X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (883) 883
Book Review (134) 134
Publication (63) 63
Book Chapter (10) 10
Newsletter (6) 6
Conference Proceeding (1) 1
Newspaper Article (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (804) 804
index medicus (736) 736
charcot-marie-tooth disease - complications (532) 532
male (493) 493
female (481) 481
adult (361) 361
charcot-marie-tooth disease (289) 289
middle aged (285) 285
charcot-marie-tooth disease - genetics (278) 278
clinical neurology (250) 250
adolescent (199) 199
neurosciences (196) 196
child (160) 160
charcot-marie-tooth disease - physiopathology (147) 147
aged (135) 135
charcot-marie-tooth disease - diagnosis (132) 132
neuropathy (118) 118
abridged index medicus (112) 112
charcot-marie-tooth disease - pathology (111) 111
mutation (110) 110
charcot-marie-tooth (92) 92
hereditary motor (92) 92
pedigree (89) 89
neurology (86) 86
surgery (77) 77
child, preschool (76) 76
orthopedics (76) 76
sensory neuropathy (70) 70
disease (67) 67
marie-tooth-disease (67) 67
phenotype (66) 66
young adult (66) 66
diagnosis (59) 59
muscular atrophy - complications (59) 59
treatment outcome (59) 59
genetic aspects (58) 58
research (57) 57
peripheral neuropathy (56) 56
animals (54) 54
mutation - genetics (53) 53
pediatrics (53) 53
retrospective studies (51) 51
care and treatment (49) 49
gene (47) 47
charcot-marie-tooth disease - surgery (46) 46
magnetic resonance imaging (46) 46
medicine & public health (45) 45
children (44) 44
follow-up studies (44) 44
mutations (44) 44
diagnosis, differential (43) 43
neural conduction (43) 43
article (41) 41
charcot–marie–tooth disease (39) 39
risk factors (39) 39
dna mutational analysis (38) 38
biopsy (37) 37
electromyography (36) 36
sural nerve - pathology (36) 36
genetics & heredity (35) 35
nervous system diseases (34) 34
complications and side effects (33) 33
medicine, general & internal (33) 33
myelin proteins - genetics (33) 33
psychiatry (32) 32
medical research (31) 31
charcot-marie-tooth disease - therapy (30) 30
gait (30) 30
pregnancy (30) 30
foot (28) 28
patients (28) 28
radiography (28) 28
rehabilitation (27) 27
genes (26) 26
health aspects (26) 26
hereditary motor and sensory neuropathy (26) 26
hereditary sensory and motor neuropathy - complications (26) 26
severity of illness index (26) 26
analysis (25) 25
gene mutations (25) 25
management (25) 25
muscle weakness - etiology (25) 25
neural conduction - physiology (25) 25
anesthesiology (24) 24
disease progression (24) 24
duplication (24) 24
family health (24) 24
genetics (24) 24
hereditary neuropathy (24) 24
hereditary sensory and motor neuropathy - genetics (24) 24
polyneuropathy (24) 24
aged, 80 and over (23) 23
charcot-marie-tooth disease - epidemiology (23) 23
foot deformities, acquired - etiology (23) 23
marie-tooth disease (23) 23
mice (23) 23
proteins (23) 23
foot deformities - etiology (22) 22
foot deformities, acquired - surgery (22) 22
gait disorders, neurologic - etiology (22) 22
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (767) 767
French (44) 44
Japanese (35) 35
Spanish (17) 17
German (10) 10
Russian (8) 8
Chinese (3) 3
Italian (3) 3
Portuguese (3) 3
Serbian (2) 2
Bulgarian (1) 1
Croatian (1) 1
Danish (1) 1
Polish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Texas Heart Institute Journal, ISSN 0730-2347, 08/2018, Volume 45, Issue 4, pp. 270 - 272
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 12/2011, Volume 365, Issue 25, pp. 2377 - 2388
The authors report that INF2 mutations are present in patients with focal segmental glomerulosclerosis (FSGS) associated with Charcot–Marie–Tooth neuropathy.... 
GLOMERULOSCLEROSIS | MEDICINE, GENERAL & INTERNAL | MYELIN | PROTEIN | NEUROPATHY | EPITHELIAL-CELLS | GENE | RHO | MEDIATED TRANSPORT | FORMIN | NEPHROPATHY | Humans | Middle Aged | Proteolipids - metabolism | Actins - metabolism | Male | Charcot-Marie-Tooth Disease - genetics | Young Adult | Kidney - metabolism | Glomerulosclerosis, Focal Segmental - etiology | Myelin and Lymphocyte-Associated Proteolipid Proteins | Adult | Female | Membrane Transport Proteins - metabolism | Microfilament Proteins - metabolism | Child | Microfilament Proteins - genetics | Charcot-Marie-Tooth Disease - complications | Schwann Cells - metabolism | Phenotype | Animals | Adolescent | Age of Onset | Heterozygote | Mice | Mutation | Myelin Proteins - metabolism | Glomerulonephritis | Gene mutations | Charcot-Marie-Tooth disease | Causes of | Genetic aspects | Research | Myelin proteins | Cdc42 protein | Disease | Exons | Genes | Amino acids | Nervous system | Neuropathy | Guanine nucleotide-binding protein | Proteins | Myelin P0 protein | Localization | Peripheral myelin protein 22 | Deoxyribonucleic acid--DNA | Kidneys | Schwann cells | Polymerization | Myelination | Genotyping | Biopsy | Glomerulus | Cytoskeleton | Genetic testing | Cytoplasm | Guanosinetriphosphatase | Index Medicus | Abridged Index Medicus | Schwann Cells | Genomics | Kidney | Charcot-Marie-Tooth Disease | Life Sciences | Proteolipids | Biochemistry, Molecular Biology | Actins | Microfilament Proteins | Membrane Transport Proteins | Myelin Proteins | Glomerulosclerosis, Focal Segmental
Journal Article
Nature Genetics, ISSN 1061-4036, 02/2010, Volume 42, Issue 2, pp. 165 - 169
Journal Article
Muscle & Nerve, ISSN 0148-639X, 02/2018, Volume 57, Issue 2, pp. 330 - 334
Introduction : Bcl‐2‐associated athanogene‐3 ( BAG3 ) mutations have been described in rare cases of rapidly progressive myofibrillar myopathies. Symptoms... 
Charcot–Marie–Tooth disease | CMT | BAG3 | axonal neuropathy myofibrillar myopathy | rigid spine syndrome | Charcot-Marie-Tooth disease | OVERDOSE | GLUTEAL COMPARTMENT SYNDROME | SATURDAY NIGHT PALSY | RHABDOMYOLYSIS | NEUROSCIENCES | IMMOBILIZATION | CLINICAL NEUROLOGY | Scoliosis - genetics | Hereditary Sensory and Motor Neuropathy - genetics | Humans | Muscular Dystrophies - genetics | Charcot-Marie-Tooth Disease - genetics | Young Adult | Electrodiagnosis | Hereditary Sensory and Motor Neuropathy - complications | Charcot-Marie-Tooth Disease - diagnostic imaging | Heart Diseases - complications | Apoptosis Regulatory Proteins - genetics | Female | Muscular Dystrophies - diagnostic imaging | Charcot-Marie-Tooth Disease - complications | Mallory Bodies - genetics | Mallory Bodies - pathology | Hereditary Sensory and Motor Neuropathy - diagnostic imaging | Muscular Dystrophies - complications | Mutation - genetics | Magnetic Resonance Imaging | Scoliosis - complications | Biopsy | Muscle, Skeletal - diagnostic imaging | Adaptor Proteins, Signal Transducing - genetics | Muscle, Skeletal - pathology | Scoliosis - diagnostic imaging | Genetic research | Genetic aspects | Diagnostic imaging | Gene mutations | Genes | EKG | Echocardiography | Bcl-2 protein | Cardiac muscle | Spine | Abnormalities | Muscles | Neuropathy | Magnetic resonance imaging | Genetic analysis | Infiltration | Mutation | Heart diseases | Index Medicus
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 09/2016, Volume 99, Issue 3, pp. 607 - 623
Journal Article
Journal Article
15.