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...

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)

Cardiovascular diseases may play a negative role in the prognosis of amyotrophic lateral sclerosis

European journal of neurology, 2018-06, Vol.25 (6), p.861-868

2018

Volltextzugriff (PDF)

PT09.2: Body Composition and Metabolic Features in the Kennedy's Disease

Clinical nutrition (Edinburgh, Scotland), 2016-09, Vol.35, p.S40-S40

2016

Volltextzugriff (PDF)

PT05.2: The Long-Term Treatment of Human Amyotrophic Lateral Sclerosis with a Modified-Ketogenic Diet

Clinical nutrition (Edinburgh, Scotland), 2016-09, Vol.35, p.S31-S31

2016

Volltextzugriff (PDF)

Emotional Lability in MND: Relationship to cognition and psychopathology and impact on caregivers

Journal of the neurological sciences, 2009-03, Vol.278 (1), p.16-20

2009

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)

45. Clinical and electrophysiological non-SPG4 spectrum of HSP

Clinical neurophysiology, 2015-01, Vol.126 (1), p.e11-e11

2015

Volltextzugriff (PDF)

Neurofilament light chain and profilin‐1 dynamics in 30 spinal muscular atrophy type 3 patients treated with nusinersen

European journal of neurology, 2024-10, Vol.31 (10), p.e16393-n/a

2024

Volltextzugriff (PDF)

Retrospective study on PET–SPECT imaging in a large cohort of myotonic dystrophy type 1 patients

Neurological sciences, 2010-12, Vol.31 (6), p.757-763

2010

Volltextzugriff (PDF)

Out-of-furnace oxidation of SiCN polymer-derived ceramic aerogel pyrolized at intermediate temperature (600–800°C)

Journal of the European Ceramic Society, 2016-02, Vol.36 (3), p.423-428

2016

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)

Lithium carbonate in amyotrophic lateral sclerosis: lack of efficacy in a dose-finding trial

Neurology, 2010-08, Vol.75 (7), p.619-625

2010

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)

Metabolic alterations in spinal and bulbar muscular atrophy

Revue neurologique, 2020-12, Vol.176 (10), p.780-787

2020

Volltextzugriff (PDF)

Novel optineurin mutations in patients with familial and sporadic amyotrophic lateral sclerosis

Journal of neurology, neurosurgery and psychiatry, 2011-11, Vol.82 (11), p.1239-1243

2011

Volltextzugriff (PDF)

New FIG4 gene mutations causing aggressive ALS

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

2018

Volltextzugriff (PDF)

Brain involvement in myotonic dystrophies: neuroimaging and neuropsychological comparative study in DM1 and DM2

Journal of neurology, 2010-08, Vol.257 (8), p.1246-1255

2010

Volltextzugriff (PDF)

P.6.4 Salbutamol tolerability and efficacy in adult type III SMA patients: Results of a multicentric, molecular and clinical, double-blind, placebo-controlled study

Neuromuscular disorders : NMD, 2013-10, Vol.23 (9), p.771-771

2013

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)

TARDBP (TDP-43) sequence analysis in patients with familial and sporadic ALS: identification of two novel mutations

European journal of neurology, 2009-06, Vol.16 (6), p.727-732

2009

Volltextzugriff (PDF)

241st ENMC international workshop: Towards a European unifying lab for Kennedy's disease. 15–17th February, 2019 Hoofddorp, The Netherlands

Neuromuscular disorders : NMD, 2019-09, Vol.29 (9), p.716-724

2019

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)

SPP1 genotype is a determinant of disease severity in Duchenne muscular dystrophy

Neurology, 2011-01, Vol.76 (3), p.219-226

2011

Volltextzugriff (PDF)

1 – 25 von 236

Suche als RSS-Feed

Aktive Filter

ThemaPhysical Sciences

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(226)
Mit Volltextzugriff
(213)

Publikationsform

Sprache

Englisch
(236)

Erscheinungsjahr

n.n

Thema

Science & Technology
(141)
Materials Science
(85)
Technology
(84)
Materials Science, Ceramics
(72)
Exact Sciences And Technology
(58)
Life Sciences & Biomedicine
(54)
Humans
(48)
Applied Sciences
(38)
Building Materials. Ceramics. Glasses
(36)
Chemical Industry And Chemicals
(36)
Neurosciences & Neurology
(35)
Male
(34)
Clinical Neurology
(33)
Female
(32)
Middle Aged
(29)
Neurosciences
(27)
Adult
(26)
Materials Science, Multidisciplinary
(23)
Neurology
(22)
Ceramic Industries
(21)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

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

Cardiovascular diseases may play a negative role in the prognosis of amyotrophic lateral sclerosis

PT09.2: Body Composition and Metabolic Features in the Kennedy's Disease

PT05.2: The Long-Term Treatment of Human Amyotrophic Lateral Sclerosis with a Modified-Ketogenic Diet

Emotional Lability in MND: Relationship to cognition and psychopathology and impact on caregivers

The role of androgen receptor gene variants on SBMA phenotype

45. Clinical and electrophysiological non-SPG4 spectrum of HSP

Neurofilament light chain and profilin‐1 dynamics in 30 spinal muscular atrophy type 3 patients treated with nusinersen

Retrospective study on PET–SPECT imaging in a large cohort of myotonic dystrophy type 1 patients

Out-of-furnace oxidation of SiCN polymer-derived ceramic aerogel pyrolized at intermediate temperature (600–800°C)

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

Lithium carbonate in amyotrophic lateral sclerosis: lack of efficacy in a dose-finding trial

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

Metabolic alterations in spinal and bulbar muscular atrophy

Novel optineurin mutations in patients with familial and sporadic amyotrophic lateral sclerosis

271st ENMC international workshop: Towards a unifying effort to fight Kennedy's disease. 20-22 October 2023, Hoofddorp, Netherlands

New FIG4 gene mutations causing aggressive ALS

Brain involvement in myotonic dystrophies: neuroimaging and neuropsychological comparative study in DM1 and DM2

P.6.4 Salbutamol tolerability and efficacy in adult type III SMA patients: Results of a multicentric, molecular and clinical, double-blind, placebo-controlled study

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

TARDBP (TDP-43) sequence analysis in patients with familial and sporadic ALS: identification of two novel mutations

241st ENMC international workshop: Towards a European unifying lab for Kennedy's disease. 15–17th February, 2019 Hoofddorp, The Netherlands

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

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

SPP1 genotype is a determinant of disease severity in Duchenne muscular dystrophy

Aktive Filter

Suchergebnisse filtern