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Acta Neurologica Scandinavica, ISSN 0001-6314, 06/2019, Volume 139, Issue 6, pp. 519 - 525
Objective: Depression and anxiety symptoms are common among patients with epilepsy, but are relatively under-researched in patients with both epilepsy and... 
Neurology | Clinical Neurology | developmental disability | mental health | seizures | anxiety disorder | depression | Journal Article | PEOPLE | RELIABILITY | PAPER | VALIDITY | CLINICAL NEUROLOGY | Medicine, Experimental | Medical research | Adults | Anxiety | Seizures (Medicine) | Epilepsy | Convulsions & seizures | Mood | Anxieties | Intellectual disabilities | Mental depression | Antiepileptic agents | Quality of life
Journal Article
Journal of Alzheimer's Disease, ISSN 1387-2877, 2017, Volume 55, Issue 2, pp. 585 - 595
Background: Frontotemporal dementia (FTD) is a heterogeneous disease both at the clinical, genetic, and pathobiological level. The underlying pathological... 
tau proteins | cerebrospinal fluid | Biomarkers | TAR DNA-binding protein 43 | Psychiatry and Mental health | Clinical Psychology | frontotemporal lobar degeneration | Geriatrics and Gerontology
Journal Article
Developmental Neurorehabilitation, ISSN 1751-8423, 2018, Volume 21, Issue 2, pp. 101 - 107
The assessment of intellectual abilities is intensive, time-consuming, and might be considered burdensome for patients. We examined psychometric qualities of... 
epilepsy | TESTS | neuropsychological assessment | WECHSLER ADULT INTELLIGENCE | psychometrics | intelligence | CHILDREN | SUBTESTS | SCORES | Developmental disability | CLINICAL-SAMPLE | SCALE | VALIDITY | EDITION
Journal Article
American Journal of Human Genetics, ISSN 0002-9297, 06/2013, Volume 92, Issue 6, pp. 946 - 954
Spinal muscular atrophy (SMA) is a heterogeneous group of neuromuscular disorders caused by degeneration of lower motor neurons. Although functional loss of... 
HEAVY-CHAIN | TRANSPORT | MARIE-TOOTH-DISEASE | NEUROPATHY | PROTEIN | GENE | DYNACTIN | BICAUDAL-D | AMYOTROPHIC-LATERAL-SCLEROSIS | MISSENSE MUTATIONS
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 11/2013, Volume 21, Issue 11, pp. 1312 - 1315
Although SPG11 is the most common complicated hereditary spastic paraplegia, our knowledge of the long-term prognosis and life expectancy is limited. We... 
mutation/genetics | hereditary spastic paraplegia | SPG11 MUTATIONS | human SPG11 protein | corpus callosum/pathology | psychoses | SPATACSIN | SPECTRUM | prognosis | THIN CORPUS-CALLOSUM | DEGENERATION
Journal Article
European journal of human genetics, ISSN 1018-4813, 2013, Volume 21, Issue 1, pp. 102 - 108
Journal Article
Nature genetics, ISSN 1061-4036, 2009, Volume 41, Issue 10, pp. 1083 - U53
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 06/2013, Volume 92, Issue 6, pp. 946 - 954
Journal Article
Nature Genetics, ISSN 1061-4036, 2010, Volume 42, Issue 2, pp. 160 - 164
Journal Article
Annals of neurology, ISSN 0364-5134, 2011, Volume 70, Issue 6, pp. 964 - 973
Journal Article
Brain, ISSN 0006-8950, 2012, Volume 135, Issue 3, pp. 723 - 735
Journal Article