homovanillic acid has been researched along with Mitochondrial Diseases 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.
Mitochondrial Diseases: Diseases caused by abnormal function of the MITOCHONDRIA. They may be caused by mutations, acquired or inherited, in mitochondrial DNA or in nuclear genes that code for mitochondrial components. They may also be the result of acquired mitochondria dysfunction due to adverse effects of drugs, infections, or other environmental causes.
| 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 Mitochondrial Diseases
| 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 Mitochondrial Diseases
| 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 |