homovanillic acid has been researched along with Electron Transport Chain Deficiencies, Mitochondrial in 4 studies
Homovanillic Acid: A 3-O-methyl ETHER of (3,4-dihydroxyphenyl)acetic acid.
homovanillate : A hydroxy monocarboxylic acid anion which is obtained by deprotonation of the carboxy group of homovanillic acid.
homovanillic acid : A monocarboxylic acid that is the 3-O-methyl ether of (3,4-dihydroxyphenyl)acetic acid. It is a catecholamine metabolite.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Mitochondrial diseases are a group of genetic disorders leading to the dysfunction of mitochondrial energy metabolism pathways." | 2.58 | Cerebrospinal fluid monoamines, pterins, and folate in patients with mitochondrial diseases: systematic review and hospital experience. ( Armstrong, J; Artuch, R; Batllori, M; García-Cazorla, A; Molero-Luis, M; Montero, R; Montoya, J; Nascimento, A; O'Callaghan, M; Ormazabal, A; Ortigoza-Escobar, JD; Palau, F; Pias, L; Ribes, A; Ruiz-Pesini, E; Sierra, C; Yubero, D, 2018) |
| "Mitochondrial disorders are clinically heterogeneous." | 1.35 | Mitochondrial diseases mimicking neurotransmitter defects. ( Artuch, R; Briones, P; Carrilho, I; Duarte, S; Garcia-Cazorla, A; Garesse, R; Montoya, J; Nascimento, A; Ormazabal, A; Pineda, M; Sala-Castellvi, P; Serrano, M, 2008) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (25.00) | 29.6817 |
| 2010's | 3 (75.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Batllori, M | 1 |
| Molero-Luis, M | 2 |
| Ormazabal, A | 3 |
| Montero, R | 1 |
| Sierra, C | 1 |
| Ribes, A | 1 |
| Montoya, J | 2 |
| Ruiz-Pesini, E | 1 |
| O'Callaghan, M | 1 |
| Pias, L | 1 |
| Nascimento, A | 2 |
| Palau, F | 1 |
| Armstrong, J | 1 |
| Yubero, D | 1 |
| Ortigoza-Escobar, JD | 1 |
| García-Cazorla, A | 3 |
| Artuch, R | 3 |
| Papandreou, A | 1 |
| Rahman, S | 1 |
| Fratter, C | 1 |
| Ng, J | 1 |
| Meyer, E | 1 |
| Carr, LJ | 1 |
| Champion, M | 1 |
| Clarke, A | 1 |
| Gissen, P | 1 |
| Hemingway, C | 1 |
| Hussain, N | 1 |
| Jayawant, S | 1 |
| King, MD | 1 |
| Lynch, BJ | 1 |
| Mewasingh, L | 1 |
| Patel, J | 1 |
| Prabhakar, P | 1 |
| Neergheen, V | 1 |
| Pope, S | 1 |
| Heales, SJR | 1 |
| Poulton, J | 1 |
| Kurian, MA | 1 |
| Serrano, M | 2 |
| Pérez-Dueñas, B | 1 |
| Pons, R | 1 |
| Duarte, S | 1 |
| Carrilho, I | 1 |
| Briones, P | 1 |
| Garesse, R | 1 |
| Sala-Castellvi, P | 1 |
| Pineda, M | 1 |
1 review available for homovanillic acid and Electron Transport Chain Deficiencies, Mitochondrial
| Article | Year |
|---|---|
Cerebrospinal fluid monoamines, pterins, and folate in patients with mitochondrial diseases: systematic review and hospital experience.
Topics: Biogenic Amines; DNA, Mitochondrial; Homovanillic Acid; Humans; Mitochondrial Diseases; Point Mutati | 2018 |
3 other studies available for homovanillic acid and Electron Transport Chain Deficiencies, Mitochondrial
| Article | Year |
|---|---|
Spectrum of movement disorders and neurotransmitter abnormalities in paediatric POLG disease.
Topics: Adolescent; Child; Child, Preschool; DNA Polymerase gamma; Female; Homovanillic Acid; Humans; Hydrox | 2018 |
Homovanillic acid in cerebrospinal fluid of 1388 children with neurological disorders.
Topics: Adolescent; Algorithms; Asphyxia Neonatorum; Brain; Central Nervous System Infections; Child; Child, | 2013 |
Mitochondrial diseases mimicking neurotransmitter defects.
Topics: Alanine; Brain; Child, Preschool; Consanguinity; Diagnosis, Differential; Dopamine Agents; Dystonia; | 2008 |