Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Raghad, Algahtani"'
Publikováno v:
Sultan Qaboos University Medical Journal, Vol 20, Iss 1, Pp 83-89 (2020)
Objectives: Faculty members are the most important resource in any institution of higher education as medical education has been, and continues to be, a priority for medical colleges in Saudi Arabia. This study aimed to assess faculty members’ perc
Externí odkaz:
https://doaj.org/article/e92fc6dfa3fc4a19ad1b4acfcb48c010
Publikováno v:
Epilepsy and Behavior Case Reports, Vol 10, Iss , Pp 1-3 (2018)
Lacosamide is one of the third-generation antiseizure drugs that block voltage-gated sodium channels by enhancing slow inactivation. The most common adverse effects of lacosamide include dizziness, headache, nausea, vomiting, diplopia, fatigue, and s
Externí odkaz:
https://doaj.org/article/5dbca0cc936844d582558afd111a3ad7
Publikováno v:
Case Reports in Medicine, Vol 2017 (2017)
Harlequin syndrome is a rare autonomic disorder characterized by unilateral facial flushing and sweating with contralateral anhidrosis induced by exercise, heat, and emotion. It is usually idiopathic but could be the first manifestation of several se
Externí odkaz:
https://doaj.org/article/38d3ce1f52e94914bcc4b9e9ad8e7b83
Publikováno v:
Case Reports in Infectious Diseases, Vol 2017 (2017)
Brucellosis is a zoonotic bacterial infection which is transmitted to humans from infected animals and is endemic in many parts of the world including Saudi Arabia. In this article, we report a case of occupational neurobrucellosis that presented wit
Externí odkaz:
https://doaj.org/article/363b9f47f0754abb8199b2c8257c8079
Autor:
Raghad Algahtani, Bader Shirah, Muhammad Imran Naseer, Mohammad H. Al-Qahtani, Angham Abdulrahman Abdulkareem, Hussein Algahtani
Publikováno v:
International Journal of Neuroscience. 131:206-211
Ataxia telangiectasia is a hereditary multisystem disorder with a wide range of symptoms and signs. It is inherited in an autosomal recessive manner due to a mutation in the ataxia telangiectasia m...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::060dfaff36f373222d2b7c21648f5cbe
https://doi.org/10.1080/00207454.2020.1736582
https://doi.org/10.1080/00207454.2020.1736582
Publikováno v:
Neurosciences
Hashimoto`s encephalopathy is a rare neurological syndrome occurring in patients with autoimmune thyroid disease. The diagnosis of Hashimoto`s encephalopathy is based on the clinical picture with the presence of serum anti-thyroid antibodies regardle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8135b7f3d2172fbd44a21d7fdd136743
https://doi.org/10.17712/nsj.2019.4.20190016
https://doi.org/10.17712/nsj.2019.4.20190016
Autor:
Bader Shirah, Mohammad H. Al-Qahtani, Angham Abdulrahman Abdulkareem, Hussein Algahtani, Muhammad Imran Naseer, Raghad Algahtani
Publikováno v:
Intractable & Rare Diseases Research. 8:142-145
Titin (TTN) is a large gene with 363 exons that encodes a large abundant protein (longest known polypeptide in nature) that is expressed in cardiac and skeletal muscles. TTN has an important role in the sarcomere organization, assembly of muscles, tr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::592091b67b63e04723b1c03c22ad905f
https://doi.org/10.5582/irdr.2019.01052
https://doi.org/10.5582/irdr.2019.01052
Autor:
Raghad Algahtani, Mohammad H. Al-Qahtani, Angham Abdulrahman Abdulkareem, Hussein Algahtani, Bader Shirah, Muhammad Imran Naseer
Publikováno v:
Intractable & Rare Diseases Research. 8:67-71
Episodic ataxia is a genetically heterogeneous neurological condition characterized by spells of incoordination and imbalance, often associated with progressive ataxia. Episodic ataxia type 2, caused by calcium voltage-gated channel subunit alpha1 A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b0320ce0f3d5ecd32edde84669dfa21
https://doi.org/10.5582/irdr.2018.01133
https://doi.org/10.5582/irdr.2018.01133
Autor:
Hussein, Algahtani, Bader, Shirah, Raghad, Algahtani, Mohammad H, Al-Qahtani, Angham Abdulrahman, Abdulkareem, Muhammad Imran, Naseer
Publikováno v:
The International journal of neuroscience. 131(2)
Ataxia telangiectasia is a hereditary multisystem disorder with a wide range of symptoms and signs. It is inherited in an autosomal recessive manner due to a mutation in the ataxia telangiectasia mutated (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::440f5e3405e187fc718216acc87a1d59
https://pubmed.ncbi.nlm.nih.gov/32172615
https://pubmed.ncbi.nlm.nih.gov/32172615
Autor:
Raghad Algahtani, Bader Shirah, Muhammad Imran Naseer, Mohammad H. Al-Qahtani, Angham Abdulrahman Abdulkareem, Hussein Algahtani
Publikováno v:
Intractable & Rare Diseases Research. 7:275-279
Ataxia with ocular apraxia type 2 is an autosomal recessive disorder caused by a mutation in the senataxin (SETX) gene. The disease is characterized by early onset cerebellar ataxia, cerebellar atrophy, axonal sensorimotor neuropathy, oculomotor apra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8b20bd6fc0445c9959d0c40f869ee9bb
https://doi.org/10.5582/irdr.2018.01107
https://doi.org/10.5582/irdr.2018.01107