EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
    1.3.5.1 | Abortion, Habitual |
26944226 |
Infertility and recurrent miscarriage with complex II deficiency-dependent mitochondrial oxidative stress in animal models. |
causal interaction
ongoing research
unassigned |
1
1
0 |
| 1.3.5.1 | Achlorhydria |
7075932 |
Gastric acid secretion, serum gastrin and parietal cell histology in hyperthyroidism. |
diagnostic usage
ongoing research
unassigned |
2
4
0 |
| 1.3.5.1 | Acidosis |
6713488 |
A morphological, enzyme-cytochemical, and physiological study of the blood-gonad barrier in the hermaphroditic snail Lymnaea stagnalis. |
ongoing research
unassigned |
2
0 |
| 1.3.5.1 | Acidosis |
10672232 |
The use of transgenic and mutant mice to study oxygen free radical metabolism. |
causal interaction
diagnostic usage
unassigned |
1
3
0 |
| 1.3.5.1 | Acidosis, Lactic |
1892363 |
Strongly succinate dehydrogenase-reactive blood vessels in muscles from patients with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes. |
diagnostic usage
ongoing research
unassigned |
2
2
0 |
| 1.3.5.1 | Acidosis, Lactic |
7616539 |
Hereditary myopathy with lactic acidosis, succinate dehydrogenase and aconitase deficiency in northern Sweden: a genealogical study. |
ongoing research
therapeutic application
unassigned |
1
1
0 |
| 1.3.5.1 | Acidosis, Lactic |
9062896 |
Expression of oxidative phosphorylation genes in muscle cell cultures from patients with mitochondrial myopathies. |
diagnostic usage
ongoing research
unassigned |
3
3
0 |
| 1.3.5.1 | Acidosis, Lactic |
14707514 |
Respiratory complex II defect in siblings associated with a symptomatic secondary block in fatty acid oxidation. |
causal interaction
diagnostic usage
unassigned |
1
1
0 |
| 1.3.5.1 | Acidosis, Lactic |
16091512 |
Predominant cerebellar volume loss as a neuroradiologic feature of pediatric respiratory chain defects. |
causal interaction
diagnostic usage
unassigned |
4
2
0 |
| 1.3.5.1 | Acidosis, Lactic |
25477904 |
Cavitating leukoencephalopathy with multiple mitochondrial dysfunction syndrome and NFU1 mutations. |
causal interaction
unassigned |
4
0 |
