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1
المؤلفون: George Ntaios, C. Tomos, Anastasia Chatzinikolaou, Paraskevi Karalazou, Stiliani Alexiou-Daniel, C. Manolopoulos, A. Nikolaidou
المصدر: Internal Medicine Journal. 38:204-206
مصطلحات موضوعية: Adult, Male, congenital, hereditary, and neonatal diseases and abnormalities, education.field_of_study, Enzyme deficiency, Greece, business.industry, Population, nutritional and metabolic diseases, Physiology, Female sex, medicine.disease, Glucosephosphate Dehydrogenase Deficiency, hemic and lymphatic diseases, parasitic diseases, Prevalence, Internal Medicine, Geographic regions, medicine, Humans, Female, Greek population, business, education, Glucose-6-phosphate dehydrogenase deficiency
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9cfcca98d7b8e39eb9f512dab599749aTest
https://doi.org/10.1111/j.1445-5994.2007.01618.xTest -
2
مصطلحات موضوعية: Male, Biomedical Research, Unclassified drug, Physiology, Cholesterol 7alpha monooxygenase, Messenger, Apolipoprotein E3, Cholesterol ester, Srebf1 gene, Ketone Bodies, Gene, Animal tissue, Feces, Mice, Hyperlipoproteinemia Type III, Cholesterol 7α-hydroxylase, Bile acid synthesis, Vitamin E, Cholesterol 7-alpha-Hydroxylase, Vitamin A, Dgat1 protein, Feces level, Retinol, Messenger RNA, Atherogenic, Cytochrome P450 isoenzyme, Lipid diet, Triacylglycerol blood level, Sterols, Cholesterol, Cholesterol blood level, Hyperlipidemia, Blood, Bile acid biosynthesis, Very low density lipoprotein, Liver, Apolipoprotein E3 (Leidein), lipids (amino acids, peptides, and proteins), Atherogenic diet, Female, Cholesterol Esters, VLDL, Acyltransferase, Lipolysis, Lipoproteins, Knockout, Sterol regulatory element binding protein 1, Bile acid, Crosses, Biosynthesis, Vitamin, Catalysis, Diacylglycerol acyltransferase, Bile Acids and Salts, Knockout mouse, Apolipoproteins E, Antioxidant activity, Genetic, Genetics, Cholesterol metabolism, Animals, Animal model, Animal experiment, Diacylglycerol O-Acyltransferase, Biology, Enzyme deficiency, mouse, Triglycerides, SREBP-1, Sterol, Apolipoproteins B, Cross breeding, Mouse mutant, Lipogenesis, Alpha tocopherol, Lipoprotein synthesis, Nonhuman, Lipid Metabolism, Diet, Metabolism, RNA, Gene expression, Controlled study, Acyltransferases
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=dris___00893::e3c199dcb96de6b5639af7c92dc8a450Test
http://resolver.tudelft.nl/uuid:8ee08125-6e90-4b58-95dc-68aff9f596e0Test -
3
المساهمون: TNO Preventie en Gezondheid
المصدر: Arteriosclerosis, Thrombosis, and Vascular Biology, 4, 24, 768-774
مصطلحات موضوعية: Apolipoprotein E, Male, Very low-density lipoprotein, Biomedical Research, Unclassified drug, Physiology, Cholesterol 7alpha monooxygenase, Apolipoprotein E3, Cholesterol ester, Srebf1 gene, Ketone Bodies, Lipoproteins, VLDL, Gene, Animal tissue, chemistry.chemical_compound, Feces, Mice, Hyperlipoproteinemia Type III, Cholesterol 7α-hydroxylase, Bile acid synthesis, Vitamin E, Cholesterol 7-alpha-Hydroxylase, Vitamin A, Mice, Knockout, Feces level, Bile acid, Retinol, Messenger RNA, Cytochrome P450 isoenzyme, Lipid diet, Triacylglycerol blood level, Sterols, Cholesterol, Cholesterol blood level, Hyperlipidemia, Blood, Bile acid biosynthesis, Very low density lipoprotein, Liver, Apolipoprotein E3 (Leidein), Lipogenesis, Cholesteryl ester, lipids (amino acids, peptides, and proteins), Atherogenic diet, Female, Cholesterol Esters, Cardiology and Cardiovascular Medicine, medicine.medical_specialty, medicine.drug_class, Acyltransferase, Lipolysis, Sterol regulatory element binding protein 1, Dgat1 protein, mouse, Biology, Cholesterol 7 alpha-hydroxylase, Biosynthesis, Vitamin, Catalysis, Diacylglycerol acyltransferase, Bile Acids and Salts, Knockout mouse, Apolipoproteins E, Antioxidant activity, Internal medicine, medicine, Genetics, Cholesterol metabolism, Animals, Animal model, Animal experiment, Diacylglycerol O-Acyltransferase, RNA, Messenger, Enzyme deficiency, Crosses, Genetic, Triglycerides, SREBP-1, Sterol, Apolipoproteins B, Cross breeding, Mouse mutant, Alpha tocopherol, Lipoprotein synthesis, Nonhuman, Lipid Metabolism, Endocrinology, Metabolism, chemistry, Diet, Atherogenic, Gene expression, Controlled study, Acyltransferases, Lipoprotein
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bbf6efd8e834969edb36dd044d3ab261Test
http://resolver.tudelft.nl/uuid:8ee08125-6e90-4b58-95dc-68aff9f596e0Test -
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المؤلفون: O. Ainoon, Nem-Yun Boo, M. S. Haliza, Z. A. Zainal Arif, S. K. Cheong
المصدر: Journal of paediatrics and child health. 31(1)
مصطلحات موضوعية: Male, congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, Enzyme deficiency, Physiology, chemistry.chemical_compound, Sex Factors, Sex factors, Risk Factors, hemic and lymphatic diseases, parasitic diseases, medicine, Ethnicity, Glucose-6-phosphate dehydrogenase, Humans, Analysis of Variance, Kuala lumpur, biology, business.industry, Infant, Newborn, Malaysia, medicine.disease, Fetal Blood, Confidence interval, Enzyme assay, Surgery, Glucosephosphate Dehydrogenase Deficiency, chemistry, Pediatrics, Perinatology and Child Health, biology.protein, Female, Analysis of variance, business, Glucose-6-phosphate dehydrogenase deficiency
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2db05a79c8a9741585d6b9286aaeea14Test
https://pubmed.ncbi.nlm.nih.gov/7748690Test -
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المؤلفون: H. J. Böhme, P. Bührdel, L. Didt
المصدر: European journal of pediatrics. 149(8)
مصطلحات موضوعية: Fructose-1,6-Diphosphatase Deficiency, Male, medicine.medical_specialty, Enzyme deficiency, medicine.medical_treatment, Exchange transfusion, Physiology, Infant, Premature, Diseases, Fructose Metabolism, Inborn Errors, Hyperbilirubinemia, Hereditary, Internal medicine, medicine, Fructose 1 6 diphosphatase, Leukocytes, Humans, biology, business.industry, Gluconeogenesis, Infant, Newborn, Infant, Enzyme assay, Hypoglycemia, Endocrinology, Fructose metabolism, Liver, Child, Preschool, Pediatrics, Perinatology and Child Health, biology.protein, Female, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43e52b19357d99bbfe51339146afcb13Test
https://pubmed.ncbi.nlm.nih.gov/2347355Test -
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المؤلفون: P V Nelson, A C Pollard, W F Carey
المصدر: Australian Journal of Experimental Biology and Medical Science. 55:253-262
مصطلحات موضوعية: Heterozygote, Enzyme deficiency, Hydrolases, business.industry, Homozygote, Clinical Biochemistry, Immunology, Infant, Physiology, Cell Biology, General Medicine, Clinical Enzyme Tests, Fibroblasts, Amniotic Fluid, Cell Line, Sphingolipidoses, Pregnancy, Prenatal Diagnosis, Humans, Medicine, Female, Lysosomes, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4060ee5ffe2192817f9a360270be9664Test
https://doi.org/10.1038/icb.1977.20Test -
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المؤلفون: Yves Nordmann, G. Aitken, H. de Verneuil
المصدر: Human Genetics. 44:145-151
مصطلحات موضوعية: Adult, Male, congenital, hereditary, and neonatal diseases and abnormalities, Erythrocytes, Enzyme deficiency, Adolescent, Carboxy-Lyases, Uroporphyrinogen III decarboxylase, Physiology, Biology, Diagnosis, Differential, Porphyrias, chemistry.chemical_compound, Uroporphyrinogen, Genetics, medicine, Humans, Uroporphyrinogen Decarboxylase, Metabolic disease, Child, skin and connective tissue diseases, Uroporphyrinogen decarboxylase activity, Genetics (clinical), Hepatoerythropoietic porphyria, nutritional and metabolic diseases, medicine.disease, humanities, Pedigree, Porphyria, chemistry, Female, Asymptomatic carrier
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0365c8f6283271442f78b44276eb222Test
https://doi.org/10.1007/bf00295407Test -
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المؤلفون: Maria Vicatou, J. L. Grech
المصدر: British journal of haematology. 25(2)
مصطلحات موضوعية: Genetics, Electrophoresis, Male, Enzyme deficiency, Incidence (epidemiology), Infant, Newborn, Physiology, Hematology, Biology, medicine.disease, language.human_language, Dehydrogenase deficiency, Infant, Newborn, Diseases, Maltese, Mediterranean Islands, Glucosephosphate Dehydrogenase Deficiency, Sex Factors, Population Surveillance, language, medicine, Humans, Female, Glucose-6-phosphate dehydrogenase deficiency
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36cd8b7255458b7c8995ae6ba1d450d6Test
https://pubmed.ncbi.nlm.nih.gov/4726905Test -
9
المؤلفون: Gino Schilirò, Florindo Mollica, Russo G, Lorenzo Pavone
المصدر: Pediatrics. 49(6)
مصطلحات موضوعية: Anemia, Hemolytic, Heterozygote, Enzyme deficiency, Erythrocytes, Anemia, Physiology, Methemoglobin, Sex Factors, Sex factors, G 6 pd deficiency, Medicine, Humans, Reduction test, Child, Sicily, business.industry, Infant, Heterozygote advantage, Favism, medicine.disease, Glucosephosphate Dehydrogenase Deficiency, Child, Preschool, Pediatrics, Perinatology and Child Health, Hemolytic crisis, Female, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e992e7ee174e78a8b3236e2edb94348eTest
https://pubmed.ncbi.nlm.nih.gov/5041319Test -
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المؤلفون: T.W. van Weerden, H.F.M. Busch, Johan F. Koster
المصدر: Neurology, 29(3), 415-416. LIPPINCOTT WILLIAMS & WILKINS
مصطلحات موضوعية: Male, Enzyme deficiency, business.industry, Paternal grandfather, media_common.quotation_subject, Age Factors, Infant, Physiology, Middle Aged, Glycogen Storage Disease, Humans, Medicine, Maltase deficiency, Female, Neurology (clinical), Girl, Glucan 1,4-alpha-Glucosidase, business, Glucosidases, media_common
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ac74997793ca435fd059512b019c35dTest
https://doi.org/10.1212/wnl.29.3.415Test