Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Sunbul, Rawda"'
Akademický článek
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Akademický článek
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Autor:
Germain, Dominique P., Al Murshedi, Fathiya, Al Jasmi, Fatma, Altarescu, Gheona, Azevedo, Olga, Barreto, Fellype C., Ezgu, Fatih, Laney, Dawn A., Moiseev, Sergey, Nochioka, Kotaro, Ouyang, Yan, Onay, Huseyin, Pavlou, Mary, Pachter, Nicholas, Politei, Juan, Sunbul, Rawda, Steeds, Rick, Yu, Wen-Chung, West, Michael L., Maski, Manish, Maksimova, Irina
Publikováno v:
In Molecular Genetics and Metabolism February 2024 141(2)
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
Akademický článek
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Autor:
Benke, Paul J, Hidalgo, Ryan J, Braffman, Bruce H, Jans, Judith, van Gassen, Koen L I, Sunbul, Rawda, El-Hattab, Ayman W
Publikováno v:
Journal of child neurology, 32(6), 543. SAGE Publications Inc.
Serine biosynthesis defects can present in a broad phenotypic spectrum ranging from Neu-Laxova syndrome, a lethal disease with multiple congenital anomalies at the severe end, to an infantile disease with severe psychomotor retardation and seizures a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::4a4fcaa00f1fd8183442223f384a3cc4
https://dspace.library.uu.nl/handle/1874/349171
https://dspace.library.uu.nl/handle/1874/349171
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
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.
Autor:
Benke PJ; 1 Joe DiMaggio Children's Hospital, Hollywood, FL, USA.; 2 Florida Atlantic University Charles E. Schmidt College of Medicine, Boca Raton, FL, USA., Hidalgo RJ; 2 Florida Atlantic University Charles E. Schmidt College of Medicine, Boca Raton, FL, USA., Braffman BH; 3 Department of Radiology, Memorial Healthcare System, Hollywood, FL, USA., Jans J; 4 Department of Genetics, University Medical Centre Utrecht, Utrecht, the Netherlands., Gassen KLIV; 4 Department of Genetics, University Medical Centre Utrecht, Utrecht, the Netherlands., Sunbul R; 5 Pediatrics Medical Genetic Unit (PMGU), Pediatrics Department, Qatif Central Hospital, Qatif, Saudi Arabia., El-Hattab AW; 6 Division of Clinical Genetics and Metabolic Disorders, Pediatrics Department, Tawam Hospital, Al-Ain, United Arab Emirates.
Publikováno v:
Journal of child neurology [J Child Neurol] 2017 May; Vol. 32 (6), pp. 543-549. Date of Electronic Publication: 2017 Jan 31.