X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (21) 21
female (20) 20
male (16) 16
adult (15) 15
index medicus (15) 15
mutation (13) 13
clinical neurology (11) 11
middle aged (11) 11
adolescent (10) 10
neurology (10) 10
aged (9) 9
genetic aspects (9) 9
genetics & heredity (8) 8
genetics (7) 7
neurosciences (7) 7
phenotype (7) 7
young adult (7) 7
child (6) 6
nervous system (5) 5
nervous system diseases (5) 5
analysis (4) 4
article (4) 4
child, preschool (4) 4
disease (4) 4
diseases (4) 4
gene mutations (4) 4
genetics, medical (4) 4
muscular dystrophy (4) 4
mutations (4) 4
neurodegeneration (4) 4
neurogenetics (4) 4
patients (4) 4
pedigree (4) 4
proteins (4) 4
sex factors (4) 4
abridged index medicus (3) 3
age distribution (3) 3
axons - pathology (3) 3
base sequence (3) 3
care and treatment (3) 3
dna mutational analysis (3) 3
genes (3) 3
health aspects (3) 3
magnetic resonance imaging (3) 3
medical genetics (3) 3
medical research (3) 3
mutation, missense (3) 3
neurologic examination (3) 3
physiological aspects (3) 3
sequence analysis, dna (3) 3
trinucleotide repeat expansion - genetics (3) 3
amino acids (2) 2
arrhythmias, cardiac - epidemiology (2) 2
binding sites (2) 2
biochemistry & molecular biology (2) 2
biopsy (2) 2
case studies (2) 2
cataract - epidemiology (2) 2
cell cycle (2) 2
clinical trials (2) 2
cross-sectional studies (2) 2
crystal structure (2) 2
deafness (2) 2
diagnosis (2) 2
disease progression (2) 2
disorder (2) 2
dna, mitochondrial - genetics (2) 2
dystrophy (2) 2
electrocardiography (2) 2
electromyography (2) 2
epilepsy (2) 2
fatigue - epidemiology (2) 2
fatigue - etiology (2) 2
gait disorders, neurologic - etiology (2) 2
gender (2) 2
genetic predisposition to disease - genetics (2) 2
genetic variation (2) 2
genomics (2) 2
genotype (2) 2
haplotypes (2) 2
heart (2) 2
hereditary diffuse leukoencephalopathy (2) 2
hereditary sensory and autonomic neuropathies - genetics (2) 2
infant (2) 2
leukodystrophy (2) 2
leukoencephalopathies - genetics (2) 2
leukoencephalopathy (2) 2
medical and health sciences (2) 2
medical imaging (2) 2
medicin och hälsovetenskap (2) 2
medicine, experimental (2) 2
mitochondrial encephalomyopathies - genetics (2) 2
mitochondrial neurogastrointestinal encephalomyopathy (2) 2
molecular medicine (2) 2
molecular sequence data (2) 2
movement disorders - epidemiology (2) 2
movement disorders - etiology (2) 2
muscular diseases - genetics (2) 2
mutation - genetics (2) 2
myoclonus (2) 2
more...
Library Location Library Location
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


British Journal of Haematology, ISSN 0007-1048, 12/2001, Volume 115, Issue 4, p. 910
Journal Article
Brain, ISSN 0006-8950, 02/2006, Volume 129, Issue 2, p. 411
  Hereditary sensory and autonomic neuropathy type I (HSAN I) is the most frequent type of hereditary neuropathy that primarily affects sensory neurons. The... 
Journal Article
No results were found for your search.

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