biotin and Acidosis
biotin has been researched along with Acidosis in 22 studies
Research
Studies (22)
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 16 (72.73) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (13.64) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 3 (13.64) | 2.80 |
Authors
| Authors | Studies |
|---|---|
| Luo, X; Xiong, Z; Zhang, G; Zhang, N; Zheng, J | 1 |
| Chao, MC; Chen, KJ; Hsiao, HP; Wu, HR | 1 |
| Aamir, M; Bibi, A; Fatima, S | 1 |
| Agrawal, M; Dahiphale, R; Jain, S | 1 |
| Boneh, A; Ciani, F; Donati, MA; Funghini, S; Malvagia, S; Morrone, A; Pasquini, E; Pela, I; Peters, H; Zammarchi, E | 1 |
| de la Sierra García-Valdecasas, M; del Portal, LR; Delgado, C; Jiménez, LM; Macías, C; Pérez, M | 1 |
| Bartlett, K | 1 |
| Bartlett, K; Leonard, JV; Ng, H | 1 |
| Baker, H; Sweetman, L; Thoene, J; Yoshino, M | 1 |
| Brewster, T; Gravel, RA; Robinson, BH; Saunders, M; Sherwood, WG | 1 |
| Raetz, H; Wolf, B | 1 |
| Bourgeay-Causse, M; Carrĕ, G; Charpentier, C; Cotisson, A; Coudĕ, FX; Frĕzal, J; Marsac, C; Munnich, A; Ogier, H; Saudubray, JM | 1 |
| Charpentier, C; Frezal, J; Marsac, C; Munnich, A; Ogier, H; Saudubray, JM | 1 |
| Bartlett, K; Clayton, B; Hyde, J; Leonard, JV; Seakins, JW; Wilson, J | 1 |
| Cohn, R; Gravel, RA; Robinson, B; Roth, K; Saunders, M; Sweetman, L | 1 |
| Brothers, V; Gerritsen, T; Rowley, BO | 1 |
| Bartlett, K; Low, LC; Seakins, JW; Shaikh, SA; Stephenson, JB | 1 |
| Bartlett, K; Dale, G; Shein, A; Wastell, HJ | 1 |
| Grier, RE; Heard, GS; Leshner, RT; McVoy, JR; Weissbecker, KA; Wolf, B | 1 |
| Draffan, GH; Gompertz, D; Hull, D; Watts, JL | 1 |
| Balgobin, L; Barnes, ND; Gompertz, D; Hull, D | 1 |
Reviews
3 review(s) available for biotin and Acidosis
| Article | Year |
|---|---|
Impaired glucose homeostasis and a novel HLCS pathogenic variant in holocarboxylase synthetase deficiency: a report of two cases and brief review.
Topics: Acidosis; Biotin; Carbon-Nitrogen Ligases; Child; Female; Glucose; Holocarboxylase Synthetase Deficiency; Homeostasis; Humans; Hypoglycemia; Infant; Mutation, Missense; Prognosis; Taiwan | 2020 |
Vitamin-responsive inborn errors of metabolism.
Topics: Acetyl-CoA Carboxylase; Acidosis; Amino Acid Metabolism, Inborn Errors; Animals; Biotin; Folic Acid; Glutaryl-CoA Dehydrogenase; Humans; Intestinal Absorption; Maple Syrup Urine Disease; Metabolism, Inborn Errors; Methemoglobinemia; Methylmalonic Acid; Oxidoreductases; Oxidoreductases Acting on CH-CH Group Donors; Propionates; Pyridoxine; Pyruvate Carboxylase Deficiency Disease; Pyruvate Kinase; Riboflavin; Tetrahydrofolate Dehydrogenase; Thiamine; Transcobalamins; Vitamin B 12; Vitamins | 1983 |
Thiamine-responsive lactic acidosis.
Topics: Acidosis; Alanine; Biotin; Carbohydrate Metabolism, Inborn Errors; Dietary Carbohydrates; Female; Humans; Hypoglycemia; Infant; Infant, Newborn; Lactates; Liver; Pyruvate Carboxylase; Pyruvate Dehydrogenase Complex; Pyruvates; Thiamine; Thioctic Acid | 1974 |
Other Studies
19 other study(ies) available for biotin and Acidosis
| Article | Year |
|---|---|
Case report of holocarboxylase synthetase deficiency (late-onset) in 2 Chinese patients.
Topics: Acidosis; Biotin; China; Dyspnea; Female; Holocarboxylase Synthetase Deficiency; Humans; Hyperglycemia; Infant; Male | 2020 |
Multiple Carboxylase Deficiency Organic Acidemia as a Cause of Infantile Seizures.
Topics: Acidosis; Biotin; Child; Female; Holocarboxylase Synthetase Deficiency; Humans; Multiple Carboxylase Deficiency; Seizures | 2021 |
Biotinidase deficiency.
Topics: Acidosis; Alopecia; Biotin; Biotinidase Deficiency; Dermatitis, Seborrheic; Epilepsy; Humans; Infant; Male | 2008 |
Clinical findings and biochemical and molecular analysis of four patients with holocarboxylase synthetase deficiency.
Topics: Acidosis; Acids; Age of Onset; Amino Acid Substitution; Binding Sites; Biotin; Biotinylation; Carbon-Nitrogen Ligases; Cells, Cultured; DNA Mutational Analysis; DNA, Complementary; Exons; Fatal Outcome; Genes; Genes, Recessive; Genotype; Holocarboxylase Synthetase Deficiency; Humans; Infant; Intellectual Disability; Introns; Male; Mutation, Missense; Phenotype; Protein Structure, Tertiary; Restriction Mapping; Skin; Substrate Specificity | 2002 |
Subacute presentation of propionic acidemia.
Topics: Acidosis; Amino Acids; Biotin; Brain; Carnitine; Diagnosis, Differential; Diet, Protein-Restricted; Disease Progression; Electrophoresis, Capillary; Gastroenteritis; Growth Disorders; Humans; Infant; Magnetic Resonance Imaging; Male; Metabolism, Inborn Errors; Propionates; Propionic Acidemia; Treatment Outcome; Vomiting | 2007 |
A combined defect of three mitochondrial carboxylases presenting as biotin-responsive 3-methylcrotonyl glycinuria and 3-hydroxyisovaleric aciduria.
Topics: Acidosis; Acyl Coenzyme A; Amino Acid Metabolism, Inborn Errors; Biotin; Butyrates; Carbon Dioxide; Carboxy-Lyases; Child, Preschool; Crotonates; Female; Fibroblasts; Glycine; Humans; Hydroxy Acids; Ligases; Mitochondria; Propionates; Pyruvate Carboxylase Deficiency Disease; Valerates | 1980 |
Biotin-responsive carboxylase deficiency associated with subnormal plasma and urinary biotin.
Topics: Acidosis; Alopecia; Ataxia; Biotin; Carbon-Carbon Ligases; Child, Preschool; Female; Humans; Ligases; Pyruvate Carboxylase Deficiency Disease; Seizures | 1981 |
Lactic acidosis in biotin-responsive multiple carboxylase deficiency caused by holocarboxylase synthetase deficiency of early and late onset.
Topics: Acidosis; Age Factors; Biotin; Carbon-Carbon Ligases; Carbon-Nitrogen Ligases; Carboxy-Lyases; Cells, Cultured; Child, Preschool; Female; Fibroblasts; Humans; Infant; Intestinal Absorption; Lactates; Lactic Acid; Ligases; Lymphocytes; Male; Methylmalonyl-CoA Decarboxylase; Pyruvate Carboxylase Deficiency Disease | 1982 |
The measurement of propionyl-CoA carboxylase and pyruvate carboxylase activity in hair roots: its use in the diagnosis of inherited biotin-dependent enzyme deficiencies.
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Biotin; Carbohydrate Metabolism, Inborn Errors; Carboxy-Lyases; Hair; Humans; Infant; Lactates; Methylmalonyl-CoA Decarboxylase; Propionates; Pyruvate Carboxylase; Pyruvates | 1983 |
Biotin dependent multiple carboxylase deficiency presenting as a congenital lactic acidosis.
Topics: Acidosis; Biotin; Female; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Lactates; Ligases; Metabolism, Inborn Errors | 1981 |
[Alopecia, chronic candidodis, mental retardation and repeated ketoacidosic comas curable by biotin administration: multiple carboxylases deficiency (author's transl)].
Topics: Acidosis; Alopecia; Biotin; Candidiasis; Coma; Female; Humans; Infant; Intellectual Disability; Ketosis; Ligases | 1980 |
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 |
Biotin-response organicaciduria. Multiple carboxylase defects and complementation studies with propionicacidemia in cultured fibroblasts.
Topics: Acidosis; Acyl Coenzyme A; Apoenzymes; Biotin; Carbon Dioxide; Carbon-Carbon Ligases; Cells, Cultured; Crotonates; Fibroblasts; Genetic Complementation Test; Humans; Ligases; Propionates; Pyruvate Carboxylase Deficiency Disease | 1979 |
The vitamin B12-deficient rat as a possible model of ketotic hyperglycinemia.
Topics: Acidosis; Animals; Biotin; Carbon Dioxide; Carboxy-Lyases; Glycine; Glycine Hydroxymethyltransferase; Ketosis; Liver; Male; Propionates; Rats; Transferases; Vitamin B 12 Deficiency | 1975 |
Biotin-reversible neurodegenerative disease in infancy.
Topics: Acidosis; Biotin; Carbon-Carbon Ligases; Carboxy-Lyases; Failure to Thrive; Female; Humans; Infant; Ligases; Methylmalonyl-CoA Decarboxylase; Muscular Diseases; Myoclonus; Pyruvate Carboxylase Deficiency Disease | 1986 |
Biotinidase deficiency: a survey of 10 cases.
Topics: Acidosis; Amidohydrolases; Biotin; Biotinidase; Female; Humans; Infant; Male; Nervous System Diseases; Opportunistic Infections; Skin Diseases; Syndrome | 1988 |
Biotinidase deficiency: initial clinical features and rapid diagnosis.
Topics: Acidosis; Amidohydrolases; Biotin; Biotinidase; Child, Preschool; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Lactates; Mass Screening; Seizures | 1985 |
Biotin-responsive beta-methylcrotonylglycinuria.
Topics: Acidosis; Administration, Oral; Amino Acid Metabolism, Inborn Errors; Biotin; Butyrates; Carbon Dioxide; Carboxy-Lyases; Chromatography, Gas; Fatty Acids; Glycine; Humans; Infant; Leucine; Male; Partial Pressure; Valerates; Valine; Vomiting | 1971 |
Biotin-responsive propionicacidaemia.
Topics: Acidosis; Biotin; Carboxy-Lyases; Child, Preschool; Chromatography, Gas; Diet Therapy; Glycine; Humans; Isoleucine; Ketones; Ligases; Male; Metabolism, Inborn Errors; Phosphotransferases; Propionates | 1970 |