X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (4) 4
index medicus (4) 4
clinical neurology (3) 3
neurosciences (3) 3
abridged index medicus (2) 2
congenital myasthenic syndromes (2) 2
female (2) 2
genetics (2) 2
male (2) 2
myasthenia gravis (2) 2
psychiatry (2) 2
adult (1) 1
autoimmune (1) 1
autosomal-dominant (1) 1
biomedicine (1) 1
brain - diagnostic imaging (1) 1
brain - pathology (1) 1
common (1) 1
congenital myasthenic syndromes, genetics (1) 1
deficiency (1) 1
deficiency causes (1) 1
dentatorubral-pallidoluysian atrophy (1) 1
diagnosis, differential (1) 1
disorders (1) 1
domain (1) 1
episodic apnea (1) 1
frameshift mutation (1) 1
gravis (1) 1
heat shock proteins (1) 1
hereditary spastic paraparesis (1) 1
identification (1) 1
leukodystrophy, metachromatic - genetics (1) 1
leukodystrophy, metachromatic - pathology (1) 1
missense mutation (1) 1
molecular-mechanisms (1) 1
motor neuron disease (1) 1
motor-neuron disease (1) 1
muscle weakness - genetics (1) 1
muscle weakness - pathology (1) 1
muscular dystrophy, facioscapulohumeral - complications (1) 1
mutation (1) 1
mutations cause (1) 1
myasthenia gravis - genetics (1) 1
myasthenia gravis - pathology (1) 1
myasthenic syndromes, congenital - genetics (1) 1
myasthenic syndromes, congenital - pathology (1) 1
myoclonic epilepsies, progressive - diagnosis (1) 1
myoclonic epilepsies, progressive - genetics (1) 1
myoclonic epilepsies, progressive - pathology (1) 1
neurobiology (1) 1
neurogenetics (1) 1
neuroimaging (1) 1
neurology (1) 1
neurosciences. biological psychiatry. neuropsychiatry (1) 1
optic atrophy (1) 1
paralysis, spastic (1) 1
pedigree (1) 1
phenotype (1) 1
recessive intellectual disability (1) 1
retinal telangiectasis - etiology (1) 1
spastic ataxias (1) 1
spastic paraplegia (1) 1
spastic paraplegia, hereditary - classification (1) 1
spastic paraplegia, hereditary - diagnosis (1) 1
spastic paraplegia, hereditary - genetics (1) 1
spastic paraplegia, hereditary - physiopathology (1) 1
spg (1) 1
therapy (1) 1
thin corpus-callosum (1) 1
x-linked hydrocephalus (1) 1
young adult (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Neurology, ISSN 0028-3878, 07/2016, Volume 87, Issue 4, pp. e39 - e39
A 21-year-old Brazilian woman presented with mild facial muscle weakness, scapular winging and an asymmetric shoulder girdle, and peroneal weakness. Medical... 
CLINICAL NEUROLOGY | Young Adult | Muscular Dystrophy, Facioscapulohumeral - complications | Retinal Telangiectasis - etiology | Female | Humans
Journal Article
NEUROLOGY, ISSN 0028-3878, 05/2016, Volume 86, Issue 18, pp. E201 - E201
A 2-year-old boy presented with delayed motor skills and language since birth. Family history disclosed consanguineous parents. Examination showed global... 
CLINICAL NEUROLOGY
Journal Article
ARQUIVOS DE NEURO-PSIQUIATRIA, ISSN 0004-282X, 09/2016, Volume 74, Issue 9, pp. 750 - 760
Journal Article
Journal Article
Arquivos de Neuro-Psiquiatria, ISSN 1678-4227, 09/2016, Volume 74, Issue 9, pp. 750 - 760
ABSTRACT Neuromuscular junction disorders represent a wide group of neurological diseases characterized by weakness, fatigability and variable degrees of... 
PSYCHIATRY | NEUROSCIENCES
Journal Article
No results were found for your search.

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