Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Zayed S. Al-Zayed"'
Autor:
Omar A. Al-Mohrej, Saeed A. Al-Jarallah, Hamad H. Al-Dakhil Allah, Rajeev Pant, Zayed S. Al-Zayed
Publikováno v:
BMC Musculoskeletal Disorders, Vol 21, Iss 1, Pp 1-5 (2020)
Abstract Background Synovial sarcoma (SS) is one of the reported sarcomas in the pediatric and adult populations. Delay in diagnosis and treatment is common in SS cases. SS may be excised before the correct diagnosis is made. Case presentation we pre
Externí odkaz:
https://doaj.org/article/3f3119caf0b54cc781955aa33da3e56b
Publikováno v:
International Journal of Surgery Case Reports
Highlights • Amelia has been associated with idiopathic scoliosis in non-syndromic patients. • VEPTR device use in management was chosen as a definitive treatment in order to preserve spinal range of motion. • Up to our knowledge there is no co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c43411aac5377cdbf3ed20f4ff6645df
https://doi.org/10.1016/j.ijscr.2020.03.007
https://doi.org/10.1016/j.ijscr.2020.03.007
Autor:
Ozair Bin Majid, Alanoud A. Albekairi, Saleh Z. Alzaid, Shahd H Almonaie, Maqsood Ahmed, Zayed S. Al-Zayed
Publikováno v:
Cureus
Introduction For Sprengel deformity, a variety of operations are available, with Woodward's procedure being a favorable option with good outcomes. This study aims to assess the outcomes of Woodward's procedure with brachial plexus monitoring to preve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c438c8f5bce241eee402506a01ab209
https://doi.org/10.7759/cureus.19797
https://doi.org/10.7759/cureus.19797
Publikováno v:
Cureus
Mullerian duct aplasia-renal agenesis-cervicothoracic somite dysplasia (MURCS) association is a rare syndrome. This unique condition consists of Mullerian duct aplasia, cervicothoracic somite dysplasia, and renal aplasia, and skeletal abnormalities m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3afd1c5a5796f6cbc5991af3fb36552c
https://doi.org/10.7759/cureus.15669
https://doi.org/10.7759/cureus.15669
Autor:
Ozair Bin Majid, Omar A Al-Mohrej, Abdullah M Alsultan, Nouf F. Alsadoun, Ali A Altalhy, Zayed S. Al-Zayed
Publikováno v:
Cureus
Introduction: In congenital anomalies of the thoracic spine, fusion in situ and hemi-epiphysiodesis are unsuitable surgical options, because three-dimensional thoracic deformity and insufficiency are uncorrectable. We aimed to evaluate the radiologic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d5f55015674945dca1e9ef4686fcfc5
https://doi.org/10.7759/cureus.14167
https://doi.org/10.7759/cureus.14167
Autor:
Yufei Shi, Huda A BinEssa, Thamer S Alhussainan, Lamya Al-Ghofaili, Anwar M Al-Rabiah, Roua A. Al-Rijjal, Minjing Zou, Brian F. Meyer, Rajeev Pant, Zayed S. Al-Zayed
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-11 (2021)
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-11 (2021)
Background Hereditary Multiple Exostoses (HME), also known as Multiple Osteochondromas (MO) is a rare genetic disorder characterized by multiple benign cartilaginous bone tumors, which are caused by mutations in the genes for exostosin glycosyltransf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba8e0f8dea3035935147214b1e54a93c
https://doi.org/10.1186/s13023-021-01738-z
https://doi.org/10.1186/s13023-021-01738-z
Autor:
Rajeev Pant, Omar A Al-Mohrej, Zayed S. Al-Zayed, Saeed A. Al-Jarallah, Hamad H. Al-Dakhil Allah
Publikováno v:
BMC Musculoskeletal Disorders, Vol 21, Iss 1, Pp 1-5 (2020)
BMC Musculoskeletal Disorders
BMC Musculoskeletal Disorders
Background Synovial sarcoma (SS) is one of the reported sarcomas in the pediatric and adult populations. Delay in diagnosis and treatment is common in SS cases. SS may be excised before the correct diagnosis is made. Case presentation we present a ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d2cfefbee2f16e3399e74dc63968d30
https://doi.org/10.1186/s12891-020-03312-3
https://doi.org/10.1186/s12891-020-03312-3
Autor:
Tariq Masoodi, Moeen Al-Sayed, Brian F. Meyer, Mohammad Al-Owain, Nadia Sakati, Hamad Al-Zaidan, Haya Al Saud, Zuhair Rhabeeni, Yousef Binamer, Zayed S. Al-Zayed, Zuhair N. Al-Hassnan, William Wade, Ruqaiah Altassan, Nadia Alhashemi, Salma M. Wakil, Mohamed A. Al-Muhaizea, Ola Khalifa, Haya Al Dosssari
Publikováno v:
American Journal of Medical Genetics Part A. 173:1009-1016
Hereditary sensory autonomic neuropathy type IV (HSAN-IV) is a rare autosomal recessive disorder that usually begins in infancy and is characterized by anhidrosis, insensitivity to noxious stimuli leading to self-mutilating behavior, and intellectual
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8873324a7a295fe9ed5569480f74de6
https://doi.org/10.1002/ajmg.a.38120
https://doi.org/10.1002/ajmg.a.38120
Cell salvage within adult and pediatric idiopathic scoliosis surgery: A random cross-sectional study
Autor:
Anwar M Al-Rabiah, Bayan Al-Torbaq, Jason Sayer, Zayed S. Al-Zayed, Omar A Al-Mohrej, Raed Hshem
Publikováno v:
SICOT-J, Vol 6, p 41 (2020)
SICOT-J
SICOT-J
Introduction: This study aimed to evaluate the use of a cell savage and its impact on the amount of allogenic blood transfused to the patients during idiopathic scoliosis surgery. Methods: A total of 142 randomly selected patients with scoliosis had
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::821c7b83ef0ef8f55f8ba5b578fa57ef
https://doi.org/10.1051/sicotj/2020038
https://doi.org/10.1051/sicotj/2020038
Autor:
Fowzan S. Alkuraya, Shinu Ansari, Nadia Al-Hashmi, Eissa Faqeih, Anas M. Alazami, Noon Mousa, Aisha Alsinani, Zayed S. Al-Zayed, Fatema Alzahrani, Mohammed Al-Owain, Ranad Shaheen, Muneera J. Alshammari
Publikováno v:
Journal of Medical Genetics. 49:630-635
Background Osteogenesis imperfecta (OI) is an hereditary bone disease in which increased bone fragility leads to frequent fractures and other complications, usually in an autosomal dominant fashion. An expanding list of genes that encode proteins rel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9dbef9bd39bde5734b932f9acd12496
https://doi.org/10.1136/jmedgenet-2012-101142
https://doi.org/10.1136/jmedgenet-2012-101142