Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Mahmoud F, Elsaid"'
Autor:
Ahmed S. Keshta, Saad I. Mallah, Khaled Al Zubaidi, Omar K. Ghorab, Mohamed S. Keshta, Dalal Alarabi, Mohammad A. Abousaleh, Mustafa Thaer Salman, Omer E. Taha, Anas A. Zeidan, Mahmoud F. Elsaid, Patrick Tang
Publikováno v:
Journal of Infection and Public Health, Vol 14, Iss 7, Pp 967-977 (2021)
The two genetically similar severe acute respiratory syndrome coronaviruses, SARS-CoV-1 and SARS-CoV-2, have each been responsible for global epidemics of vastly different scales. Although both viruses arose from similar origins, they quickly diverge
Externí odkaz:
https://doaj.org/article/4e2cb467cb3b4945ba260d4602ff7ed6
Autor:
Dalal Alarabi, Ahmed S. Keshta, Patrick Tang, Omer E. Taha, Mohamed S. Keshta, Omar Ghorab, Khaled Al Zubaidi, Saad I. Mallah, Mahmoud F. Elsaid, Mustafa Thaer Salman, Anas A. Zeidan, Mohammad A. Abousaleh
Publikováno v:
Journal of Infection and Public Health
Journal of Infection and Public Health, Vol 14, Iss 7, Pp 967-977 (2021)
Journal of Infection and Public Health, Vol 14, Iss 7, Pp 967-977 (2021)
The two genetically similar severe acute respiratory syndrome coronaviruses, SARS-CoV-1 and SARS-CoV-2, have each been responsible for global epidemics of vastly different scales. Although both viruses arose from similar origins, they quickly diverge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::404a59c8c044f8289845fff40897d6c0
https://pubmed.ncbi.nlm.nih.gov/34130121
https://pubmed.ncbi.nlm.nih.gov/34130121
Autor:
M. Elizabeth Ross, M. Al Mureikhi, Tawfeg Ben-Omran, Alice Abdel Aleem, Mahmoud F. Elsaid, Khalid Ibrahim, Nader Chalhoub, Hooman Kamel
Publikováno v:
Clinical Genetics. 93:387-391
We report a consanguineous Arab family with three affected siblings who display a disorder of global developmental delay, learning difficulties, facial dysmorphism, hearing impairments, and cataract. The clinical phenotype was associated with charact
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ad115e9d3c145371e0849d02eb3f128f
https://doi.org/10.1111/cge.13122
https://doi.org/10.1111/cge.13122
Autor:
Christopher A. Walsh, Mariam Almureikhi, A. James Barkovich, Nada Alaaraj, Tawfeg Ben-Omran, Shenela Lakhani, Jennifer N. Partlow, Ryan N. Doan, Muna Al Saffar, Mahmoud F. Elsaid
Publikováno v:
European Journal of Medical Genetics. 60:245-249
Arthrogryposis multiplex congenital, the occurrence of multiple joint contractures at birth, can in some cases be accompanied by insufficient myelination of peripheral nerves, muscular hypotonia, reduced tendon reflexes, and respiratory insufficiency
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5aadf62692ab45aba7827376e619f5dc
https://doi.org/10.1016/j.ejmg.2017.02.006
https://doi.org/10.1016/j.ejmg.2017.02.006
Autor:
Rana Al Shami, Noora ElMudehki, Vidya Nair, Khalid Ibrahim, Alice AbdelAleem, Mahmoud F. Elsaid, Khalid Mohamed
Publikováno v:
Congenital Dystrophies - Neuromuscular Disorders Precision Medicine: Genomics to Care and Cure.
Introduction: Mutations in genes-encoding collagen VI-a chain are known to cause congenital muscular dystrophies, (CMDs). Aim: Screening for COL6A mutations in CMDs’ patients. Methods: WGS, Sanger sequencing, plasmids-construction, Western-blot and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f8925fc2f83c221bf43c246703e0b66e
https://doi.org/10.5339/qproc.2020.nmd.25
https://doi.org/10.5339/qproc.2020.nmd.25
Autor:
Mahmoud F. Elsaid
Publikováno v:
Congenital Dystrophies - Neuromuscular Disorders Precision Medicine: Genomics to Care and Cure.
Although muscular diseases are monogenetic disorders, inherited in an autosomal recessive (AR), dominant or X-linked pattern, the marked variability in genetics and presentations can be identified within the same category of a subtype and among patie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce4d29f292eb502812fc5f502561ade3
https://doi.org/10.5339/qproc.2020.nmd.5
https://doi.org/10.5339/qproc.2020.nmd.5
Autor:
Fatima Al Musafri, Reem Babiker Mohamed, Sheikh Dr. Mohamed Bin Hamad Al-Thani, Alice Abdel Aleem, Gustavo Dziewczapolski, Mahmoud F. Elsaid, Hamda Qotba
Publikováno v:
Congenital Dystrophies - Neuromuscular Disorders Precision Medicine: Genomics to Care and Cure.
Neuromuscular disorders (NMDs) present a large group of primary muscle weakness’ diseases that progressively affect the subjects’ walking and movements’ abilities. Associated extra-muscular involvements constitute chronic co-morbidities that di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c49e665dcf45613da239d5a769765b84
https://doi.org/10.5339/qproc.2020.nmd.4
https://doi.org/10.5339/qproc.2020.nmd.4
Autor:
Reem Babiker Mohamed, Rana al-Shami, Mahmoud F. Elsaid, Omar Osman, M. Elizabeth Ross, Noora AlMudheki, Khalid Mohamed, Khalid Ibrahim, Nader Chalhoub, Osama Elalamy, Omer F. Kuzu, Alice Abdel Aleem, Almahdi Chakroun
Publikováno v:
Neuromuscular disorders : NMD. 30(6)
Congenital LAMA2 related muscular dystrophy (LAMA2-RD), the most commonly recognized type of congenital muscular dystrophies, has been described in patients' cohorts from Europe and the UK but not from Middle-Eastern. This study aimed to reveal the p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::875c99aec7790778571273e453d840f8
https://pubmed.ncbi.nlm.nih.gov/32444167
https://pubmed.ncbi.nlm.nih.gov/32444167
Autor:
Alice Abdel Aleem, Hussein Kamel, Yasmin A. Mohamoud, Mahmoud F. Elsaid, Tawfeg Ben-Omran, Pankaj Kumar, Khalid Ibrahim, M. Elizabeth Ross, Karsten Suhre, Iman K. Al-Azwani, Nader Chalhoub, Eman K. Al-Dous, Joel A. Malek
Publikováno v:
Annals of Neurology. 81:68-78
Objective Exome sequences account for only 2% of the genome and may overlook mutations causing disease. To obtain a more complete view, whole genome sequencing (WGS) was analyzed in a large consanguineous family in which members displayed autosomal r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::df57224d38f93413ef391f4b69b1023b
https://doi.org/10.1002/ana.24826
https://doi.org/10.1002/ana.24826
Publikováno v:
Open Journal of Immunology. :33-38
Introduction: Ataxia telangiectasia (AT) is a rare disease characterized by immunodeficiency and neurological manifestations. Ataxia, resulting from cerebella atrophy, runs a progressive incapacitating course. Clinical monitoring of the disease cours
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::11b4060b30771023e6cd1a93f7d6f47f
https://doi.org/10.4236/oji.2015.51004
https://doi.org/10.4236/oji.2015.51004