المؤلفون: Wilke, Matheus V. M. B., De Kleine, Ruben H., Wietasch, J.K.G., Van Amerongen, Cynthia C. A., Blokzijl, Hans, Van Spronsen, Francjan J., Schwartz, Ida V. D., Derks, Terry G. J.

المصدر: Wilke , M V M B , De Kleine , R H , Wietasch , J K G , Van Amerongen , C C A , Blokzijl , H , Van Spronsen , F J , Schwartz , I V D & Derks , T G J 2016 , ' Orthotopic liver transplantation in glycogen storage disease type la: Perioperative glucose and lactate homeostasis ' , Journal of Inborn Errors of Metabolism and Screening , vol. 4 . https://doi.org/10.1177/2326409816649599Test

مصطلحات موضوعية: Familial amyloid polyneuropathy, Glucose blood, Glycogen storage disease type la, Hypoglycemia, Lactic acidemia, Liver transplantation, glucose, lactic acid, adult, article, bleeding, carbohydrate intake, clinical article, controlled study, female, glucose homeostasis, glycogen storage disease type 1, glycogen storage disease type 1a, human, lactic acidosis, male, priority journal, retrospective study, young adult

وصف الملف: application/pdf

العلاقة: https://research.rug.nl/en/publications/dda7cb58-fa8e-4405-87b6-4c6ae3d57feaTest

الإتاحة: https://doi.org/10.1177/2326409816649599Test
https://hdl.handle.net/11370/dda7cb58-fa8e-4405-87b6-4c6ae3d57feaTest
https://research.rug.nl/en/publications/dda7cb58-fa8e-4405-87b6-4c6ae3d57feaTest
https://pure.rug.nl/ws/files/121254112/Orthotopic_Liver_Transplantation_in_Glycogen_Storage_Disease_Type_1a.pdfTest

المصدر: Journal of Inborn Errors of Metabolism and Screening. 4

مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, carbohydrate intake, retrospective study, glycogen storage disease type 1, Glycogen storage disease type la, male, Lactic acidemia, glucose homeostasis, controlled study, human, glucose, clinical article, Liver transplantation, glycogen storage disease type 1a, adult, lactic acid, article, nutritional and metabolic diseases, bleeding, Hypoglycemia, Glucose blood, lactic acidosis, female, priority journal, Familial amyloid polyneuropathy, young adult

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=dris___00893::c88b58fd3501bd4b80d2dd03b7263885Test
https://hdl.handle.net/11370/dda7cb58-fa8e-4405-87b6-4c6ae3d57feaTest

المؤلفون: Chan, EWY

مصطلحات موضوعية: Article, Plasmodium Falciparum, Malaria, Laboratory Test, Human, Glycogen Storage Disease Type 1, Female, Drug Substitution, Clinical Feature, Case Report, Adult

العلاقة: Journal of Pharmacy Practice and Research; http://www.scopus.com/mlt/select.url?eid=2-s2.0-33746151229&selection=ref&src=s&origin=recordpageTest; Journal Of Pharmacy Practice And Research, 2006, v. 36 n. 2, p. 134-135; 135; eid_2-s2.0-33746151229; 134; http://hdl.handle.net/10722/145483Test; 36

الإتاحة: http://hdl.handle.net/10722/145483Test

المؤلفون: Joris P. J. Slaets, Froukje L. Ubels, Andries J. Smit, Jan Peter Rake, G. Peter A. Smit

المساهمون: Health Psychology Research (HPR), Groningen Kidney Center (GKC), Vascular Ageing Programme (VAP)

المصدر: European Journal of Pediatrics, 161, S62-S64. SPRINGER

مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Arteriosclerosis, glycogen storage disease type 1, CHILDREN, Familial hypercholesterolemia, Glycogen Storage Disease Type I, albuminuria, Internal medicine, medicine, Humans, Glycogen storage disease, FAMILIAL HYPERCHOLESTEROLEMIA, HYPERLIPIDEMIA, Proteinuria, medicine.diagnostic_test, Vascular disease, business.industry, hyperlipidaemia, ADULTS, medicine.disease, RAMIPRIL, Blood pressure, Endocrinology, Pediatrics, Perinatology and Child Health, Cardiology, Albuminuria, cardiovascular system, Female, Microalbuminuria, medicine.symptom, atherosclerosis, Lipid profile, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6550d6270dd094d8868643f07109c026Test
https://research.rug.nl/en/publications/a76c1c57-b6b0-4fd7-83df-761d8f5669e7Test

المؤلفون: Borhane Annabi, Hisayuki Hiraiwa, Ke-Jian Lei, Ruti Parvari, Eli Hershkovitz, Janice Yang Chou, Shimon Moses, Mihael H. Polymeropoulos, Brian C. Mansfield, Tsuneyuki Ubagai, Hanna Mandel, Moshe Fryman

المصدر: The American Journal of Human Genetics. (2):400-405

مصطلحات موضوعية: Genetic Markers, Male, Glycogen-storage disease type 1, congenital, hereditary, and neonatal diseases and abnormalities, Neutropenia, Genes, Recessive, Locus (genetics), Glycogen Storage Disease Type I, Biology, Consanguinity, Chromosome 11, Gene mapping, Genetic linkage, Microsomes, Glycogen Storage Disease Type Ib, Ethnicity, medicine, Genetics, Humans, Glycogen storage disease, Family, Genetics(clinical), Gene, Genetics (clinical), Glycogen storage disease type I, Polymorphism, Genetic, Chromosomes, Human, Pair 11, Chromosome Mapping, nutritional and metabolic diseases, medicine.disease, Pedigree, Genetic marker, Female, von Gierke disease, Chromosome Deletion, Lod Score, Glucose-6-phosphatase, Linkage analysis, Microsatellite Repeats, Research Article

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cda9f0c663a87582ff622262832c0b2eTest