X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (4642) 4642
Publication (413) 413
Book Chapter (56) 56
Newsletter (46) 46
Book Review (42) 42
Book / eBook (19) 19
Conference Proceeding (13) 13
Magazine Article (5) 5
Government Document (3) 3
Dissertation (2) 2
Reference (2) 2
Web Resource (2) 2
Data Set (1) 1
Paper (1) 1
Streaming Video (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (3023) 3023
male (1958) 1958
female (1708) 1708
animals (1587) 1587
index medicus (1548) 1548
acidosis (1294) 1294
adult (864) 864
lactic-acidosis (718) 718
hydrogen-ion concentration (647) 647
rats (597) 597
middle aged (586) 586
adolescent (403) 403
child (402) 402
mutation (396) 396
clinical neurology (385) 385
infant (374) 374
pathology (372) 372
neurosciences (367) 367
acidosis - pathology (366) 366
pediatrics (356) 356
acidosis - metabolism (352) 352
infant, newborn (351) 351
research (340) 340
metabolism (333) 333
brain - pathology (332) 332
child, preschool (332) 332
lactic acidosis (331) 331
acidosis - etiology (307) 307
aged (305) 305
mice (290) 290
physiology (285) 285
dna, mitochondrial - genetics (282) 282
encephalopathy (266) 266
urology & nephrology (263) 263
magnetic resonance imaging (253) 253
analysis (249) 249
disease (246) 246
hypoxia (244) 244
medicine (244) 244
biopsy (243) 243
cell biology (236) 236
physiological aspects (235) 235
diagnosis (234) 234
kidney - pathology (232) 232
time factors (232) 232
research article (230) 230
myopathy (227) 227
mitochondria (224) 224
risk factors (223) 223
genetics & heredity (222) 222
stroke-like episodes (221) 221
care and treatment (219) 219
mitochondrial dna (218) 218
disease models, animal (217) 217
metabolic acidosis (213) 213
rats, sprague-dawley (210) 210
acidosis - complications (206) 206
health aspects (205) 205
biochemistry & molecular biology (199) 199
multidisciplinary sciences (191) 191
article (190) 190
ischemia (187) 187
metabolic-acidosis (178) 178
pregnancy (174) 174
melas (170) 170
point mutation (169) 169
children (167) 167
brain (166) 166
muscle, skeletal - pathology (166) 166
cells, cultured (165) 165
liver - pathology (165) 165
blood (163) 163
acidosis - chemically induced (161) 161
renal tubular-acidosis (161) 161
apoptosis (160) 160
endocrinology & metabolism (160) 160
medicine, research & experimental (159) 159
cancer (158) 158
acidosis, lactic - pathology (156) 156
proteins (156) 156
surgery (154) 154
syndrome (153) 153
genetic aspects (151) 151
fatal outcome (150) 150
acidosis - physiopathology (149) 149
diagnosis, differential (149) 149
expression (149) 149
medicine, general & internal (149) 149
science (145) 145
dna (144) 144
mortality (144) 144
oncology (143) 143
phenotype (138) 138
cattle (137) 137
retrospective studies (134) 134
treatment outcome (134) 134
melas syndrome - genetics (133) 133
diabetes (132) 132
hematology (132) 132
rats, wistar (132) 132
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (4384) 4384
German (91) 91
Japanese (78) 78
French (76) 76
Spanish (38) 38
Russian (27) 27
Italian (18) 18
Polish (9) 9
Chinese (8) 8
Dutch (6) 6
Portuguese (6) 6
Bulgarian (3) 3
Ukrainian (3) 3
Hebrew (2) 2
Hungarian (2) 2
Korean (2) 2
Romanian (2) 2
Swedish (2) 2
Turkish (2) 2
Czech (1) 1
Danish (1) 1
Finnish (1) 1
Norwegian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Human Pathology, ISSN 0046-8177, 2015, Volume 49, pp. 27 - 32
Summary Complex I deficiency causes Leigh syndrome, fatal infant lactic acidosis, and neonatal cardiomyopathy. Mutations in more than 100 nuclear DNA and... 
Pathology | Metabolic disease | Lethal neonatal lactic acidosis | Whole-exome sequencing | Mitochondriopathy | Complex I deficiency | ACAD9 defect | Mitochondrial hyperplasia | Multiorgan failure | DIAGNOSIS | CARDIOMYOPATHY | PATHOLOGY | GENE | DNA | EXPRESSION | Immunohistochemistry | Fibroblasts - enzymology | Diaphragm - pathology | Mitochondria, Heart - pathology | Electron Transport Complex I - deficiency | Humans | Hyperplasia | Male | Cardiomyopathy, Hypertrophic - enzymology | Acyl-CoA Dehydrogenases - genetics | Leigh Disease - pathology | Muscle Weakness - genetics | Amino Acid Metabolism, Inborn Errors - genetics | Autopsy | DNA Mutational Analysis | Electron Transport Complex I - genetics | Fatal Outcome | Muscle Weakness - pathology | Acyl-CoA Dehydrogenases - deficiency | Amino Acid Metabolism, Inborn Errors - pathology | Kidney Tubules - pathology | Infant, Newborn | Multiple Organ Failure - pathology | Acyl-CoA Dehydrogenase - genetics | Cardiomyopathy, Hypertrophic - genetics | Genetic Predisposition to Disease | Mitochondria, Liver - pathology | Mitochondria, Heart - enzymology | Fibroblasts - pathology | Leigh Disease - genetics | Acidosis, Lactic - pathology | Cardiomyopathy, Hypertrophic - diagnosis | Mitochondrial Diseases - enzymology | Phenotype | Acyl-CoA Dehydrogenase - deficiency | Kidney Tubules - enzymology | Acidosis - diagnosis | Multiple Organ Failure - enzymology | Acidosis - genetics | Amino Acid Metabolism, Inborn Errors - enzymology | Mitochondrial Diseases - pathology | Muscle Weakness - diagnosis | Acidosis, Lactic - genetics | Cause of Death | Acidosis, Lactic - enzymology | Amino Acid Metabolism, Inborn Errors - diagnosis | DNA, Mitochondrial - genetics | Muscle Weakness - enzymology | Transfection | Mitochondrial Diseases - genetics | Mitochondria, Muscle - enzymology | Mitochondria, Muscle - pathology | Leigh Disease - enzymology | Cells, Cultured | Multiple Organ Failure - genetics | Codon, Nonsense | Mitochondria, Liver - enzymology | Multiple Organ Failure - diagnosis | Diaphragm - enzymology | Acidosis - pathology | Leigh Disease - diagnosis | Acidosis - enzymology | Mitochondrial Diseases - diagnosis | Acidosis, Lactic - diagnosis | Cardiomyopathy, Hypertrophic - pathology | Infants (Newborn) | Muscles | Genetic aspects | Mitochondrial DNA | Liver | Heart | Urine | Cytochrome | Antigens | Enzymes | Cytomegalovirus | Cardiomyopathy | Data bases | Defects | Musculoskeletal system | Rodents | Fibroblasts | Oxidation | Mutation | Metabolic disorders | Deoxyribonucleic acid--DNA
Journal Article
European journal of human genetics : EJHG, ISSN 1018-4813, 09/2015, Volume 23, Issue 9, pp. 1254 - 1258
Coenzyme Q10 deficiency is a clinically and genetically heterogeneous disorder, with manifestations that may range from fatal neonatal multisystem failure, to... 
Mitochondrial Diseases - pathology | Muscle Weakness - diagnosis | Acidosis, Lactic - genetics | Humans | Ubiquinone - deficiency | Muscle Weakness - blood | Proteinuria - pathology | Muscle Weakness - genetics | Intellectual Disability - genetics | Proteinuria - blood | Intellectual Disability - blood | Alkyl and Aryl Transferases - genetics | Ubiquinone - blood | Fatal Outcome | Muscle Weakness - pathology | Acidosis, Lactic - blood | Ataxia - blood | Female | Ataxia - genetics | Alkyl and Aryl Transferases - deficiency | Infant, Newborn | Ataxia - pathology | Mitochondria, Muscle - genetics | Mitochondrial Diseases - genetics | Gene Expression | Muscle, Skeletal - enzymology | Mitochondria, Muscle - enzymology | Mitochondria, Muscle - pathology | Ubiquinone - analogs & derivatives | Intellectual Disability - pathology | Ubiquinone - genetics | Proteinuria - genetics | Acidosis, Lactic - pathology | Ataxia - diagnosis | Hepatic Insufficiency - blood | Sequence Analysis, DNA | Renal Aminoacidurias - pathology | Point Mutation | Hepatic Insufficiency - pathology | Hepatic Insufficiency - genetics | Consanguinity | Renal Aminoacidurias - genetics | Muscle, Skeletal - pathology | Mitochondrial Diseases - blood | Mitochondrial Diseases - diagnosis | Renal Aminoacidurias - blood | Neonates | Cell culture | Intensive care | Laboratories | Genomics | Liver | Childrens health | Aciduria | Ventricles (cerebral) | Biosynthesis | Genetic screening | Electron transport chain | Mitochondria | Coenzyme Q10 | Encephalopathy | Fibroblasts | Genetics | Complementation | Supplementation | Diagnosis | Lactic acidosis | Echocardiography | Electron microscopy | Metabolism | Patients | Pregnancy | Cristae | Mutation | Ventricle | Acidosis | Proteinuria | Life Sciences | Human health and pathology | Short Report
Journal Article
Cellular and Molecular Life Sciences, ISSN 1420-682X, 08/2017, Volume 74, Issue 15, pp. 2761 - 2771
Although surgical excision, chemo-, and radiotherapy are clearly advanced, tumors may relapse due to cells of the so-called "minimal residual disease". Indeed,... 
Dormancy | Tumor microenvironment | Acidosis | CANCER-CELLS | LACTIC-ACID | STEM-CELLS | BIOCHEMISTRY & MOLECULAR BIOLOGY | RADIATION-INDUCED APOPTOSIS | CELL BIOLOGY | EPITHELIAL-MESENCHYMAL TRANSITION | HUMAN GLIOBLASTOMA CELLS | IN-VIVO | HUMAN-MELANOMA CELLS | PUMP INHIBITOR PANTOPRAZOLE | EXTRACELLULAR PH | Immunologic Surveillance | Neoplasm, Residual - pathology | Acidosis - immunology | Cell Proliferation | Prognosis | Humans | Neoplastic Stem Cells - immunology | Tumor Microenvironment | Killer Cells, Natural - pathology | Neoplasm Recurrence, Local - etiology | Neovascularization, Pathologic - etiology | Neovascularization, Pathologic - pathology | T-Lymphocytes, Cytotoxic - pathology | Neoplasm Recurrence, Local - immunology | Neoplasm Recurrence, Local - pathology | Acidosis - complications | Neoplasms - therapy | Killer Cells, Natural - immunology | Neoplastic Stem Cells - pathology | Neoplasm, Residual - immunology | Neovascularization, Pathologic - immunology | T-Lymphocytes, Cytotoxic - immunology | Animals | Neoplasms - immunology | Acidosis - pathology | Neoplasm, Residual - complications | Neoplasms - pathology | Apoptosis | Hydrogen-Ion Concentration | Chemotherapy | Killer cells | Cancer | Therapy | Target recognition | Tumor cells | Minimal residual disease | Cytotoxicity | Radio | Acidity | Radiation therapy | Tissues | Patients | Cells | Immunology | Acids | Lymphocytes | Surgery | Clusters | Remission | Natural killer cells | Tumors
Journal Article
Neurology, ISSN 0028-3878, 2014, Volume 82, Issue 23, pp. 2063 - 2071
Journal Article
Current Opinion in Allergy and Clinical Immunology, ISSN 1528-4050, 06/2014, Volume 14, Issue 3, pp. 217 - 221
PURPOSE OF REVIEWTo raise awareness among healthcare providers about the clinical and laboratory findings in acute and chronic food protein-induced... 
Rice allergy | Food allergy | Food anaphylaxis | Food protein-induced enterocolitis syndrome | CHALLENGE | MANAGEMENT | ALLERGY | food protein-induced enterocolitis syndrome | food anaphylaxis | rice allergy | IMMUNOLOGY | food allergy | COWS MILK | FEATURES | Hypoalbuminemia - pathology | Humans | Hypoalbuminemia - etiology | Methemoglobinemia - diagnosis | Methemoglobinemia - physiopathology | Male | Methemoglobinemia - etiology | Anemia - physiopathology | Eosinophilia - pathology | Thrombocytosis - blood | Failure to Thrive - pathology | Failure to Thrive - diagnosis | Enterocolitis - diagnosis | Methemoglobinemia - blood | Eosinophilia - physiopathology | Acute Disease | Eosinophilia - etiology | Enterocolitis - physiopathology | Anemia - diagnosis | Thrombocytosis - etiology | Hypoalbuminemia - diagnosis | Acidosis - diagnosis | Dietary Proteins - adverse effects | Chronic Disease | Enterocolitis - pathology | Anemia - blood | Diarrhea - physiopathology | Eosinophilia - blood | Failure to Thrive - blood | Enterocolitis - blood | Failure to Thrive - etiology | Anemia - pathology | Enterocolitis - etiology | Diarrhea - pathology | Methemoglobinemia - pathology | Diarrhea - blood | Acidosis - physiopathology | Hypoalbuminemia - blood | Failure to Thrive - physiopathology | Thrombocytosis - pathology | Anemia - etiology | Eosinophilia - diagnosis | Acidosis - etiology | Acidosis - blood | Thrombocytosis - physiopathology | Syndrome | Thrombocytosis - diagnosis | Diarrhea - diagnosis | Weight Loss | Acidosis - pathology | Diarrhea - etiology | Hypoalbuminemia - physiopathology | Edited by Alessandro Fiocchi and Julie Wang | FOOD ALLERGY
Journal Article
Journal of Forensic and Legal Medicine, ISSN 1752-928X, 2008, Volume 16, Issue 4, pp. 173 - 177
Journal Article
Pediatric Nephrology, ISSN 0931-041X, 11/2014, Volume 29, Issue 11, pp. 2139 - 2146
Journal Article
American Journal of Tropical Medicine and Hygiene, ISSN 0002-9637, 04/2013, Volume 88, Issue 4, pp. 747 - 756
Journal Article