Zobrazeno 1 - 10
of 244
pro vyhledávání: '"Al-Odaib A"'
Autor:
Sakati Nadia, Al-Odaib Ali, Al-Habit Ola, Colak Dilek, Alshidi Tarfa A, AbuDheim Nada, Al-Dosari Naji, Al-Zahrani Jawaher, Meyer Brian, Ozand Pinar T, Kaya Namik
Publikováno v:
Molecular Cytogenetics, Vol 4, Iss 1, p 9 (2011)
Abstract Background Genomic imbalances of the 12q telomere are rare; only a few patients having 12q24.31-q24.33 deletions were reported. Interestingly none of these were mosaic. Although some attempts have been made to establish phenotype/genotype in
Externí odkaz:
https://doaj.org/article/7ed7c61239bb44c590e4a86801bd1ce2
Autor:
Daghestani Maha H, Warsy Arjumand, Daghestani Mazin H, Al-odaib Ali N, Eldali Abdelmoneim, Al-Eisa Nadia A, Al-zhrani Sabah
Publikováno v:
Lipids in Health and Disease, Vol 9, Iss 1, p 90 (2010)
Abstract Background β2-adrenoceptor (β2AR) gene polymorphism glutamine 27 glutamic acid (Gln27Glu) and Arg16Gly were reported to have an association with obesity and obesity related disorders in some population. We evaluated Gln27Glu polymorphism i
Externí odkaz:
https://doaj.org/article/8e6c8c8359f74efda123493b33bb4c0e
Autor:
Majid Alfadhel, Muhammad Umair, Bader Almuzzaini, Saif Alsaif, Sulaiman A. AlMohaimeed, Maher A. Almashary, Wardah Alharbi, Latifah Alayyar, Abdulrahman Alasiri, Mariam Ballow, Abdulkareem AlAbdulrahman, Monira Alaujan, Marwan Nashabat, Ali Al‐Odaib, Waleed Altwaijri, Ahmed Al‐Rumayyan, Muhammad T. Alrifai, Ahmed Alfares, Mohammed AlBalwi, Brahim Tabarki
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 6, Iss 10, Pp 2097-2103 (2019)
Abstract Background Biotin–thiamine‐responsive basal ganglia disease (BTBGD) is an autosomal recessive neurometabolic disorder mostly presented in children. The disorder is described as having subacute encephalopathy with confusion, dystonia, and
Externí odkaz:
https://doaj.org/article/96e539f8f7c14fda9b2b9706c9f85dd7
Autor:
Guo, Yiran, Kartawinata, Melissa, Li, Jiankang, Pickett, Hilda A., Teo, Juliana, Kilo, Tatjana, Barbaro, Pasquale M., Keating, Brendan, Chen, Yulan, Tian, Lifeng, Al-Odaib, Ahmad, Reddel, Roger R., Christodoulou, John, Xu, Xun, Hakonarson, Hakon *, Bryan, Tracy M. *
Publikováno v:
In Blood 30 October 2014 124(18):2767-2774
Incidence of newborn screening disorders among 56632 infants in Central Saudi Arabia. A 6-year study
Autor:
Sulaiman A. AlMohaimeed, Amer N. Ammari, Maher Almashary, Lujane Alahaideb, Amal Alhashem, Fahad M. Alharbi, Horia AlMalawi, Aida I. Al-Aqeel, Wafa Elsheikh, Sarar Mohamed, Ali Al-Odaib
Publikováno v:
Saudi Medical Journal, Vol 41, Iss 7, Pp 703-708 (2020)
Objectives: To determine the incidence of newborn screening (NBS) disorders and to study the key performance indicators of the program. Methods: This retrospective single-center study enrolled all infants who underwent NBS from January 2012 to Decemb
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8996ee55aa8368dfa7c3f2468a31b03
https://smj.org.sa/index.php/smj/article/view/smj.2020.7.25147/12069
https://smj.org.sa/index.php/smj/article/view/smj.2020.7.25147/12069
Autor:
Alquraini, Turki1, Al-Odaib, Ali2, Al-Dhalaan, Hesham2, Merza, Haniah1, Mahoney, Gerald3 gjm14@case.edu
Publikováno v:
International Journal of Disability, Development & Education. May2019, Vol. 66 Issue 3, p233-248. 16p. 4 Charts, 2 Graphs.
Autor:
Faten Almutairi, Tarek Mustafa Owaidah, Najmeh Ahangari, Nada Al-Ahmadi, Leslie E. Sanderson, Henry Houlden, Romulo Mombach, Mazhor Al-Dosary, Anoud Abdulmalik Albader, Banan Al-Younes, Osama M. Mustafa, Tainá Regina Damaceno Silveira, Dilek Colak, Namik Kaya, Miriam Schmidts, Hazem Ghebeh, Herma C. van der Linde, Robin Palvadeau, Aida M. Bertoli-Avella, Raghda M Sabbagh, Rawan Almass, Hesham Aldhalaan, Maryam Najafi, Bashayer Alawam, Aljouhra AlHargan, Kristina Lanko, Aljohara Alharbi, Maysoon Alsagob, Bedri Karakas, Reza Maroofian, A. Nazli Basak, Khalid AlAhmadi, Ali Al-Odaib, Arndt Rolfs, Mohammad A. Al-Muhaizea, Elena Perenthaler, Najim Ameziane, Dinu Antony, Futwan Al-Mohanna, Albandary Al-Bakheet, Faisal S. BinHumaid, Anita Nikoncuk, Nikolas A Kühn, Dorota Monies, Ehsan Ghayoor Karimiani, Hamad Al-Zaidan, Tjakko J. van Ham, Ewa Goljan, Luana Gabriela Dalla Rosa Vieira, Jill A. Rosenfeld, Salmo Raskin, Dürdane Aksoy, Brian F. Meyer, Tahsin Stefan Barakat, Daniah Trabzuni, Stefan T. Arold
Publikováno v:
Brain, 144(3), 769-780. Oxford University Press
Brain
Brain
Membrane trafficking is a complex, essential process in eukaryotic cells responsible for protein transport and processing. Deficiencies in vacuolar protein sorting (VPS) proteins, key regulators of trafficking, cause abnormal intracellular segregatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3829cf3b4e450f526ad567f2a5f9dda5
https://pure.eur.nl/en/publications/e4916caa-5909-4a69-8c0c-11eb8621c0a0
https://pure.eur.nl/en/publications/e4916caa-5909-4a69-8c0c-11eb8621c0a0
Autor:
Colak, Dilek, Al-Dhalaan, Hesham, Nester, Michael, AlBakheet, AlBandary, Al-Younes, Banan, Al-Hassnan, Zohair, Al-Dosari, Mohammad, Chedrawi, Aziza, Al-Owain, Muhammad, AbuDheim, Nada, Al-Alwan, Laila, Al-Odaib, Ali, Ozand, Pinar, Inan, Mehmet Sait, Kaya, Namik
Publikováno v:
In Genomics 2011 97(1):19-28
Autor:
Kaya, Namik *, Imtiaz, Faiqa, Colak, Dilek, Al-Sayed, Moeenaldeen, Al-Odaib, Ali, Al-Zahrani, Fatma, Al-Mubarak, Bashayer R., Al-Owain, Mohammad, Al-Dhalaan, Hesham, Chedrawi, Aziza, Al-Hassnan, Zuhair, Coskun, Serdar, Sakati, Nadia, Ozand, Pinar, Meyer, Brian F.
Publikováno v:
In Genetics in Medicine September 2008 10(9):675-684
Autor:
Kaya, Namik, Al-Owain, Mohammad, AlBakheet, AlBandary, Colak, Dilek, Al-Odaib, Ali, Imtiaz, Faiqa, Coskun, Serdar, Al-Sayed, Moeenaldeen, Al-Hassnan, Zuhair, Al-Zaidan, Hamad, Meyer, Brian, Ozand, Pinar
Publikováno v:
In European Journal of Medical Genetics 2008 51(6):558-565