biotin has been researched along with Acquired Metabolic Diseases, Brain in 9 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (22.22) | 18.7374 |
| 1990's | 4 (44.44) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 3 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Lopez-Marin, L | 1 |
| Chen, J; Chen, SZ; Fan, CH; Li, R; Liu, XM; Sang, Y | 1 |
| Bellanger, A; Brice, A; Debs, R; Degos, B; Depienne, C; Galanaud, D; Keren, B; Lyon-Caen, O; Rastetter, A; Sedel, F | 1 |
| Glasgow, AM; Higgins, JJ; Kerr, DS; Lusk, M | 1 |
| Amir, N; Elpeleg, ON; Eshel, G; Gibson, KM; Livne, M | 1 |
| Dulac, O; Gautier, A; Héron, B; Ponsot, G | 1 |
| Bousounis, DP; Camfield, PR; Wolf, B | 1 |
| Bachmann, C; Baumgartner, ER; Blauenstein, U; Probst, A; Suormala, TM; Vest, M; Wick, H | 1 |
| Bressman, S; Brin, M; Eisenberg, M; Fahn, S; Maltese, W | 1 |
1 review(s) available for biotin and Acquired Metabolic Diseases, Brain
| Article | Year |
|---|---|
[Metabolic approach in epileptic encephalopathies in infants].
Topics: Age of Onset; Biotin; Brain Diseases, Metabolic; Brain Diseases, Metabolic, Inborn; Child, Preschool; Creatine; Diagnostic Techniques, Neurological; Epilepsy; Fetal Diseases; Holocarboxylase Synthetase Deficiency; Humans; Hypoxia-Ischemia, Brain; Infant; Infant, Newborn; Pyridoxaminephosphate Oxidase; Pyridoxine; Seizures | 2017 |
8 other study(ies) available for biotin and Acquired Metabolic Diseases, Brain
| Article | Year |
|---|---|
Screening of Inherited Metabolic Disorders in Infants with Infantile Spasms.
Topics: Amino Acid Metabolism, Inborn Errors; Anticonvulsants; Biotin; Brain; Brain Diseases, Metabolic; Chromatography, Gas; Developmental Disabilities; Epilepsy; Female; Glutaryl-CoA Dehydrogenase; Humans; Infant; Liver; Liver Function Tests; Magnetic Resonance Imaging; Male; Mass Screening; Mass Spectrometry; Metabolic Diseases; Phenylketonurias; Spasms, Infantile; Succinate-Semialdehyde Dehydrogenase; Tomography, X-Ray Computed | 2015 |
Biotin-responsive basal ganglia disease in ethnic Europeans with novel SLC19A3 mutations.
Topics: Adult; Basal Ganglia; Basal Ganglia Diseases; Biotin; Brain Diseases, Metabolic; DNA Mutational Analysis; Dystonia; Epilepsy; Europe; Female; Genetic Markers; Genetic Predisposition to Disease; Genotype; Humans; Magnetic Resonance Imaging; Male; Membrane Transport Proteins; Mutation; Portugal; Thiamine; Treatment Outcome; Vitamin B Complex; White People | 2010 |
MRI, clinical, and biochemical features of partial pyruvate carboxylase deficiency.
Topics: Biotin; Brain; Brain Diseases, Metabolic; Child; Child, Preschool; Consanguinity; Fibroblasts; Follow-Up Studies; Humans; Infant; Infant, Newborn; Lymphocytes; Magnetic Resonance Imaging; Male; Neurologic Examination; Phenotype; Pyruvate Carboxylase; Pyruvate Carboxylase Deficiency Disease | 1994 |
Holocarboxylase synthetase deficiency: a treatable metabolic disorder masquerading as cerebral palsy.
Topics: Biotin; Brain Diseases, Metabolic; Carbon-Nitrogen Ligases; Carnitine; Cerebral Palsy; Follow-Up Studies; Humans; Infant; Ligases; Male; Neurologic Examination; Prenatal Diagnosis; Psychomotor Disorders; Triplets | 1994 |
[Biotinidase deficiency. Progressive encephalopathy curable with biotin].
Topics: Amidohydrolases; Biotin; Biotinidase; Brain Diseases, Metabolic; Epilepsy; Humans; Infant; Male | 1993 |
Reversal of brain atrophy with biotin treatment in biotinidase deficiency.
Topics: Amidohydrolases; Atrophy; Biotin; Biotinidase; Brain; Brain Diseases, Metabolic; Child, Preschool; Electroencephalography; Female; Follow-Up Studies; Humans; Infant; Magnetic Resonance Imaging; Male; Neurologic Examination; Tomography, X-Ray Computed | 1993 |
Biotinidase deficiency: a cause of subacute necrotizing encephalomyelopathy (Leigh syndrome). Report of a case with lethal outcome.
Topics: Amidohydrolases; Biotin; Biotinidase; Brain Diseases, Metabolic; Carboxy-Lyases; Cerebral Cortex; Diagnosis, Differential; Female; Humans; Infant; Kidney; Leigh Disease; Liver; Respiratory Sounds | 1989 |
Biotin-responsive encephalopathy with myoclonus, ataxia, and seizures.
Topics: Adult; Amidohydrolases; Ataxia; Biotin; Biotinidase; Brain Diseases, Metabolic; Electroencephalography; Electromyography; Female; Hearing Loss; Humans; Myoclonus; Pyruvate Carboxylase; Seizures | 1986 |