X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
medical and health sciences (58) 58
medicin och hälsovetenskap (58) 58
humans (49) 49
index medicus (46) 46
female (38) 38
male (35) 35
clinical neurology (29) 29
medicin (27) 27
neurology (27) 27
neurosciences (27) 27
clinical medicine (26) 26
klinisk medicin (26) 26
medicine (26) 26
adult (25) 25
middle aged (24) 24
neurologi (24) 24
mutation (22) 22
pedigree (20) 20
genetics & heredity (16) 16
sweden (11) 11
adolescent (10) 10
dna, mitochondrial - genetics (10) 10
myopathy (10) 10
abridged index medicus (9) 9
biochemistry & molecular biology (9) 9
genes, dominant (9) 9
muscle, skeletal - pathology (9) 9
point mutation (9) 9
age of onset (8) 8
aged (8) 8
brain - pathology (8) 8
genetics (8) 8
magnetic resonance imaging (8) 8
mitochondrial myopathy (8) 8
base sequence (7) 7
dna mutational analysis (7) 7
family (7) 7
internal medicine (7) 7
mutation - genetics (7) 7
progressive external ophthalmoplegia (7) 7
gene (6) 6
molecular sequence data (6) 6
multiple deletions (6) 6
muscular diseases - genetics (6) 6
mutations (6) 6
ophthalmoplegia, chronic progressive external - genetics (6) 6
phenotype (6) 6
autonomic symptoms (5) 5
biopsy (5) 5
brain (5) 5
cerebellar ataxia (5) 5
child, preschool (5) 5
dermatologi och venerologi, klinisk genetik, invärtesmedicin (5) 5
dermatology and venerology,clinical genetics, internal medicine (5) 5
disease (5) 5
dna polymerase gamma (5) 5
dna-directed dna polymerase - genetics (5) 5
invärtesmedicin (5) 5
mitochondria (5) 5
mitochondrial dna (5) 5
mitochondrial myopathies - genetics (5) 5
narcolepsy - genetics (5) 5
pathology (5) 5
progressive multiple-sclerosis (5) 5
sequence deletion (5) 5
adult-onset leukodystrophy (4) 4
ataxia (4) 4
atrophy (4) 4
child (4) 4
deafness (4) 4
deafness - genetics (4) 4
dna (4) 4
exome sequencing (4) 4
gene deletion (4) 4
genetic linkage (4) 4
lamin type b - genetics (4) 4
mitochondrial myopathies - metabolism (4) 4
muscle (4) 4
muscle, skeletal - metabolism (4) 4
proteins (4) 4
spinocerebellar degenerations - genetics (4) 4
syndrome (4) 4
young adult (4) 4
alexander-disease (3) 3
amino acid sequence (3) 3
anestesi och intensivvård (3) 3
anesthesiology and intensive care (3) 3
arrhythmogenic right ventricular dysplasia - genetics (3) 3
autosomal dominant leukodystrophy (3) 3
autosomal-dominant (3) 3
basic medicine (3) 3
blotting, southern (3) 3
cardiomyopathy (3) 3
caveolin-3 (3) 3
deletions (3) 3
dementia (3) 3
desmin (3) 3
disease progression (3) 3
duplication (3) 3
encephalomyopathy (3) 3
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal Article
Muscle and Nerve, ISSN 0148-639X, 01/2011, Volume 43, Issue 1, p. 144
Journal Article
Muscle & Nerve, ISSN 0148-639X, 01/2011, Volume 43, Issue 1, pp. 144 - 144
Journal Article
Muscle & Nerve, ISSN 0148-639X, 01/2011, Volume 43, Issue 1, pp. 144 - 144
Journal Article
Muscle and Nerve, ISSN 0148-639X, 2011, Volume 43, Issue 1, pp. 144 - 144
Journal Article
Muscle & Nerve, ISSN 0148-639X, 01/2011, Volume 43, Issue 1, p. 144
Journal Article
Human Mutation, ISSN 1059-7794, 04/2013, Volume 34, Issue 4, pp. 572 - 577
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 09/2012, Volume 20, Issue 9, pp. 984 - 985
Journal Article
Annals of Neurology, ISSN 0364-5134, 09/2015, Volume 78, Issue 3, pp. 412 - 425
Journal Article
Journal Article
Human Mutation, ISSN 1059-7794, 08/2013, Volume 34, Issue 8, pp. 1160 - 1171
Journal Article
Brain, ISSN 0006-8950, 2012, Volume 135, Issue 6, pp. 1682 - 1694
Journal Article
No results were found for your search.

Cannot display more than 1000 results, please narrow the terms of your search.