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...

Adaptive functional reorganization in amyotrophic lateral sclerosis: coexisting degenerative and compensatory changes

European journal of neurology, 2020-01, Vol.27 (1), p.121-128

2020

Volltextzugriff (PDF)

Spinal cord multi‐parametric magnetic resonance imaging for survival prediction in amyotrophic lateral sclerosis

European journal of neurology, 2017-08, Vol.24 (8), p.1040-1046

2017

Volltextzugriff (PDF)

Insights into the genetic epidemiology of spinal and bulbar muscular atrophy: prevalence estimation and multiple founder haplotypes in the Veneto Italian region

European journal of neurology, 2019-03, Vol.26 (3), p.519-524

2019

Volltextzugriff (PDF)

Kennedy disease (X-linked recessive bulbospinal neuronopathy): A comprehensive review from pathophysiology to therapy

Revue neurologique, 2017-05, Vol.173 (5), p.326-337

2017

Volltextzugriff (PDF)

Unimpaired Neuropsychological Performance and Enhanced Memory Recall in Patients with Sbma: A Large Sample Comparative Study

Scientific reports, 2018-09, Vol.8 (1), p.13627-8, Article 13627

2018

Volltextzugriff (PDF)

Clinical correlations and long‐term follow‐up in 100 patients with sarcoglycanopathies

European journal of neurology, 2021-02, Vol.28 (2), p.660-669

2021

Volltextzugriff (PDF)

New FIG4 gene mutations causing aggressive ALS

European journal of neurology, 2018-03, Vol.25 (3), p.e41-e42

2018

Volltextzugriff (PDF)

Quantitative brainstem and spinal MRI in amyotrophic lateral sclerosis: implications for predicting noninvasive ventilation needs

Journal of neurology, 2024-03, Vol.271 (3), p.1235-1246

2024

Volltextzugriff (PDF)

The role of AR polyQ tract in male breast carcinoma: lesson from an SBMA case

Annals of oncology, 2017-05, Vol.28 (5), p.1160-1161

2017

Volltextzugriff (PDF)

The role of androgen receptor gene variants on SBMA phenotype

Journal of the neurological sciences, 2015-10, Vol.357, p.e231-e231

2015

Volltextzugriff (PDF)

Right hemisphere dysfunction and emotional processing in ALS: an fMRI study

Journal of neurology, 2010-12, Vol.257 (12), p.1970-1978

2010

Volltextzugriff (PDF)

No effect of AR polyG polymorphism on spinal and bulbar muscular atrophy phenotype

European journal of neurology, 2016-06, Vol.23 (6), p.1134-1136

2016

Volltextzugriff (PDF)

ALS risk but not phenotype is affected by ataxin-2 intermediate length polyglutamine expansion

Neurology, 2011-06, Vol.76 (23), p.2030-2031

2011

Volltextzugriff (PDF)

The blurred scenario of motor neuron disorders linked to Spatacsin mutations: a case report

European journal of neurology, 2014-10, Vol.21 (10), p.e85-e86

2014

Volltextzugriff (PDF)

Motor neuron disease of very long disease duration or Charcot–Marie–Tooth disease? A novel phenotype related to the SOD1 p.E22G variant

Revue neurologique, 2017-12, Vol.173 (10), p.671-673

2017

Volltextzugriff (PDF)

No evidence of cardiomyopathy in spinal and bulbar muscular atrophy

Acta neurologica Scandinavica, 2013-12, Vol.128 (6), p.e30-e32

2013

Volltextzugriff (PDF)

CAG repeat length in androgen receptor gene is not associated with amyotrophic lateral sclerosis

European journal of neurology, 2012-10, Vol.19 (10), p.1373-1375

2012

Volltextzugriff (PDF)

P438 Multimodal evaluation of the effect of salbutamol on walking capacity in ambulatory individuals with ALS: insights from the phase 2 WALKALS study

Neuromuscular disorders : NMD, 2023-10, Vol.33, p.S187-S187

2023

Volltextzugriff (PDF)

Muscle and not neuronal biomarkers correlate with severity in spinal and bulbar muscular atrophy

Neurology, 2019-03, Vol.92 (11), p.e1205

2019

Volltextzugriff (PDF)

P.173 Preliminary natural history quantitative MRI data in lower limb muscle and heart of patients with limb-girdle muscular dystrophy type R9

Neuromuscular disorders : NMD, 2022-10, Vol.32, p.S117

2022

Volltextzugriff (PDF)

Genetic Variation in KIFAP3 Is Associated with an Upper Motor Neuron-Predominant Phenotype in Amyotrophic Lateral Sclerosis

Neuro-degenerative diseases, 2011-01, Vol.8 (6), p.491-495

2011

Volltextzugriff (PDF)

P.217 Cervical spinal cord MRI parameters as predictors of early degeneration in asymptomatic C9Orf72 carriers: a longitudinal study

Neuromuscular disorders : NMD, 2022, Vol.32, p.S134-S135

2022

Volltextzugriff (PDF)

P125 Quantitative MRI in upper limb muscles of patients with dysferlinopathy: 6-months and 12-months longitudinal data from the natural history Jain COS 2 project

Neuromuscular disorders : NMD, 2023-10, Vol.33, p.S78-S79

2023

Volltextzugriff (PDF)

P283 Natural history of limb girdle muscular dystrophy R9: one-year follow-up of a European cohort

Neuromuscular disorders : NMD, 2023-10, Vol.33, p.S114-S114

2023

Volltextzugriff (PDF)

P.163 Quantitative MRI in upper limb muscle of patients with dysferlinopathy: preliminary baseline results of the natural history study Jain COS2

Neuromuscular disorders : NMD, 2022-10, Vol.32, p.S114-S115

2022

Volltextzugriff (PDF)

1 – 25 von 110

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(101)
Mit Volltextzugriff
(92)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(74)
Life Sciences & Biomedicine
(41)
Humans
(38)
Technology
(31)
Engineering
(27)
Female
(27)
Male
(26)
Neurosciences & Neurology
(24)
Clinical Neurology
(23)
Middle Aged
(22)
Mechanics
(21)
Adult
(19)
Exact Sciences And Technology
(18)
Neurosciences
(18)
Engineering, Multidisciplinary
(17)
Physics
(16)
Aged
(15)
Fundamental Areas Of Phenomenology
(15)
Computer Science
(13)
Computer Science, Interdisciplinary Applications
(13)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Adaptive functional reorganization in amyotrophic lateral sclerosis: coexisting degenerative and compensatory changes

Spinal cord multi‐parametric magnetic resonance imaging for survival prediction in amyotrophic lateral sclerosis

Insights into the genetic epidemiology of spinal and bulbar muscular atrophy: prevalence estimation and multiple founder haplotypes in the Veneto Italian region

Kennedy disease (X-linked recessive bulbospinal neuronopathy): A comprehensive review from pathophysiology to therapy

Unimpaired Neuropsychological Performance and Enhanced Memory Recall in Patients with Sbma: A Large Sample Comparative Study

Clinical correlations and long‐term follow‐up in 100 patients with sarcoglycanopathies

New FIG4 gene mutations causing aggressive ALS

Quantitative brainstem and spinal MRI in amyotrophic lateral sclerosis: implications for predicting noninvasive ventilation needs

The role of AR polyQ tract in male breast carcinoma: lesson from an SBMA case

The role of androgen receptor gene variants on SBMA phenotype

Right hemisphere dysfunction and emotional processing in ALS: an fMRI study

No effect of AR polyG polymorphism on spinal and bulbar muscular atrophy phenotype

ALS risk but not phenotype is affected by ataxin-2 intermediate length polyglutamine expansion

The blurred scenario of motor neuron disorders linked to Spatacsin mutations: a case report

Motor neuron disease of very long disease duration or Charcot–Marie–Tooth disease? A novel phenotype related to the SOD1 p.E22G variant

No evidence of cardiomyopathy in spinal and bulbar muscular atrophy

CAG repeat length in androgen receptor gene is not associated with amyotrophic lateral sclerosis

P438 Multimodal evaluation of the effect of salbutamol on walking capacity in ambulatory individuals with ALS: insights from the phase 2 WALKALS study

Muscle and not neuronal biomarkers correlate with severity in spinal and bulbar muscular atrophy

P.173 Preliminary natural history quantitative MRI data in lower limb muscle and heart of patients with limb-girdle muscular dystrophy type R9

Genetic Variation in KIFAP3 Is Associated with an Upper Motor Neuron-Predominant Phenotype in Amyotrophic Lateral Sclerosis

P.217 Cervical spinal cord MRI parameters as predictors of early degeneration in asymptomatic C9Orf72 carriers: a longitudinal study

P125 Quantitative MRI in upper limb muscles of patients with dysferlinopathy: 6-months and 12-months longitudinal data from the natural history Jain COS 2 project

P283 Natural history of limb girdle muscular dystrophy R9: one-year follow-up of a European cohort

P.163 Quantitative MRI in upper limb muscle of patients with dysferlinopathy: preliminary baseline results of the natural history study Jain COS2

Suchergebnisse filtern