X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (337) 337
Publication (81) 81
Book Chapter (22) 22
Patent (13) 13
Book / eBook (8) 8
Book Review (6) 6
Conference Proceeding (6) 6
Dissertation (4) 4
Newspaper Article (3) 3
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (153) 153
index medicus (117) 117
clinical neurology (110) 110
neurosciences (92) 92
male (89) 89
female (84) 84
adult (65) 65
charcot-marie-tooth disease - genetics (59) 59
middle aged (59) 59
charcot-marie-tooth disease (57) 57
animals (54) 54
article (53) 53
mutation (52) 52
neuropathy (47) 47
charcot-marie-tooth disease - physiopathology (42) 42
adolescent (36) 36
aged (36) 36
abridged index medicus (34) 34
marie-tooth-disease (33) 33
child (32) 32
mice (31) 31
charcot-marie-tooth disease - pathology (30) 30
phenotype (29) 29
neurology (23) 23
charcot-marie-tooth disease - diagnosis (22) 22
young adult (20) 20
gene (19) 19
hereditary motor (19) 19
mutation - genetics (19) 19
child, preschool (18) 18
pedigree (18) 18
myelin (17) 17
research (17) 17
schwann-cells (17) 17
mutations (16) 16
peripheral neuropathy (16) 16
amino acid sequence (15) 15
genetics & heredity (15) 15
proteins (15) 15
rats (15) 15
reliability (15) 15
sensory neuropathy (15) 15
analysis (14) 14
disease (14) 14
genetic aspects (14) 14
genetics (14) 14
molecular sequence data (14) 14
myelin p0 protein - genetics (14) 14
myelin proteins - genetics (14) 14
severity of illness index (14) 14
aged, 80 and over (13) 13
cmt (13) 13
disease progression (13) 13
nervous system diseases (13) 13
neural conduction - physiology (13) 13
age (12) 12
major structural protein (12) 12
medical research (12) 12
patients (12) 12
physiological aspects (12) 12
surgery (12) 12
charcot-marie-tooth disease - complications (11) 11
charcot-marie-tooth disease - metabolism (11) 11
charcot-marie-tooth disease - therapy (11) 11
charcot–marie–tooth disease (11) 11
congenital, hereditary, and neonatal diseases and abnormalities (11) 11
diagnosis (11) 11
expression (11) 11
original (11) 11
peripheral nervous system diseases - genetics (11) 11
protein (11) 11
schwann cells (11) 11
axons - pathology (10) 10
cells, cultured (10) 10
charcot-marie-tooth (10) 10
electrophysiology (10) 10
hereditary neuropathy (10) 10
multidisciplinary sciences (10) 10
neural conduction (10) 10
schwann cells - metabolism (10) 10
studies (10) 10
children (9) 9
cmt1a (9) 9
cohort studies (9) 9
disease models, animal (9) 9
genetic testing (9) 9
history (9) 9
neurons (9) 9
pressure palsies (9) 9
subtypes (9) 9
biochemistry & molecular biology (8) 8
clinical trials (8) 8
cmt neuropathy score (8) 8
disability evaluation (8) 8
duplication (8) 8
earth drilling (8) 8
earth drilling, e.g. deep drilling (8) 8
fixed constructions (8) 8
gene expression (8) 8
genotype (8) 8
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Robarts - Stacks (4) 4
UofT at Mississauga - Stacks (4) 4
Faculty of Information - Stacks (2) 2
UTL at Downsview - May be requested (2) 2
UofT at Scarborough - Stacks (2) 2
Collection Dvlpm't (Acquisitions) - Closed Orders (1) 1
Gerstein Science - Stacks (1) 1
Robarts - Searching (1) 1
St. Michael's College (John M. Kelly) - 2nd Floor (1) 1
Trinity College (John W Graham) - Stacks (1) 1
Trinity College (John W Graham) - Storage (1) 1
Victoria University E.J. Pratt - Stacks (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Brain, ISSN 0006-8950, 09/2018, Volume 141, Issue 9, pp. e71 - e71
Journal Article
Brain Research, ISSN 0006-8993, 10/2019, p. 146491
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 01/2018, Volume 128, Issue 1, p. 110
Journal Article
Neurology, ISSN 0028-3878, 02/2018, Volume 90, Issue 6, pp. 257 - 259
Sandelius et al.(1) identify neurofilament light (NfL) as a potential biomarker for different types of Charcot-Marie-Tooth disease (CMT) in the current issue... 
CHAIN | CLINICAL NEUROLOGY | PROTEIN | Biomarkers | Intermediate Filaments | Humans | Charcot-Marie-Tooth Disease
Journal Article
Muscle & Nerve, ISSN 0148-639X, 12/2017, Volume 56, Issue 6, pp. 1092 - 1095
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 01/2018, Volume 128, Issue 1, pp. 110 - 112
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 4/2016, Volume 113, Issue 17, pp. 4552 - 4554
Journal Article
Muscle & Nerve, ISSN 0148-639X, 12/2015, Volume 52, Issue 6, pp. 1110 - 1113
Journal Article
Muscle & Nerve, ISSN 0148-639X, 10/2016, Volume 54, Issue 4, pp. 728 - 732
Journal Article
Muscle & Nerve, ISSN 0148-639X, 11/2015, Volume 52, Issue 5, pp. 905 - 908
Journal Article
Muscle & Nerve, ISSN 0148-639X, 04/2014, Volume 49, Issue 4, pp. 478 - 482
Journal Article
Muscle & Nerve, ISSN 0148-639X, 10/2013, Volume 48, Issue 4, pp. 604 - 622
Journal Article
Journal of clinical neurophysiology : official publication of the American Electroencephalographic Society, ISSN 0736-0258, 11/2017, Volume 34, Issue 6, pp. 508 - 511
Journal Article
Journal of Neurology, Neurosurgery & Psychiatry, ISSN 0022-3050, 04/2015, Volume 86, Issue 4, pp. 362 - 362
  Mutations in the neurofilament light chain (NEFL) gene cause CMT2E or CMT1F 5 6 by disrupting the axonal cytoskeleton; NEFL is not expressed in myelin.... 
SURGERY | MARIE-TOOTH-DISEASE | SUBTYPES | PSYCHIATRY | CLINICAL NEUROLOGY | Female | Male | Charcot-Marie-Tooth Disease - diagnostic imaging | Humans | Peripheral Nerves - diagnostic imaging | Ultrasonography | Studies | Clinical trials | Ultrasonic imaging | Mutation
Journal Article
Journal of Neuromuscular Diseases, ISSN 2214-3599, 2018, Volume 5, Issue 1, pp. 99 - 104
Introduction: Mutations in the gene encoding DNA polymerase gamma (POLG) impair its ability to proofread mitochondrial DNA (mtDNA) during replication [1]. This... 
asymmetric ataxia | POLG mutation | mitochondrial mutation | Cerebellum | Executive function | DNA polymerase | Cerebellar ataxia | Epilepsy | Mitochondrial DNA | Neuropathy | Mental depression | Polyneuropathy | Genetic screening | DNA biosynthesis | Pathogenicity | Sensorimotor system | Ataxia | Mutation | Deoxyribonucleic acid--DNA | DNA-directed DNA polymerase | Seizures
Journal Article
Journal of neuromuscular diseases, ISSN 2214-3599, 12/2017
Mutations in the gene encoding DNA polymerase gamma (POLG) impair its ability to proofread mitochondrial DNA (mtDNA) during replication [1]. This results in a... 
Journal Article
Current Opinion in Neurology, ISSN 1350-7540, 10/2004, Volume 17, Issue 5, pp. 579 - 585
Purpose of review The purpose of this review is to assist neurologists, neuroscientists and other interested readers in following the expanding volume of... 
Charcot-Marie-Tooth | Axonal transport | Neurons | Schwann cells | Protein trafficking | protein trafficking | PHENOTYPE | MODEL | neurons | NEUROSCIENCES | CLINICAL NEUROLOGY | MEMBER | GENE | MOTOR NEUROPATHY | DYNACTIN | axonal transport | HSP22 | MUTATIONS | GTP Phosphohydrolases | Humans | Glycine-tRNA Ligase - genetics | Protein Transport - physiology | Protein Tyrosine Phosphatases - metabolism | rab GTP-Binding Proteins - genetics | Mitochondrial Proteins - genetics | Charcot-Marie-Tooth Disease - genetics | Heat-Shock Proteins - genetics | Protein Tyrosine Phosphatases - genetics | Ascorbic Acid - therapeutic use | Mitochondrial Proteins - metabolism | Nerve Fibers, Myelinated - pathology | Membrane Proteins - metabolism | Nuclear Proteins - genetics | Nerve Fibers, Myelinated - metabolism | rab GTP-Binding Proteins - metabolism | Membrane Proteins - genetics | Progesterone - antagonists & inhibitors | Heat-Shock Proteins - metabolism | Axonal Transport - physiology | Nuclear Proteins - metabolism | Schwann Cells - pathology | Schwann Cells - metabolism | Charcot-Marie-Tooth Disease - drug therapy | Glycine-tRNA Ligase - metabolism | Transcription Factors - genetics | Charcot-Marie-Tooth Disease - pathology | Protein Tyrosine Phosphatases, Non-Receptor | Myelin Proteins - genetics | Transcription Factors - metabolism | Animals | Charcot-Marie-Tooth Disease - physiopathology | Myelin Proteins - metabolism
Journal Article
No results were found for your search.

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