biotin has been researched along with Focal Neurologic Deficits in 4 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 4 (100.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Allen, RJ; Goodman, SI; Grier, RE; Howell, DM; Hurst, DL; Kien, CL; Parker, WD; Wolf, B | 1 |
Kien, CL; Swick, HM | 1 |
Heard, GS; Jefferson, LG; Nance, WE; Proud, VK; Weissbecker, KA; Wolf, B | 1 |
Eldjarn, L; Jellum, E; Pande, H; Stokke, O; Waaler, PE | 1 |
4 other study(ies) available for biotin and Focal Neurologic Deficits
Article | Year |
---|---|
Phenotypic variation in biotinidase deficiency.
Topics: Amidohydrolases; Biotin; Biotinidase; Carboxy-Lyases; Child, Preschool; Female; Humans; Infant; Infant, Newborn; Male; Neurologic Manifestations; Skin Manifestations | 1983 |
Biotin deficiency with neurologic and cutaneous manifestations but without organic aciduria.
Topics: Acids; Biotin; Child, Preschool; Humans; Male; Neurologic Manifestations; Skin Manifestations | 1983 |
Clinical findings in four children with biotinidase deficiency detected through a statewide neonatal screening program.
Topics: Amidohydrolases; Biotin; Biotinidase; Child, Preschool; Female; Humans; Infant; Infant, Newborn; Male; Metabolism, Inborn Errors; Neurologic Manifestations; Pilot Projects; Skin Manifestations; Virginia | 1985 |
Beta-methylcrotonyl-CoA carboxylase deficiency: a new metabolic error in leucine degradation.
Topics: Amino Acid Metabolism, Inborn Errors; Biotin; Bronchopneumonia; Butyrates; Carbon Dioxide; Carbon-Carbon Ligases; Chromatography, Gas; Diet Therapy; Female; Glycine; Humans; Infant; Leucine; Ligases; Mass Spectrometry; Neurologic Manifestations; Odorants; Pentanols; Valerates | 1972 |