A Novel c.973G>T Mutation in the ε-subunit of the Acetylcholine Receptor Causing Congenital Myasthenic Syndrome in an Iranian Family

por Karimzadeh, P, Parvizi Omran, S, Ghaedi, H, Omrani, MD
Publicado en Balkan J Med Genet (2019)

A novel mutation and variable phenotypic expression in a large consanguineous pedigree with Jalili syndrome

por Rahimi-Aliabadi, S, Daftarian, N, Ahmadieh, H, Emamalizadeh, B, Jamshidi, J, Tafakhori, A, Ghaedi, H, Noroozi, R, Taghavi, S, Ahmadifard, A, Alehabib, E, Andarva, M, Shokraeian, P, Atakhorrami, M, Darvish, H
Publicado en Eye (Lond) (2016)

Hepatitis B Virus Infection in Patients with Blood Disorders: A Concise Review in Pediatric Study

por Mansouri, N, Movafagh, A, Sayad, A, Ghafouri-Fard, S, Darvish, H, Zare-Abdollahi, D, Emamalizadeh, B, Shahvaisizadeh, F, Ghaedi, H, Bastami, M, Kayyal, M, Hashemi, M, Heidari, MH, Nejatizadeh, A, Zamani, M
Publicado en Iran J Ped Hematol Oncol (2014)