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: Yoshihiro Horii, Michinori Ito, Seiko Kitamura, Takahiko Saijo, Ichiro Yokota, Etsuo Naito, Yasuhiro Kuroda, Yukiko Ogawa, Junko Matsuda, Eiko Takada

المصدر: Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. (1):79-84

مصطلحات موضوعية: Male, Pyruvate decarboxylation, Pyruvate dehydrogenase complex deficiency, Pyruvate Dehydrogenase Complex, Biology, chemistry.chemical_compound, Lactic acidemia, Thiamine treatment, medicine, Humans, Point Mutation, Lactic Acid, Lymphocytes, Thiamine, Child, Pyruvate Dehydrogenase Complex Deficiency Disease, Molecular Biology, Cells, Cultured, Binding Sites, Infant, food and beverages, Exons, Pyruvate dehydrogenase complex, medicine.disease, Molecular biology, Pyruvate dehydrogenase deficiency, chemistry, TPP binding region, Molecular Medicine, E1α subunit, Thiamine pyrophosphate, Pyruvate Decarboxylase, Pyruvate decarboxylase, Thiamine pyrophosphate binding

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c3e3947c09e5d66d273e3315f213dc3Test