UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

A randomized clinical trial to evaluate the effects of rasagiline on depressive symptoms in non-demented Parkinson's disease patients

European journal of neurology, 2015-08, Vol.22 (8), p.1184-1191

2015

Volltextzugriff (PDF)

Combining olfactory test and motion analysis sensors in Parkinson's disease preclinical diagnosis: a pilot study

Acta neurologica Scandinavica, 2018-02, Vol.137 (2), p.204-211

2018

Volltextzugriff (PDF)

A cross-sectional multicenter study of cognitive and behavioural features in multiple system atrophy patients of the parkinsonian and cerebellar type

Journal of Neural Transmission, 2013-04, Vol.120 (4), p.613-618

2013

Volltextzugriff (PDF)

Validation of the Italian version of the Non Motor Symptoms Scale for Parkinson's disease

Parkinsonism & related disorders, 2017-01, Vol.34, p.38-42

2017

Volltextzugriff (PDF)

Intercepting Parkinson disease non-motor subtypes: A proof-of-principle study in a clinical setting

Journal of the neurological sciences, 2018-05, Vol.388, p.186-191

2018

Volltextzugriff (PDF)

Early-onset parkinsonism associated with PINK1 mutations: frequency, genotypes, and phenotypes

Neurology, 2005-07, Vol.65 (1), p.87-95

2005

Volltextzugriff (PDF)

DJ-1( PARK7), a novel gene for autosomal recessive, early onset parkinsonism

Neurological sciences, 2003-10, Vol.24 (3), p.159-160

2003

Volltextzugriff (PDF)

The G6055A (G2019S) mutation in LRRK2 is frequent in both early and late onset Parkinson’s disease and originates from a common ancestor

Journal of medical genetics, 2005-11, Vol.42 (11), p.e65-e65

2005

Volltextzugriff (PDF)

Adaptation and psychometric properties of the Italian version of the Non-Motor Symptoms Questionnaire for Parkinson’s disease

Neurological sciences, 2017-04, Vol.38 (4), p.673-678

2017

Volltextzugriff (PDF)

Lack of association between IL-1β, TNF-α, and IL-10 gene polymorphisms and sporadic Parkinson's disease in an Italian cohort

Acta neurologica Scandinavica, 2011-09, Vol.124 (3), p.176-181

2011

Volltextzugriff (PDF)

A Wide Variety of Mutations in the Parkin Gene Are Responsible for Autosomal Recessive Parkinsonism in Europe

Human molecular genetics, 1999-04, Vol.8 (4), p.567-574

1999

Volltextzugriff (PDF)

Donepezil in the treatment of hallucinations and delusions in Parkinson's disease

Neurological sciences, 2002-04, Vol.23 (1), p.41-43

2002

Volltextzugriff (PDF)

A case-control study on Alzheimer's disease and exposure to anesthesia

Neurological sciences, 2002-04, Vol.23 (1), p.11-14

2002

Volltextzugriff (PDF)

2.011 DIFFUSION TENSOR IMAGING STUDY IN PARKINSON'S DISEASE WITH IMPULSE CONTROL DISORDERS

Parkinsonism & related disorders, 2012, Vol.18, p.S93-S93

2012

Volltextzugriff (PDF)

Parkinsonism after Chronic Exposure to the Fungicide Maneb (Manganese ethylene-bis-dithiocarbamate)

Scandinavian Journal of Work, Environment ＆ Health, 1994-08, Vol.20 (4), p.301-305

1994

Volltextzugriff (PDF)

Mutation in the SYNJ1 Gene Associated with Autosomal Recessive, Early-Onset Parkinsonism

Human mutation, 2013-09, Vol.34 (9), p.1208-1215

2013

Volltextzugriff (PDF)

P1.123 Cognitive function in Parkinson's disease patients with Dopamine Dysregulation syndrome

Parkinsonism & related disorders, 2009, Vol.15, p.S60-S60

2009

Volltextzugriff (PDF)

P.2.c.008 Assessment of tolerability and efficacy of duloxetine in the treatment of depressed patients with Parkinson's disease

European neuropsychopharmacology, 2010, Vol.20, p.S372-S372

2010

Volltextzugriff (PDF)

A study of five candidate genes in Parkinson’s disease and related neurodegenerative disorders

Neurology, 1999-10, Vol.53 (7), p.1415-1415

1999

Volltextzugriff (PDF)

P1.170 Autonomic cardiovascular disfunction in early Parkinson's disease

Parkinsonism & related disorders, 2009, Vol.15, p.S72-S73

2009

Volltextzugriff (PDF)

DAT gene polymorphisms (rs28363170, rs393795) and levodopa-induced dyskinesias in Parkinson's disease

Neuroscience letters, 2019-01, Vol.690, p.83-88

2019

Volltextzugriff (PDF)

Genome-wide scan linkage analysis for Parkinson’s disease: the European genetic study of Parkinson’s disease

Journal of medical genetics, 2004-12, Vol.41 (12), p.900-907

2004

Volltextzugriff (PDF)

Mutations in the DJ-1 Gene Associated with Autosomal Recessive Early-Onset Parkinsonism

Science (American Association for the Advancement of Science), 2003-01, Vol.299 (5604), p.256-259

2003

Volltextzugriff (PDF)

Pseudo-dominant inheritance and exon 2 triplication in a family with parkin gene mutations

Neurology, 2001-09, Vol.57 (5), p.924-927

2001

Volltextzugriff (PDF)

1 – 25 von 346

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(305)
Mit Volltextzugriff
(266)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(4)
... seit 90 Tagen
(7)

Menü

Weitere Dienste

Einstellungen

A randomized clinical trial to evaluate the effects of rasagiline on depressive symptoms in non-demented Parkinson's disease patients

Combining olfactory test and motion analysis sensors in Parkinson's disease preclinical diagnosis: a pilot study

A cross-sectional multicenter study of cognitive and behavioural features in multiple system atrophy patients of the parkinsonian and cerebellar type

Validation of the Italian version of the Non Motor Symptoms Scale for Parkinson's disease

Intercepting Parkinson disease non-motor subtypes: A proof-of-principle study in a clinical setting

Early-onset parkinsonism associated with PINK1 mutations: frequency, genotypes, and phenotypes

DJ-1( PARK7), a novel gene for autosomal recessive, early onset parkinsonism

The G6055A (G2019S) mutation in LRRK2 is frequent in both early and late onset Parkinson’s disease and originates from a common ancestor

Adaptation and psychometric properties of the Italian version of the Non-Motor Symptoms Questionnaire for Parkinson’s disease

Lack of association between IL-1β, TNF-α, and IL-10 gene polymorphisms and sporadic Parkinson's disease in an Italian cohort

A Wide Variety of Mutations in the Parkin Gene Are Responsible for Autosomal Recessive Parkinsonism in Europe

Donepezil in the treatment of hallucinations and delusions in Parkinson's disease

A case-control study on Alzheimer's disease and exposure to anesthesia

2.011 DIFFUSION TENSOR IMAGING STUDY IN PARKINSON'S DISEASE WITH IMPULSE CONTROL DISORDERS

Parkinsonism after Chronic Exposure to the Fungicide Maneb (Manganese ethylene-bis-dithiocarbamate)

Mutation in the SYNJ1 Gene Associated with Autosomal Recessive, Early-Onset Parkinsonism

P1.123 Cognitive function in Parkinson's disease patients with Dopamine Dysregulation syndrome

Phenotype, genotype, and worldwide genetic penetrance of LRRK2 -associated Parkinson's disease: a case-control study

P.2.c.008 Assessment of tolerability and efficacy of duloxetine in the treatment of depressed patients with Parkinson's disease

A study of five candidate genes in Parkinson’s disease and related neurodegenerative disorders

P1.170 Autonomic cardiovascular disfunction in early Parkinson's disease

DAT gene polymorphisms (rs28363170, rs393795) and levodopa-induced dyskinesias in Parkinson's disease

Genome-wide scan linkage analysis for Parkinson’s disease: the European genetic study of Parkinson’s disease

Mutations in the DJ-1 Gene Associated with Autosomal Recessive Early-Onset Parkinsonism

Pseudo-dominant inheritance and exon 2 triplication in a family with parkin gene mutations

Suchergebnisse filtern