UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 48

Sortiert nach

Age-specific penetrance of LRRK2 G2019S in the Michael J. Fox Ashkenazi Jewish LRRK2 Consortium

Neurology, 2015-07, Vol.85 (1), p.89

2015

Volltextzugriff (PDF)

Analysis of an early-onset Parkinson's disease cohort for DJ-1 mutations

Movement disorders, 2004-07, Vol.19 (7), p.796-800

2004

Volltextzugriff (PDF)

Application of the Movement Disorder Society prodromal criteria in healthy G2019S‐LRRK2 carriers

Movement disorders, 2018-07, Vol.33 (6), p.966-973

2018

Volltextzugriff (PDF)

The association between Mediterranean diet adherence and Parkinson's disease

Movement disorders, 2012-05, Vol.27 (6), p.771-774

2012

Volltextzugriff (PDF)

Association of glucocerebrosidase mutations with dementia with lewy bodies

Archives of neurology (Chicago), 2009-05, Vol.66 (5), p.578

2009

Volltextzugriff (PDF)

Body mass index in essential tremor

Archives of neurology (Chicago), 2002-08, Vol.59 (8), p.1273

2002

Volltextzugriff (PDF)

Case-control study of the parkin gene in early-onset Parkinson disease

Archives of neurology (Chicago), 2006-04, Vol.63 (4), p.548

2006

Volltextzugriff (PDF)

Clinical and dopamine transporter imaging characteristics of non-manifest LRRK2 and GBA mutation carriers in the Parkinson's Progression Markers Initiative (PPMI): a cross-sectional study

Lancet neurology, 2020-01, Vol.19 (1), p.71-80

2020

Volltextzugriff (PDF)

Construction and validation of a Parkinson's disease mutation genotyping array for the Parkin gene

Movement disorders, 2007-05, Vol.22 (7), p.932-937

2007

Volltextzugriff (PDF)

Contribution of aging to the severity of different motor signs in Parkinson disease

Archives of neurology (Chicago), 2005-03, Vol.62 (3), p.467

2005

Volltextzugriff (PDF)

Differences in performance on English and Hebrew versions of the MoCA in Parkinson's patients

Clinical parkinsonism & related disorders, 2020-01, Vol.3, p.100042, Article 100042

2020

Volltextzugriff (PDF)

Estimation of genetic risk function with covariates in the presence of missing genotypes

Statistics in medicine, 2017-09, Vol.36 (22), p.3533-3546

2017

Volltextzugriff (PDF)

Estimation of genetic risk function with covariates in the presence of missing genotypes: A. J. LEE et al

Statistics in medicine, 2017-09, Vol.36 (22), p.3533-3546

2017

Volltextzugriff (PDF)

Evidence for increased completed suicide in first-degree relatives of LRRK2 G2019S mutation Parkinson's disease

Journal of neurology, neurosurgery and psychiatry, 2019-07, Vol.90 (7), p.843

2019

Volltextzugriff (PDF)

Familial aggregation of early‐ and late‐onset Parkinson's disease

Annals of neurology, 2003-10, Vol.54 (4), p.507-513

2003

Volltextzugriff (PDF)

Genetic and Clinical Predictors of Deep Brain Stimulation in Young-Onset Parkinson's Disease

Movement disorders clinical practice (Hoboken, N.J.), 2016-09, Vol.3 (5), p.465-471

2016

Volltextzugriff (PDF)

Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes

Human molecular genetics, 2014-09, Vol.23 (17), p.4693-4702

2014

Volltextzugriff (PDF)

Genomewide Association Studies of LRRK2 Modifiers of Parkinson's Disease

Annals of neurology, 2021-07, Vol.90 (1), p.76-88

2021

Volltextzugriff (PDF)

Increased rate of sporadic and recurrent rare genic copy number variants in P arkinson's disease among A shkenazi J ews

Molecular genetics & genomic medicine, 2013-09, Vol.1 (3), p.142-154

2013

Volltextzugriff (PDF)

Increased rate of sporadic and recurrent rare genic copy number variants in Parkinson's disease among Ashkenazi Jews

Molecular genetics & genomic medicine, 2013-09, Vol.1 (3), p.142-154

2013

Volltextzugriff (PDF)

Interest in Genetic Testing in Ashkenazi Jewish Parkinson’s Disease Patients and Their Unaffected Relatives

Journal of genetic counseling, 2015-04, Vol.24 (2), p.238-246

2015

Volltextzugriff (PDF)

1 – 25 von 48

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(38)
Mit Volltextzugriff
(34)

Publikationsform

Artikel
(48)

Sprache

Englisch
(48)
Japanisch
(5)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Age-specific penetrance of LRRK2 G2019S in the Michael J. Fox Ashkenazi Jewish LRRK2 Consortium

Analysis of an early-onset Parkinson's disease cohort for DJ-1 mutations

Application of the Movement Disorder Society prodromal criteria in healthy G2019S‐LRRK2 carriers

The association between Mediterranean diet adherence and Parkinson's disease

Association of glucocerebrosidase mutations with dementia with lewy bodies

Association of Olfactory Performance With Motor Decline and Age at Onset in People With Parkinson Disease and the LRRK2 G2019S Variant

Body mass index in essential tremor

Cancer outcomes among Parkinson's disease patients with leucine rich repeat kinase 2 mutations, idiopathic Parkinson's disease patients, and nonaffected controls

Case-control study of the parkin gene in early-onset Parkinson disease

Clinical and dopamine transporter imaging characteristics of non-manifest LRRK2 and GBA mutation carriers in the Parkinson's Progression Markers Initiative (PPMI): a cross-sectional study

Cognitive and motor function in long-duration PARKIN-associated Parkinson disease

Construction and validation of a Parkinson's disease mutation genotyping array for the Parkin gene

Contribution of aging to the severity of different motor signs in Parkinson disease

Differences in performance on English and Hebrew versions of the MoCA in Parkinson's patients

Estimation of genetic risk function with covariates in the presence of missing genotypes

Estimation of genetic risk function with covariates in the presence of missing genotypes: A. J. LEE et al

Evidence for increased completed suicide in first-degree relatives of LRRK2 G2019S mutation Parkinson's disease

Familial aggregation of early‐ and late‐onset Parkinson's disease

Frequency of known mutations in early-onset Parkinson disease: implication for genetic counseling: the consortium on risk for early onset Parkinson disease study

Genetic and Clinical Predictors of Deep Brain Stimulation in Young-Onset Parkinson's Disease

Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes

Genomewide Association Studies of LRRK2 Modifiers of Parkinson's Disease

Increased rate of sporadic and recurrent rare genic copy number variants in P arkinson's disease among A shkenazi J ews

Increased rate of sporadic and recurrent rare genic copy number variants in Parkinson's disease among Ashkenazi Jews

Interest in Genetic Testing in Ashkenazi Jewish Parkinson’s Disease Patients and Their Unaffected Relatives

Suchergebnisse filtern