X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (4230) 4230
Book Review (621) 621
Publication (162) 162
Newsletter (145) 145
Book Chapter (26) 26
Magazine Article (16) 16
Conference Proceeding (3) 3
Data Set (1) 1
Dissertation (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
humans (3104) 3104
index medicus (3013) 3013
rhabdomyolysis (2896) 2896
male (2130) 2130
adult (1330) 1330
female (1307) 1307
rhabdomyolysis - diagnosis (990) 990
rhabdomyolysis - etiology (990) 990
middle aged (896) 896
rhabdomyolysis - chemically induced (592) 592
risk factors (576) 576
diagnosis (563) 563
aged (501) 501
acute kidney injury - etiology (480) 480
medicine, general & internal (466) 466
creatine kinase - blood (463) 463
adolescent (440) 440
rhabdomyolysis - complications (435) 435
abridged index medicus (417) 417
acute-renal-failure (391) 391
diagnosis, differential (380) 380
rhabdomyolysis - therapy (379) 379
care and treatment (332) 332
animals (319) 319
exercise (316) 316
child (295) 295
complications and side effects (290) 290
case studies (287) 287
health aspects (285) 285
acute renal failure (276) 276
creatine kinase (275) 275
research (268) 268
myopathy (265) 265
medicine & public health (263) 263
treatment outcome (263) 263
young adult (256) 256
surgery (253) 253
pediatrics (252) 252
urology & nephrology (251) 251
acute kidney injury (247) 247
retrospective studies (235) 235
myoglobinuria (231) 231
clinical neurology (229) 229
case report (228) 228
rhabdomyolysis - physiopathology (219) 219
hydroxymethylglutaryl-coa reductase inhibitors - adverse effects (208) 208
acute kidney injury - therapy (202) 202
acute kidney injury - diagnosis (201) 201
acute disease (195) 195
muscle, skeletal - pathology (190) 190
rhabdomyolysis - blood (190) 190
statins (189) 189
pharmacology & pharmacy (186) 186
rhabdomyolysis - pathology (183) 183
myoglobin (171) 171
child, preschool (165) 165
aged, 80 and over (163) 163
neurosciences (161) 161
medicine (160) 160
patients (160) 160
anesthesiology (154) 154
emergency medicine (150) 150
exertional rhabdomyolysis (146) 146
mortality (145) 145
veterinary sciences (145) 145
biopsy (144) 144
children (143) 143
internal medicine (141) 141
skeletal-muscle (139) 139
analysis (137) 137
creatine (137) 137
time factors (137) 137
management (136) 136
muscles (136) 136
compartment syndrome (133) 133
malignant hyperthermia (133) 133
rhabdomyolysis - epidemiology (128) 128
disease (127) 127
muscle (127) 127
prognosis (127) 127
fatal outcome (126) 126
risk (125) 125
horses (124) 124
urine (124) 124
medical research (123) 123
mutation (122) 122
magnetic resonance imaging (121) 121
complications (119) 119
drug therapy (119) 119
metabolism (117) 117
renal failure (117) 117
muscular diseases - chemically induced (112) 112
therapy (112) 112
biomarkers - blood (111) 111
renal dialysis (110) 110
kidneys (108) 108
drug interactions (107) 107
follow-up studies (107) 107
simvastatin (107) 107
causes of (106) 106
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (3874) 3874
German (121) 121
French (118) 118
Spanish (92) 92
Japanese (66) 66
Italian (25) 25
Korean (23) 23
Portuguese (15) 15
Polish (11) 11
Dutch (10) 10
Norwegian (9) 9
Danish (8) 8
Russian (7) 7
Chinese (6) 6
Turkish (6) 6
Czech (5) 5
Serbian (4) 4
Hebrew (3) 3
Hungarian (3) 3
Croatian (2) 2
Lithuanian (2) 2
Romanian (2) 2
Bulgarian (1) 1
Finnish (1) 1
Icelandic (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Clinical Imaging, ISSN 0899-7071, 11/2019, Volume 58, pp. 166 - 169
We report the case of a 36 year old male who demonstrated extensive high attenuation in the muscles of the chest wall and neck on a noncontrast chest CT. The... 
Rhabdomyolysis | Index Medicus
Journal Article
Pediatrics, ISSN 0031-4005, 02/2013, Volume 131, Issue 2, pp. e629 - e634
Folate and vitamin B-12 metabolism are essential for de novo purine synthesis, and several defects in these pathways have been associated with... 
Cobalamin | Megaloblast | Hemolytic uremic syndrome | Folate | Immunodeficiency | folate | DEFECTS | cobalamin | GENE | megaloblast | TRANSCOBALAMIN-II DEFICIENCY | ABNORMALITIES | PEDIATRICS | immunodeficiency | PATIENT | hemolytic uremic syndrome | Peripheral Nervous System Diseases - diagnosis | Leukopenia - diagnosis | Lipid Metabolism, Inborn Errors - genetics | Pneumonia, Pneumocystis - diagnosis | Humans | 3-Hydroxyacyl CoA Dehydrogenases - genetics | Vitamin B 12 - therapeutic use | DNA Mutational Analysis | Sulfadoxine - therapeutic use | Cardiomyopathies - diagnosis | Infant, Newborn | Cardiomyopathies - drug therapy | Mitochondrial Myopathies | Retinitis Pigmentosa - drug therapy | Trimethoprim - therapeutic use | Combined Modality Therapy | Bone Marrow Examination | Sequence Analysis, DNA | Retinitis Pigmentosa - diagnosis | Severe Combined Immunodeficiency - genetics | Pneumonia, Pneumocystis - genetics | Immunization, Passive | Leukopenia - drug therapy | Genetic Carrier Screening | Peripheral Nervous System Diseases - drug therapy | Mitochondrial Trifunctional Protein - deficiency | Anemia, Megaloblastic - genetics | Minor Histocompatibility Antigens | Lipid Metabolism, Inborn Errors - drug therapy | Leukopenia - genetics | Infant | Rhabdomyolysis | Cardiomyopathies - genetics | Anemia, Megaloblastic - diagnosis | Female | Drug Therapy, Combination | Peripheral Nervous System Diseases - genetics | Methylenetetrahydrofolate Dehydrogenase (NADP) - genetics | Hydroxocobalamin - therapeutic use | Pneumonia, Pneumocystis - drug therapy | Severe Combined Immunodeficiency - diagnosis | Lipid Metabolism, Inborn Errors - diagnosis | Severe Combined Immunodeficiency - drug therapy | Retinitis Pigmentosa - genetics | Opportunistic Infections - genetics | Opportunistic Infections - diagnosis | Exome - genetics | Opportunistic Infections - drug therapy | Anemia, Megaloblastic - drug therapy | 3-Hydroxyacyl CoA Dehydrogenases - deficiency | Drug Combinations | Nervous System Diseases | Care and treatment | Gene mutations | Research | Nucleotide sequencing | Diagnosis | Vitamin B12 | Hemolytic-uremic syndrome | DNA sequencing | Pediatrics | Immunology | Vitamin B | Genetics | Mutation | Drug therapy | Metabolism | Index Medicus | Abridged Index Medicus
Journal Article
Journal of Craniofacial Surgery, ISSN 1049-2275, 12/2015, Volume 27, Issue 1, pp. e48 - e50
Journal Article
European Journal of Internal Medicine, ISSN 0953-6205, 2006, Volume 18, Issue 2, pp. 90 - 100
Abstract Rhabdomyolysis is defined as a pathological condition of skeletal muscle cell damage leading to the release of toxic intracellular material into the... 
Internal Medicine | Rhabdomyolysis | Energy depletion | Diagnosis | Calcium | Cell death
Journal Article
EUROPEAN JOURNAL OF INTERNAL MEDICINE, ISSN 0953-6205, 03/2007, Volume 18, Issue 2, pp. 90 - 100
Rhabdomyolysis is defined as a pathological condition of skeletal muscle cell damage leading to the release of toxic intracellular material into the blood... 
OXIDATIVE STRESS | calcium | cell death | diagnosis | ACUTE-RENAL-FAILURE | energy depletion | PERMEABILITY TRANSITION | CELL-DEATH | SKELETAL-MUSCLE | MEDICINE, GENERAL & INTERNAL | rhabdomyolysis | NEUROMUSCULAR MANIFESTATIONS | CA2 | DRUG-INDUCED RHABDOMYOLYSIS | DISEASE
Journal Article
Internal Medicine Journal, ISSN 1444-0903, 09/2019, Volume 49, Issue 9, pp. 1081 - 1091
Hyperlipidaemia is a major risk factor for cardiovascular morbidity and mortality. 3‐hydroxy‐3‐methylglutaryl coenzyme‐A reductase inhibitors (‘statins’) are... 
cardiovascular disease | statin intolerance | statin | alternative therapy | lipid | Complications and side effects | Enzymes | Low density lipoproteins | Mortality | Statins | Cardiovascular agents | Lipoproteins (low density) | Apheresis | Hyperlipidemia | Rhabdomyolysis | Management | Morbidity | Risk factors | Cholesterol | Intolerance | Diagnosis | Cardiovascular diseases | Myopathy | Reductase | Index Medicus
Journal Article
Acta Paediatrica, ISSN 0803-5253, 05/2016, Volume 105, Issue 5, pp. 549 - 554
Journal Article
Journal of special operations medicine : a peer reviewed journal for SOF medical professionals, ISSN 1553-9768, 09/2016, Volume 16, Issue 3, pp. 65 - 71
Exertional rhabdomyolysis (ER) is a medical condition whereby damage to skeletal muscle is induced by excessive physical activity in otherwise healthy... 
Fluid Therapy | Primary Prevention | Rhabdomyolysis - diagnosis | Exercise | Military Personnel | Rhabdomyolysis - epidemiology | Humans | Rhabdomyolysis - therapy | Risk Factors | Rhabdomyolysis - prevention & control
Journal Article
Journal of the American Veterinary Medical Association, ISSN 0003-1488, 02/2000, Volume 216, Issue 4, pp. 554 - 558
Journal Article
Ophthalmology, ISSN 0161-6420, 10/2016, Volume 123, Issue 10, pp. 2183 - 2195
Purpose To assess long-term effects of genotype on chorioretinopathy severity in patients with mitochondrial trifunctional protein (MTP) disorders. Design... 
AMPLITUDE-DECORRELATION ANGIOGRAPHY | COA DEHYDROGENASE | OPTICAL COHERENCE TOMOGRAPHY | FATTY-ACID OXIDATION | STRATEGY | OPTIMAL DIETARY THERAPY | OPHTHALMOLOGY | RETINOPATHY | G1528C MUTATION | SPECTRUM | 3-HYDROXYACYL-COA DEHYDROGENASE-DEFICIENCY | Lipid Metabolism, Inborn Errors - genetics | Prognosis | Follow-Up Studies | Humans | Child, Preschool | Rhabdomyolysis - complications | Infant | Male | Nervous System Diseases - genetics | Nervous System Diseases - diagnosis | Young Adult | Cardiomyopathies - genetics | Rhabdomyolysis - diagnosis | Visual Fields | Cardiomyopathies - diagnosis | Adult | Female | Retrospective Studies | Mitochondrial Myopathies - diagnosis | Child | Choroid Diseases - genetics | Fluorescein Angiography | Electroretinography | Mitochondrial Trifunctional Protein - genetics | Mitochondrial Myopathies - complications | Tomography, Optical Coherence | Lipid Metabolism, Inborn Errors - diagnosis | Genotype | Choroid Diseases - etiology | Visual Acuity | Forecasting | Nervous System Diseases - complications | Mitochondrial Myopathies - genetics | Mitochondrial Trifunctional Protein - metabolism | Rhabdomyolysis - genetics | Adolescent | Cardiomyopathies - complications | Lipid Metabolism, Inborn Errors - complications | Choroid Diseases - diagnosis | Fundus Oculi | Mitochondrial Trifunctional Protein - deficiency | Index Medicus
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 04/2018, Volume 123, Issue 4, pp. 441 - 448
Journal Article
Western Journal of Emergency Medicine, ISSN 1936-900X, 2016, Volume 17, Issue 6, pp. 801 - 804
Journal Article
Zhongguo xiu fu chong jian wai ke za zhi = Zhongguo xiufu chongjian waike zazhi = Chinese journal of reparative and reconstructive surgery, ISSN 1002-1892, 06/2018, Volume 32, Issue 6, pp. 703 - 706
Journal Article
No results were found for your search.

Cannot display more than 1000 results, please narrow the terms of your search.