biotin has been researched along with Central Nervous System Disease in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (40.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (40.00) | 29.6817 |
| 2010's | 1 (20.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Geoffroy, CG; Kim, JJ; Kim, ND; Meves, JM; Zheng, B | 1 |
| Bouhasin, J; Knutsen, A; Puetz, J | 1 |
| Kostulas, V; Link, H; Olsson, T | 1 |
| Bartlett, K; Clayton, B; Hyde, J; Leonard, JV; Seakins, JW; Wilson, J | 1 |
| Alvarez, JG; Guerra, A; Navarro, PC; Ortiz, FJ | 1 |
5 other study(ies) available for biotin and Central Nervous System Disease
| Article | Year |
|---|---|
Oligodendrocytic but not neuronal Nogo restricts corticospinal axon sprouting after CNS injury.
Topics: Age Factors; Animals; Axons; Biotin; Central Nervous System Diseases; Dextrans; Disease Models, Animal; Food Deprivation; Functional Laterality; Gray Matter; Mice; Mice, Inbred C57BL; Mice, Transgenic; Neurogenesis; Neurons; Nogo Proteins; Oligodendroglia; Pyramidal Tracts; Recovery of Function; Transduction, Genetic; Vesicular Glutamate Transport Protein 1 | 2018 |
Congenital deficiency of vitamin K-dependent coagulation factors associated with central nervous system anomalies.
Topics: Arnold-Chiari Malformation; Biotin; Blood Coagulation Disorders; Blood Coagulation Factors; Central Nervous System Diseases; Factor IX; Factor VII; Factor X; Female; Humans; Infant, Newborn; Male; Multiple Carboxylase Deficiency; Pregnancy; Prothrombin; Vitamin K | 2004 |
Improved detection of oligoclonal IgG in cerebrospinal fluid by isoelectric focusing in agarose, double-antibody peroxidase labeling, and avidin-biotin amplification.
Topics: Avidin; Biotin; Central Nervous System Diseases; Collodion; Fluorescent Antibody Technique; Humans; Immunoenzyme Techniques; Immunoglobulin G; Indicators and Reagents; Infections; Isoelectric Focusing; Multiple Sclerosis; Rosaniline Dyes; Sepharose | 1984 |
Inherited disorders of 3-methylcrotonyl CoA carboxylation.
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Biotin; Carbon-Carbon Ligases; Central Nervous System Diseases; Female; Humans; Infant; Infant, Newborn; Leucine; Ligases | 1981 |
Cutaneous and neurologic manifestations of biotinidase deficiency.
Topics: Amidohydrolases; Biotin; Biotinidase; Central Nervous System Diseases; Consanguinity; Diagnosis, Differential; Humans; Infant, Newborn; Male; Skin Diseases | 2000 |