adenine has been researched along with Hereditary Optic Neuroretinopathy in 3 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "This mutation can also cause MELAS syndrome (which encompasses mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke), and other genetic factors may contribute to the clinical expression." | 1.34 | A MELAS-associated ND1 mutation causing leber hereditary optic neuropathy and spastic dystonia. ( Bettink-Remeijer, MW; de Coo, IF; Hendrickx, A; Hintzen, RQ; Maat-Kievit, A; Schoonderwoerd, KC; Sluiter, W; Smeets, HJ; Spruijt, L, 2007) |
| "We therefore suspected Leber's hereditary optic neuropathy (LHON) and thus performed a PCR analysis of the mitochondrial DNA." | 1.33 | [Hyperintense optic nerve lesion on T2-weighted MRI imaging in the acute stage of Leber's hereditary optic neuropathy: a case report]. ( Fujikawa, A; Honda, H; Ochi, M; Satoh, A; Tomita, I; Tsujihata, M, 2006) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Kim, JY | 1 |
| Hwang, JM | 1 |
| Park, SS | 1 |
| Honda, H | 1 |
| Tsujihata, M | 1 |
| Ochi, M | 1 |
| Satoh, A | 1 |
| Tomita, I | 1 |
| Fujikawa, A | 1 |
| Spruijt, L | 1 |
| Smeets, HJ | 1 |
| Hendrickx, A | 1 |
| Bettink-Remeijer, MW | 1 |
| Maat-Kievit, A | 1 |
| Schoonderwoerd, KC | 1 |
| Sluiter, W | 1 |
| de Coo, IF | 1 |
| Hintzen, RQ | 1 |
3 other studies available for adenine and Hereditary Optic Neuroretinopathy
| Article | Year |
|---|---|
Mitochondrial DNA C4171A/ND1 is a novel primary causative mutation of Leber's hereditary optic neuropathy with a good prognosis.
Topics: Adenine; Adolescent; Child; Cytosine; DNA, Mitochondrial; Female; Humans; Male; Middle Aged; NADH De | 2002 |
[Hyperintense optic nerve lesion on T2-weighted MRI imaging in the acute stage of Leber's hereditary optic neuropathy: a case report].
Topics: Acute Disease; Adenine; Diagnosis, Differential; DNA, Mitochondrial; Guanine; Humans; Magnetic Reson | 2006 |
A MELAS-associated ND1 mutation causing leber hereditary optic neuropathy and spastic dystonia.
Topics: Adenine; Adult; DNA, Mitochondrial; Dystonia; Female; Guanine; Humans; MELAS Syndrome; Muscle Spasti | 2007 |