UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 33

Sortiert nach

A further case with chronic hemolysis, CIDP and lethal cerebral vasculitis due to a CD59 mutation

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S143-S143

2016

Volltextzugriff (PDF)

T.I.3 The rationale for immunosuppressive treatment in DMD

Neuromuscular disorders : NMD, 2008-10, Vol.18 (9), p.830-830

Korinthenberg, R

2008

Volltextzugriff (PDF)

Hammersmith Functional Motor Scale and Motor Function Measure-20 in non ambulant SMA patients

Neuromuscular disorders : NMD, 2014-04, Vol.24 (4), p.347-352

2014

Volltextzugriff (PDF)

Six minute walk test in type III spinal muscular atrophy: A 12 month longitudinal study

Neuromuscular disorders : NMD, 2013-08, Vol.23 (8), p.624-628

2013

Volltextzugriff (PDF)

Somatropin treatment of spinal muscular atrophy: A placebo-controlled, double-blind crossover pilot study

Neuromuscular disorders : NMD, 2014-02, Vol.24 (2), p.134-142

2014

Volltextzugriff (PDF)

Six minute walk test in type III spinal muscular atrophy: A 12month longitudinal study

Neuromuscular disorders : NMD, 2013-08, Vol.23 (8), p.624-628

2013

Volltextzugriff (PDF)

The TREAT-NMD Advisory Committee for Therapeutics (TACT): An innovative de-risking model to foster orphan drug development

Neuromuscular disorders : NMD, 2015-10, Vol.25, p.S271-S271

2015

Volltextzugriff (PDF)

P.188 - A further case with chronic hemolysis, CIDP and lethal cerebral vasculitis due to a CD59 mutation

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S143-S143

2016

Volltextzugriff (PDF)

G.P.2 Mutations in the human isoprenoid synthase domain containing gene are a common cause of congenital and limb girdle muscular dystrophies

Neuromuscular disorders : NMD, 2012-10, Vol.22 (9), p.812-812

2012

Volltextzugriff (PDF)

G.P.3.09 Mutation in PDHA1 gene mimicking a Guillain-Barré-Syndrome

Neuromuscular disorders : NMD, 2008-10, Vol.18 (9), p.754-754

2008

Volltextzugriff (PDF)

M.P.1.09 TREAT-NMD Clinical Trials Coordination Centre: Efficiency of networking

Neuromuscular disorders : NMD, 2009-09, Vol.19 (8), p.548-549

2009

Volltextzugriff (PDF)

P3.52 FOR-DMD: double-blind randomized trial to optimize steroid regime in Duchenne Muscular Dystrophy (DMD)

Neuromuscular disorders : NMD, 2010-10, Vol.20 (9), p.657-657

2010

Volltextzugriff (PDF)

T.P.3.08 The TREAT-NMD Clinical Trials Coordination Centre (CTCC)

Neuromuscular disorders : NMD, 2008-10, Vol.18 (9), p.796-796

2008

Volltextzugriff (PDF)

Facing the genetic heterogeneity in neuromuscular disorders: Linkage analysis as an economic diagnostic approach towards the molecular diagnosis

Neuromuscular disorders : NMD, 2006-01, Vol.16 (1), p.4-13

2006

Volltextzugriff (PDF)

P.77 - Severe congenital myopathy with myasthenic features and lethal neurodegeneration – A new ALG14-related phenotype?

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S112-S112

2016

Volltextzugriff (PDF)

G.P.4.14 Clinical variability in siblings with calpainopathy (LGMD2A)

Neuromuscular disorders : NMD, 2007, Vol.17 (9), p.791-791

2007

Volltextzugriff (PDF)

G.P.284 - The TREAT-NMD Advisory Committee for Therapeutics (TACT): An innovative de-risking model to foster orphan drug development

Neuromuscular disorders : NMD, 2015-10, Vol.25, p.S271-S271

2015

Volltextzugriff (PDF)

Inhibitory conditioning stimulus in transcranial magnetic stimulation reduces the number of excited spinal motor neurons

Clinical neurophysiology, 2001-10, Vol.112 (10), p.1810-1813

2001

Volltextzugriff (PDF)

Post-traumatic syndrome after minor head injury cannot be predicted by neurological investigations

Brain & development (Tokyo. 1979), 2004-03, Vol.26 (2), p.113-117

2004

Volltextzugriff (PDF)

Fast corticospinal system and motor performance in children: conduction proceeds skill

Pediatric neurology, 1998-09, Vol.19 (3), p.217-221

1998

Volltextzugriff (PDF)

Cerebral regional hypometabolism caused by propofol-induced sedation in children with severe myoclonic epilepsy: a study using fluorodeoxyglucose positron emission tomography and statistical parametric mapping

Neuroscience letters, 2002-12, Vol.335 (2), p.79-82

2002

Volltextzugriff (PDF)

A case of childhood Pompe disease demonstrating phenotypic variability of p.Asp645Asn

Neuromuscular disorders : NMD, 2004-06, Vol.14 (6), p.371-374

2004

Volltextzugriff (PDF)

Towards harmonisation of outcome measures for DMD and SMA within TREAT-NMD; Report of three expert workshops: TREAT-NMD/ENMC Workshop on outcome measures, 12th–13th May 2007, Naarden, The Netherlands; TREAT-NMD Workshop on outcome measures in experimental trials for DMD, 30th June–1st July 2007, Naarden, The Netherlands; Conjoint Institute of Myology TREAT-NMD Meeting on physical activity monitoring in neuromuscular disorders, 11th July 2007, Paris, France

Neuromuscular disorders : NMD, 2008-11, Vol.18 (11), p.894-903

2008

Volltextzugriff (PDF)

Congenital muscular dystrophy

Brain & development (Tokyo. 1979), 1983, Vol.5 (4), p.429-429

1983

Volltextzugriff (PDF)

Efficacy of lamotrigine and vigabatrin in drug-resistant epilepsies of childhood

Pediatric neurology, 1999-11, Vol.21 (5), p.802-807

1999

Volltextzugriff (PDF)

1 – 25 von 33

Suche als RSS-Feed

Aktive Filter

KollektionElsevier Journal Backfiles on ScienceDirect (DFG Nationallizenzen)

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(32)
Mit Volltextzugriff
(33)

Publikationsform

Artikel
(32)
Berichte
(1)

Sprache

Englisch
(33)
Japanisch
(1)

Erscheinungsjahr

n.n

Thema

Neurology
(17)
Humans
(16)
Life Sciences & Biomedicine
(15)
Science & Technology
(15)
Neurosciences & Neurology
(13)
Clinical Neurology
(12)
Child
(11)
Male
(11)
Adult
(7)
Biological And Medical Sciences
(7)
Female
(7)
Neurosciences
(7)
Adolescent
(6)
Child, Preschool
(6)
Pediatrics
(5)
Medical Sciences
(4)
Fundamental And Applied Biological Sciences. Psychology
(3)
Outcome Measures
(3)
Spinal Muscular Atrophy
(3)
Young Adult
(3)

15 weitere anzeigen...

Weniger anzeigen...

Kollektion

Elsevier ScienceDirect Journals Complete
(33)
IngentaConnect
(31)
MEDLINE
(16)
IngentaConnect Journals
(14)
Single Journals
(2)
Business Source Ultimate
(1)
Psychology & Behavioral Sciences Collection
(1)
Journals@Ovid Complete
(1)

3 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

4 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

A further case with chronic hemolysis, CIDP and lethal cerebral vasculitis due to a CD59 mutation

T.I.3 The rationale for immunosuppressive treatment in DMD

Hammersmith Functional Motor Scale and Motor Function Measure-20 in non ambulant SMA patients

Six minute walk test in type III spinal muscular atrophy: A 12 month longitudinal study

Somatropin treatment of spinal muscular atrophy: A placebo-controlled, double-blind crossover pilot study

Six minute walk test in type III spinal muscular atrophy: A 12month longitudinal study

The TREAT-NMD Advisory Committee for Therapeutics (TACT): An innovative de-risking model to foster orphan drug development

P.188 - A further case with chronic hemolysis, CIDP and lethal cerebral vasculitis due to a CD59 mutation

G.P.2 Mutations in the human isoprenoid synthase domain containing gene are a common cause of congenital and limb girdle muscular dystrophies

G.P.3.09 Mutation in PDHA1 gene mimicking a Guillain-Barré-Syndrome

M.P.1.09 TREAT-NMD Clinical Trials Coordination Centre: Efficiency of networking

P3.52 FOR-DMD: double-blind randomized trial to optimize steroid regime in Duchenne Muscular Dystrophy (DMD)

T.P.3.08 The TREAT-NMD Clinical Trials Coordination Centre (CTCC)

Facing the genetic heterogeneity in neuromuscular disorders: Linkage analysis as an economic diagnostic approach towards the molecular diagnosis

P.77 - Severe congenital myopathy with myasthenic features and lethal neurodegeneration – A new ALG14-related phenotype?

G.P.4.14 Clinical variability in siblings with calpainopathy (LGMD2A)

G.P.284 - The TREAT-NMD Advisory Committee for Therapeutics (TACT): An innovative de-risking model to foster orphan drug development

Inhibitory conditioning stimulus in transcranial magnetic stimulation reduces the number of excited spinal motor neurons

Post-traumatic syndrome after minor head injury cannot be predicted by neurological investigations

Fast corticospinal system and motor performance in children: conduction proceeds skill

Cerebral regional hypometabolism caused by propofol-induced sedation in children with severe myoclonic epilepsy: a study using fluorodeoxyglucose positron emission tomography and statistical parametric mapping

A case of childhood Pompe disease demonstrating phenotypic variability of p.Asp645Asn

Congenital muscular dystrophy

Efficacy of lamotrigine and vigabatrin in drug-resistant epilepsies of childhood

Aktive Filter

Suchergebnisse filtern