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1دورية أكاديمية
المؤلفون: Betzler, SB, Koh, AL, Lotsch, BV, Sinclair, R, Scheu, C
المصدر: ACS Applied Nano Materials. 3(9)
مصطلحات موضوعية: environmental TEM, solid-state oxidation, dislocation-mediated transformation, niobium oxide, crystal defects
وصف الملف: application/pdf
URL الوصول: https://escholarship.org/uc/item/85w5v3pm
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2دورية أكاديمية
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3دورية أكاديمية
المؤلفون: Stockman, Alan C., Koh, Al Tee
المصدر: Canadian Journal of Economics; Feb86, Vol. 19 Issue 1, p23, 12p
مصطلحات موضوعية: LABOR contracts, WAGE payment systems, FOREIGN exchange rates, BALANCE of trade
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4دورية أكاديمية
المؤلفون: Sinclair, R, Koh, AL, Kempen, P, Jung, HJ
المصدر: Microscopy & Microanalysis; Jul2009 Supplement 2, Vol. 15 Issue S2, p1200-1201, 2p
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5دورية أكاديمية
المؤلفون: Koh, AL, Watanabe, M, Sinclair, R
المصدر: Microscopy & Microanalysis; Jul2009 Supplement 2, Vol. 15 Issue S2, p432-433, 2p
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6دورية أكاديمية
المؤلفون: Cheng DT; Respiratory Medicine Service, Department of Paediatrics, KK Women's and Children's Hospital, Singapore.; Paediatric Academic Clinical Programme, Duke-NUS Medical School, Singapore., Yeo TH; Paediatric Academic Clinical Programme, Duke-NUS Medical School, Singapore.; Neurology Service, Department of Paediatrics, KK Women's and Children's Hospital, Singapore., Seng MS; Paediatric Academic Clinical Programme, Duke-NUS Medical School, Singapore.; Haematology/Oncology Service, Department of Paediatrics, KK Women's and Children's Hospital, Singapore., Teoh OH; Respiratory Medicine Service, Department of Paediatrics, KK Women's and Children's Hospital, Singapore.; Paediatric Academic Clinical Programme, Duke-NUS Medical School, Singapore., Lee S; Paediatric Anaesthesia Service, KK Women's and Children's Hospital, Singapore., Koh AL; Paediatric Academic Clinical Programme, Duke-NUS Medical School, Singapore.; Genetics Service, Department of Paediatrics, KK Women's and Children's Hospital, Singapore.
المصدر: Singapore medical journal [Singapore Med J] 2024 Jun 28. Date of Electronic Publication: 2024 Jun 28.
نوع المنشور: Journal Article
بيانات الدورية: Publisher: Wolters Kluwer - Medknow Country of Publication: India NLM ID: 0404516 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2737-5935 (Electronic) Linking ISSN: 00375675 NLM ISO Abbreviation: Singapore Med J Subsets: MEDLINE
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7تقرير
المؤلفون: Yap JYC; Nephrology Service, Department of Pediatrics, KK Women's and Children's Hospital, Singapore, Singapore.; Pediatric Academic Clinical Programme, Duke-NUS Medical School, Singapore, Singapore., Lim JY; Pediatric Academic Clinical Programme, Duke-NUS Medical School, Singapore, Singapore.; Genetics Service, Department of Pediatrics, KK Women's and Children's Hospital, Singapore, Singapore., Bhatia A; Department of Maternal-Fetal Medicine, KK Women's and Children's Hospital, Singapore, Singapore., Tan VKJ; Department of Maternal-Fetal Medicine, KK Women's and Children's Hospital, Singapore, Singapore., Koo S; Pediatric Academic Clinical Programme, Duke-NUS Medical School, Singapore, Singapore.; KK Research Centre, KK Women's and Children's Hospital, Singapore, Singapore., Nishimura G; Department of Radiology, Musashino-Yowakai Hospital, Tokyo, Japan., Moosa S; Faculty of Medicine and Health Sciences, Division of Molecular Biology and Human Genetics, Stellenbosch University, Cape Town, South Africa.; Department of Medical Genetics, Tygerberg Hospital, Cape Town, South Africa., Koh AL; Pediatric Academic Clinical Programme, Duke-NUS Medical School, Singapore, Singapore.; Genetics Service, Department of Pediatrics, KK Women's and Children's Hospital, Singapore, Singapore., Tan EC; Pediatric Academic Clinical Programme, Duke-NUS Medical School, Singapore, Singapore.; Department of Maternal-Fetal Medicine, KK Women's and Children's Hospital, Singapore, Singapore., Fong N; Pediatric Academic Clinical Programme, Duke-NUS Medical School, Singapore, Singapore.; Genetics Service, Department of Pediatrics, KK Women's and Children's Hospital, Singapore, Singapore., Jamuar SS; Pediatric Academic Clinical Programme, Duke-NUS Medical School, Singapore, Singapore.; Genetics Service, Department of Pediatrics, KK Women's and Children's Hospital, Singapore, Singapore.
المصدر: American journal of medical genetics. Part A [Am J Med Genet A] 2024 Feb; Vol. 194 (2), pp. 358-362. Date of Electronic Publication: 2023 Oct 06.
نوع المنشور: Case Reports; Research Support, Non-U.S. Gov't
بيانات الدورية: Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE
مواضيع طبية MeSH: Osteogenesis Imperfecta*/genetics , Hyperostosis, Cortical, Congenital* , Fetal Diseases*, Infant, Newborn ; Humans ; Female ; Pregnancy ; Mutation ; Membrane Proteins/genetics ; Collagen Type I/genetics ; Bone and Bones/pathology
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8دورية أكاديمية
المؤلفون: Heng TYJ; Department of Paediatrics, KK Women's and Children's Hospital., Ow JR; Institute of Molecular and Cell Biology (IMCB), Agency for Science, Technology and Research (A*STAR)., Koh AL; Genetics Service, Department of Paediatrics, KK Women's and Children's Hospital.; SingHealth Duke-NUS Paediatric Academic Clinical Programme, Duke-NUS Medical School., Lim JSC; Biochemical Genetics and National Expanded Newborn Screening, Department of Pathology and Laboratory Medicine, KK Women's and Children's Hospital., Ong CBK; Department of Nutrition and Dietetics, KK Women's and Children's Hospital., Goh JCY; Division of Nursing - Nursing Clinical Services, KK Women's and Children's Hospital., Lim JY; Genetics Service, Department of Paediatrics, KK Women's and Children's Hospital., Chiou FK; SingHealth Duke-NUS Paediatric Academic Clinical Programme, Duke-NUS Medical School.; Gastroenterology, Hepatology & Nutrition Service, Department of Paediatrics, KK Women's and Children's Hospital., Jamuar SS; Genetics Service, Department of Paediatrics, KK Women's and Children's Hospital.; SingHealth Duke-NUS Paediatric Academic Clinical Programme, Duke-NUS Medical School.; SingHealth Duke-NUS Institute of Precision Medicine, National Heart Centre Singapore, Republic of Singapore.
المصدر: Clinical dysmorphology [Clin Dysmorphol] 2024 Jan 01; Vol. 33 (1), pp. 43-49. Date of Electronic Publication: 2023 Oct 13.
نوع المنشور: Case Reports; Journal Article
بيانات الدورية: Publisher: Lippincott Williams & Wilkins Country of Publication: England NLM ID: 9207893 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1473-5717 (Electronic) Linking ISSN: 09628827 NLM ISO Abbreviation: Clin Dysmorphol Subsets: MEDLINE
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9دورية أكاديمية
المؤلفون: Leow EH; Nephrology Service, Department of Paediatrics, KK Women's and Children's Hospital, Singapore, Singapore., Chong SL; Nephrology Service, Department of Paediatrics, KK Women's and Children's Hospital, Singapore, Singapore., Tan ES; Genetics Service, Department of Paediatrics, KK Women's and Children's Hospital, Singapore, Singapore., Koh AL; Genetics Service, Department of Paediatrics, KK Women's and Children's Hospital, Singapore, Singapore., Cham BWM; Genetics Service, Department of Paediatrics, KK Women's and Children's Hospital, Singapore, Singapore., Yap CJY; Nephrology Service, Department of Paediatrics, KK Women's and Children's Hospital, Singapore, Singapore., Ng YH; Nephrology Service, Department of Paediatrics, KK Women's and Children's Hospital, Singapore, Singapore.
المصدر: Nephrology (Carlton, Vic.) [Nephrology (Carlton)] 2023 Dec; Vol. 28 (12), pp. 649-654. Date of Electronic Publication: 2023 Aug 24.
نوع المنشور: Case Reports; Journal Article; Review
بيانات الدورية: Publisher: Blackwell Science Country of Publication: Australia NLM ID: 9615568 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1440-1797 (Electronic) Linking ISSN: 13205358 NLM ISO Abbreviation: Nephrology (Carlton) Subsets: MEDLINE
مواضيع طبية MeSH: Microscopy* , Urolithiasis*/diagnosis , Urolithiasis*/genetics, Child ; Humans ; Male ; Adenine/therapeutic use ; Adenine/urine ; Adenine Phosphoribosyltransferase/genetics ; Adenine Phosphoribosyltransferase/urine ; Urinalysis
SCR Disease Name: Adenine phosphoribosyltransferase deficiency
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10دورية أكاديمية
المؤلفون: Wong MST; Lee Kong Chian School of Medicine, Nanyang Technological University., Thomas T; Neurology Service, Department of Paediatrics, KK Women's and Children's Hospital.; SingHealth Duke-NUS Paediatric Academic Clinical Programme., Lim JY; SingHealth Duke-NUS Paediatric Academic Clinical Programme.; Genetics Service, Department of Paediatrics, KK Women's and Children's Hospital.; SingHealth Duke-NUS Genomic Medicine Centre., Kam S; SingHealth Duke-NUS Paediatric Academic Clinical Programme.; Genetics Service, Department of Paediatrics, KK Women's and Children's Hospital.; SingHealth Duke-NUS Genomic Medicine Centre., Teo JX; SingHealth Duke-NUS Institute of Precision Medicine., Ching J; Cardiovascular and Metabolic Disorders Programme, Duke-NUS Medical School.; KK Research Centre, KK Women's and Children's Hospital., Goh CYJ; Division of Nursing - Nursing Clinical Services, Genetics Specialty Nurse, KK Women's and Children's Hospital, Singapore, Singapore., Jamuar SS; Lee Kong Chian School of Medicine, Nanyang Technological University.; SingHealth Duke-NUS Paediatric Academic Clinical Programme.; Genetics Service, Department of Paediatrics, KK Women's and Children's Hospital.; SingHealth Duke-NUS Genomic Medicine Centre.; SingHealth Duke-NUS Institute of Precision Medicine., Lim WK; SingHealth Duke-NUS Genomic Medicine Centre.; SingHealth Duke-NUS Institute of Precision Medicine., Koh AL; Lee Kong Chian School of Medicine, Nanyang Technological University.; SingHealth Duke-NUS Paediatric Academic Clinical Programme.; Genetics Service, Department of Paediatrics, KK Women's and Children's Hospital.; SingHealth Duke-NUS Genomic Medicine Centre.
المصدر: Clinical dysmorphology [Clin Dysmorphol] 2023 Jul 01; Vol. 32 (3), pp. 106-111. Date of Electronic Publication: 2023 May 01.
نوع المنشور: Review; Journal Article
بيانات الدورية: Publisher: Lippincott Williams & Wilkins Country of Publication: England NLM ID: 9207893 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1473-5717 (Electronic) Linking ISSN: 09628827 NLM ISO Abbreviation: Clin Dysmorphol Subsets: MEDLINE
مواضيع طبية MeSH: Ceramides* , Neurodegenerative Diseases*/pathology, Humans ; Brain/diagnostic imaging ; Brain/pathology ; Mutation, Missense ; Seizures/pathology