicado 2022

Genetic insights into PHARC syndrome: identification of a novel frameshift mutation in ABHD12

por Daneshi, Ahmad, Garshasbi, Masoud, Farhadi, Mohammad, Falavarjani, Khalil Ghasemi, Vafaee-Shahi, Mohammad, Almadani, Navid, Zabihi, MohammadSina, Ghalavand, Mohammad Amin, Falah, Masoumeh
Publicado 2023