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1دورية أكاديمية
المؤلفون: Bindi, Verónica, Eiroa, Hernán D., Crespo, Carolina, Martinez, María, Bay, Luisa
المصدر: Journal of Inborn Errors of Metabolism and Screening. January 2021 9
مصطلحات موضوعية: Glycogen storage disease I, growth, metabolic control, Complications, liver adenoma, Hypertriglyceridemia, Lactic acidemia, nephropathy
وصف الملف: text/html
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2دورية أكاديمية
المؤلفون: Castaño Amores, Celia, Nieto-Gómez, Pelayo
المصدر: Ars Pharmaceutica (Internet); Vol. 63 No. 2 (2022); 126-131 ; Ars Pharmaceutica (Internet); Vol. 63 Núm. 2 (2022); 126-131 ; 2340-9894 ; 0004-2927
مصطلحات موضوعية: fumarase deficiency, lactic acidemia, organic aciduria, ketogenic diet, metabolic disease, déficit de fumarasa, acidemia láctica, aciduria orgánica, dieta cetogénica, enfermedad metabólica
وصف الملف: application/pdf; text/xml
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3دورية أكاديمية
المؤلفون: Verónica Bindi, Hernán D. Eiroa, Carolina Crespo, María Martinez, Luisa Bay
المصدر: Journal of Inborn Errors of Metabolism and Screening, Vol 9 (2021)
مصطلحات موضوعية: Glycogen storage disease I, growth, metabolic control, Complications, liver adenoma, Hypertriglyceridemia, Lactic acidemia, nephropathy, Medicine (General), R5-920
وصف الملف: electronic resource
العلاقة: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S2326-45942021000100307&tlng=enTest; https://doaj.org/toc/2326-4594Test
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4دورية أكاديمية
المؤلفون: Wilke, Matheus V. M. B., Kleine, Ruben H. de, Wietasch, J. K. G., Amerongen, Cynthia C. A. van, Blokzijl, Hans, Spronsen, Francjan J. van, Schwartz, Ida V. D., Derks, Terry G. J.
المصدر: Journal of Inborn Errors of Metabolism and Screening. January 2016 4
مصطلحات موضوعية: glycogen storage disease type 1a, liver transplantation, familial amyloid polyneuropathy, glucose blood, hypoglycemia, lactic acidemia
وصف الملف: text/html
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5دورية أكاديمية
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
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 -
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المؤلفون: María Martinez, Verónica Bindi, Carolina Crespo, Luisa Bay, Hernán Eiroa
المصدر: Journal of Inborn Errors of Metabolism and Screening, Vol 9 (2021)
Journal of Inborn Errors of Metabolism and Screening v.9 2021
Journal of Inborn Errors of Metabolism and Screening
Instituto Genética para Todos (IGPT)
instacron:IGPTمصطلحات موضوعية: medicine.medical_specialty, Medicine (General), Complications, Endocrinology, Diabetes and Metabolism, growth, Hypoglycemia, Carbohydrate metabolism, Gastroenterology, Nephropathy, chemistry.chemical_compound, R5-920, Internal medicine, Lactic acidemia, medicine, Genetics (clinical), Glycogen storage disease I, Hypertriglyceridemia, Glycogen storage disease type I, Triglyceride, business.industry, metabolic control, medicine.disease, chemistry, Metabolic control analysis, Pediatrics, Perinatology and Child Health, Cohort, nephropathy, business, liver adenoma
وصف الملف: text/html
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c56d6a9df990cfd6f8b8981cc8d9e1bTest
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S2326-45942021000100307&tlng=enTest -
7دورية أكاديمية
المؤلفون: Ogasahara, Saburo, Engel, Andrew G., Frens, David, Mack, Diane
المصدر: Proceedings of the National Academy of Sciences of the United States of America, 1989 Apr 01. 86(7), 2379-2382.
الوصول الحر: https://www.jstor.org/stable/33482Test
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8دورية أكاديمية
المؤلفون: Ceban, Emil, Cojocaru, Victor, Condrea, Dinu, Ursul, Sergiu, Cojocaru, Doriana, Uncuţa, Andrei, Gutium, Corina, Rusu, Victoria, Todiraș, Mihail
مصطلحات موضوعية: COVID-19, ferritin, ARDS, lactic acidemia, disease severity
وصف الملف: application/pdf
العلاقة: CEBAN, Emil, COJOCARU, Victor, CONDREA, Dinu, et al. Rolul feritinei în determinarea gradului de severitate al pacienţilor critici, suferinzi de COVID-19, plasaţi în Unităţile de Terapie Intensivă = The role of ferritin in determining the severity of critical patients with COVID-19 admitted in Intensive Care Units. In: Revista de Ştiinţe ale Sănătăţii din Moldova. 2020, vol. 23(1), pp. 136-145. ISSN 2345-1467.; https://stiinta.usmf.md/sites/default/files/2020-08/MJHS_23%281%29.pdfTest; http://repository.usmf.md/./handle/20.500.12710/11441Test
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المؤلفون: Wilke,Matheus V. M. B., Kleine,Ruben H. de, Wietasch,J. K. G., Amerongen,Cynthia C. A. van, Blokzijl,Hans, Spronsen,Francjan J. van, Schwartz,Ida V. D., Derks,Terry G. J.
المصدر: Journal of Inborn Errors of Metabolism and Screening, Volume: 4, Article number: e150014, Published: 30 MAY 2019
Journal of Inborn Errors of Metabolism and Screening v.4 2016
Journal of Inborn Errors of Metabolism and Screening
Instituto Genética para Todos (IGPT)
instacron:IGPTمصطلحات موضوعية: glucose blood, congenital, hereditary, and neonatal diseases and abnormalities, familial amyloid polyneuropathy, hypoglycemia, liver transplantation, glycogen storage disease type 1a, nutritional and metabolic diseases, lactic acidemia
وصف الملف: text/html
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::f4b8a49250ad4b6e528fe86f0b7d1a3eTest
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S2326-45942016000100304&lng=en&tlng=enTest -
10دورية أكاديمية
المؤلفون: Scholte, H.R. (Hans), Busch, H.F.M. (Herman), Bakker, H.D. (Henk), Bogaard, J.M. (Jan), Luyt-Houwen, I.E.M. (I. E M), Kuyt, L.P. (L.)
المصدر: Biochimica et Biophysica Acta - Molecular Basis of Disease vol. 1271 no. 1, pp. 75-83
مصطلحات موضوعية: Carnitine, Complex I deficiency, Encephalomyopathy, Lactic acidemia, Mitochondrion, Myopathy, Oxidative phosphorylation, Riboflavin
وصف الملف: application/pdf
العلاقة: http://repub.eur.nl/pub/66958Test; urn:hdl:1765/66958
الإتاحة: https://doi.org/10.1016/0925-4439Test(95)00013-T
http://repub.eur.nl/pub/66958Test