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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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

Analysis of Copy Number Variations in Patients with Autism Using Cytogenetic and MLPA Techniques: Report of 16p13. 1p13. 3 and 10q26. 3 Duplications

Saghar Ghasemi Firouzabadi, Roshanak Vameghi, Roxana Kariminejad, Hossein Darvish, Susan Banihashemi, Mahboubeh Firouzkouhi Moghaddam, Peyman Jamali, Hassan Farbod Mofidi Tehrani, Hossein Dehghani, Mohammad Reza Raeisoon, Mehrnaz Narooie-Nejad, Javad Jamshidi, Abbas Tafakhori, Saeid Sadabadi, Farkhondeh Behjati
2016 International Journal of Molecular and Cellular Medicine

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

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
2017/2/21 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
2017/2/25 Neurological Research

Omentin Val109Asp polymorphism and risk of coronary artery disease

Javad Jamshidi, Mehrdad Ghanbari, Ali Asnaashari, Nosaybeh Jafari, Gholam Abbas Valizadeh
2017/3 Asian Cardiovascular and Thoracic Annals

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

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

Vitamin D receptor gene rs4334089 polymorphism and Parkinson’s disease in Iranian population

Atena Fazeli, Marzieh Motallebi, Javad Jamshidi, Abolfazl Movafagh, Hamid Ghaedi, Babak Emamalizadeh, Kaveh Kashani, Hossein Darvish
2016/8/31 Basal Ganglia

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

Phaeohyphomycosis due to Dematiaceous Fungi A Review of the Literature

Mohammad Hosein Afsarian, Tahereh Shokohi, Mehdi Arzanlou, Mehdi Taheri Sarvtin, Hamid Badali
2012/9/15 Journal of Mazandaran University of Medical Sciences

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
2017/2/21 Genetic Testing and Molecular Biomarkers
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