3-methylglutaconic acid has been researched along with Luft Disease in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 4 (80.00) | 18.2507 |
| 2000's | 1 (20.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Armstrong, DL; Scaglia, F; Scheuerle, AE; Sweetman, L; Towbin, JA; Wong, LJ | 1 |
| Besley, GT; Broadhead, DM; Heptinstall, LE; Lendon, M; Phillips, B; Till, J | 1 |
| Deufel, T; Duran, M; Endres, W; Gibson, KM; Hadorn, HB; Ibel, H; Kennaway, NG; Paetzke, I | 1 |
| Barth, PG; Vreken, P; Wanders, RJ | 1 |
| Allen, JT; Cantlay, AM; Lunt, PW; Newbury-Ecob, RA; Shokrollahi, K; Steward, CG | 1 |
1 review(s) available for 3-methylglutaconic acid and Luft Disease
| Article | Year |
|---|---|
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 |
4 other study(ies) available for 3-methylglutaconic acid and Luft Disease
| Article | Year |
|---|---|
Neonatal presentation of ventricular tachycardia and a Reye-like syndrome episode associated with disturbed mitochondrial energy metabolism.
Topics: Biomarkers; Carnitine; DNA, Mitochondrial; Female; Glutarates; Humans; Infant, Newborn; Mitochondrial Myopathies; Mutation; Orotic Acid; Reye Syndrome; Tachycardia, Ventricular | 2002 |
Mitochondrial complex deficiencies in a male with cardiomyopathy and 3-methylglutaconic aciduria.
Topics: Amino Acid Metabolism, Inborn Errors; Cardiomyopathies; Child; DNA Mutational Analysis; Electron Transport; Fatal Outcome; Glutarates; Humans; Male; Mitochondria, Muscle; Mitochondrial Myopathies | 1995 |
Multiple respiratory chain abnormalities associated with hypertrophic cardiomyopathy and 3-methylglutaconic aciduria.
Topics: Acidosis, Lactic; Cardiomyopathy, Hypertrophic; Electron Transport Complex IV; Glutarates; Humans; Hydro-Lyases; Infant; Leucine; Male; Meglutol; Metabolism, Inborn Errors; Mitochondrial Myopathies; Respiration Disorders | 1993 |
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 |