Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Sahar Sharaf"'
Autor:
Ebtesam Mohamed Fahmy, Mohamed Elsayed Elawady, Sahar Sharaf, Sarah Heneidy, Rania Shehata Ismail
Publikováno v:
The Egyptian Journal of Neurology, Psychiatry and Neurosurgery, Vol 57, Iss 1, Pp 1-5 (2021)
Abstract Background Accumulating data have suggested that vitamin D receptor (VDR) gene is a pretender gene for vulnerability to Parkinson disease (PD). This study aimed to assess the relationship of VDR gene polymorphisms (FokI and ApaI) with PD. Fi
Externí odkaz:
https://doaj.org/article/435d34f78c8b49e38ca7b3fecd270084
Autor:
Ebtesam Mohamed Fahmy, Mohamed Elsayed Elawady, Sahar Sharaf, Sarah Heneidy, Rania Shehata Ismail
Publikováno v:
The Egyptian Journal of Neurology, Psychiatry and Neurosurgery, Vol 56, Iss 1, Pp 1-4 (2020)
Abstract Background Vitamin D is suggested to play an important role in neurodegenerative disorders. Objective To examine the association between serum 25 vitamin D3 and Parkinson’s disease (PD). Materials and methods Fifty patients suffering from
Externí odkaz:
https://doaj.org/article/661bd38215c044d18c6fd284c3736167
Autor:
Mona Fathy, Arwa M. Darweesh, Sahar Sharaf, Hadeel M. El-Hanafi, Fayek M. Ghaleb, Iman A. Fahmy, Shadia M. Hussein
Publikováno v:
Bulletin of the National Research Centre, Vol 44, Iss 1, Pp 1-7 (2020)
Abstract Background Glaucoma is the second leading cause of blindness in the world with primary open-angle glaucoma (POAG) that is the most prevalent type. Brain-derived neurotrophic factor (BDNF) is a member of the neurotrophin family synthesized by
Externí odkaz:
https://doaj.org/article/0b244fb648a7487eae2f41fd6323a7ad
Publikováno v:
In Egyptian Pediatric Association Gazette June 2015 63(2):63-68
Publikováno v:
International Journal of Clinical Cardiology. 6
Publikováno v:
Online Journal of Cardiovascular Research. 1
Autor:
Iman, Elbanhawy, Ebtesam Mohamed, Fahmy, Sahar, Sharaf, Rania Shehata, Ismail, Karim, Elmehdawy
Publikováno v:
Acta neurologica Belgica. 121(1)
Memory, cognition and visuospatial aspects of temporal lobe epilepsy (TLE) have not been fully analyzed yet. From among the huge growing population of circulating apoproteins analyzed in TLE, apolipoprotein E (APOE) was discovered; however, its role
Autor:
Fatma, Elmougy, Sahar, Sharaf, Mona, Hafez, Ahmed, Khattab, Hazem, Abou-Yousef, Marwa, Elsharkawy, Heba, Baz, Sherif, Ekladious, Balsam, Sherif, Noha, Musa, Yasmin, Elshiwy, Alaa, Afif, Mona, Abdullatif, Ghada, Thabet, Normeen, Rady, Amany, Ibrahim, Hend, Soliman
Publikováno v:
Annals of the New York Academy of Sciences. 1415(1)
CYP21A2 genotyping remains an important element in the diagnosis and management of congenital adrenal hyperplasia, and establishing accurate genotype-phenotype correlations has facillitated adequate genetic counseling and prenatal management for at-r