thymine has been researched along with Encephalomyelitis, Subacute Necrotizing in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 4 (100.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| de Vries, DD | 1 |
| van Engelen, BG | 1 |
| Gabreëls, FJ | 1 |
| Ruitenbeek, W | 1 |
| van Oost, BA | 1 |
| Degoul, F | 1 |
| François, D | 1 |
| Diry, M | 1 |
| Ponsot, G | 1 |
| Desguerre, I | 1 |
| Héron, B | 1 |
| Marsac, C | 1 |
| Moutard, ML | 1 |
| Seller, A | 1 |
| Kennedy, CR | 1 |
| Temple, IK | 1 |
| Brown, GK | 1 |
| Chakrapani, A | 1 |
| Heptinstall, L | 1 |
| Walter, J | 1 |
4 other studies available for thymine and Encephalomyelitis, Subacute Necrotizing
| Article | Year |
|---|---|
A second missense mutation in the mitochondrial ATPase 6 gene in Leigh's syndrome.
Topics: Base Sequence; Cytosine; DNA, Mitochondrial; Female; Humans; Leigh Disease; Male; Molecular Sequence | 1993 |
A near homoplasmic T8993G mtDNA mutation in a patient with atypic Leigh syndrome not present in the mother's tissues.
Topics: Child, Preschool; DNA, Mitochondrial; Female; Guanine; Humans; Leigh Disease; Mothers; Point Mutatio | 1997 |
Leigh syndrome resulting from de novo mutation at position 8993 of mitochondrial DNA.
Topics: DNA, Mitochondrial; Fatal Outcome; Guanine; Humans; Infant, Newborn; Leigh Disease; Male; Point Muta | 1997 |
A family with Leigh syndrome caused by the rarer T8993C mutation.
Topics: Cytosine; DNA, Mitochondrial; Humans; Infant; Leigh Disease; Male; Point Mutation; Proton-Translocat | 1998 |