X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (31) 31
clinical neurology (23) 23
neurosciences (20) 20
index medicus (19) 19
female (18) 18
middle aged (18) 18
male (16) 16
adult (15) 15
neurology (12) 12
aged (10) 10
medicine & public health (9) 9
myotonic dystrophy (9) 9
musculoskeletal diseases (8) 8
myasthenia gravis (7) 7
myotonic dystrophy - pathology (7) 7
animals (6) 6
medicine (6) 6
myotonic dystrophy - genetics (6) 6
abridged index medicus (5) 5
care and treatment (5) 5
diagnosis (5) 5
differentiation (5) 5
messenger-rna (5) 5
mri (5) 5
myopathy (5) 5
neurology. diseases of the nervous system (5) 5
neuroradiology (5) 5
research (5) 5
rna-binding proteins - genetics (5) 5
rna-binding proteins - metabolism (5) 5
therapy (5) 5
usage (5) 5
cell line (4) 4
congenital, hereditary, and neonatal diseases and abnormalities (4) 4
ctg repeats (4) 4
double-blind (4) 4
genetic aspects (4) 4
intravenous immunoglobulin (4) 4
magnetic resonance imaging (4) 4
mice (4) 4
molecular-basis (4) 4
multiple-sclerosis (4) 4
mutation (4) 4
mycophenolate-mofetil (4) 4
myotonic dystrophy - metabolism (4) 4
myotonic dystrophy - physiopathology (4) 4
pathology (4) 4
phosphorylation (4) 4
region (4) 4
research article (4) 4
triplet repeat (4) 4
znf9 (4) 4
article (3) 3
celf1 protein (3) 3
cell biology (3) 3
corpus callosum (3) 3
dm2 (3) 3
efficacy (3) 3
expansion (3) 3
expression (3) 3
family medicine (3) 3
immunosuppression (3) 3
immunotherapy (3) 3
increases translation (3) 3
internal medicine (3) 3
muscle, skeletal - pathology (3) 3
myotonic dystrophy - classification (3) 3
neuropsychology (3) 3
orthopedics (3) 3
patients (3) 3
pediatrics (3) 3
phenotype (3) 3
plasma-exchange (3) 3
questionnaire (3) 3
rating-scale (3) 3
restless legs syndrome (3) 3
review (3) 3
rituximab (3) 3
translation (3) 3
treatment (3) 3
treatment outcome (3) 3
young adult (3) 3
abnormalities (2) 2
acetylcholine-receptor (2) 2
antibodies (2) 2
atrophy (2) 2
beta (2) 2
biochemistry & molecular biology (2) 2
brain (2) 2
brain - pathology (2) 2
case report (2) 2
case studies (2) 2
central nervous system (2) 2
chronic inflammatory demyelinating polyneuropathy (2) 2
chronic inflammatory demyelinating polyradiculoneuropathy (2) 2
complications and side effects (2) 2
cug-binding protein (2) 2
cugbp1 (2) 2
cyclin d3 (2) 2
data mining (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


2015, ISBN 9783662442395
Angeborene Muskelerkrankungen gehören zu den „Orphan Diseases“, die von der Pädiatrie zunehmend in die Erwachsenenmedizin hinein reichen -  darunter die... 
Medicine | Neurology | Pediatrics | Internal medicine | Orthopedics | Family medicine
Web Resource
PLoS ONE, ISSN 1932-6203, 06/2015, Volume 10, Issue 6, p. e0130352
Objectives Central nervous system involvement is one important clinical aspect of myotonic dystrophy type 1 and 2 (DM1 and DM2). We assessed CNS involvement... 
MULTIPLE-SCLEROSIS | ABNORMALITIES | MRI | ALZHEIMERS-DISEASE | MULTIDISCIPLINARY SCIENCES | VOLUME | TEMPORAL-LOBE ATROPHY | MYOPATHY | RATING-SCALE | BRAIN | Atrophy - diagnostic imaging | Cognition Disorders - physiopathology | Depression - physiopathology | Atrophy - physiopathology | White Matter - physiopathology | Cognition Disorders - diagnostic imaging | Humans | Middle Aged | Male | Cerebral Cortex - diagnostic imaging | Myotonic Dystrophy - diagnostic imaging | Cerebral Cortex - physiopathology | Gray Matter - diagnostic imaging | Radiography | Mesencephalon - diagnostic imaging | Myotonic Dystrophy - physiopathology | White Matter - diagnostic imaging | Sleep | Gray Matter - physiopathology | Adult | Female | Aged | Depression - diagnostic imaging | Mesencephalon - physiopathology | Comparative analysis | Depression, Mental | Cerebellum | Brain | Pons | Peptides | Brain stem | Central nervous system | Cognitive ability | Impairment | Mental depression | Functional magnetic resonance imaging | Sleepiness | Enlargement | Cortex (visual) | Patients | Studies | Restless legs syndrome | Neurology | Hospitals | Myotonic dystrophy | Brain damage | Mutation | Morphometry | Short term memory | Neurosciences | Correlation | Nuclear magnetic resonance--NMR | Demography | Mesencephalon | Daytime | Spatial discrimination | Cortex (somatosensory) | Flexibility | Atrophy | Cortex (frontal) | Spectrum analysis | Population | Sleep and wakefulness | Age | Cortex (cingulate) | Medical imaging | Corpus callosum | Hemispheric laterality | Brain research | Magnetic resonance imaging | Neural networks | Dystrophy | Ventricle | Alzheimers disease | Spatial memory | Nuclear magnetic resonance | NMR
Journal Article
Therapeutic Advances in Neurological Disorders, ISSN 1756-2856, 02/2019, Volume 12, p. 175628641983224
Myasthenia gravis (MG) is an autoantibody-mediated disease that compromises the acetylcholine receptors or associated structures of the postsynaptic membrane... 
treatment | unmet need | disability | tolerability | side effects | definition | refractory myasthenia gravis | quality of life | burden | TRANSSTERNAL THYMECTOMY | FOLLOW-UP | SYMPTOMS | ACETYLCHOLINE-RECEPTOR | CLINICAL NEUROLOGY | PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY | INTRAVENOUS IMMUNOGLOBULIN | THORACOSCOPIC THYMECTOMY | CORTICOSTEROID-THERAPY | RITUXIMAB | QUALITY-OF-LIFE
Journal Article
Muscle & Nerve, ISSN 0148-639X, 06/2007, Volume 35, Issue 6, pp. 712 - 724
Journal Article
Journal of Neurology, ISSN 0340-5354, 9/2017, Volume 264, Issue 9, pp. 2010 - 2020
Journal Article
PLOS ONE, ISSN 1932-6203, 03/2019, Volume 14, Issue 3, p. e0213381
Objectives The aim of this study was to examine the natural history of brain involvement in adult-onset myotonic dystrophies type 1 and 2 (DM1, DM2). Methods... 
DAYTIME SLEEPINESS | MULTIPLE-SCLEROSIS | ABNORMALITIES | MULTIDISCIPLINARY SCIENCES | WORKSHOP REPORT | RATING-SCALE | TYPE-1 | WHITE-MATTER CHANGES | CEREBRAL INVOLVEMENT | VOXEL-BASED MORPHOMETRY | IMPAIRMENT | Neuroimaging | Case studies | Usage | Care and treatment | Middle aged persons | Myotonic dystrophy | Development and progression | Health aspects | Risk factors
Journal Article