glutaric acid has been researched along with Brain Diseases, Metabolic, Familial in 23 studies
glutaric acid: RN given refers to parent cpd
glutaric acid : An alpha,omega-dicarboxylic acid that is a linear five-carbon dicarboxylic acid.
| Excerpt | Relevance | Reference |
|---|---|---|
| " Antiquitin deficiency is the most common form of pyridoxine-dependent epilepsy." | 5.05 | Inherited Disorders of Lysine Metabolism: A Review. ( Bouchereau, J; Schiff, M, 2020) |
| "Her symptoms consisted of a few convulsions between 2." | 1.33 | [Glutaric aciduria type 1 with normal evolution: follow-up of one case until adult age]. ( Garcia-Segura, JM; Merinero, B; Pascual-Castroviejo, I; Pascual-Pascual, SI; Ugarte, M; Velazquez, R; Viaño, J, 2005) |
| "Glutaric aciduria type 1 is an inborn error of lysine, hydroxylysine, and tryptophan metabolism caused by deficiency of glutaryl-coenzyme A dehydrogenase." | 1.32 | Glutaric aciduria type 1: proton magnetic resonance spectroscopy findings. ( Cakmakçi, H; Dirik, E; Kurul, S, 2004) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 22 (95.65) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (4.35) | 2.80 |
| Authors | Studies |
|---|---|
| Bouchereau, J | 1 |
| Schiff, M | 1 |
| Olivera, S | 1 |
| Fernandez, A | 1 |
| Latini, A | 2 |
| Rosillo, JC | 1 |
| Casanova, G | 1 |
| Wajner, M | 2 |
| Cassina, P | 1 |
| Barbeito, L | 1 |
| Kamate, M | 1 |
| Patil, VD | 1 |
| Chetal, V | 1 |
| Hattiholi, V | 1 |
| Kölker, S | 4 |
| Hoffmann, GF | 5 |
| Koeller, DM | 2 |
| Okun, JG | 2 |
| Lund, TM | 1 |
| Christensen, E | 1 |
| Kristensen, AS | 1 |
| Schousboe, A | 1 |
| Lund, AM | 1 |
| Korman, SH | 1 |
| Salomons, GS | 1 |
| Gutman, A | 1 |
| Brooks, R | 1 |
| Jakobs, C | 1 |
| Kurul, S | 1 |
| Cakmakçi, H | 1 |
| Dirik, E | 1 |
| Patil, N | 1 |
| Shinde, S | 1 |
| Karande, S | 1 |
| Kulkarni, M | 1 |
| Gerstner, B | 1 |
| Gratopp, A | 1 |
| Marcinkowski, M | 1 |
| Sifringer, M | 1 |
| Obladen, M | 1 |
| Bührer, C | 1 |
| Pascual-Castroviejo, I | 1 |
| Pascual-Pascual, SI | 1 |
| Merinero, B | 1 |
| Ugarte, M | 1 |
| Garcia-Segura, JM | 1 |
| Viaño, J | 1 |
| Velazquez, R | 1 |
| Ferreira, Gda C | 1 |
| Viegas, CM | 1 |
| Schuck, PF | 1 |
| Tonin, A | 1 |
| Ribeiro, CA | 1 |
| Coelho, Dde M | 1 |
| Dalla-Costa, T | 1 |
| Wyse, AT | 1 |
| Wannmacher, CM | 1 |
| Vargas, CR | 1 |
| Hedlund, GL | 1 |
| Longo, N | 1 |
| Pasquali, M | 1 |
| Sauer, SW | 2 |
| Zinnanti, WJ | 2 |
| Lazovic, J | 2 |
| Wolpert, EB | 1 |
| Antonetti, DA | 1 |
| Smith, MB | 1 |
| Connor, JR | 2 |
| Woontner, M | 2 |
| Goodman, SI | 2 |
| Cheng, KC | 2 |
| Bishop, FS | 1 |
| Liu, JK | 1 |
| McCall, TD | 1 |
| Brockmeyer, DL | 1 |
| Housman, C | 1 |
| LaNoue, K | 1 |
| O'Callaghan, JP | 1 |
| Simpson, I | 1 |
| Jacobs, RE | 1 |
| Zschocke, J | 1 |
| Quak, E | 1 |
| Guldberg, P | 1 |
| Ahlemeyer, B | 1 |
| Krieglstein, J | 1 |
| Hartley, LM | 1 |
| Khwaja, OS | 1 |
| Verity, CM | 1 |
| Knapp, JF | 1 |
| Soden, SE | 1 |
| Dasouki, MJ | 1 |
| Walsh, IR | 1 |
| Piatt, JH | 1 |
| Frim, D | 1 |
4 reviews available for glutaric acid and Brain Diseases, Metabolic, Familial
| Article | Year |
|---|---|
Inherited Disorders of Lysine Metabolism: A Review.
Topics: 2-Aminoadipic Acid; Aldehyde Dehydrogenase; Amino Acid Metabolism, Inborn Errors; Arginine; Brain; B | 2020 |
Pathomechanisms of neurodegeneration in glutaryl-CoA dehydrogenase deficiency.
Topics: Amino Acid Metabolism, Inborn Errors; Animals; Brain Diseases, Metabolic, Inborn; Child, Preschool; | 2004 |
Glutaric acidemia type 1.
Topics: Amino Acid Metabolism, Inborn Errors; Animals; Brain Diseases, Metabolic, Inborn; Carnitine; Glutara | 2006 |
Glutaric aciduria type 1 presenting as bilateral subdural hematomas mimicking nonaccidental trauma. Case report and review of the literature.
Topics: Brain Diseases, Metabolic, Inborn; Brain Injuries; Diagnosis, Differential; Female; Glutarates; Glut | 2007 |
19 other studies available for glutaric acid and Brain Diseases, Metabolic, Familial
| Article | Year |
|---|---|
Astrocytic proliferation and mitochondrial dysfunction induced by accumulated glutaric acidemia I (GAI) metabolites: possible implications for GAI pathogenesis.
Topics: Amino Acid Metabolism, Inborn Errors; Animals; Animals, Newborn; Anthracenes; Antioxidants; Astrocyt | 2008 |
'Glutaric aciduria type I--an easily diagnosable and treatable metabolic disorder'.
Topics: Amino Acid Metabolism, Inborn Errors; Brain Diseases, Metabolic, Inborn; Child, Preschool; Female; G | 2009 |
Adult onset glutaric aciduria type I presenting with a leukoencephalopathy.
Topics: Adult; Age of Onset; Animals; Brain; Brain Diseases, Metabolic, Inborn; Child; Disease Models, Anima | 2003 |
On the neurotoxicity of glutaric, 3-hydroxyglutaric, and trans-glutaconic acids in glutaric acidemia type 1.
Topics: Animals; Brain Diseases, Metabolic, Inborn; Cell Death; Cells, Cultured; Cerebral Cortex; Corpus Str | 2004 |
D-2-hydroxyglutaric aciduria and glutaric aciduria type 1 in siblings: coincidence, or linked disorders?
Topics: Brain Diseases, Metabolic, Inborn; Child, Preschool; Female; Glutarates; Glutaryl-CoA Dehydrogenase; | 2004 |
Glutaric aciduria type 1: proton magnetic resonance spectroscopy findings.
Topics: Brain Diseases, Metabolic, Inborn; Glutarates; Glutaryl-CoA Dehydrogenase; Humans; Infant; Magnetic | 2004 |
Glutaric aciduria type I associated with learning disability.
Topics: Brain; Brain Diseases, Metabolic, Inborn; Child; Glutarates; Humans; Learning Disabilities; Magnetic | 2004 |
Glutaric acid and its metabolites cause apoptosis in immature oligodendrocytes: a novel mechanism of white matter degeneration in glutaryl-CoA dehydrogenase deficiency.
Topics: Amino Acid Chloromethyl Ketones; Animals; Apoptosis; Base Sequence; Brain Diseases, Metabolic, Inbor | 2005 |
[Glutaric aciduria type 1 with normal evolution: follow-up of one case until adult age].
Topics: Basal Ganglia; Brain; Brain Chemistry; Brain Diseases, Metabolic, Inborn; Carnitine; Cells, Cultured | 2005 |
Glutaric acid administration impairs energy metabolism in midbrain and skeletal muscle of young rats.
Topics: Animals; Brain Diseases, Metabolic, Inborn; Carbon Dioxide; Carbon Radioisotopes; Creatine Kinase; D | 2005 |
Lysine intake and neurotoxicity in glutaric aciduria type I: towards a rationale for therapy?
Topics: Amino Acid Metabolism, Inborn Errors; Animals; Brain Diseases, Metabolic, Inborn; Diet; Disease Mode | 2006 |
New insights for glutaric aciduria type I.
Topics: Amino Acid Metabolism, Inborn Errors; Animals; Brain Diseases, Metabolic, Inborn; Diet; Disease Mode | 2006 |
Biochemistry and bioenergetics of glutaryl-CoA dehydrogenase deficiency.
Topics: Acyl Coenzyme A; Animals; Blood-Brain Barrier; Brain; Brain Diseases, Metabolic, Inborn; Capillary P | 2007 |
Mechanism of age-dependent susceptibility and novel treatment strategy in glutaric acidemia type I.
Topics: Aging; Amino Acid Metabolism, Inborn Errors; Animals; Brain Diseases, Metabolic, Inborn; Child; Diet | 2007 |
Mutation analysis in glutaric aciduria type I.
Topics: Brain Diseases, Metabolic, Inborn; DNA Mutational Analysis; Electrophoresis, Polyacrylamide Gel; Exo | 2000 |
Maturation-dependent neurotoxicity of 3-hydroxyglutaric and glutaric acids in vitro: a new pathophysiologic approach to glutaryl-CoA dehydrogenase deficiency.
Topics: Animals; Antibodies; Brain Diseases, Metabolic, Inborn; Cells, Cultured; Chick Embryo; Dizocilpine M | 2000 |
Glutaric aciduria type 1 and nonaccidental head injury.
Topics: Brain Diseases, Metabolic, Inborn; Child Abuse; Craniocerebral Trauma; Diagnosis, Differential; Drai | 2001 |
A 9-month-old baby with subdural hematomas, retinal hemorrhages, and developmental delay.
Topics: Brain Diseases, Metabolic, Inborn; Child Abuse; Developmental Disabilities; Diagnosis, Differential; | 2002 |
Glutaric aciduria type 1 and nonaccidental head injury.
Topics: Brain Diseases, Metabolic, Inborn; Craniocerebral Trauma; Diagnosis, Differential; Glutarates; Gluta | 2002 |