X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (3628) 3628
Book Review (853) 853
Publication (414) 414
Book / eBook (86) 86
Book Chapter (72) 72
Newsletter (63) 63
Newspaper Article (59) 59
Conference Proceeding (23) 23
Dissertation (2) 2
Magazine Article (1) 1
Reference (1) 1
Report (1) 1
Web Resource (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (3171) 3171
humans (2742) 2742
male (1484) 1484
muscular dystrophy (1396) 1396
female (1307) 1307
animals (1162) 1162
clinical neurology (1067) 1067
neurosciences (1032) 1032
adult (1005) 1005
muscle, skeletal - pathology (972) 972
mutation (914) 914
middle aged (712) 712
mice (697) 697
child (623) 623
skeletal-muscle (617) 617
adolescent (607) 607
muscular dystrophies - genetics (597) 597
phenotype (586) 586
muscle, skeletal - metabolism (557) 557
genetic aspects (533) 533
muscular dystrophies - pathology (496) 496
proteins (483) 483
gene (482) 482
neurology (471) 471
muscles (450) 450
biopsy (443) 443
cell biology (433) 433
muscular-dystrophy (426) 426
mutations (416) 416
pathology (415) 415
genetics & heredity (409) 409
muscular dystrophies, limb-girdle - genetics (406) 406
child, preschool (397) 397
research (381) 381
girdle muscular-dystrophy (376) 376
muscle proteins - genetics (361) 361
myopathy (359) 359
biochemistry & molecular biology (353) 353
musculoskeletal system (342) 342
expression (336) 336
aged (335) 335
analysis (331) 331
disease (322) 322
muscular dystrophies, limb-girdle - pathology (309) 309
dystrophin (305) 305
immunohistochemistry (298) 298
muscular dystrophies - metabolism (296) 296
pedigree (293) 293
diagnosis (289) 289
muscle (289) 289
magnetic resonance imaging (286) 286
dysferlin (284) 284
disease models, animal (283) 283
abridged index medicus (280) 280
duchenne muscular-dystrophy (277) 277
genetics (273) 273
article (270) 270
skeletal muscle (264) 264
mutation - genetics (263) 263
young adult (261) 261
genes (254) 254
gene expression (251) 251
muscular diseases - pathology (250) 250
cardiomyopathy (248) 248
rodents (248) 248
muscle, skeletal - physiopathology (245) 245
dystrophy (241) 241
muscular diseases - genetics (237) 237
dna mutational analysis (234) 234
medicine (232) 232
membrane proteins - genetics (228) 228
medicine, research & experimental (225) 225
muscle proteins - metabolism (222) 222
duchenne muscular dystrophy (217) 217
protein (217) 217
muscles - pathology (209) 209
physiological aspects (209) 209
glycoprotein complex (198) 198
dilated cardiomyopathy (197) 197
research article (196) 196
infant (195) 195
muscular dystrophies - diagnosis (191) 191
muscular dystrophies - physiopathology (186) 186
dystrophin - genetics (184) 184
health aspects (182) 182
mice, knockout (180) 180
musculoskeletal diseases (176) 176
neuromuscular diseases (173) 173
gene mutations (170) 170
alpha-dystroglycan (167) 167
diagnosis, differential (167) 167
mice, inbred c57bl (166) 166
membrane proteins - metabolism (164) 164
glycosylation (163) 163
multidisciplinary sciences (162) 162
utrophin (162) 162
care and treatment (157) 157
limb-girdle muscular dystrophy (157) 157
dystroglycan (154) 154
life sciences (152) 152
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (69) 69
Holland Bloorview Kids Rehabilitation - Stacks (11) 11
Humber River Regional Hospital - Church Stacks (2) 2
Providence Healthcare - Stacks (2) 2
Collection Dvlpm't (Acquisitions) - Vendor file (1) 1
Mt Sinai Hospital - Online (1) 1
Mt Sinai Hospital - Pathology (1) 1
Providence Healthcare - Reference (1) 1
Sunnybrook Health Sciences Centre - Holland Reference (1) 1
Sunnybrook Health Sciences Centre - Holland Stacks (1) 1
Sunnybrook Health Sciences Centre - Online (1) 1
Sunnybrook Health Sciences Centre - Sunnybrook Stacks (1) 1
Toronto East General Hospital - Stacks (1) 1
UTL at Downsview - May be requested (1) 1
UofT Schools - Stacks (1) 1
West Park Healthcare Centre - Stacks (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (3805) 3805
Japanese (24) 24
Spanish (15) 15
French (11) 11
German (8) 8
Chinese (5) 5
Italian (4) 4
Portuguese (4) 4
Russian (2) 2
Polish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Nature Genetics, ISSN 1061-4036, 04/2012, Volume 44, Issue 4, pp. 450 - 455
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 2014, Volume 23, Issue 15, pp. 4103 - 4110
Journal Article
Journal Article
Brain, ISSN 0006-8950, 2013, Volume 136, Issue 1, pp. 269 - 281
Journal Article
PLoS ONE, ISSN 1932-6203, 02/2014, Volume 9, Issue 2, pp. e90377 - e90377
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 07/2013, Volume 93, Issue 1, pp. 181 - 190
Myopathies are a clinically and etiologically heterogeneous group of disorders that can range from limb girdle muscular dystrophy (LGMD) to syndromic forms... 
HUTTERITE POPULATION | COMPLEX | TRANSPORT | MUTANTS | DANON-DISEASE | GENE | GENETICS & HEREDITY | COMPONENTS | LINKAGE ANALYSIS | GOLGI | IDENTIFICATION | Sequence Deletion | Vesicular Transport Proteins - metabolism | Humans | Endoplasmic Reticulum - metabolism | Male | Multiprotein Complexes - genetics | Golgi Apparatus - pathology | Syria | Intellectual Disability - genetics | Exome | Young Adult | Endoplasmic Reticulum - pathology | Multiprotein Complexes - metabolism | Lysosomes - metabolism | Muscular Dystrophies, Limb-Girdle - genetics | Adult | Female | Ataxia - genetics | Muscular Dystrophies, Limb-Girdle - pathology | Lysosome-Associated Membrane Glycoproteins - metabolism | RNA Splice Sites | Creatine Kinase - blood | Endoplasmic Reticulum - genetics | Movement Disorders - pathology | Vesicular Transport Proteins - genetics | Chromosome Mapping | Muscular Diseases - pathology | Protein Transport | Homozygote | Pedigree | Adolescent | Lysosome-Associated Membrane Glycoproteins - genetics | Protein Binding | Golgi Apparatus - metabolism | Consanguinity | Movement Disorders - genetics | Muscular Diseases - genetics | Lysosomal-Associated Membrane Protein 2 | Golgi Apparatus - genetics | Gene mutations | Physiological aspects | Child development deviations | Muscle diseases | Genetic aspects | Research | Developmental disabilities | Learning disabilities | Genomes | Glycoproteins | Mutation | Motor ability | Index Medicus | Report
Journal Article
American Journal of Pathology, The, ISSN 0002-9440, 2016, Volume 186, Issue 9, pp. 2429 - 2448
Journal Article
Journal Article