X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (1531) 1531
Publication (147) 147
Book Chapter (42) 42
Book Review (18) 18
Conference Proceeding (8) 8
Book / eBook (4) 4
Dissertation (1) 1
Journal / eJournal (1) 1
Magazine Article (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (1198) 1198
progressive external ophthalmoplegia (849) 849
female (582) 582
dna, mitochondrial - genetics (548) 548
male (541) 541
index medicus (489) 489
clinical neurology (476) 476
adult (446) 446
mitochondrial dna (416) 416
middle aged (393) 393
mutation (374) 374
neurosciences (359) 359
ophthalmoplegia, chronic progressive external - genetics (327) 327
kearns-sayre syndrome (266) 266
aged (230) 230
disease (214) 214
genetics & heredity (203) 203
dna polymerase gamma (195) 195
mitochondrial diseases - genetics (192) 192
biochemistry & molecular biology (190) 190
adolescent (185) 185
mitochondria (183) 183
dna-directed dna polymerase - genetics (182) 182
chronic progressive external ophthalmoplegia (175) 175
point mutation (165) 165
animals (147) 147
myopathy (141) 141
phenotype (139) 139
child (137) 137
mtdna (134) 134
muscle, skeletal - pathology (134) 134
deletions (130) 130
multiple deletions (130) 130
hereditary optic neuropathy (128) 128
gene deletion (124) 124
mutations (122) 122
dna (121) 121
neurology (121) 121
molecular sequence data (118) 118
ophthalmology (116) 116
ophthalmoplegia, chronic progressive external - pathology (116) 116
pedigree (113) 113
genetic aspects (112) 112
ophthalmoplegia, chronic progressive external - diagnosis (108) 108
cytochrome-c-oxidase (106) 106
mitochondrial disease (106) 106
stroke-like episodes (106) 106
biopsy (100) 100
ophthalmoplegia, chronic progressive external - complications (100) 100
base sequence (98) 98
mutation - genetics (98) 98
ragged-red fibers (98) 98
ophthalmoplegia (97) 97
dna mutational analysis (95) 95
cell biology (94) 94
gene (93) 93
lactic-acidosis (93) 93
mitochondrial myopathy (92) 92
mitochondrial myopathies - genetics (89) 89
sequence deletion (89) 89
mitochondria - genetics (86) 86
research (85) 85
mitochondrial diseases (84) 84
magnetic resonance imaging (83) 83
skeletal-muscle (83) 83
dna, mitochondrial - metabolism (82) 82
mitochondria - metabolism (79) 79
polg (78) 78
child, preschool (76) 76
genetics (75) 75
polymerase chain reaction (75) 75
diagnosis, differential (74) 74
mitochondrial encephalomyopathies - genetics (74) 74
article (73) 73
diagnosis (73) 73
oxidative phosphorylation (73) 73
ophthalmoplegia, chronic progressive external - physiopathology (72) 72
paralysis (72) 72
dna replication (71) 71
infant (70) 70
polg mutations (69) 69
genes (68) 68
kearns-sayre syndrome - genetics (67) 67
kearns-sayre-syndrome (67) 67
mitochondrial-dna (67) 67
pathology (66) 66
aged, 80 and over (65) 65
analysis (65) 65
amino acid sequence (64) 64
melas (64) 64
muscle (64) 64
dna-directed dna polymerase - metabolism (62) 62
genomes (62) 62
medicine & public health (62) 62
dna deletions (61) 61
gene mutations (61) 61
young adult (61) 61
autosomal-dominant (60) 60
eye (59) 59
muscle, skeletal - metabolism (58) 58
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (1418) 1418
Japanese (38) 38
Spanish (32) 32
German (25) 25
French (20) 20
Italian (6) 6
Chinese (5) 5
Portuguese (5) 5
Czech (3) 3
Hungarian (3) 3
Russian (3) 3
Polish (2) 2
Romanian (2) 2
Turkish (2) 2
Dutch (1) 1
Korean (1) 1
Swedish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Brain, ISSN 0006-8950, 5/2014, Volume 137, Issue 5, pp. 1323 - 1336
Journal Article
JAMA Neurology, ISSN 2168-6149, 11/2013, Volume 70, Issue 11, pp. 1429 - 1431
Journal Article
Current neurology and neuroscience reports, 06/2016, Volume 16, Issue 6, p. 53
Progressive external ophthalmoplegia (PEO), marked by progressive bilateral ptosis and diffuse reduction in ocular motility, represents a finding of... 
Diagnosis, Differential | Genetic Testing | Biopsy | Humans | Treatment Outcome | Ophthalmoplegia, Chronic Progressive External - genetics | Ophthalmoplegia, Chronic Progressive External - diagnosis | Disease Progression
Journal Article
by Wu, Y and Kang, L and Wu, HL and Hou, Y and Wang, ZX
CHINESE MEDICAL JOURNAL, ISSN 0366-6999, 05/2019, Volume 132, Issue 10, pp. 1202 - 1207
Background: Chronic progressive external ophthalmoplegia (CPEO) is a mitochondrial encephalomyopathy caused by multiple mtDNA abnormalities. There is little... 
OCT | MACULA | Optical coherence tomography | NERVE-FIBER LAYER | ALZHEIMERS-DISEASE | Retina | Nerve fiber layer | MILD COGNITIVE IMPAIRMENT | Chronic progressive external ophthalmoplegia | MEDICINE, GENERAL & INTERNAL | RETINAL ATROPHY | ASSOCIATION | THICKNESS | SEVERITY | PARKINSONS-DISEASE | Original
Journal Article
by Lv, ZY and Xu, XM and Cao, XF and Wang, Q and Sun, DF and Tian, WJ and Yang, Y and Wang, YZ and Hao, YL
MEDICINE, ISSN 0025-7974, 12/2017, Volume 96, Issue 48, p. e8869
Rationale: Chronic progressive external ophthalmoplegia (CPEO) is a classical mitochondrial ocular disorder characterized by bilateral progressive ptosis and... 
16S rRNA | DIAGNOSIS | MANAGEMENT | RETT-SYNDROME | MRI | C2835T | DISORDERS | 12S rRNA | chronic progressive external ophthalmoplegia plus | C960del | MEDICINE, GENERAL & INTERNAL | DNA | DISEASE | mitochondrial
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 08/2009, Volume 85, Issue 2, pp. 290 - 295
Journal Article
Brain, ISSN 0006-8950, 2/2008, Volume 131, Issue 2, pp. 329 - 337
Journal Article
International Ophthalmology, ISSN 0165-5701, 1/2019, Volume 39, Issue 1, pp. 213 - 217
To report midterm outcomes of strabismus strategy for management of diplopia in chronic progressive external ophthalmoplegia and specific surgical planning... 
Chronic progressive external ophthalmoplegia | Strabismus surgery | Ophthalmology | Medicine & Public Health | Diplopia management in CPEO | OPHTHALMOLOGY | MANAGEMENT | Medical colleges | Diplopia | Strabismus | Health aspects | Children's hospitals | Alignment | Motility | Preservation | Kidnapping | Surgery | Asthenopia | Impairment | Ophthalmoplegia | Patients
Journal Article
Multiple Sclerosis Journal, ISSN 1352-4585, 5/2019, Volume 25, Issue 6, pp. 879 - 882
Evidence from genetic and pathologic studies suggests that mitochondrial dysfunction occurs in multiple sclerosis (MS). Furthermore, cases of MS have been... 
demyelinating disease | multiple sclerosis | mitochondrial disease | oxidative stress | neurogenetics | Progressive external ophthalmoplegia | NEUROSCIENCES | CLINICAL NEUROLOGY | Ophthalmoplegia | Multiple sclerosis | Mitochondria
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 2006, Volume 78, Issue 6, pp. 1026 - 1034
Journal Article
Mitochondrion, ISSN 1567-7249, 09/2019
Journal Article
Journal Article
18.