Zobrazeno 1 - 4
of 4
pro vyhledávání: '"AlThihli, Khalid"'
Publikováno v:
Sultan Qaboos University Medical Journal
Propionic acidaemia (PPA) is a disorder of amino acid and odd-chain fatty acid metabolism. Hypoglycaemia is a more commonly described finding rather than hyperglycaemia during metabolic decompensation of PPA. There is a high mortality rate in patient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::829f0aa3cb2d00b505d899ba37ff7ee6
http://europepmc.org/articles/PMC8631204
http://europepmc.org/articles/PMC8631204
Autor:
Almannai, Mohammed, Felemban, Rana, Saleh, Mohammed A, Faqeih, Eissa A, Alasmari, Ali, AlHashem, Amal, Mohamed, Sarar, Sunbul, Rawda, Al-Murshedi, Fathiya, AlThihli, Khalid, Eyaid, Wafaa, Ali, Rehab, Ben-Omran, Tawfeg, Blau, Nenad, El-Hattab, Ayman W, Alfadhel, Majid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______885::461047d2bb3339fbcb9ce24bf1a365c5
https://doi.org/10.5167/uzh-180681
https://doi.org/10.5167/uzh-180681
Autor:
AlThihli, Khalid, Rudkin, Teresa, Carson, Nancy, Poulin, Chantal, Melançon, Serge, Der Kaloustian, Vazken M.
Publikováno v:
American Journal of Medical Genetics. Part A; September 2008, Vol. 146 Issue: 18 p2412-2416, 5p
Autor:
Almannai M; Section of Medical Genetics, Children's Hospital, King Fahad Medical City, Riyadh, Saudi Arabia., Felemban R; Section of Medical Genetics, Children's Hospital, King Fahad Medical City, Riyadh, Saudi Arabia., Saleh MA; Section of Medical Genetics, Children's Hospital, King Fahad Medical City, Riyadh, Saudi Arabia., Faqeih EA; Section of Medical Genetics, Children's Hospital, King Fahad Medical City, Riyadh, Saudi Arabia., Alasmari A; Section of Medical Genetics, Children's Hospital, King Fahad Medical City, Riyadh, Saudi Arabia., AlHashem A; Department of Pediatric, Prince Sultan Medical Military City, Riyadh, Saudi Arabia; Department of Anatomy and Cell Biology, College of Medicine, Alfaisal University, Riyadh, Saudi Arabia., Mohamed S; Department of Pediatric, Prince Sultan Medical Military City, Riyadh, Saudi Arabia., Sunbul R; Pediatrics Medical Genetic Unit (PMGU), Pediatrics Department, Qatif Central Hospital, Qatif, Saudi Arabia., Al-Murshedi F; Department of Genetics, College of Medicine, Sultan Qaboos University, Muscat, Sultanate of Oman., AlThihli K; Department of Genetics, College of Medicine, Sultan Qaboos University, Muscat, Sultanate of Oman., Eyaid W; Division of Genetics, Department of Pediatrics, King Abdulaziz Medical City, Ministry of National Guard-Health Affairs (MNGHA), Riyadh, Saudi Arabia., Ali R; Clinical and Metabolic Genetics Section, Department of Pediatrics, Hamad Medical Corporation, Doha, Qatar., Ben-Omran T; Clinical and Metabolic Genetics Section, Department of Pediatrics, Hamad Medical Corporation, Doha, Qatar., Blau N; Dietmar-Hopp-Metabolic Center, University Children's Hospital, Heidelberg, Germany; Division of Metabolism, University Children's Hospital Zurich, Switzerland., El-Hattab AW; Department of Clinical Sciences, College of Medicine, University of Sharjah, Sharjah, United Arab Emirates; Genetics Clinics, KidsHeart Medical Center, Dubai, United Arab Emirates., Alfadhel M; Division of Genetics, Department of Pediatrics, King Abdulaziz Medical City, Ministry of National Guard-Health Affairs (MNGHA), Riyadh, Saudi Arabia; King Abdullah International Medical Research Center (KAIMRC), Riyadh, Saudi Arabia; College of Medicine, King Saud Bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia. Electronic address: dralfadhelm@gmail.com.
Publikováno v:
Pediatric neurology [Pediatr Neurol] 2019 Jul; Vol. 96, pp. 40-47. Date of Electronic Publication: 2019 Feb 18.