| Diseases | Rating | Bibliogr. | Expand |
---|
1 | MELAS Syndrome | 100 | + + | |
2 | Acidosis, Lactic | 38 | + + | |
3 | Mitochondrial Myopathies | 18 | + + | |
4 | Acidosis | 12 | + + | |
5 | Muscular Diseases | 10 | + + | |
6 | Mitochondrial Encephalomyopathies | 6 | + + | |
7 | Cerebrovascular Disorders | 6 | + + | |
8 | Stroke | 4 | + + | |
9 | Arteriolosclerosis | 3 | + + | |
10 | Cytochrome-c Oxidase Deficiency | 3 | + + | |
11 | MERRF Syndrome | 3 | + + | |
12 | Acidosis, Renal Tubular | 3 | + + | |
13 | Ophthalmoplegia, Chronic Progressive External | 3 | + + | |
14 | Neuromuscular Diseases | 3 | + + | |
15 | Brain Diseases | 3 | + + | |
16 | Syndrome | 2 | + + | |
17 | Kearns-Sayre Syndrome | 2 | + + | |
18 | Mitochondrial Diseases | 2 | + + | |
19 | Epilepsies, Myoclonic | 2 | + + | |
20 | Muscle Weakness | 1 | + + | |
21 | Deafness | 1 | + + | |
22 | Muscle Hypotonia | 1 | + + | |
23 | Acidosis, Respiratory | 1 | + + | |
24 | Hyperemia | 1 | + + | |
25 | Ophthalmoplegia | 1 | + + | |
26 | Congenital Disorders of Glycosylation | 1 | + + | |
27 | Diabetes Mellitus | 1 | + + | |
28 | Atrophy | 1 | + + | |
29 | Fanconi Syndrome | 1 | + + | |
30 | Cardiomyopathy, Hypertrophic, Familial | 1 | + + | |
31 | Cardiomyopathies | 1 | + + | |
32 | Brain Diseases, Metabolic | 1 | + + | |
33 | Intestinal Pseudo-Obstruction | 1 | + + | |
34 | Anemia, Sideroblastic | 1 | + + | |
35 | Thiamine Deficiency | 1 | + + | |
36 | Seizures | 1 | + + | |
37 | Disease Progression | 1 | + + | |
38 | Genetic Predisposition to Disease | 1 | + + | |
39 | Diabetes Mellitus, Type 2 | 1 | + + | |
40 | Dysphonia | 1 | + + | |
41 | Diabetes Mellitus, Type 1 | 1 | + + | |
42 | Epilepsy, Tonic-Clonic | 1 | + + | |