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Drugs, ISSN 0012-6667, 2/2019, Volume 79, Issue S1, pp. 17 - 21
Neuropathology of hepatic encephalopathy (HE) in cirrhosis is primarily astroglial in nature characterized by Alzheimer type 2 astrocytosis together with... 
Pharmacotherapy | Internal Medicine | Medicine & Public Health | Pharmacology/Toxicology | PATHOGENESIS | AMMONIA | HYPERAMMONEMIA | LIVER | GABA | RATS | PHARMACOLOGY & PHARMACY | NECROSIS-FACTOR-ALPHA | TOXICOLOGY | BINDING-SITES | BRAIN | Liver Cirrhosis - drug therapy | Hepatic Encephalopathy - metabolism | Neurotransmitter Agents - antagonists & inhibitors | Ammonia - metabolism | Basal Ganglia - physiopathology | gamma-Aminobutyric Acid - metabolism | Humans | Hepatic Encephalopathy - physiopathology | Cerebellum - physiopathology | Hepatic Encephalopathy - drug therapy | Manganese - metabolism | Thalamus - physiopathology | Liver Cirrhosis - metabolism | Liver Cirrhosis - physiopathology | Inflammation - physiopathology | Cerebellum | Neuroimaging | Metabolic rate | Coma | Brain | Neurosciences | Basal ganglia | Dehydrogenases | Neuropathology | Pathogenesis | Liver | Systematic review | Antagonists | Activation | Reduction | γ-Aminobutyric acid | Encephalopathy | Hepatology | Thalamus | Movement disorders | Enzymes | Cortex (cingulate) | Medical imaging | Deactivation | Central nervous system diseases | Inflammation | Metabolism | Ganglia | Microglia | Neurology | Ammonia | Cirrhosis | Neurotransmitters | Gliosis | Medical prognosis | TNF inhibitors | Binding sites | Hepatic encephalopathy | Manganese | Review
Journal Article
Journal of Pediatric Gastroenterology and Nutrition, ISSN 0277-2116, 06/2013, Volume 56, Issue 6, pp. 675 - 681
OBJECTIVES:Congenital portosystemic shunts (CPSSs) are rare but increasingly recognized as a cause of important multisystem morbidity. We present new cases and... 
liver tumor | hepatopulmonary syndrome | encephalopathy | pulmonary hypertension | congenital portosystemic shunt | PORTAL-VEIN | LIVER-TRANSPLANTATION | PATENT DUCTUS VENOSUS | CLINICAL PRESENTATIONS | HEPATOCELLULAR-CARCINOMA | NUTRITION & DIETETICS | AMPLATZER VASCULAR PLUG | ABERNETHY MALFORMATION | PEDIATRICS | TRANSCATHETER CLOSURE | INTRAPULMONARY SHUNT | GASTROENTEROLOGY & HEPATOLOGY | Humans | Portal Vein - physiopathology | Infant | Young Adult | Liver Neoplasms - epidemiology | Vascular Malformations - therapy | Portal Vein - abnormalities | Nervous System Malformations - physiopathology | Abnormalities, Multiple - epidemiology | Hepatopulmonary Syndrome - epidemiology | Adult | Child | Hyperammonemia - etiology | Nervous System Malformations - therapy | Comorbidity | Hypertension, Pulmonary - epidemiology | Abnormalities, Multiple - physiopathology | Nervous System Malformations - epidemiology | Vascular Malformations - epidemiology | Abnormalities, Multiple - therapy | Abnormalities, Multiple - diagnosis | Adolescent | Nervous System Malformations - diagnosis | Heart Defects, Congenital - epidemiology | Vascular Malformations - diagnosis | Heart Defects, Congenital - diagnosis | Heart Defects, Congenital - physiopathology | Heart Defects, Congenital - therapy | Vascular Malformations - physiopathology
Journal Article
Journal Article
Journal Article
Annals of Nutrition and Metabolism, ISSN 0250-6807, 12/2016, Volume 68, Issue 3, pp. 1 - 4
The metabolic roles of carnitine have been greatly clarified over the past 50 years, and it is now well established that carnitine is a key player in... 
Carnitine Deficiency Disorders in Pediatrics | Carnitine deficiency | Inborn errors of metabolism | Metabolic disorders | Carnitine | NUTRITION & DIETETICS | ENDOCRINOLOGY & METABOLISM | DEFICIENCY | Lipid Metabolism, Inborn Errors - diet therapy | History, 21st Century | Humans | Lipid Metabolism, Inborn Errors - drug therapy | Cardiomyopathies - prevention & control | Infant | Carnitine - history | Lipid Metabolism, Inborn Errors - history | Metabolism, Inborn Errors - history | Cardiomyopathies - physiopathology | Deficiency Diseases - diet therapy | Carnitine - deficiency | Muscular Diseases - physiopathology | Orphan Drug Production - history | Adult | Muscular Diseases - history | Muscular Diseases - prevention & control | Dietary Supplements - adverse effects | Child | Carnitine Acyltransferases - history | Carnitine - administration & dosage | Hyperammonemia - physiopathology | Cardiomyopathies - history | Cardiomyopathies - diet therapy | History, 20th Century | Carnitine Acyltransferases - deficiency | Clinical Trials as Topic | Deficiency Diseases - prevention & control | Hyperammonemia - history | Hyperammonemia - prevention & control | Nutritional Sciences - history | Deficiency Diseases - history | Hyperammonemia - diet therapy | Metabolism, Inborn Errors - diet therapy | Carnitine - adverse effects | Lipid Metabolism, Inborn Errors - physiopathology | Administration, Intravenous | Muscular Diseases - diet therapy | Energy Metabolism | Carnitine - therapeutic use | Deficiency Diseases - physiopathology | Metabolism, Inborn Errors - drug therapy | Metabolism, Inborn Errors - physiopathology | Child Nutrition Sciences - history
Journal Article
Journal Article
Hepatology, ISSN 0270-9139, 10/2008, Volume 48, Issue 4, pp. 1202 - 1212
Journal Article
Journal Article
Heart Rhythm, ISSN 1547-5271, 2016, Volume 13, Issue 1, pp. 165 - 174
Journal Article
Journal Article
Glia, ISSN 0894-1491, 05/2007, Volume 55, Issue 7, pp. 758 - 771
Journal Article