X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (3398) 3398
Publication (246) 246
Book Chapter (32) 32
Book Review (27) 27
Dissertation (3) 3
Book / eBook (2) 2
Conference Proceeding (2) 2
Journal / eJournal (2) 2
Magazine Article (2) 2
Newspaper Article (2) 2
Data Set (1) 1
Paper (1) 1
Reference (1) 1
Trade Publication Article (1) 1
Web Resource (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
hyperammonemia (2265) 2265
humans (1881) 1881
male (1262) 1262
index medicus (1163) 1163
female (972) 972
animals (867) 867
ammonia (828) 828
ammonia - blood (528) 528
neurosciences (506) 506
rats (502) 502
hepatic encephalopathy (453) 453
adult (449) 449
encephalopathy (423) 423
metabolism (390) 390
pediatrics (386) 386
middle aged (385) 385
hyperammonemia - etiology (360) 360
biochemistry & molecular biology (329) 329
liver (318) 318
child (314) 314
hepatic-encephalopathy (309) 309
brain (302) 302
hyperammonemia - metabolism (300) 300
infant, newborn (295) 295
endocrinology & metabolism (273) 273
infant (269) 269
gastroenterology & hepatology (258) 258
genetics & heredity (254) 254
child, preschool (252) 252
glutamine (251) 251
adolescent (242) 242
hyperammonemia - chemically induced (242) 242
clinical neurology (241) 241
hyperammonemia - diagnosis (241) 241
brain - metabolism (236) 236
hyperammonemia - complications (233) 233
rats, wistar (226) 226
mutation (225) 225
neurology (223) 223
ornithine transcarbamylase deficiency (223) 223
urea (222) 222
ammonia - metabolism (220) 220
diagnosis (219) 219
aged (218) 218
medicine, research & experimental (210) 210
children (195) 195
hyperammonemia - drug therapy (191) 191
urea cycle disorders (191) 191
glutamate (189) 189
valproic acid (187) 187
valproic acid - adverse effects (187) 187
mice (184) 184
treatment outcome (183) 183
urea cycle (183) 183
biochemistry, general (182) 182
analysis (181) 181
hyperammonemia - therapy (179) 179
cirrhosis (178) 178
hyperammonemia - blood (178) 178
hyperammonemia - genetics (172) 172
enzymes (167) 167
acute liver-failure (162) 162
hyperammonemia - physiopathology (160) 160
oncology (159) 159
risk factors (159) 159
carnitine (155) 155
physiological aspects (155) 155
medicine & public health (154) 154
health aspects (152) 152
liver diseases (151) 151
biomedicine (150) 150
amino acids (149) 149
hepatic encephalopathy - metabolism (149) 149
disease models, animal (147) 147
pharmacology & pharmacy (146) 146
therapy (146) 146
care and treatment (145) 145
deficiency (137) 137
medicine, general & internal (137) 137
research (137) 137
article (136) 136
urea - metabolism (134) 134
hepatic encephalopathy - etiology (133) 133
coma (126) 126
liver cirrhosis (126) 126
oxidative stress (122) 122
astrocytes (121) 121
metabolic diseases (121) 121
in-vivo (119) 119
inborn-errors (118) 118
anticonvulsants - adverse effects (117) 117
hyperammonemia - pathology (115) 115
diagnosis, differential (114) 114
glutamine - metabolism (112) 112
hepatic encephalopathy - physiopathology (112) 112
gene (111) 111
mutations (111) 111
internal medicine (106) 106
epilepsy (104) 104
glutamic acid - metabolism (103) 103
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (3114) 3114
Japanese (76) 76
Spanish (71) 71
French (51) 51
German (50) 50
Chinese (19) 19
Korean (18) 18
Italian (11) 11
Portuguese (6) 6
Polish (5) 5
Turkish (4) 4
Norwegian (3) 3
Russian (3) 3
Czech (1) 1
Dutch (1) 1
Finnish (1) 1
Hebrew (1) 1
Romanian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Gastroenterology, ISSN 0016-5085, 2010, Volume 139, Issue 2, pp. 675 - 684
Background & Aims Hyperammonemia and inflammation cooperate to induce neurological alterations in hepatic encephalopathy. Recent studies in animal models... 
Gastroenterology and Hepatology | Neuroinflammation | Bile Duct-Ligation | Hyperammonemia | Hepatic Encephalopathy | LEARNING-ABILITY | ALZHEIMERS-DISEASE | PATHOLOGY | MODELS | INFLAMMATION | CIRRHOTIC-PATIENTS | GASTROENTEROLOGY & HEPATOLOGY | IBUPROFEN RESTORES | BRAIN | Inflammation - pathology | Rats, Wistar | Male | Motor Activity | Anti-Inflammatory Agents, Non-Steroidal - pharmacology | Hyperammonemia - pathology | Learning | Hyperammonemia - drug therapy | Cognition Disorders - prevention & control | Ligation | Microglia - immunology | Inflammation - drug therapy | Cognition Disorders - etiology | Inflammation Mediators - metabolism | Microglia - pathology | Behavior, Animal - drug effects | Hepatic Encephalopathy - etiology | Cognition Disorders - immunology | Cognition Disorders - psychology | Disease Models, Animal | Ibuprofen - pharmacology | Inflammation - psychology | Quaternary Ammonium Compounds | Cognition Disorders - pathology | Rats | Inflammation - immunology | Bile Ducts - surgery | Cognition - drug effects | Inflammation - etiology | Hepatic Encephalopathy - prevention & control | Hepatic Encephalopathy - pathology | Animals | Hepatic Encephalopathy - immunology | Hyperammonemia - complications | Hyperammonemia - immunology | Brain - pathology | Hepatic Encephalopathy - psychology | Brain - immunology | Hyperammonemia - psychology | Cell Movement | Mitogens | Prostaglandins E | Nitric oxide | Hepatic encephalopathy
Journal Article
2017, Clinics in developmental medicine (unnumbered), ISBN 9781909962835, xxv, 225 pages
Among the vast body of literature that has grown around Rett syndrome, this volume is the first to be aimed at both clinicians and researchers. It presents a... 
Rett syndrome | Treatment
Book
Case report - Valproate-induced hyperammonemic encephalopathy with normal liver function, 12/2005
Hyperammonemic encephalopathy with normal liver function is an uncommon serious adverse effect of valproate therapy. We retrospectively analyzed the case... 
Valproate, Hyperammonemia, Hyperammonemic encephalopathy
Journal
Orphanet Journal of Rare Diseases, ISSN 1750-1172, 2012, Volume 7, Issue 1, pp. 32 - 32
Journal Article
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 4/2015, Volume 112, Issue 17, pp. 5521 - 5526
Journal Article
Orphanet Journal of Rare Diseases, ISSN 1750-1172, 08/2016, Volume 11, Issue 1, p. 116
Journal Article
PLoS ONE, ISSN 1932-6203, 07/2013, Volume 8, Issue 7, p. e60581
Most conditions detected by expanded newborn screening result from deficiency of one of the enzymes that degrade acyl-coenzyme A (CoA) esters in mitochondria.... 
RAT-LIVER | 3-HYDROXY-3-METHYLGLUTARYL-COA LYASE | INHIBITION | METABOLISM | COENZYME-A PROFILES | PYRUVATE-CARBOXYLASE | QUANTIFICATION | MULTIDISCIPLINARY SCIENCES | DEFICIENT MICE | LYASE HL | SPECTROMETRY | Hyperammonemia - metabolism | Humans | Hypoglycemia - mortality | Acetyl Coenzyme A - genetics | Acyl Coenzyme A - genetics | Hepatocytes - metabolism | Mitochondria - ultrastructure | Genes, Lethal | Mitochondria - genetics | Pyruvic Acid - metabolism | Hyperammonemia - mortality | Gene Order | Hypoglycemia - genetics | Gene Targeting | Hyperammonemia - genetics | Leucine - metabolism | Carbon Dioxide - metabolism | Liver - metabolism | Acyl Coenzyme A - deficiency | Metabolome | Mitochondria - metabolism | Gene Knockout Techniques | Hypoglycemia - metabolism | Acetyl Coenzyme A - metabolism | Mice, Knockout | Peroxisomes | Phenotype | Animals | Gluconeogenesis - genetics | Metabolic Networks and Pathways | Models, Biological | Lethargy | Mice | Enzymes | Esters | Metabolites | Glutamate | Analysis | Organic acids | Glutamic acid | Inborn errors of metabolism | Ketogenesis | Laboratories | Liver | Pyruvic acid | Leucine | Defects | Degradation | Proteins | Mitochondria | Rodents | Coenzyme A | Chemical synthesis | Gluconeogenesis | Urine | Medical research | Incubation | Hyperammonemia | Hypoglycemia | Metabolism | Fatty acids | Studies | Urea | Hepatocytes | Carboxylation | Scientific imaging | Mass spectrometry | Acetyl Coenzyme A | Life Sciences | Hépatology and Gastroenterology | Carbon Dioxide | Human health and pathology | Pyruvic Acid | Acyl Coenzyme A
Journal Article
Annals of internal medicine, ISSN 0003-4819, 02/2018, Volume 168, Issue 4, p. 306
Journal Article
Recurrent stupor due to lysinuric protein intolerance, 12/2005
Recurrent stupor in children is an uncommon clinical problem with a wide differential diagnosis; inherited metabolic disorders account for a vast majority. We... 
Lysinuric protein intolerance, hyperammonemia, recurrent stupor
Journal
Journal Article
Clinical Toxicology, ISSN 1556-3650, 2/2009, Volume 47, Issue 2, pp. 101 - 111
Introduction. Valproic acid (VPA) is a broad-spectrum antiepileptic drug that is now used commonly for several other neurological and psychiatric indications.... 
Antidotes | Valproic acid | Hepatotoxicity |