سوابق علمی و پژوهشی - دانشگاه علوم پزشکی فسا

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Javad Jamshidi
جواد جمشیدی
(Javad Jamshidi)
کارشناسی ارشد
دانشکده پزشکی, گروه بیوشیمی و ژنتیک
j.jamshidi@fums.ac.ir

جستجو رزومه

مقاله ها

Behnam Safarpour Lima, Hamid Ghaedi, Narsis Daftarian, Hamid Ahmadieh, Javad Jamshidi, Mehdi Khorrami, Rezvan Noroozi, Nasim Sohrabifar, Farhad Assarzadegan, Omid Hesami, Shaghayegh Taghavi, Azadeh Ahmadifard, Minoo Atakhorrami, Simin Rahimi-Aliabadi, Neda Shahmohammadibeni, Elham Alehabib, Monavvar Andarva, Hossein Darvish, Babak Emamalizadeh, Date:2016/1/7
AuthorsBehnam Safarpour Lima, Hamid Ghaedi, Narsis Daftarian, Hamid Ahmadieh, Javad Jamshidi, Mehdi Khorrami, Rezvan Noroozi, Nasim Sohrabifar, Farhad Assarzadegan, Omid Hesami, Shaghayegh Taghavi, Azadeh Ahmadifard, Minoo Atakhorrami, Simin Rahimi-Aliabadi, Neda Shahmohammadibeni, Elham Alehabib, Monavvar Andarva, Hossein Darvish, Babak Emamalizadeh
Date2016/1/7
PublisherElsevier Masson
DescriptionAbstract Wolfram syndrome is one of the rare autosomal recessive, progressive, rnneurodegenerative disorders, characterized by diabetes mellitus and optic atrophy. Several rnother features are observed in patients including deafness, ataxia, and peripheral rnneuropathy. A gene called WFS1 is identified on chromosome 4p, responsible for Wolfram rnsyndrome. We investigated a family consisted of parents and 8 children, which 5 of them rnhave been diagnosed for Wolfram syndrome. WFS1 gene in all family members was ...