Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Rana Al Shami"'
Autor:
Anood Alassaf, Rana Al Shami, Jehan Al Rayahi, William Mifsud, Khalid Al-Kharazi, Abdulqadir J. Nashwan
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 75, Iss , Pp 102071- (2021)
Three years old boy presented with recurrent severe abdominal pain. He was treated for constipation and the pain resolved. Later he developed a limitation of neck movements. Investigations revealed a spinal cord mass. After surgical resection, histop
Externí odkaz:
https://doaj.org/article/e6ed438967694206b93250a7840a8415
Autor:
Rana Al-Shami, Adnan Al-Mutawkkil
Publikováno v:
International Journal of Advanced Research in Computer Science. 11:31-37
More recently, computing storage systems have started implementing an erasure code approach in storing big data due to its many advantages such as reducing storage cost, providing fault tolerance, and reliability. However, many challenges and open is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ae762e81c8742842b08dbd1bcab0ea13
https://doi.org/10.26483/ijarcs.v11i5.6650
https://doi.org/10.26483/ijarcs.v11i5.6650
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:
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
Publikováno v:
International Journal of Central Nervous System Disease. :7
The COVID-19 pandemic, caused by Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2), spread in few months from a small focus in Wuhan (Hubei province, China) to over 28 million people worldwide , COVID-19 is often more severe in people 60+y
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::570da95f40357d1f287403ec5a4dcf45
https://doi.org/10.28933/ijcnsd-2021-05-0505
https://doi.org/10.28933/ijcnsd-2021-05-0505
Publikováno v:
International Journal of Case Reports. :211
Background: SYNGAP1, which encodes a RAS-GTPase-activating protein, is located on the short arm of chromosome 6.Mutations of the SYNGAP1 gene were first identified in 2009 in patients with nonsyndromic intellectual disability (ID) acquired microcepha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1902fd52e5ecb048aa6db0b74efed664
https://doi.org/10.28933/ijcr-2021-03-3007
https://doi.org/10.28933/ijcr-2021-03-3007
Autor:
Rihab Alozeib, Rana al-Shami, Hanem Abdullah, Abdulrahman Al-Debs, Patrick Tang, Ahlam Ahmed, Azhar Alamri, Sondos Altaraqji
Publikováno v:
International Journal of Pediatric Research and Reviews. :36
Most reported cases of coronavirus disease 2019 (COVID-19) in children aged
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f2ba04f8e9ba7d52ad50b45748e5ce4a
https://doi.org/10.28933/ijoprr-2021-06-0505
https://doi.org/10.28933/ijoprr-2021-06-0505
Autor:
Sondos Altaraqji, Rana al-Shami
Publikováno v:
International Journal of Case Reports. :210
Chromosomal abnormalities involving deletions and duplications are known to cause severe developmental disorders, including mental retardation, dysmorphism, and seizures, in children. As the technique of array-based comparative genomic hybridization
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::43b0d18b21ff0a3d84ca59cebeb40b43
https://doi.org/10.28933/ijcr-2021-03-3005
https://doi.org/10.28933/ijcr-2021-03-3005
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
Publikováno v:
Indian Journal of Child Health. :61-62
We describe a child who presented with a respiratory illness in the influenza pandemic season and was found to be positive for the influenza A, he developed neurological manifestations of cranial nerve palsies and was found to have radiological evide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a66ace04d1c74ed0665df9ed80775916
https://doi.org/10.32677/ijch.2018.v05.i01.015
https://doi.org/10.32677/ijch.2018.v05.i01.015