Page last updated: 2024-09-05

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. Journal of pediatric endocrinology & metabolism : JPEM, 2020, Nov-26, Volume: 33, Issue:11 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. Advances in clinical chemistry, 1983, Volume: 23 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. Nutrition reviews, 1974, Volume: 32, Issue:3 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. Medicine, 2020, Volume: 99, Issue:18 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. Journal of the College of Physicians and Surgeons--Pakistan : JCPSP, 2021, Volume: 31, Issue:1 Topics: Acidosis; Biotin; Child; Female; Holocarboxylase Synthetase Deficiency; Humans; Multiple Carboxylase Deficiency; Seizures	2021
Biotinidase deficiency. Indian pediatrics, 2008, Volume: 45, Issue:9 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. American journal of medical genetics, 2002, Jul-22, Volume: 111, Issue:1 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. Journal of child neurology, 2007, Volume: 22, Issue:12 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. Clinica chimica acta; international journal of clinical chemistry, 1980, Jan-15, Volume: 100, Issue:2 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. The New England journal of medicine, 1981, Apr-02, Volume: 304, Issue:14 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. The Journal of pediatrics, 1982, Volume: 101, Issue:4 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. Clinica chimica acta; international journal of clinical chemistry, 1983, May-09, Volume: 130, Issue:1 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. European journal of pediatrics, 1981, Volume: 137, Issue:2 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)]. Annales de medecine interne, 1980, Volume: 131, Issue:7 Topics: Acidosis; Alopecia; Biotin; Candidiasis; Coma; Female; Humans; Infant; Intellectual Disability; Ketosis; Ligases	1980
Inherited disorders of 3-methylcrotonyl CoA carboxylation. Archives of disease in childhood, 1981, Volume: 56, Issue:1 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. The Journal of clinical investigation, 1979, Volume: 64, Issue:6 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. Pediatric research, 1975, Volume: 9, Issue:10 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. Australian paediatric journal, 1986, Volume: 22, Issue:1 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. Archives of disease in childhood, 1988, Volume: 63, Issue:10 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. Annals of neurology, 1985, Volume: 18, Issue:5 Topics: Acidosis; Amidohydrolases; Biotin; Biotinidase; Child, Preschool; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Lactates; Mass Screening; Seizures	1985
Biotin-responsive beta-methylcrotonylglycinuria. Lancet (London, England), 1971, Jul-03, Volume: 2, Issue:7714 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. Lancet (London, England), 1970, Aug-01, Volume: 2, Issue:7666 Topics: Acidosis; Biotin; Carboxy-Lyases; Child, Preschool; Chromatography, Gas; Diet Therapy; Glycine; Humans; Isoleucine; Ketones; Ligases; Male; Metabolism, Inborn Errors; Phosphotransferases; Propionates	1970