X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
clinical neurology (6) 6
index medicus (5) 5
humans (4) 4
child (3) 3
d4z4 (3) 3
facioscapulohumeral dystrophy (3) 3
muscular dystrophy, facioscapulohumeral - physiopathology (3) 3
abnormalities (2) 2
adolescent (2) 2
adult (2) 2
age of onset (2) 2
atypical features (2) 2
diagnosis (2) 2
disease (2) 2
epilepsy (2) 2
female (2) 2
follow-up studies (2) 2
hearing-loss (2) 2
infant (2) 2
infantile fshd (2) 2
male (2) 2
muscular dystrophy, facioscapulohumeral - genetics (2) 2
muscular-dystrophy (2) 2
natural history (2) 2
neuromuscular diseases (2) 2
neurosciences (2) 2
pediatrics (2) 2
phenotype (2) 2
quality of life (2) 2
4q35-facioscapulohumeral muscular-dystrophy (1) 1
6-minute walk test (1) 1
abridged index medicus (1) 1
atypical parkinsonism (1) 1
cardiac & cardiovascular systems (1) 1
child, preschool (1) 1
children (1) 1
clinical-features (1) 1
coats syndrome (1) 1
cohort studies (1) 1
complications and side effects (1) 1
congenital, hereditary, and neonatal diseases and abnormalities (1) 1
development and progression (1) 1
duchenne muscular-dystrophy (1) 1
dystrophy (1) 1
early onset (1) 1
early onset; facioscapulohumeral dystrophy; infantile fshd; pediatrics, perinatology and child health; neurology; neurology; genetics (1) 1
early-onset fshd (1) 1
expiration (1) 1
facial diplegia (1) 1
facioscapulohumeral muscular dystrophy (1) 1
facioscapulohumeral muscular-dystrophy (1) 1
fatigue (1) 1
flattening (1) 1
fshd (1) 1
gene (1) 1
gene-environment interaction (1) 1
genetic heterogeneity (1) 1
genotype (1) 1
genotypes (1) 1
health aspects (1) 1
hearing loss (1) 1
heart (1) 1
hereditary spastic paraplegia (1) 1
infant, newborn (1) 1
lung (1) 1
lungs (1) 1
management (1) 1
mental-retardation (1) 1
middle aged (1) 1
mobius-syndrome (1) 1
motor skills - physiology (1) 1
motor task performance (1) 1
multiple system atrophy (1) 1
muscle ultrasound (1) 1
muscles (1) 1
muscular dystrophies (1) 1
muscular dystrophy (1) 1
muscular dystrophy, facioscapulohumeral - complications (1) 1
muscular dystrophy, facioscapulohumeral - psychology (1) 1
muscular dystrophy, facioscapulohumeral - therapy (1) 1
muscular fatigue (1) 1
musculoskeletal diseases (1) 1
mutation (1) 1
natural-history (1) 1
neurological disorders (1) 1
neuromuscular disorders (1) 1
observational study (1) 1
onset (1) 1
paediatrics (1) 1
pain (1) 1
parkinsons-disease (1) 1
patients (1) 1
phenotypes (1) 1
population surveillance (1) 1
posture (1) 1
prospective studies (1) 1
psychogenic movement-disorders (1) 1
pulmonary function (1) 1
pulmonary/respiratory (1) 1
quality-of-life (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Annals of Neurology, ISSN 0364-5134, 2018, Volume 84, Issue 5, pp. 627 - 637
Objective Facioscapulohumeral dystrophy (FSHD) is one of the most frequent heritable muscular dystrophies, with a large variety in age at onset and disease... 
HEARING-LOSS | DIAGNOSIS | 6-MINUTE WALK TEST | D4Z4 | FATIGUE | DISEASE | MUSCLE ULTRASOUND | DUCHENNE MUSCULAR-DYSTROPHY | QUALITY-OF-LIFE | NEUROSCIENCES | CLINICAL NEUROLOGY | CHILDREN | Phenotypes | Abnormalities | Epilepsy | Muscles | Fatigue | Retina | Motor task performance | Patients | Hearing loss | Muscular fatigue | Quality of life | Pain | Ultrasonography | Dystrophy | Children | Mutation | Genotypes | Natural history
Journal Article
Neurology, ISSN 0028-3878, 12/2018
OBJECTIVETo assess the relation between age at onset and disease severity in facioscapulohumeral muscular dystrophy (FSHD). METHODSIn this prospective... 
Journal Article
Neurology, ISSN 0028-3878, 2019, Volume 92, Issue 4, pp. e378 - e385
OBJECTIVE: To assess the relation between age at onset and disease severity in facioscapulohumeral muscular dystrophy (FSHD). METHODS: In this prospective... 
HEART | TYPE-1 | D4Z4 | CLINICAL NEUROLOGY
Journal Article
Respiratory Medicine, ISSN 0954-6111, 2017, Volume 126, pp. 130 - 131
Journal Article
Journal Article
European Journal of Paediatric Neurology, ISSN 1090-3798, 09/2018, Volume 22, Issue 5, pp. 782 - 785
To assess the long-term natural course of early-onset facioscapulohumeral dystrophy (FSHD), which is important for patient management and trial-readiness, and... 
Infantile FSHD | Facioscapulohumeral dystrophy | Early-onset FSHD | Neuromuscular disorders | Natural history | DIAGNOSIS | MUSCULAR-DYSTROPHY | PHENOTYPE | PEDIATRICS | CLINICAL NEUROLOGY | Muscular Dystrophy, Facioscapulohumeral - complications | Phenotype | Follow-Up Studies | Humans | Middle Aged | Adolescent | Age of Onset | Adult | Female | Male
Journal Article
Nature Reviews. Neurology, ISSN 1759-4758, 2018, Volume 14, Issue 3, pp. 183 - 189
Neurological disorders of gait, balance and posture are both debilitating and common. Adequate recognition of these so-called disorders of axial mobility is... 
MULTIPLE SYSTEM ATROPHY | PSYCHOGENIC MOVEMENT-DISORDERS | ATYPICAL PARKINSONISM | MANAGEMENT | HEREDITARY SPASTIC PARAPLEGIA | ABNORMALITIES | CLINICAL-FEATURES | NATURAL-HISTORY | STEP INITIATION | CLINICAL NEUROLOGY | PARKINSONS-DISEASE | Neurological disorders | Posture
Journal Article
No results were found for your search.

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