biotin has been researched along with Metabolic Diseases in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (25.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 2 (50.00) | 24.3611 |
| 2020's | 1 (25.00) | 2.80 |
| Authors | Studies |
|---|---|
| Dong, H; Guan, H; Jin, Y; Kang, L; Li, D; Li, X; Liu, Y; Song, J; Yang, Y; Zhang, Y; Zhou, C | 1 |
| Chen, J; Chen, SZ; Fan, CH; Li, R; Liu, XM; Sang, Y | 1 |
| Campistol, J; Castiñeiras, D; Couce, ML; Fraga, JM; García Cazorla, A; García Silva, MT; Martín-Hernández, E; Navarrete, R; Pérez, B; Pérez-Cerdá, C; Pineda, M; Ugarte, M | 1 |
| Diamantopoulos, N; Heard, GS; Painter, MJ; Roe, C; Wolf, B | 1 |
4 other study(ies) available for biotin and Metabolic Diseases
| Article | Year |
|---|---|
Eleven novel mutations and clinical characteristics in seven Chinese patients with thiamine metabolism dysfunction syndrome.
Topics: Asian People; Biotin; Brain; Brain Diseases; Child, Preschool; DNA, Mitochondrial; Female; High-Throughput Nucleotide Sequencing; Humans; Infant; Ketoglutaric Acids; Leigh Disease; Magnetic Resonance Imaging; Male; Membrane Transport Proteins; Metabolic Diseases; Mitochondrial Membrane Transport Proteins; Thiamin Pyrophosphokinase; Thiamine | 2020 |
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 |
[Clinical and genetic findings in patients with biotinidase deficiency detected through newborn screening or selective screening for hearing loss or inherited metabolic disease].
Topics: Adolescent; Biotin; Biotinidase; Biotinidase Deficiency; Child, Preschool; Hearing Loss; Humans; Infant; Infant, Newborn; Metabolic Diseases; Mutation; Neonatal Screening; Vitamin B Complex | 2011 |
Biotinidase deficiency: accumulation of lactate in the brain and response to physiologic doses of biotin.
Topics: Amidohydrolases; Biotin; Biotinidase; Brain; Child; Humans; Lactates; Male; Metabolic Diseases | 1986 |