المؤلفون: Gregory Guthrie, Charlotte Lauridsen, Douglas G. Burrin, Shaji Chacko, Barbara Stoll, Jogchum Plat

المساهمون: Nutrition and Movement Sciences, RS: NUTRIM - R1 - Obesity, diabetes and cardiovascular health

المصدر: American Journal of Physiology-Gastrointestinal and Liver Physiology, 318(1), G41-G52. American Physiological Society
Guthrie, G, Stoll, B, Chacko, S, Lauridsen, C, Plat, J & Burrin, D G 2020, ' Rifampicin, not vitamin E, suppresses parenteral nutrition-associated liver disease development through the pregnane X receptor pathway in piglets ', American Journal of Physiology: Gastrointestinal and Liver Physiology, vol. 318, no. 1, pp. G41-G52 . https://doi.org/10.1152/ajpgi.00193.2019
Am J Physiol Gastrointest Liver Physiol

مصطلحات موضوعية: 0301 basic medicine, Parenteral Nutrition, Physiology, medicine.medical_treatment, Sus scrofa, parenteral nutrition-associated liver disease, INFANTS, vitamin E, Pharmacology, Liver Diseases/etiology, rifampicin, Liver disease, chemistry.chemical_compound, ABC TRANSPORTERS, Liver/drug effects, Cytochrome P-450 CYP3A, Glucuronosyltransferase, Phospholipids, FISH-OIL, Hyperbilirubinemia, Pregnane X receptor, Liver Diseases, ALPHA-TOCOPHEROL, Gastroenterology, Pregnane X Receptor, Cytochrome P-450 CYP3A/metabolism, Fish oil, Liver, FAT OVERLOAD SYNDROME, ACID, alfa-tocopherol, Emulsions, Rifampin, medicine.drug, Research Article, Signal Transduction, EXPRESSION, Fat Emulsions, Intravenous, Bile Acids and Salts/biosynthesis, Hyperbilirubinemia/etiology, METABOLISM, Bile Acids and Salts, 03 medical and health sciences, Pregnane X Receptor/agonists, Cholestasis, Physiology (medical), medicine, Animals, Vitamin E/pharmacology, 030109 nutrition & dietetics, Hepatology, business.industry, Vitamin E, bile acid metabolism, Cholestasis/etiology, LIPID EMULSION, medicine.disease, Soybean Oil, Disease Models, Animal, 030104 developmental biology, Parenteral nutrition, chemistry, Animals, Newborn, Glucuronosyltransferase/metabolism, BILE, alpha-Tocopherol, business, Rifampin/pharmacology, cholestasis, Rifampicin

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50d93c23b8e62b533153371662603600
https://doi.org/10.1152/ajpgi.00193.2019

المؤلفون: Omarsdottir, Sif, Ljunggren, Östen, Mallmin, Hans, Michaëlsson, Karl, Lööf, Lars

المصدر: European Journal of Gastroenterology and Hepathology. 14(1):43-8

مصطلحات موضوعية: Adult, Aged, 80 and over, Bone Density, Cholecalciferol/blood, Chronic Disease, Female, Femur Neck, Humans, Hyperbilirubinemia/etiology, Liver Diseases/blood/*complications/physiopathology, Lumbar Vertebrae, Male, Middle Aged, Osteoporosis/*etiology, Prospective Studies, MEDICINE, MEDICIN

وصف الملف: print

URL الوصول: https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-74837
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Retrieve&list_uids=11782574&dopt=Citation

المؤلفون: Abdul-Razzak, KK, Almomany, EM, Nusier, MK, Obediat, AD, Salim, AM

المصدر: GMS German Medical Science; VOL: 6; DOC10 /20080924/

مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, GLUCOSEPHOSPHATE DEHYDROGENASE/genetics, INFANT, NEWBORN, vitamin C, G6PD-Mangel, vitamin E, HYPERBILIRUBINEMIA, Glucose-6-Phosphat-Dehydrogenase-Mangel, GLUCOSEPHOSPHAT-DEHYDROGENASE/Genetik, VITAMIN E/Blut, hemic and lymphatic diseases, G6PD deficiency, GLUCOSEPHOSPHATE DEHYDROGENASE DEFICIENCY/metabolism, HEMOLYSIS, GLUKOSEPHOSPHAT-DEHYDROGENASEMANGEL/Stoffwechsel, MENSCH, nutritional and metabolic diseases, VITAMIN E/blood, HUMANS, Bilirubin, HÄMOLYSE, ASCORBIC ACID/blood, HYPERBILIRUBINÄMIE, ASCORBINSÄURE/Blut, KIND, NEUGEBORENES, glucose-6-phosphate dehydrogenase deficiency, ddc: 610, HYPERBILIRUBINEMIA/*etiology, HYPERBILIRUBINÄMIE/*Ätiologie

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______1175::1096d0535a2015e578d05cf22e4cf16f
http://www.egms.de/en/journals/gms/2008-6/000055.shtml

المؤلفون: González, M, Iglesias, J, Ribalta, J, Reyes, H, Hernández, I, Bianchi, M, Andrighetti, F, Molina, C., TIRIBELLI, CLAUDIO

المساهمون: González, M, Iglesias, J, Tiribelli, Claudio, Ribalta, J, Reyes, H, Hernández, I, Bianchi, M, Andrighetti, F, Molina, C.

مصطلحات موضوعية: Pregnancy Complications/drug therapy, Hyperbilirubinemia/etiology, Intrahepatic/drug therapy, Pilot Projects, Cholagogues and Choleretics/pharmacokinetics, Severity of Illness Index, Cholagogues and Choleretics/therapeutic use, Hyperbilirubinemia/drug therapy, Cholagogues and Choleretics/administration & dosage, Liver Function Tests, Pregnancy, Recurrence, Intrahepatic/blood, Humans, Bicyclo Compounds, Cholestasis, Intrahepatic/complications, Terpenes, Heterocyclic, Infant, Newborn, Bile Acids and Salts/blood, Pruritus/etiology, Pruritus/drug therapy, Female, Bicyclo Compounds, Heterocyclic, Bile Acids and Salts/blood, Cholagogues and Choleretics/administration & dosage, Cholagogues and Choleretics/pharmacokinetics, Cholagogues and Choleretics/therapeutic use, Cholestasis, Intrahepatic/blood, Cholestasis, Intrahepatic/complications, Cholestasis, Intrahepatic/drug therapy, Female, Humans, Hyperbilirubinemia/drug therapy, Hyperbilirubinemia/etiology, Infant, Newborn, Liver Function Tests, Pilot Projects, Pregnancy, Pregnancy Complications/drug therapy, Pruritus/drug therapy, Pruritus/etiology, Recurrence, Severity of Illness Index, Terpenes

وصف الملف: STAMPA

URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::b17fe13747f04632e0a8fef41550a856
http://hdl.handle.net/11368/2847851

المؤلفون: Geronooz, I., Scheen, André, Senterre, Jacques

المصدر: Revue Médicale de Liège, 54(6), 517-21. Liège, Belgique: Hopital de Baviere (1999).

مصطلحات موضوعية: Abortion, Spontaneous/etiology, Adult, Congenital Abnormalities/etiology, Developmental Disabilities/etiology, Diabetes Mellitus/etiology, Diabetes, Gestational/complications, Female, Fetal Diseases/etiology, Humans, Hyperbilirubinemia/etiology, Infant, Newborn, Infant, Newborn, Diseases/etiology, Obesity/etiology, Pregnancy, Pregnancy Outcome, Respiratory Distress Syndrome, Newborn/etiology, Human health sciences :: Pediatrics, Sciences de la santé humaine :: Pédiatrie, Human health sciences :: Endocrinology, metabolism & nutrition, Sciences de la santé humaine :: Endocrinologie, métabolisme & nutrition

URL الوصول: https://orbi.uliege.be/handle/2268/12562

المؤلفون: Evagellos Liberopoulos, Eleni Bairaktari, Moses Elisaf

المصدر: Nephron. 91:532-533

مصطلحات موضوعية: Male, medicine.medical_specialty, medicine.medical_treatment, Renal function, Gastroenterology, Diagnosis, Differential, Normal renal function, Internal medicine, medicine, Humans, Aged, Antibacterial agent, Hyperbilirubinemia/etiology/*physiopathology, Chemotherapy, business.industry, Febrile illness, Kidney Diseases/*etiology, medicine.disease, Fever/etiology/physiopathology, Tubulointerstitial Nephritis, Leptospirosis, Kidney Tubules, Proximal/*physiopathology, Surgery, Acute Disease, business, Leptospirosis/complications/*diagnosis, Kidney disease

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b18f9a9704b5fbe805f1e811572c1919
https://doi.org/10.1159/000064304

عناروين إضافية: Antioxidative Vitamine und Glucose-6-Phosphat-Dehydrogenase-Mangel bei ausgereiften Neugeborenen

المصدر: GMS German Medical Science; VOL: 6; DOC10 /20080924/

مصطلحات الفهرس: HYPERBILIRUBINEMIA, HYPERBILIRUBINEMIA/*etiology, GLUCOSEPHOSPHATE DEHYDROGENASE DEFICIENCY/metabolism, GLUCOSEPHOSPHATE DEHYDROGENASE/genetics, ASCORBIC ACID/blood, VITAMIN E/blood, HEMOLYSIS, HUMANS, INFANT, NEWBORN, HYPERBILIRUBINÄMIE, HYPERBILIRUBINÄMIE/*Ätiologie, GLUKOSEPHOSPHAT-DEHYDROGENASEMANGEL/Stoffwechsel, GLUCOSEPHOSPHAT-DEHYDROGENASE/Genetik, ASCORBINSÄURE/Blut, VITAMIN E/Blut, HÄMOLYSE, MENSCH, KIND, NEUGEBORENES, bilirubin, vitamin C, vitamin E, glucose-6-phosphate dehydrogenase deficiency, G6PD deficiency, Bilirubin, Vitamin C, Vitamin E, Glucose-6-Phosphat-Dehydrogenase-Mangel, G6PD-Mangel, ddc: 610, article

URL: http://www.egms.de/en/journals/gms/2008-6/000055.shtml
Abdul-Razzak KK, Nusier MK, Obediat AD, Salim AM. Antioxidant vitamins and hyperbilirubinemia in neonates. GMS Ger Med Sci. 2007;5:Doc03. Available from: http://www.egms.de/en/gms/2007-5/000039.shtml
Baydas G, Karatas F, Gursu MF, Bozkurt HA, Ilhan N, Yasar A, Canatan H. Antioxidant vitamin levels in term and preterm infants and their relation to maternal vitamin status. Arch Med Res. 2002;33(3):276-80. DOI: 10.1016/S0188-4409(02)00356-9
Beutler E. Glucose-6-phosphate dehydrogenase deficiency: a historical perspective. Blood. 2008;111(1):16-24. DOI: 10.1182/blood-2007-04-077412
Bizzarro MJ, Colson E, Ehrenkranz RA. Differential diagnosis and management of anemia in the newborn. Pediatr Clin North Am. 2004;51(4):1087-107, xi. DOI: 10.1016/j.pcl.2004.03.006
Brouillard RP. Measurement of red blood cell life-span. JAMA. 1974;230(9):1304-5. DOI: 10.1001/jama.230.9.1304
Catignani GL, Bieri JG. Simultaneous determination of retinol and alpha-tocopherol in serum or plasma by liquid chromatography. Clin Chem. 1983;29(4):708-12.
Chan AC, Chow CK, Chiu D. Interaction of antioxidants and their implication in genetic anemia. Proc Soc Exp Biol Med. 1999;222(3):274-82. DOI: 10.1046/j.1525-1373.1999.d01-144.x
Connolly AM, Volpe JJ. Clinical features of bilirubin encephalopathy. Clin Perinatol. 1990;17(2):371-9.
Frank JE. Diagnosis and Management of G6PD Deficiency. Am Fam Physician. 2005;72(7):1277-82
Gaetani GF, Rolfo M, Arena S, Mangerini R, Meloni GF, Ferraris AM. Active Involvement of Catalase During Hemolytic Crises of Favism. Blood. 1996;88(3):1084-8.
Gordon-Smith EC. Investigation of the hereditary haemolytic anemia. In: Dacie JV, Lewis SM, editors. Practical haematology. Edinburgh: Churchill Livingstone, 1984. p. 152-78.
Gross SJ. Vitamin E and neonatal bilirubinemia. Pediatrics. 1979;64(3):321-3.
Jablonska-Skwiecinska E, Lewandowska I, Plochocka D, Topczewski J, Zimowski JG, Klopocka J, Burzynska B. Several mutations including two novel mutations of the glucose-6-phosphate dehydrogenase gene in Polish G6PD deficient subjects with chronic nonspherocytic hemolytic anemia, acute hemolytic anemia, and favism. Hum Mutat. 1999;14(6):477-84. DOI: 10.1002/(SICI)1098-1004(199912)14:6<477::AID-HUMU6>3.0.CO;2-X
Jalloh S, Van Rostenberghe H, Yusoff NM, Ghazali S, Nik Ismail NZ, Matsuo M, Wahab NA, Nishio H. Poor correlation between hemolysis and jaundice in glucose 6-phosphate dehydrogenase-deficient babies. Pediatr Int. 2005;47(3):258-61. DOI: 10.1111/j.1442-200x.2005.02052.x
Kaplan M, Vreman HJ, Hammerman C, Leiter C, Abramov A, Stevenson DK. Contribution of haemolysis to jaundice in Sephardic Jewish glucose-6-phosphate dehydrogenase deficient neonates. Br J Haematol. 1996;93(4):822-7.
Kilic M, Turgut M, Taskin E, Cekmen M, Aygun AD. Nitric oxide levels and antioxidant enzyme activities in jaundices of premature infants. Cell Biochem Funct. 2004;22(5):339-42. DOI: 10.1002/cbf.1112
Kondo H, Takahashi M, Niki E. Peroxynitrite-induced hemolysis of human erythrocytes and its inhibition by antioxidants. FEBS Lett. 1997;413(2):236-8. DOI: 10.1016/S0014-5793(97)00922-8
Kwok CJ, Martin AC, Au SW, Lam VM. G6PDdb, an integrated database of glucose-6-phosphate dehydrogenase (G6PD) mutations. Hum Mutat. 2002;19(3):217-24. DOI: 10.1002/humu.10036
Laosombat V, Sattayasevana B, Chotsampancharoen T, Wongchanchailert M. Glucose-6-Phosphate Dehydrogenase Variants Associated with Favism in Thai Children. Int J Hematol. 2006;83(2):139-43. DOI: 10.1532/IJH97.A20513
Lau HK, Li CH, Lee AC. Acute massive haemolysis in children with glucose-6-phosphate dehydrogenase deficiency. Hong Kong Med J. 2006;12(2):149-51.
Lim F, Vulliamy T, Abdalla SH. An Ashkenazi Jewish woman presenting with favism. J Clin Pathol. 2005;58(3):317-9. DOI: 10.1136/jcp.2004.017426
Manco L, Gonçalves P, Macedo-Ribeiro S, Seabra C, Melo P, Ribeiro ML. Two new glucose-6-phosphate dehydrogenase mutations causing chronic hemolysis. Haematologica. 2005;90(8):1135-6.
McCormick DB, Green HL. The vitamins. In: Burtis CA, Ashwood ER, editors. Tietz text book of clinical chemistry. Philadelphia: Saunders; 1999. p. 999-1028.
Mehta A, Mason PJ, Vulliamy TJ. Glucose-6-phosphate dehydrogenase deficiency. Baillieres Best Pract Res Clin Haematol. 2000;13(1):21-38. DOI: 10.1053/beha.1999.0055
Niki E, Yamamoto Y, Komuro E, Sato K. Membrane damage due to lipid oxidation. Am J Clin Nutr. 1991;53(1 Suppl):201S-205S.
Niki E, Komuro E, Takahashi M, Urano S, Ito E, Terao K. Oxidative hemolysis of erythrocytes and its inhibition by free radical scavengers. J Biol Chem. 1988;263(36):19809-14.
Ojo CO, Dawodu AH, Osifo BO. Vitamin E deficiency in the pathogenesis of haemolysis and hyperbilirubinaemia of neonatal jaundice. J Trop Pediatr. 1986;32(5):251-4.
Pearson HA. Life-span of the fetal red blood cell. J Pediatr. 1967;70(2):166-71. DOI: 10.1016/S0022-3476(67)80410-4
Strain JJ, Mulholland CW. Vitamin C and vitamin E - synergistic interaction in vivo? EXS. 1992;62:419-22.
Turan Y. Prevalence of erythrocyte glucose-6-phosphate dehydrogenase (G6PD) deficiency in the population of western Turkey. Arch Med Res. 2006;37(7):880-2. DOI: 10.1016/j.arcmed.2006.03.005
Turgut M, Basaran O, Cekmen M, Karatas F, Kurt A, Aygün AD. Oxidant and antioxidant levels in preterm newborns with idiopathic hyperbilirubinemia. J Paediatr Child Health. 2004;40(11):633-7. DOI: 10.1111/j.1440-1754.2004.00489.x
Usanga EA, Ameen R. Glucose-6-Phosphate Dehydrogenase Deficiency in Kuwait, Syria, Egypt, Iran, Jordan and Lebanon. Hum Hered. 2000;50(3):158-61. DOI: 10.1159/000022906
Valaes T. Severe neonatal jaundice associated with glucose-6-phosphate dehydrogenase deficiency: pathogenesis and global epidemiology. Acta Paediatr Suppl. 1994;394:58-76. DOI: 10.1111/j.1651-2227.1994.tb13216.x
Vanderpas J, Vertongen F. Erythrocyte vitamin E is oxidized at a lower peroxide concentration in neonates than in adults. Blood. 1985;66(6):1272-7.
Weng YH, Chou YH, Lien RI. Hyperbilirubinemia in healthy neonates with glucose-6-phosphate dehydrogenase deficiency. Early Hum Dev. 2003;71(2):129-36. DOI: 10.1016/S0378-3782(03)00002-1
Yeruchimovich M, Shapira B, Mimouni FB, Dollberg S. Neonatal Nucleated Red Blood Cells in G6PD Deficiency. Am J Perinatol. 2002;19(4):215-9. DOI: 10.1055/s-2002-28485

مصطلحات الفهرس: Adult, Aged, Aged; 80 and over, Bone Density, Cholecalciferol/blood, Chronic Disease, Female, Femur Neck, Humans, Hyperbilirubinemia/etiology, Liver Diseases/blood/*complications/physiopathology, Lumbar Vertebrae, Male, Middle Aged, Osteoporosis/*etiology, Prospective Studies, Medical and Health Sciences, Medicin och hälsovetenskap, Article in journal, info:eu-repo/semantics/article, text

URL: http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-74837
European Journal of Gastroenterology and Hepathology, 0954-691X, 2002, 14:1, s. 43-8