Zobrazeno 1 - 10
of 64
pro vyhledávání: '"Ibrahim A, Alorainy"'
Autor:
Farid Alzhrani, Hassan Alassiry, Ibrahim A Alorainy, Fahad B Albadr, Yassin Abdulsamad, Ahmad Aldhaferi
Publikováno v:
Journal of Nature and Science of Medicine, Vol 5, Iss 1, Pp 40-43 (2022)
Objectives: Cochlear implantation provides significant benefits to patients with postmeningitis deafness; however, the prediction of the outcome is difficult. Therefore, the goal was to investigate whether there is a correlation between cochlear impl
Externí odkaz:
https://doaj.org/article/deacf5fd06c64fc896b6c16cac274bcf
Autor:
Malak Ali Alghamdi, Hicham Benabdelkamel, Afshan Masood, Narjes Saheb Sharif-Askari, Mahmood Y. Hachim, Hamad Alsheikh, Muddathir H. Hamad, Mustafa A. Salih, Fahad A. Bashiri, Khalid Alhasan, Tarek Kashour, Pilar Guatibonza Moreno, Sabine Schröder, Vasiliki Karageorgou, Aida M. Bertoli-Avella, Hisham Alkhalidi, Dima Z. Jamjoom, Ibrahim A. Alorainy, Assim A. Alfadda, Rabih Halwani
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Galloway-Mowat syndrome is a rare autosomal recessive disease characterized by a unique combination of renal and neurological manifestations, including early-onset steroid-resistant nephrotic syndrome, microcephaly, psychomotor delay, and gyral abnor
Externí odkaz:
https://doaj.org/article/8db6644c11c4473ea480bba4e547fa50
Autor:
Mustafa A. Salih, Muddathir H. Hamad, Marco Savarese, Ibrahim A. Alorainy, Abdullah S. Al-Jarallah, Hisham Alkhalidi, Hanan AlQudairy, Anoud Albader, Amal Jahz Alotaibi, Maysoon Alsagob, Albandary Al-Bakheet, Dilek Colak, Bjarne Udd, Namik Kaya
Publikováno v:
Genetic Testing and Molecular Biomarkers. 25:757-764
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::10dd34776b6b84cac76c375a9a086b10
https://doi.org/10.1089/gtmb.2021.0085
https://doi.org/10.1089/gtmb.2021.0085
Publikováno v:
Aljouf University Medical Journal. 7:29-36
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::60e1d8d1be6190dffc86c4174c1e1b43
https://doi.org/10.12816/0056998
https://doi.org/10.12816/0056998
Publikováno v:
Indian Journal of Radiology and Imaging, Vol 20, Iss 03, Pp 174-181 (2010)
About 3 to 10% of pregnancies are complicated by glycemic control abnormalities. Maternal diabetes results in significantly greater risk for antenatal, perinatal, and neonatal morbidity and mortality, as well as congenital malformations. The number o
Externí odkaz:
https://doaj.org/article/8f228db8449843758208cec1cfc58b52
Publikováno v:
Journal of Family and Community Medicine, Vol 17, Iss 2, Pp 96-102 (2010)
This paper is an attempt to produce a guide for improving the quality of Multiple Choice Questions (MCQs) used in undergraduate and postgraduate assessment. Multiple Choice Questions type is the most frequently used type of assessment worldwide. Well
Externí odkaz:
https://doaj.org/article/96aba1d307c94b859af269a3ba8a86a5
Publikováno v:
The American Journal of Case Reports
Patient: Female, 32 Final Diagnosis: Progressive multifocal leukoencephalopathy Symptoms: Progressive behavioral changes • seizures Medication: — Clinical Procedure: Management Specialty: Neurology Objective: Rare disease Background: Progressive
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01b8711d75bfd356ac86b3f511c64885
https://doi.org/10.12659/ajcr.911521
https://doi.org/10.12659/ajcr.911521
Autor:
Abdulmajeed AlDrees, Jumanah Al-Sufayan, Albandary Al-Bakheet, Salah A. Elmalik, Ibrahim A. Alorainy, Mohammed Zain Seidahmed, Dilek Colak, Namik Kaya, Ibrahim M. Ghozzi, Muddathir H. Hamad, Mustafa A. Salih
Publikováno v:
BMC Neurology
BMC Neurology, Vol 20, Iss 1, Pp 1-7 (2020)
BMC Neurology, Vol 20, Iss 1, Pp 1-7 (2020)
Background Homozygous frameshift mutation in RUBCN (KIAA0226), known to result in endolysosomal machinery defects, has previously been reported in a single Saudi family with autosomal recessive spinocerebellar ataxia (Salih ataxia, SCAR15, OMIM # 615
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6c5e1d242fc34c7e335c4a179becd38
https://doi.org/10.1186/s12883-020-01761-w
https://doi.org/10.1186/s12883-020-01761-w
Autor:
Nicholas W. Wood, Saif Alshahrani, Dilek Colak, Michael C. Kruer, Kshitij Mankad, Zuhair Rahbeeni, Rozeena Huma, Khushnooda Ramzan, Rawan Almass, Stanislav Groppa, Moeenaldeen Al-Sayed, Indran Davagnanam, Fuad Almutairi, Maha S Al-Shammari, Maria Puiu, E Ghayoor Karimiani, N. Kaya, Stephanie Efthymiou, Nourelhoda A Haridy, M Beiraghi Toosi, Alya Qari, Muddathir H. Hamad, Mustafa A. Salih, Maysoon Alsagob, Somayeh Bakhtiari, Jessika Johannsen, Tatjana Bierhals, Reza Maroofian, Katja Kloth, Adela Chirita-Emandi, Henry Houlden, N T Malintan, Faiqa Imtiaz, Ibrahim A. Alorainy, Jana Vandrovcova, Laila AlQuait, Hamad Al-Zaidan, Viorica Chelban
Publikováno v:
European Journal of Neurology
Background and purpose\ud Hypomyelinating leukodystrophies are a heterogeneous group of genetic disorders with a wide spectrum of phenotypes and a high rate of genetically unsolved cases. Bi‐allelic mutations in NKX6‐2 were recently linked to spa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a074b70a1bf1d6a7a437cc5a7084b5ca
https://openaccess.sgul.ac.uk/id/eprint/111215/6/Chelban_et_al-2019-European_Journal_of_Neurology.pdf
https://openaccess.sgul.ac.uk/id/eprint/111215/6/Chelban_et_al-2019-European_Journal_of_Neurology.pdf
Autor:
May L. Griebel, Klaus Schmitz-Abe, Anh Thu N. Lam, Abdullah Abu Jamea, Caroline D. Robson, Mauricio R. Delgado, Sarah Servattalab, Mohammad Asif Dogar, Ibrahim A. Alorainy, A. James Barkovich, Maya Peeva, Saumya Shekhar Jamuar, Marie Drottar, Kyriacos Markianos, Khaled K. Abu-Amero, Zayed Al Zayed, Elizabeth C. Engle, P. Ellen Grant, Alissa M. D'Gama, Wai-Man Chan, Christopher A. Walsh, Nancy J. Clegg, Ed S. Lein, Timothy W. Yu, Wendy L. Ward, Thomas M. Bosley
Publikováno v:
Nature genetics
Motor, sensory, and integrative activities of the brain are coordinated by a series of midline-bridging neuronal commissures whose development is tightly regulated. Here we report a new human syndrome in which these commissures are widely disrupted,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::810f6d374273cf3a5e7ec3c2d4ae6bab
https://doi.org/10.1038/ng.3804
https://doi.org/10.1038/ng.3804