UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 48

Sortiert nach

Critical illness polyneuromyopathy: the electrophysiological components of a complex entity

Intensive care medicine, 2003-09, Vol.29 (9), p.1505-1514

2003

Link zum Volltext

Verfügbarkeit prüfen

ISPD gene mutations are a common cause of congenital and limb-girdle muscular dystrophies

Brain (London, England : 1878), 2013, Vol.136 (Pt 1), p.269-281

2013

Link zum Volltext

Verfügbarkeit prüfen

Generation of two Duchenne muscular dystrophy patient-specific induced pluripotent stem cell lines DMD02 and DMD03 (MUNIi001-A and MUNIi003-A)

Stem cell research, 2019-10, Vol.40, p.101562-101562, Article 101562

2019

Link zum Volltext

Verfügbarkeit prüfen

Autosomal recessive limb-girdle muscular dystrophies in the Czech Republic

BMC neurology, 2014-08, Vol.14 (1), p.154-154, Article 154

2014

Link zum Volltext

Verfügbarkeit prüfen

COMPASS-U Global Heat Balance Calculations

IEEE transactions on plasma science, 2023-03, Vol.51 (3), p.922-926

2023

Link zum Volltext
IEEE_Xplore

COMPASS-U Global Heat Balance Calculations

IEEE transactions on plasma science, 2022-12, Vol.51 (3)

2022

Link zum Volltext

Verfügbarkeit prüfen

Mutations in the SPTLC2 Subunit of Serine Palmitoyltransferase Cause Hereditary Sensory and Autonomic Neuropathy Type I

American journal of human genetics, 2010-10, Vol.87 (4), p.513-522

2010

Link zum Volltext

Verfügbarkeit prüfen

CLCN1 mutations in Czech patients with myotonia congenita, in silico analysis of novel and known mutations in the human dimeric skeletal muscle chloride channel

PloS one, 2013-12, Vol.8 (12), p.e82549-e82549

2013

Link zum Volltext

Verfügbarkeit prüfen

X-linked Charcot-Marie-Tooth disease: Phenotypic expression of a novel mutation Ile127Ser in the GJB1 (connexin 32) gene

Muscle & nerve, 2005-02, Vol.31 (2), p.252-255

2005

Link zum Volltext

Verfügbarkeit prüfen

Risk factors for critical illness polyneuromyopathy

Journal of neurology, 2005-03, Vol.252 (3), p.343-351

2005

Link zum Volltext

Verfügbarkeit prüfen

Analysis of histopathologic and molecular pathologic findings in Czech LGMD2A patients

Muscle & nerve, 2006-03, Vol.33 (3), p.424-432

2006

Link zum Volltext

Verfügbarkeit prüfen

First dedicated observations of runaway electrons in the COMPASS tokamak

Nukleonika, 2015-06, Vol.60 (2), p.249-255

2015

Link zum Volltext

Verfügbarkeit prüfen

COMPARISON BETWEEN 2D TURBULENCE MODEL ESEL AND EXPERIMENTAL DATA FROM AUG AND COMPASS TOKAMAKS

Acta polytechnica (Prague, Czech Republic : 1992), 2015-01, Vol.55 (2), p.128-135

2015

Link zum Volltext

Verfügbarkeit prüfen

Papillary fibroelastoma originating from the free left ventricular wall as the cause of recurrent stroke: Description of the case and literature review

Cor et vasa (English ed.), 2016-10, Vol.58 (5), p.e466-e469

2016

Link zum Volltext

Verfügbarkeit prüfen

Efficacy of pregabalin in neuropathic pain in paediatric oncological patients

European journal of paediatric neurology, 2009-07, Vol.13 (4), p.332-336

2009

Link zum Volltext

Verfügbarkeit prüfen

Clinical and electrophysiological findings and long-term outcomes in paediatric patients with critical illness polyneuromyopathy

European journal of paediatric neurology, 2006-07, Vol.10 (4), p.176-181

2006

Link zum Volltext

Verfügbarkeit prüfen

Histopathological features in subsequent muscle biopsies in a warmblood mare with myotonic dystrophy

The Veterinary quarterly, 2012-09, Vol.32 (3-4), p.187-192

2012

Link zum Volltext

Verfügbarkeit prüfen

European Cross-Sectional Survey of Current Care Practices for Duchenne Muscular Dystrophy Reveals Regional and Age-Dependent Differences

Journal of neuromuscular diseases, 2016-11, Vol.3 (4), p.517-527

2016

Link zum Volltext

Verfügbarkeit prüfen

An unusual case of congenital muscular dystrophy with normal serum CK level, external ophtalmoplegia, and white matter changes on brain MRI

European journal of paediatric neurology, 2007-11, Vol.11 (6), p.381-384

2007

Link zum Volltext

Verfügbarkeit prüfen

Toxoplasmosis of the central nervous systems after allogeneic stem cell transplantation

Časopis lékařů českých, 2010, Vol.149 (4), p.184-188

2010

Link zum Volltext

Verfügbarkeit prüfen

Membranózní defekt komorového septa s hemodynamikou defektu Gerbodeho typu při perforaci septálního cípu trikuspidální chlopně

Cor et vasa (English ed.), 2009-05, Vol.51 (5), p.358-359

2009

Link zum Volltext

Verfügbarkeit prüfen

NH3-modified swelling of silica-filled silicone rubber

Journal of applied polymer science, 1979-05, Vol.23 (9), p.2681-2694

1979

Link zum Volltext

Verfügbarkeit prüfen

Bound rubber and "crepe hardening" in silicone rubber

Journal of applied polymer science, 1977-12, Vol.21 (12), p.3211-3222

1977

Link zum Volltext

Verfügbarkeit prüfen

NH 3 ‐modified swelling of silica‐filled silicone rubber

Journal of applied polymer science, 1980-06, Vol.25 (6), p.1261-1261

1980

Link zum Volltext

Verfügbarkeit prüfen

NH3-modified swelling of silica-filled silicone rubber

Journal of applied polymer science, 1980-06, Vol.25 (6), p.1261-1261

1980

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 48

Suche als RSS-Feed

Aktive Filter

KollektionElsevier Journal Backfiles on ScienceDirect (DFG Nationallizenzen)

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(47)
Mit Volltextzugriff
(47)

Publikationsform

Artikel
(47)
Tagungsberichte
(1)

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Critical illness polyneuromyopathy: the electrophysiological components of a complex entity

ISPD gene mutations are a common cause of congenital and limb-girdle muscular dystrophies

Generation of two Duchenne muscular dystrophy patient-specific induced pluripotent stem cell lines DMD02 and DMD03 (MUNIi001-A and MUNIi003-A)

Autosomal recessive limb-girdle muscular dystrophies in the Czech Republic

COMPASS-U Global Heat Balance Calculations

COMPASS-U Global Heat Balance Calculations

Mutations in the SPTLC2 Subunit of Serine Palmitoyltransferase Cause Hereditary Sensory and Autonomic Neuropathy Type I

CLCN1 mutations in Czech patients with myotonia congenita, in silico analysis of novel and known mutations in the human dimeric skeletal muscle chloride channel

X-linked Charcot-Marie-Tooth disease: Phenotypic expression of a novel mutation Ile127Ser in the GJB1 (connexin 32) gene

Risk factors for critical illness polyneuromyopathy

Analysis of histopathologic and molecular pathologic findings in Czech LGMD2A patients

First dedicated observations of runaway electrons in the COMPASS tokamak

COMPARISON BETWEEN 2D TURBULENCE MODEL ESEL AND EXPERIMENTAL DATA FROM AUG AND COMPASS TOKAMAKS

Papillary fibroelastoma originating from the free left ventricular wall as the cause of recurrent stroke: Description of the case and literature review

Efficacy of pregabalin in neuropathic pain in paediatric oncological patients

Clinical and electrophysiological findings and long-term outcomes in paediatric patients with critical illness polyneuromyopathy

Histopathological features in subsequent muscle biopsies in a warmblood mare with myotonic dystrophy

European Cross-Sectional Survey of Current Care Practices for Duchenne Muscular Dystrophy Reveals Regional and Age-Dependent Differences

An unusual case of congenital muscular dystrophy with normal serum CK level, external ophtalmoplegia, and white matter changes on brain MRI

Toxoplasmosis of the central nervous systems after allogeneic stem cell transplantation

Membranózní defekt komorového septa s hemodynamikou defektu Gerbodeho typu při perforaci septálního cípu trikuspidální chlopně

NH3-modified swelling of silica-filled silicone rubber

Bound rubber and "crepe hardening" in silicone rubber

NH 3 ‐modified swelling of silica‐filled silicone rubber

NH3-modified swelling of silica-filled silicone rubber

Aktive Filter

Suchergebnisse filtern