Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Soha Yazbek"'
Autor:
Abla M Sibai, Neil V Singh, Samer Jabbour, Shadi Saleh, Sawsan Abdulrahim, Farah Naja, Soha Yazbek
Publikováno v:
PLoS ONE, Vol 12, Iss 6, p e0178401 (2017)
To review trends in non-communicable (NCD) research output in the Arab region, in terms of quantity and quality, study design, setting and focus. We also examined differences by time and place, and assessed gaps between research output and NCD burden
Externí odkaz:
https://doaj.org/article/2eeb719589a84be7b6ad37b69b954a43
Publikováno v:
J Community Genet
BACKGROUND: The MENA region is disproportionately affected by genetic disease. The aim of this research is to scope the region for evidence of genetic services and public health interventions to identify geographic gaps, and to provide a descriptive
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66ae32a3894022314b2a1c14d7b01f8d
https://europepmc.org/articles/PMC9947218/
https://europepmc.org/articles/PMC9947218/
Publikováno v:
The Lancet Haematology. 10:e91-e92
Publikováno v:
Journal of Immigrant and Minority Health. 22:1347-1367
The aim of this systematic review is to provide physicians and researchers with a comprehensive list of reported genetic disorders in patients of Syrian origin-those who have become part of the largest displaced population globally-and to highlight t
Publikováno v:
American Journal of Medical Genetics Part A
The coronavirus disease 2019 (COVID-19) emerged in early 2020 and since, has brought about tremendous cost to economies and healthcare systems universally. Reports of pediatric patients with inherited conditions and COVID-19 infections are emerging.
Autor:
Gregory Antonios, Dania B Awad, Firas Kobeissy, Rami Mahfouz, Rémi Safi, Marwan M El-Sabban, Perla Z Zgheib, Soha Yazbek, Brigitte Wex
Publikováno v:
Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry
Molecules
Volume 23
Issue 6
Molecules, Vol 23, Iss 6, p 1350 (2018)
Molecules
Volume 23
Issue 6
Molecules, Vol 23, Iss 6, p 1350 (2018)
SLC35B4, solute receptor for UDP-N-acetylglucosamine and UDP-xylose, is associated with diabetes and predisposing conditions. This study investigated the localization of SLC35B4 and compared the differential expression between a knockdown of SLC35B4
Autor:
Farah Naja, Samer Jabbour, Shadi Saleh, Sawsan Abdulrahim, Abla M. Sibai, Soha Yazbek, Neil Singh
Publikováno v:
PLoS ONE
PLoS ONE, Vol 12, Iss 6, p e0178401 (2017)
PLoS ONE, Vol 12, Iss 6, p e0178401 (2017)
Objectives To review trends in non-communicable (NCD) research output in the Arab region, in terms of quantity and quality, study design, setting and focus. We also examined differences by time and place, and assessed gaps between research output and
Publikováno v:
Cellular and molecular biology (Noisy-le-Grand, France). 63(3)
Familial Mediterranean Fever (FMF) is an autosomal recessive autoinflammatory disease affecting people of Mediterranean ancestry. The disease is caused by mutations in the MEFV gene located on chromosome 16p13.3. The aim of this pilot study was to as
Publikováno v:
Journal of Community Genetics. 6:83-105
The review lists the genetic diseases reported in Lebanese individuals, surveys genetic programs and services, and highlights the absence of basic genetic health services at the individual and community level. The incidence of individual diseases is
Autor:
Soha Yazbek, Roy A. Khalaf, Sarah Khansa, Rouba Hoteit, Amira S. Sabbagh, Rami Mahfouz, Nady El Hajj, Dina Shammaa, Zaher K. Otrock
Publikováno v:
Gene. 525:136-140
Aims The Natural Killer Cell Immunoglobulin-like Receptor (KIR) genotype profiling in Follicular Lymphoma has not been reported before in the literature. Materials and methods DNA extracted from 20 Follicular Lymphoma patients and 62 healthy controls