glutaric acid and riboflavin

glutaric acid has been researched along with riboflavin in 19 studies

Research

Studies (19)

Timeframe	Studies, this research(%)	All Research%
pre-1990	5 (26.32)	18.7374
1990's	4 (21.05)	18.2507
2000's	10 (52.63)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Bennett, MJ; Goodman, SI; Hale, DE; Pollitt, RJ; Vamecq, J	1
Bell, RB; Brownell, AK; Engel, AG; Frerman, FE; Goodman, SI; Roe, CR; Seccombe, DW; Snyder, FF	1
Iafolla, AK; Kahler, SG	1
Divry, P; Gregersen, N; Mathieu, M; Vianey-Liaud, C	1
Bartlett, K; Eyre, JA; Fisher, J; Gardner-Medwin, D; Johnson, MA; Turnbull, DM; Watmough, NJ	1
Bolhuis, PA; de Visser, M; Luyt-Houwen, IE; Oey, PL; Scholte, HR; Schutgens, RB; Vaandrager-Verduin, MH; Veder, HA	1
Blom, W; Giesberts, MA; Mooy, PD; Przyrembel, H; Scholte, HR; van Gelderen, HH	1
Rohr, F; Warman, ML; Yannicelli, S	1
Ciceri, E; Garavaglia, B; Moroni, I; Rimoldi, M; Uziel, G	1
Gunji, T; Koga, Y; Nonaka, I; Shimizu, N; Tojo, M; Yamaguchi, S	1
Corral, I; Gimeno, A; Martínez Castrillo, JC; Martínez-Pardo, M	1
Christensen, E; de Koning, TJ; Dorland, L; Hoffmann, GF; Knerr, I; Müller, P; Rascher, W; Trautmann, U; Trefz, FK; Wündisch, GF; Zschocke, J	1
Liang, Y; Liu, L; Luo, XP; Wang, MT; Wei, H	1
Luo, F; Sun, JP; Yang, YJ; Yu, XH; Zhong, L	1
Chen, LH; Jong, YJ; Lai, CL; Liang, WC; Tsai, KB	1
Garcia-Segura, JM; Merinero, B; Pascual-Castroviejo, I; Pascual-Pascual, SI; Ugarte, M; Velazquez, R; Viaño, J	1
Garcia Pérez, A; Martínez Granero, MA; Martínez-Pardo, M; Parra, E	1
Bain, MD; Chalmers, RA; Zschocke, J	1
Berger, R; de Sain-van der Velden, MG; Dorland, L; Ruiter, JP; Spliet, WG; Testerink, N; van der Kolk, JH; Votion, DM; Wanders, RJ; Westermann, CM; Wijnberg, ID	1

Reviews

2 review(s) available for glutaric acid and riboflavin

Article	Year
The inborn errors of mitochondrial fatty acid oxidation. Journal of inherited metabolic disease, 1987, Volume: 10 Suppl 1 Topics: Carnitine; Diagnosis, Differential; Electron-Transferring Flavoproteins; Fatty Acid Desaturases; Fatty Acids; Flavoproteins; Glutarates; Humans; Iron-Sulfur Proteins; Lipid Metabolism, Inborn Errors; Microbodies; Mitochondria; Multienzyme Complexes; Oxidation-Reduction; Oxidoreductases Acting on CH-NH Group Donors; Riboflavin	1987
Nutrition support for glutaric acidemia type I. Journal of the American Dietetic Association, 1994, Volume: 94, Issue:2 Topics: Amino Acid Metabolism, Inborn Errors; Carnitine; Child; Child, Preschool; Dietary Proteins; Female; Food, Formulated; Glutarates; Glutaryl-CoA Dehydrogenase; Humans; Infant; Infant, Newborn; Lysine; Male; Mitochondria; Oxidoreductases; Oxidoreductases Acting on CH-CH Group Donors; Riboflavin; Tryptophan	1994

Article

Year

The inborn errors of mitochondrial fatty acid oxidation.

Journal of inherited metabolic disease, 1987, Volume: 10 Suppl 1

Topics: Carnitine; Diagnosis, Differential; Electron-Transferring Flavoproteins; Fatty Acid Desaturases; Fatty Acids; Flavoproteins; Glutarates; Humans; Iron-Sulfur Proteins; Lipid Metabolism, Inborn Errors; Microbodies; Mitochondria; Multienzyme Complexes; Oxidation-Reduction; Oxidoreductases Acting on CH-NH Group Donors; Riboflavin

1987

Nutrition support for glutaric acidemia type I.

Journal of the American Dietetic Association, 1994, Volume: 94, Issue:2

Topics: Amino Acid Metabolism, Inborn Errors; Carnitine; Child; Child, Preschool; Dietary Proteins; Female; Food, Formulated; Glutarates; Glutaryl-CoA Dehydrogenase; Humans; Infant; Infant, Newborn; Lysine; Male; Mitochondria; Oxidoreductases; Oxidoreductases Acting on CH-CH Group Donors; Riboflavin; Tryptophan

1994

Other Studies

17 other study(ies) available for glutaric acid and riboflavin

Article	Year
Atypical riboflavin-responsive glutaric aciduria, and deficient peroxisomal glutaryl-CoA oxidase activity: a new peroxisomal disorder. Journal of inherited metabolic disease, 1991, Volume: 14, Issue:2 Topics: Acyl-CoA Oxidase; Cells, Cultured; Child, Preschool; Fatty Acids; Female; Fibroblasts; Gas Chromatography-Mass Spectrometry; Glutarates; Humans; Lysine; Microbodies; Oxidation-Reduction; Oxidoreductases; Riboflavin	1991
Electron transfer flavoprotein: ubiquinone oxidoreductase (ETF:QO) deficiency in an adult. Neurology, 1990, Volume: 40, Issue:11 Topics: Acidosis; Adult; Carnitine; Electron-Transferring Flavoproteins; Fatty Acid Desaturases; Female; Glutarates; Humans; Iron-Sulfur Proteins; Lipid Metabolism, Inborn Errors; Multienzyme Complexes; Muscular Diseases; Oxidoreductases Acting on CH-NH Group Donors; Reye Syndrome; Riboflavin	1990
Megalencephaly in the neonatal period as the initial manifestation of glutaric aciduria type I. The Journal of pediatrics, 1989, Volume: 114, Issue:6 Topics: Amino Acid Metabolism, Inborn Errors; Brain; Carnitine; Female; Glutarates; Glutaryl-CoA Dehydrogenase; Humans; Infant, Newborn; Oxidoreductases; Oxidoreductases Acting on CH-CH Group Donors; Riboflavin	1989
Lipid storage myopathy due to glutaric aciduria type II: treatment of a potentially fatal myopathy. Developmental medicine and child neurology, 1988, Volume: 30, Issue:5 Topics: Carnitine; Female; Glutarates; Glutaryl-CoA Dehydrogenase; Glycine; Humans; Infant; Lipid Metabolism; Metabolic Diseases; Muscles; Muscular Diseases; Oxidoreductases; Oxidoreductases Acting on CH-CH Group Donors; Riboflavin	1988
Riboflavin-responsive lipid-storage myopathy and glutaric aciduria type II of early adult onset. Neurology, 1986, Volume: 36, Issue:3 Topics: Adolescent; Carnitine; Child; Fatty Acids; Female; Fibroblasts; Glutarates; Humans; Infant; Lipid Metabolism; Metabolic Diseases; Mitochondria, Muscle; Muscular Diseases; Pedigree; Riboflavin	1986
Glutaric aciduria type II: treatment with riboflavine, carnitine and insulin. European journal of pediatrics, 1984, Volume: 143, Issue:2 Topics: Biopsy; Carnitine; Fatty Acid Desaturases; Glutarates; Humans; Hypoglycemia; Infant; Insulin; Male; Metabolism, Inborn Errors; Muscle Hypotonia; Muscles; Riboflavin	1984
Riboflavin-responsive glutaric aciduria type II presenting as a leukodystrophy. Pediatric neurology, 1995, Volume: 13, Issue:4 Topics: Child, Preschool; Glutarates; Humans; Leukoencephalopathy, Progressive Multifocal; Magnetic Resonance Imaging; Male; Phenotype; Riboflavin	1995
[A case of riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency (glutaric aciduria type II)]. No to hattatsu = Brain and development, 2000, Volume: 32, Issue:2 Topics: Acyl-CoA Dehydrogenases; Biomarkers; Carnitine; Child; Electron-Transferring Flavoproteins; Fatty Acids; Glutarates; Humans; Iron-Sulfur Proteins; Lipid Metabolism, Inborn Errors; Male; Multienzyme Complexes; Oxidoreductases Acting on CH-NH Group Donors; Riboflavin	2000
[Glutaric aciduria type I: diagnosis in adulthood and phenotypic variability]. Neurologia (Barcelona, Spain), 2001, Volume: 16, Issue:8 Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Brain; Brain Diseases, Metabolic; Carnitine; Fibroblasts; Glutarates; Glutaryl-CoA Dehydrogenase; Humans; Infant; Magnetic Resonance Imaging; Movement Disorders; Oxidoreductases; Oxidoreductases Acting on CH-CH Group Donors; Riboflavin; Tomography, X-Ray Computed	2001
Glutaric aciduria type III: a distinctive non-disease? Journal of inherited metabolic disease, 2002, Volume: 25, Issue:6 Topics: Amino Acid Metabolism, Inborn Errors; Child; Child, Preschool; Chromosome Deletion; Diarrhea; Fasting; Female; Glutarates; Humans; Liver; Lysine; Male; Pipecolic Acids; Riboflavin	2002
[Late-onset riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency (glutaric aciduria type II)]. Zhonghua er ke za zhi = Chinese journal of pediatrics, 2003, Volume: 41, Issue:12 Topics: Acyl-CoA Dehydrogenase; Adolescent; Age of Onset; Child; Female; Gas Chromatography-Mass Spectrometry; Glutarates; Humans; Metabolism, Inborn Errors; Photosensitizing Agents; Riboflavin; Treatment Outcome	2003
[Glutaric aciduria type I: report of a case]. Zhonghua er ke za zhi = Chinese journal of pediatrics, 2004, Volume: 42, Issue:7 Topics: Amino Acid Metabolism, Inborn Errors; Diagnosis, Differential; Diet; Glutarates; Humans; Infant; Male; Riboflavin; Treatment Outcome	2004
Riboflavin-responsive glutaric aciduria type II with recurrent pancreatitis. Pediatric neurology, 2004, Volume: 31, Issue:3 Topics: Acyl-CoA Dehydrogenase; Adult; Female; Glutarates; Humans; Male; Metabolism, Inborn Errors; Pancreatitis; Pedigree; Recurrence; Riboflavin	2004
[Glutaric aciduria type 1 with normal evolution: follow-up of one case until adult age]. Neurologia (Barcelona, Spain), 2005, Volume: 20, Issue:4 Topics: Basal Ganglia; Brain; Brain Chemistry; Brain Diseases, Metabolic, Inborn; Carnitine; Cells, Cultured; Child Development; Child, Preschool; Chromosomes, Human, Pair 19; Corpus Callosum; Female; Fibroblasts; Follow-Up Studies; Glutarates; Glutaryl-CoA Dehydrogenase; Heterozygote; Humans; Intelligence; Lactic Acid; Magnetic Resonance Imaging; Mutation, Missense; Oxidoreductases Acting on CH-CH Group Donors; Riboflavin; Seizures; Sequence Deletion	2005
[Macrocephaly the first manifestation of glutaric aciduria type I: the importance of early diagnosis]. Neurologia (Barcelona, Spain), 2005, Volume: 20, Issue:5 Topics: Brain; Brain Diseases, Metabolic; Carnitine; Diagnosis, Differential; Glutarates; Humans; Infant; Magnetic Resonance Imaging; Male; Riboflavin; Time Factors	2005
Riboflavin-responsive glutaryl CoA dehydrogenase deficiency. Molecular genetics and metabolism, 2006, Volume: 88, Issue:1 Topics: Adult; Amino Acid Metabolism, Inborn Errors; Amino Acid Substitution; Child; Child, Preschool; Fatal Outcome; Female; Glutarates; Glutaryl-CoA Dehydrogenase; Humans; Infant; Male; Protein Structure, Quaternary; Riboflavin	2006
Acquired multiple Acyl-CoA dehydrogenase deficiency in 10 horses with atypical myopathy. Neuromuscular disorders : NMD, 2008, Volume: 18, Issue:5 Topics: Acyl-CoA Dehydrogenase; Acyl-CoA Dehydrogenases; Animals; Butyric Acid; Butyryl-CoA Dehydrogenase; Carnitine; Chromatography, High Pressure Liquid; Female; Gas Chromatography-Mass Spectrometry; Glutarates; Horse Diseases; Horses; Isovaleryl-CoA Dehydrogenase; Lactic Acid; Male; Microscopy, Electron; Microscopy, Fluorescence; Muscles; Muscular Diseases; Riboflavin	2008