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Bone, ISSN 8756-3282, 1985
Journal
Journal Article
Arteriosclerosis, thrombosis, and vascular biology, ISSN 1079-5642, 12/2007, Volume 27, Issue 12, pp. 2684 - 2690
Oxidative stress | Inflammatory response | Insulin-like growth factor | Apolipoprotein E | Atherosclerosis | Peripheral Vascular Disease | Life Sciences & Biomedicine | Hematology | Cardiovascular System & Cardiology | Science & Technology | Cardiology. Vascular system | Cardiovascular system | Investigative techniques, diagnostic techniques (general aspects) | General and cellular metabolism. Vitamins | Diseases of the peripheral vessels. Diseases of the vena cava. Miscellaneous | Atherosclerosis (general aspects, experimental research) | Pharmacology. Drug treatments | Biological and medical sciences | Investigative techniques of hemodynamics | Medical sciences | Blood and lymphatic vessels | Tumor Necrosis Factor-alpha - metabolism | Inflammation - pathology | Phosphorylation | Apolipoproteins E - deficiency | Antioxidants - metabolism | Atherosclerosis - genetics | Humans | Aorta - metabolism | RNA, Messenger - metabolism | Stem Cells - metabolism | Anti-Inflammatory Agents - metabolism | Apolipoproteins E - metabolism | Inflammation - metabolism | Dietary Fats - administration & dosage | Insulin-Like Growth Factor I - administration & dosage | Superoxides - metabolism | Anti-Inflammatory Agents - administration & dosage | Dinoprost - analogs & derivatives | Proto-Oncogene Proteins c-akt - metabolism | Interleukin-6 - metabolism | Disease Models, Animal | Recombinant Proteins - metabolism | Atherosclerosis - pathology | Dinoprost - urine | Macrophages - pathology | Endothelial Cells - metabolism | Mice, Inbred C57BL | Cells, Cultured | Nitric Oxide Synthase Type III | Atherosclerosis - metabolism | Disease Progression | Mice, Knockout | Aorta - pathology | Macrophages - metabolism | Animals | Apolipoproteins E - genetics | Antioxidants - administration & dosage | Inflammation - genetics | Stem Cells - pathology | Inflammation - prevention & control | Mice | Oxidative Stress - drug effects | Endothelial Cells - pathology | Atherosclerosis - prevention & control | Insulin-Like Growth Factor I - metabolism | Nitric Oxide Synthase Type II - metabolism | Index Medicus
Journal Article
Journal Article
Movement disorders, ISSN 0885-3185, 05/2019, Volume 34, Issue 5, pp. 598 - 613
inborn errors of metabolism | treatment | movement disorders | neurotransmitter disorders | neurogenetics | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Amino Acid Metabolism, Inborn Errors - complications | Niemann-Pick Disease, Type C - therapy | Hepatolenticular Degeneration - therapy | Monosaccharide Transport Proteins - deficiency | Amino Acid Metabolism, Inborn Errors - physiopathology | Humans | Folic Acid Deficiency - therapy | Hepatolenticular Degeneration - physiopathology | Vitamin E Deficiency - therapy | Dystonic Disorders - complications | Brain Diseases, Metabolic - diagnosis | Vitamin E Deficiency - diagnosis | Xanthomatosis, Cerebrotendinous - diagnosis | Basal Ganglia Diseases - diagnosis | Carbohydrate Metabolism, Inborn Errors - therapy | Dystonia - etiology | Carbohydrate Metabolism, Inborn Errors - diagnosis | Parkinsonian Disorders - physiopathology | Chorea - physiopathology | Dystonia - physiopathology | Metabolic Diseases - diagnosis | Ataxia - diagnosis | Carbohydrate Metabolism, Inborn Errors - physiopathology | Metabolism, Inborn Errors - diagnosis | Folic Acid Deficiency - complications | Movement Disorders - physiopathology | Brain Diseases, Metabolic - physiopathology | Basal Ganglia Diseases - therapy | Ataxia - complications | Muscle Spasticity - physiopathology | Xanthomatosis, Cerebrotendinous - complications | Metabolic Diseases - complications | Metabolism, Inborn Errors - complications | Metabolism, Inborn Errors - physiopathology | Brain Diseases, Metabolic - complications | Glutaryl-CoA Dehydrogenase - deficiency | Carbohydrate Metabolism, Inborn Errors - complications | Ataxia - etiology | Hepatolenticular Degeneration - diagnosis | Metabolism, Inborn Errors - therapy | Niemann-Pick Disease, Type C - physiopathology | Parkinsonian Disorders - etiology | Amino Acid Metabolism, Inborn Errors - diagnosis | Brain Diseases, Metabolic - therapy | Xanthomatosis, Cerebrotendinous - therapy | Metabolic Diseases - therapy | Metabolic Diseases - physiopathology | Myoclonus - etiology | Vitamin E Deficiency - complications | Niemann-Pick Disease, Type C - diagnosis | Dystonic Disorders - physiopathology | Dystonic Disorders - therapy | Hepatolenticular Degeneration - complications | Vitamin E Deficiency - physiopathology | Ataxia - physiopathology | Ataxia - therapy | Chorea - etiology | Amino Acid Metabolism, Inborn Errors - therapy | Basal Ganglia Diseases - complications | Folic Acid Deficiency - physiopathology | Myoclonus - physiopathology | Muscle Spasticity - etiology | Dystonic Disorders - diagnosis | Basal Ganglia Diseases - physiopathology | Movement Disorders - etiology | Xanthomatosis, Cerebrotendinous - physiopathology | Folic Acid Deficiency - diagnosis | Niemann-Pick Disease, Type C - complications | Dystonic Disorders - etiology | Metabolism, Inborn errors of | Education | Mortality | Finance | Physiological aspects | Creatine | Movement disorders | Energy metabolism | Inborn errors of metabolism | Lysosomal storage diseases | Metabolism | Autophagy | Morbidity | Quality of life | Phenomenology | Psychiatrists | Differential diagnosis | Children | Phagocytosis | Index Medicus
Journal Article