Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Shokoufeh Abdollahi"'
Autor:
Feng Yan, Cedric Tremblay, Francine Garret-Bakelman, Jesslyn Saw, Matthew P. McCormack, Shokoufeh Abdollahi, Pieter Van Vlierberghe, David Powell, Nicholas C. Wong, David J. Curtis
Publikováno v:
Blood. 140:5898-5899
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e665f8a18e5e2d795378890eb2ad69eb
https://doi.org/10.1182/blood-2022-169201
https://doi.org/10.1182/blood-2022-169201
Autor:
Shokoufeh Abdollahi, Javad Jamshidi, Abbas Tafakhori, Hossein Darvish, Elham Alehabib, Marjan Chapi, Somayeh Alinaghi, Amir Hossein Johari, Hamid Ghaedi
Publikováno v:
European Journal of Medical Genetics. 60:578-582
Waardenburg anophthalmia syndrome (WAS) is a rare disorder that mostly affects the eyes and distal limbs. In the current study we reported two Iranian patients with WAS. The first case was a 26-year-old girl with unilateral anophthalmia, bilateral ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b71d13e0d745379b944d35314f40a11
https://doi.org/10.1016/j.ejmg.2017.08.006
https://doi.org/10.1016/j.ejmg.2017.08.006
Autor:
Bahia-Namavar Jahromi, Shiva Poorang, Najmeh Moein-Vaziri, Zahra Anvar, Mahnaz Banaei, Seyed Mohammad Bagher Tabei, Seyed Alireza Dastgheib, Behrouz Gharesi-Fard, Shokoufeh Abdollahi
Publikováno v:
Clinical laboratory. 64(7)
BACKGROUND Recurrent pregnancy loss (RPL) defined as three or more consecutive spontaneous miscarriages before the 20th week of gestation is caused by different factors including genetic and epigenetic background. However the involvement of paternal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16ddd1fb7b0abe03b7aba03e66c37ec1
https://pubmed.ncbi.nlm.nih.gov/30146842
https://pubmed.ncbi.nlm.nih.gov/30146842
Autor:
Helmut Butzkueven, Jeannette Lechner-Scott, John A. Hamilton, Vicki E. Maltby, Tomas Kalincik, Jim Stankovich, Mastura Monif, Terence J. O'Brien, Shokoufeh Abdollahi
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 90:A42.3-A42
IntroductionCladribine Tablets (Mavenclad®) is nucleoside analogue of deoxyadenosine, and an oral treatment for relapsing remitting MS (RRMS). In RRMS clinical trials, Cladribine has been shown to reduce brain atrophy, relapse rates, and new lesions
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c1f3b55534a306f41840e7894dd245ba
https://doi.org/10.1136/jnnp-2019-anzan.116
https://doi.org/10.1136/jnnp-2019-anzan.116
Autor:
Shahram Torkamandi, Shaghayegh Taghavi, Saeed Mohammadihosseinabad, Mohammad Reza Abbaszadegan, Neda Shahmohammadibeni, Shokoufeh Abdollahi, Marzieh Motallebi, Negar Pedram, Leyla HaghNejad, Masoumeh Amini Gavenaroudi, Ehsan Ahmadi, Abolfazl Movafagh, Hamid Ghaedi, Babak Emamalizadeh, Amir Ehtesham Shafiei Zarneh, Atena Fazeli, Gholam Ali Shahidi, Hossein Darvish, Javad Jamshidi, Alireza Zare Bidoki, Abbas Tafakhori
Publikováno v:
Journal of the Neurological Sciences. 355:72-74
DNA variations in the fibroblast growth factor 20 gene have been reported to be associated with Parkinson's disease (PD). The rs12720208, a functional SNP located in the 3'UTR region of the gene, was reported as a risk factor for PD. A number of stud
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60763c4a51a0fb9278bccfe9e686f52f
https://doi.org/10.1016/j.jns.2015.05.020
https://doi.org/10.1016/j.jns.2015.05.020
Autor:
Mahnoosh Rahimi, Mahnaz Shahmohammadibeni, Hossein Ali Shahmohammadibeni, Monavvar Andarva, Javad Jamshidi, Hajar Eftekhari, Haleh Akhavan-Niaki, Babak Emamalizadeh, Mahmoud Shekari Khaniani, Azadeh Ahmadifard, Ehteram Khademi, Shaghayegh Taghavi, Alireza Zare Bidoki, Hossein Darvish, Neda Shahmohammadibeni, Amir Ehtesham Shafiei Zarneh, Abbas Tafakhori, Atena Fazeli, Minoo Atakhorrami, Marzieh Motallebi, Tahereh Dadkhah, Elham Alehabib, Simin Rahimi-Aliabadi, Shokoufeh Abdollahi
Publikováno v:
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 37(5)
Parkinson's disease (PD) is the second most prevalent neurodegenerative disorder. Both genetic and environmental factors are involved in the etiology of the disease. Many studies have revealed the susceptibility genes and variations for PD which need
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::560834c8f76d74818e75ae469d17a41e
https://pubmed.ncbi.nlm.nih.gov/26732583
https://pubmed.ncbi.nlm.nih.gov/26732583
Autor:
Shahmohammadibeni, Neda1, Rahimi-Aliabadi, Simin2, Jamshidi, Javad3, Emamalizadeh, Babak2, Shahmohammadibeni, Hossein4, Zare Bidoki, Alireza5, Akhavan-Niaki, Haleh1, Eftekhari, Hajar1, Abdollahi, Shokoufeh6, Shekari Khaniani, Mahmoud, Shahmohammadibeni, Mahnaz1, Fazeli, Atena2, Motallebi, Marzieh2, Taghavi, Shaghayegh2, Ahmadifard, Azadeh2, Shafiei Zarneh, Amir2, Andarva, Monavvar2, Dadkhah, Tahereh1, Khademi, Ehteram1, Alehabib, Elham2
Publikováno v:
Neurological Sciences. May2016, Vol. 37 Issue 5, p731-736. 6p. 4 Charts.
Autor:
Poorang, Shiva, Abdollahi, Shokoufeh, Anvar, Zahra, Tabei, Seyed M. B., Jahromi, Bahia-Namavar, Moein-Vaziri, Najmeh, Gharesi-Fard, Behrouz, Banaei, Mahnaz, Dastgheib, Seyed A.
Publikováno v:
Clinical Laboratory; 2018, Vol. 64 Issue 7/8, p1121-1128, 8p