3-methylglutaconic acid has been researched along with Cardiomyopathy, Congestive in 12 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 5 (41.67) | 18.2507 |
| 2000's | 5 (41.67) | 29.6817 |
| 2010's | 2 (16.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Greenwood, J; Hakim, S; Platt, J; Ronvelia, D; Zaragoza, MV | 1 |
| Anikster, Y; Barth, PG; Duran, M; Morava, E; Sperl, W; Wevers, RA; Wortmann, SB; Zschocke, J | 1 |
| Burlina, AB; Catuogno, S; Pellegrino, P; Prioli, MD; Rugolotto, S; Toniolo, D | 1 |
| Henry, AE; Kelly, RI; Mazzocco, MM | 1 |
| Boulton, ME; Brownstein, DG; Davies, JR; Davies, VJ; Hogan, V; Hollins, AJ; Moat, SJ; Nichols, PP; Piechota, M; Powell, KA; Votruba, M; White, KE; Wride, MA; Yip, W | 1 |
| Blazek, G; Finsterer, J; Stollberger, C | 1 |
| Brown, G; Johnson, A; Land, JM; Ostman-Smith, I | 1 |
| Kleinle, S; Krähenbühl, S; Liechti-Gallati, S; Ruesch, S; Schaffner, T; Weber, J; Wermuth, B; Wiesmann, UN | 1 |
| Barth, PG; Vreken, P; Wanders, RJ | 1 |
| Allen, JT; Cantlay, AM; Lunt, PW; Newbury-Ecob, RA; Shokrollahi, K; Steward, CG | 1 |
| Iinuma, K; Kitoh, T; Ohura, T; Ohya, N; Sakamoto, O | 1 |
| Cheatham, JP; Clark, BJ; Kelley, RI; Nigro, MA; Powell, BR; Sherwood, GW; Sladky, JT; Swisher, WP | 1 |
2 review(s) available for 3-methylglutaconic acid and Cardiomyopathy, Congestive
| Article | Year |
|---|---|
Inborn errors of metabolism with 3-methylglutaconic aciduria as discriminative feature: proper classification and nomenclature.
Topics: Abnormalities, Multiple; Barth Syndrome; Cardiomyopathy, Dilated; Cerebellar Ataxia; Chorea; Diagnosis, Differential; Glutarates; Humans; Metabolism, Inborn Errors; Optic Atrophy; Spastic Paraplegia, Hereditary; Terminology as Topic | 2013 |
X-linked cardioskeletal myopathy and neutropenia (Barth syndrome)-MIM 302060.
Topics: Cardiomyopathy, Dilated; Child; Genetic Linkage; Glutarates; Growth Disorders; Humans; Male; Mitochondrial Myopathies; Mutation; Neutropenia; Syndrome; X Chromosome | 1999 |
10 other study(ies) available for 3-methylglutaconic acid and Cardiomyopathy, Congestive
| Article | Year |
|---|---|
Intrafamilial variability for novel TAZ gene mutation: Barth syndrome with dilated cardiomyopathy and heart failure in an infant and left ventricular noncompaction in his great-uncle.
Topics: Acyltransferases; Barth Syndrome; Cardiolipins; Cardiomyopathy, Dilated; Codon, Nonsense; Exons; Genetic Heterogeneity; Glutarates; Heart Defects, Congenital; Heart Failure; Humans; Infant; Male; Middle Aged; Myocardium; Neutropenia; Pedigree; Transcription Factors | 2012 |
Long-term treatment of Barth syndrome with pantothenic acid: a retrospective study.
Topics: Acyltransferases; Adolescent; Cardiomyopathy, Dilated; Child; Child, Preschool; Follow-Up Studies; Glutarates; Granulocyte Colony-Stimulating Factor; Heart Transplantation; Humans; Infant; Male; Mutation; Neutropenia; Pantothenic Acid; Proteins; Retrospective Studies; Syndrome; Transcription Factors; Treatment Failure | 2003 |
Barth syndrome is associated with a cognitive phenotype.
Topics: Cardiomyopathy, Dilated; Child; Child, Preschool; Cholesterol; Cognition Disorders; Genotype; Glutarates; Growth Disorders; Humans; Male; Musculoskeletal Diseases; Neuropsychological Tests; Neutropenia; Phenotype; Severity of Illness Index; Syndrome | 2007 |
A missense mutation in the murine Opa3 gene models human Costeff syndrome.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acid Sequence; Animals; Base Sequence; Brain; Cardiomyopathy, Dilated; Disease Models, Animal; Glutarates; Humans; Mice; Mice, Inbred C3H; Molecular Sequence Data; Mutation, Missense; Optic Atrophy, Autosomal Dominant; Optic Nerve; Phenotype; Point Mutation; Proteins; Retinal Ganglion Cells; Reverse Transcriptase Polymerase Chain Reaction; Spinal Cord; Syndrome; Transcription, Genetic; Visual Acuity | 2008 |
Prevalence of Barth syndrome in adult left ventricular hypertrabeculation / noncompaction.
Topics: Adult; Cardiomyopathy, Dilated; Comorbidity; Female; Genetic Diseases, X-Linked; Glutarates; Heart Ventricles; Humans; Leukocyte Count; Male; Neuromuscular Diseases; Neutropenia; Retrospective Studies; Syndrome | 2008 |
Dilated cardiomyopathy due to type II X-linked 3-methylglutaconic aciduria: successful treatment with pantothenic acid.
Topics: Amino Acid Metabolism, Inborn Errors; Cardiomyopathy, Dilated; Electrocardiography; Genetic Linkage; Glutarates; Humans; Infant, Newborn; Male; Pantothenic Acid; X Chromosome | 1994 |
Combined 3-methylglutaconic and 3-hydroxy-3-methylglutaric aciduria with endocardial fibroelastosis and dilatative cardiomyopathy in male and female siblings with partial deficiency of complex II/III in fibroblasts.
Topics: Cardiomyopathy, Dilated; DNA, Mitochondrial; Electron Transport Complex II; Electron Transport Complex III; Endocardium; Female; Fibroblasts; Glutarates; Humans; Infant; Liver; Male; Meglutol; Mitochondria, Heart; Multienzyme Complexes; Muscle Hypotonia; Myocardium; Oxidoreductases; Point Mutation; Succinate Dehydrogenase | 1996 |
Genetic analysis of the G4.5 gene in families with suspected Barth syndrome.
Topics: Cardiomyopathy, Dilated; DNA Mutational Analysis; Failure to Thrive; Genetic Linkage; Glutarates; Humans; Infant; Infant, Newborn; Male; Mitochondrial Myopathies; Mutagenesis, Insertional; Mutation, Missense; Neutropenia; Pedigree; Syndrome; X Chromosome | 1999 |
Novel missense mutation (R94S) in the TAZ ( G4.5) gene in a Japanese patient with Barth syndrome.
Topics: Acyltransferases; Cardiomyopathy, Dilated; DNA Mutational Analysis; DNA Primers; DNA-Binding Proteins; Glutarates; Humans; Infant; Japan; Male; Muscular Diseases; Mutation; Mutation, Missense; Neutropenia; Polymerase Chain Reaction; Proteins; Syndrome; Transcription Factors; X Chromosome | 2002 |
X-linked dilated cardiomyopathy with neutropenia, growth retardation, and 3-methylglutaconic aciduria.
Topics: Adult; Cardiomyopathy, Dilated; Child; Child, Preschool; Chromatography, High Pressure Liquid; Fumarates; Glutarates; Growth Disorders; Heart Failure; Humans; Male; Meglutol; Muscular Diseases; Neutropenia; Pedigree; Syndrome; X Chromosome | 1991 |