UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 55

Sortiert nach

Hereditary spastic paraplegia: clinical features and pathogenetic mechanisms

Lancet neurology, 2008-12, Vol.7 (12), p.1127-1138

2008

Link zum Volltext

Verfügbarkeit prüfen

A systematic evaluation of integration free reprogramming methods for deriving clinically relevant patient specific induced pluripotent stem (iPS) cells

PloS one, 2013-11, Vol.8 (11), p.e81622-e81622

2013

Link zum Volltext

Verfügbarkeit prüfen

Association between diabetes and subsequent Parkinson disease: A record-linkage cohort study

Neurology, 2018-07, Vol.91 (2), p.e139

2018

Link zum Volltext

Verfügbarkeit prüfen

A Metabolic Study of Huntington's Disease

PloS one, 2016-01, Vol.11 (1), p.e0146480-e0146480

2016

Link zum Volltext

Verfügbarkeit prüfen

SGCE mutations cause psychiatric disorders: clinical and genetic characterization

Brain (London, England : 1878), 2013, Vol.136 (Pt 1), p.294-303

2013

Link zum Volltext

Verfügbarkeit prüfen

Pathological Relevance of Post-Translationally Modified Alpha-Synuclein (pSer87, pSer129, nTyr39) in Idiopathic Parkinson's Disease and Multiple System Atrophy

Cells (Basel, Switzerland), 2022-03, Vol.11 (5), p.906

2022

Link zum Volltext

Verfügbarkeit prüfen

Effects of age and cognition on a cross-cultural paediatric adaptation of the Sniffin' Sticks Identification Test

PloS one, 2015-08, Vol.10 (8), p.e0131641-e0131641

2015

Link zum Volltext

Verfügbarkeit prüfen

A 24-Hour Study of the Hypothalamo-Pituitary Axes in Huntington's Disease

PloS one, 2015-10, Vol.10 (10), p.e0138848-e0138848

2015

Link zum Volltext

Verfügbarkeit prüfen

What sample sizes for reliability and validity studies in neurology?

Journal of neurology, 2012-12, Vol.259 (12), p.2681-2694

2012

Link zum Volltext

Verfügbarkeit prüfen

Neuropathologic Validation and Diagnostic Accuracy of Presynaptic Dopaminergic Imaging in the Diagnosis of Parkinsonism

Neurology, 2024-06, Vol.102 (11), p.e209453

2024

Link zum Volltext

Verfügbarkeit prüfen

Final Exon Frameshift Biallelic PTPN23 Variants Are Associated with Microcephalic Complex Hereditary Spastic Paraplegia

Brain sciences, 2021-05, Vol.11 (5), p.614

2021

Link zum Volltext

Verfügbarkeit prüfen

Recent Advances in the Molecular Pathogenesis of Dystonia-Plus Syndromes and Heredodegenerative Dystonias

Current neuropharmacology, 2013-01, Vol.11 (1), p.30-40

2013

Link zum Volltext

Verfügbarkeit prüfen

Elevated salivary protein in Parkinson's disease and salivary DJ-1 as a potential marker of disease severity

Parkinsonism & related disorders, 2015-10, Vol.21 (10), p.1251-1255

2015

Link zum Volltext

Verfügbarkeit prüfen

TorsinA and dystonia: from nuclear envelope to synapse

Journal of neurochemistry, 2009-06, Vol.109 (6), p.1596-1609

2009

Link zum Volltext

Verfügbarkeit prüfen

Human spastin has multiple microtubule‐related functions

Journal of neurochemistry, 2005-12, Vol.95 (5), p.1411-1420

2005

Link zum Volltext

Verfügbarkeit prüfen

The cervical dystonia impact profile (CDIP-58): can a Rasch developed patient reported outcome measure satisfy traditional psychometric criteria?

Health and quality of life outcomes, 2008-08, Vol.6 (1), p.58-58, Article 58

2008

Link zum Volltext

Verfügbarkeit prüfen

Heterozygous missense mutations in BSCL2 are associated with distal hereditary motor neuropathy and Silver syndrome

Nature genetics, 2004-03, Vol.36 (3), p.271-276

2004

Link zum Volltext

Verfügbarkeit prüfen

Characterization of a novel TYMP splice site mutation associated with mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)

Neuromuscular disorders : NMD, 2009-02, Vol.19 (2), p.151-154

2009

Link zum Volltext

Verfügbarkeit prüfen

DRPLA in Europe

Nature genetics, 1994-03, Vol.6 (3), p.225-225

1994

Link zum Volltext

Verfügbarkeit prüfen

A numerical study of the development mechanisms of polar lows

Tellus. Series A, Dynamic meteorology and oceanography, 1985-10, Vol.37A (5), p.460-477

1985

Link zum Volltext

Verfügbarkeit prüfen

Genomic analysis of individual differences in ethanol drinking: evidence for non-genetic factors in C57BL/6 mice

PloS one, 2011-06, Vol.6 (6), p.e21100

2011

Link zum Volltext

Verfügbarkeit prüfen

Recent Advances in the Molecular Pathogenesis of Dystonia-Plus Syndromes and Heredodegenerative Dystonias

Current neuropharmacology, 2013-01, Vol.11 (1), p.30-40

2013

Link zum Volltext

Verfügbarkeit prüfen

Treatment of on/off switches in the adjoint method: FDDA experiments with a simple model

Tellus. Series A, Dynamic meteorology and oceanography, 1993-10, Vol.45 (5), p.525-538

1993

Link zum Volltext

Verfügbarkeit prüfen

Structural and Hydrogeological Controls on Hydrocarbon and Brine Migration into Drinking Water Aquifers in Southern New York

Ground water, 2018-03, Vol.56 (2), p.225-244

2018

Link zum Volltext

Verfügbarkeit prüfen

Fluid management with a simplified conservative protocol for the acute respiratory distress syndrome

Critical care medicine, 2015-02, Vol.43 (2), p.288-295

2015

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 55

Suche als RSS-Feed

Aktive Filter

KollektionIngentaConnect Journals

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(55)
Mit Volltextzugriff
(49)

Publikationsform

Artikel
(55)

Sprache

Englisch
(55)
Japanisch
(11)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Hereditary spastic paraplegia: clinical features and pathogenetic mechanisms

A systematic evaluation of integration free reprogramming methods for deriving clinically relevant patient specific induced pluripotent stem (iPS) cells

Association between diabetes and subsequent Parkinson disease: A record-linkage cohort study

A Metabolic Study of Huntington's Disease

SGCE mutations cause psychiatric disorders: clinical and genetic characterization

Pathological Relevance of Post-Translationally Modified Alpha-Synuclein (pSer87, pSer129, nTyr39) in Idiopathic Parkinson's Disease and Multiple System Atrophy

Effects of age and cognition on a cross-cultural paediatric adaptation of the Sniffin' Sticks Identification Test

A 24-Hour Study of the Hypothalamo-Pituitary Axes in Huntington's Disease

What sample sizes for reliability and validity studies in neurology?

Neuropathologic Validation and Diagnostic Accuracy of Presynaptic Dopaminergic Imaging in the Diagnosis of Parkinsonism

Final Exon Frameshift Biallelic PTPN23 Variants Are Associated with Microcephalic Complex Hereditary Spastic Paraplegia

Recent Advances in the Molecular Pathogenesis of Dystonia-Plus Syndromes and Heredodegenerative Dystonias

Elevated salivary protein in Parkinson's disease and salivary DJ-1 as a potential marker of disease severity

TorsinA and dystonia: from nuclear envelope to synapse

Human spastin has multiple microtubule‐related functions

The cervical dystonia impact profile (CDIP-58): can a Rasch developed patient reported outcome measure satisfy traditional psychometric criteria?

Heterozygous missense mutations in BSCL2 are associated with distal hereditary motor neuropathy and Silver syndrome

Characterization of a novel TYMP splice site mutation associated with mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)

DRPLA in Europe

A numerical study of the development mechanisms of polar lows

Genomic analysis of individual differences in ethanol drinking: evidence for non-genetic factors in C57BL/6 mice

Recent Advances in the Molecular Pathogenesis of Dystonia-Plus Syndromes and Heredodegenerative Dystonias

Treatment of on/off switches in the adjoint method: FDDA experiments with a simple model

Structural and Hydrogeological Controls on Hydrocarbon and Brine Migration into Drinking Water Aquifers in Southern New York

Fluid management with a simplified conservative protocol for the acute respiratory distress syndrome

Aktive Filter

Suchergebnisse filtern