glutaric acid has been researched along with Brain Diseases in 11 studies
glutaric acid: RN given refers to parent cpd
glutaric acid : An alpha,omega-dicarboxylic acid that is a linear five-carbon dicarboxylic acid.
Brain Diseases: Pathologic conditions affecting the BRAIN, which is composed of the intracranial components of the CENTRAL NERVOUS SYSTEM. This includes (but is not limited to) the CEREBRAL CORTEX; intracranial white matter; BASAL GANGLIA; THALAMUS; HYPOTHALAMUS; BRAIN STEM; and CEREBELLUM.
| Excerpt | Relevance | Reference |
|---|---|---|
| "The association of macrocephaly, dystonia, and bilateral temporal arachnoid cysts, shown either by computed tomography or magnetic resonance imaging, seems to be diagnostic of glutaric aciduria type 1." | 5.29 | Macrocephaly, dystonia, and bilateral temporal arachnoid cysts: glutaric aciduria type 1. ( Casas, C; Fernández, MA; Martínez-Lage, JF; Poza, M; Puche, A; Rodriguez Costa, T, 1994) |
| "A 9-month-old patient was admitted with encephalopathy and acute loss of acquired motor skills during the course of COVID-19 disease." | 1.62 | COVID-19 triggered encephalopathic crisis in a patient with glutaric aciduria type 1. ( Ahmadzada, S; Aktuglu-Zeybek, C; Kiykim, E; Yalcinkaya, C; Zubarioglu, T, 2021) |
| "The association of macrocephaly, dystonia, and bilateral temporal arachnoid cysts, shown either by computed tomography or magnetic resonance imaging, seems to be diagnostic of glutaric aciduria type 1." | 1.29 | Macrocephaly, dystonia, and bilateral temporal arachnoid cysts: glutaric aciduria type 1. ( Casas, C; Fernández, MA; Martínez-Lage, JF; Poza, M; Puche, A; Rodriguez Costa, T, 1994) |
| "Glutaric aciduria type I is an autosomal recessive metabolic disorder of children associated with severe dystonic motor disturbances and degeneration in the cerebral cortex, striatum and cerebellum." | 1.27 | Hypothesis: a role for quinolinic acid in the neuropathology of glutaric aciduria type I. ( Heyes, MP, 1987) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (27.27) | 18.7374 |
| 1990's | 4 (36.36) | 18.2507 |
| 2000's | 3 (27.27) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (9.09) | 2.80 |
| Authors | Studies |
|---|---|
| Zubarioglu, T | 1 |
| Ahmadzada, S | 1 |
| Yalcinkaya, C | 1 |
| Kiykim, E | 1 |
| Aktuglu-Zeybek, C | 1 |
| Mühlhausen, C | 1 |
| Ergün, S | 1 |
| Strauss, KA | 1 |
| Koeller, DM | 1 |
| Crnic, L | 1 |
| Woontner, M | 1 |
| Goodman, SI | 3 |
| Ullrich, K | 1 |
| Braulke, T | 1 |
| Naughten, ER | 1 |
| Mayne, PD | 1 |
| Monavari, AA | 1 |
| Sulaiman, G | 1 |
| Croke, DT | 1 |
| Sternberg, B | 1 |
| Frenkel, AL | 1 |
| Plouin, P | 1 |
| Monod, N | 1 |
| Norenberg, MD | 1 |
| Küpfer, A | 1 |
| Aeschlimann, C | 1 |
| Wermuth, B | 1 |
| Cerny, T | 1 |
| Martínez-Lage, JF | 1 |
| Casas, C | 1 |
| Fernández, MA | 1 |
| Puche, A | 1 |
| Rodriguez Costa, T | 1 |
| Poza, M | 1 |
| Vion-Dury, J | 1 |
| Salvan, AM | 1 |
| Confort-Gouny, S | 1 |
| Cozzone, PJ | 1 |
| Kölker, S | 1 |
| Ahlemeyer, B | 1 |
| Krieglstein, J | 1 |
| Hoffmann, GF | 1 |
| Mandel, H | 1 |
| Braun, J | 1 |
| el-Peleg, O | 1 |
| Christensen, E | 1 |
| Berant, M | 1 |
| Heyes, MP | 1 |
1 review available for glutaric acid and Brain Diseases
| Article | Year |
|---|---|
Vascular dysfunction as an additional pathomechanism in glutaric aciduria type I.
Topics: Amino Acid Metabolism, Inborn Errors; Animals; Brain Diseases; Cerebrovascular Circulation; Glutarat | 2004 |
10 other studies available for glutaric acid and Brain Diseases
| Article | Year |
|---|---|
COVID-19 triggered encephalopathic crisis in a patient with glutaric aciduria type 1.
Topics: Amino Acid Metabolism, Inborn Errors; Brain; Brain Diseases; Brain Diseases, Metabolic; Carnitine; C | 2021 |
Glutaric aciduria type I: outcome in the Republic of Ireland.
Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Brain Diseases; Child; Child, Preschool; Fe | 2004 |
[Diagnoses to consider in newborn infants with inactive EEG tracings].
Topics: Brain Diseases; Cerebral Hemorrhage; Electroencephalography; Encephalomalacia; Glutarates; Heart Def | 1983 |
Glutaric acidemia as a cause of striatal necrosis in childhood.
Topics: Brain Diseases; Child; Corpus Striatum; Glutarates; Glutaryl-CoA Dehydrogenase; Humans; Necrosis; Ox | 1983 |
Prophylaxis and reversal of ifosfamide encephalopathy with methylene-blue.
Topics: Administration, Oral; Adolescent; Antidotes; Bone Neoplasms; Brain Diseases; Drug Overdose; Female; | 1994 |
Macrocephaly, dystonia, and bilateral temporal arachnoid cysts: glutaric aciduria type 1.
Topics: Arachnoid Cysts; Brain; Brain Diseases; Carnitine; Dystonia; Female; gamma-Aminobutyric Acid; Glutar | 1994 |
Atlas of brain proton magnetic resonance spectra. Part II: Inherited metabolic encephalopathies.
Topics: Adipates; Adult; Anatomy, Artistic; Argininosuccinic Acid; Argininosuccinic Aciduria; Brain; Brain D | 1998 |
Evaluation of trigger factors of acute encephalopathy in glutaric aciduria type I: fever and tumour necrosis factor-alpha.
Topics: Animals; Brain Diseases; Cells, Cultured; Chick Embryo; Dose-Response Relationship, Drug; Fever; Glu | 2000 |
Glutaric aciduria type I. Brain CT features and a diagnostic pitfall.
Topics: Amino Acid Metabolism, Inborn Errors; Brain; Brain Diseases; Glutarates; Humans; Infant; Male; Tomog | 1991 |
Hypothesis: a role for quinolinic acid in the neuropathology of glutaric aciduria type I.
Topics: Brain Diseases; Child; Glutarates; Glutaryl-CoA Dehydrogenase; Humans; Neurotoxins; Oxidoreductases; | 1987 |