دانشکده پیراپزشکی - دانشگاه علوم پزشکی و خدمات درمانی فسا

دانشکده پیراپزشکی دانشگاه علوم پزشکی فسا

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تقويم آموزشي نيمسال اول 1395-1394

تقويم آموزشي نيمسال اول 1395-1394

تقويم آموزشي نيمسال اول 1395-1394

آغاز سال تحصيلي جديد مبارك

آغاز سال تحصيلي جديد مبارك

دانشكده پيراپزشكي آغاز فصل بهار علم و دانش و فصل شكفتن شكوفه هاي آگاهي را به تمامي دانشجويان و تلاشگران عرصه علوم پزشكي تبريك مي گويد.

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PHAEOHYPOMYCOSIS DUE TO DEMATIACEOUS FUNGI; A REVIEW OF THE LITERATURES

MOHAMMAD HOSEIN AFSARIAN, TAHEREH SHOKOHI, MAHDI ARZANLOU, SARVTIN MEHDI TAHERI, HAMID BADALI
2012/1/1

Emery-Dreifuss Muscular Dystrophy: a Report of a Large Family with 11 Affected Individuals.

Azadeh Ahmadifard, Javad Jamshidi, Abbas Tafakhori, Reza Mollazadeh, Zeinab Falsafi, Hossein Darvish
2016 International journal of molecular and cellular medicine

Association of β-Secretase Functional Polymorphism with Risk of Schizophrenia

Simin Rahimi-Aliabadi, Neda Shahmohammadibeni, Javad Jamshidi, Ehsan Esmaili Shandiz, Reza Mirfakhraie, Mina Ohadi, Farhad Ramezani Nejad, Nader Mansoori, Mohammad Taheri, Fatemeh Gholipour, Susan Moudi, Gouya Tayebi, Shahram Divsalar, Hossein Darvish, Abolfazl Movafagh
2017/4/1 Genetic Testing and Molecular Biomarkers

RAB7L1 promoter polymorphism and risk of Parkinson’s disease; a case-control study

Ali Khaligh, Maryam Goudarzian, Alireza Moslem, Amirhosein Mehrtash, Javad Jamshidi, Hossein Darvish, Babak Emamalizadeh
2017/5/4 Neurological Research

Association of renin–angiotensin–aldosterone system gene polymorphisms with left ventricular hypertrophy in patients with heart failure with preserved ejection fraction: A case–control study

Ehsan Bahramali, Negar Firouzabadi, Mona Rajabi, Alireza Manafi, Mehrdad Zarghami, Seyyed Mohammad Mousavi, Javad Jamshidi
2017/5/14 Clinical and Experimental Hypertension

Support for “Disease-Only” Genotypes and Excess of Homozygosity at the CYTH4 Primate-Specific GTTT-Repeat in Schizophrenia

Ehteram Khademi, Elham Alehabib, Ehsan Esmaili Shandiz, Azadeh Ahmadifard, Monavvar Andarva, Javad Jamshidi, Simin Rahimi-Aliabadi, Ramin Pouriran, Farhad Ramezani Nejad, Nader Mansoori, Neda Shahmohammadibeni, Shaghyegh Taghavi, Parasto Shokraeian, Haleh Akhavan-Niaki, Coro Paisán-Ruiz, Hossein Darvish, Mina Ohadi
2017/7/19 Genetic Testing and Molecular Biomarkers

c. 376G> A mutation in WFS1 gene causes Wolfram syndrome without deafness

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
2016/2/29 European journal of medical genetics

PTRHD1 (C2orf79) mutations lead to autosomal‐recessive intellectual disability and parkinsonism

Hamidreza Khodadadi, Luis J Azcona, Vajiheh Aghamollaii, Mir Davood Omrani, Masoud Garshasbi, Shaghayegh Taghavi, Abbas Tafakhori, Gholam Ali Shahidi, Javad Jamshidi, Hossein Darvish, Coro Paisán‐Ruiz
2017/2/1 Movement Disorders

A Clinical and Molecular Genetic Study of 50 Families with Autosomal Recessive Parkinsonism Revealed Known and Novel Gene Mutations

Shaghayegh Taghavi, Rita Chaouni, Abbas Tafakhori, Luis J Azcona, Saghar Ghasemi Firouzabadi, Mir Davood Omrani, Javad Jamshidi, Babak Emamalizadeh, Gholam Ali Shahidi, Mona Ahmadi, Seyed Amir Hassan Habibi, Azadeh Ahmadifard, Atena Fazeli, Marzieh Motallebi, Peyman Petramfar, Saeed Askarpour, Shiva Askarpour, Hossein Ali Shahmohammadibeni, Neda Shahmohammadibeni, Hajar Eftekhari, Amir Ehtesham Shafiei Zarneh, Saeed Mohammadihosseinabad, Mehdi Khorrami, Safa Najmi, Ahmad Chitsaz, Parasto Shokraeian, Hossein Ehsanbakhsh, Jalal Rezaeidian, Reza Ebrahimi Rad, Faranak Madadi, Monavvar Andarva, Elham Alehabib, Minoo Atakhorrami, Seyed Erfan Mortazavi, Zahra Azimzadeh, Mahdis Bayat, Amir Mohammad Besharati, Mohammad Ali Harati-Ghavi, Samareh Omidvari, Zahra Dehghani-Tafti, Faraz Mohammadi, Banafsheh Mohammad Hossein Pour, Hamid Noorollahi Moghaddam, Ehsan Esmaili Shandiz, Arman Habibi, Zahra Taherian-Esfahani, Hossein Darvish, Coro Paisßn-Ruiz
2017/5/13 Molecular Neurobiology

The analysis of association between SNCA, HUSEYO and CSMD1 gene variants and Parkinson’s disease in Iranian population

Neda Shahmohammadibeni, Simin Rahimi-Aliabadi, Javad Jamshidi, Babak Emamalizadeh, Hossein Ali Shahmohammadibeni, Alireza Zare Bidoki, Haleh Akhavan-Niaki, Hajar Eftekhari, Shokoufeh Abdollahi, Mahmoud Shekari Khaniani, Mahnaz Shahmohammadibeni, Atena Fazeli, Marzieh Motallebi, Shaghayegh Taghavi, Azadeh Ahmadifard, Amir Ehtesham Shafiei Zarneh, Monavvar Andarva, Tahereh Dadkhah, Ehteram Khademi, Elham Alehabib, Mahnoosh Rahimi, Abbas Tafakhori, Minoo Atakhorrami, Hossein Darvish
2016/5/1 Neurological Sciences

Association of ACE gene D polymorphism with left ventricular hypertrophy in patients with diastolic heart failure: a case–control study

Ehsan Bahramali, Mona Rajabi, Javad Jamshidi, Seyyed Mohammad Mousavi, Mehrdad Zarghami, Alireza Manafi, Negar Firouzabadi
2016/2/1 BMJ open

Comparison of Breastfeeding Patterns in Women with Normal Vaginal Delivery and Cesarean Section

SHAHNAZ KARIMI, KALYANI MAJID NAJAFI, MOHAMMAD MAHDI NAGHIZADEH, FARHOUD NEKOEE, MOJGAN KAMALI
2011/1/1
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