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...

Muscle histology vs MRI in Duchenne muscular dystrophy

Neurology, 2011-01, Vol.76 (4), p.346-353

2011

Volltextzugriff (PDF)

Update on the management of Duchenne muscular dystrophy

Archives of disease in childhood, 2008-11, Vol.93 (11), p.986-990

2008

Volltextzugriff (PDF)

Natural history of Ullrich congenital muscular dystrophy

Neurology, 2009-07, Vol.73 (1), p.25-31

2009

Volltextzugriff (PDF)

Randomized, double-blind, placebo-controlled trial of phenylbutyrate in spinal muscular atrophy

Neurology, 2007-01, Vol.68 (1), p.51-55

2007

Volltextzugriff (PDF)

Comparative analysis of antisense oligonucleotide sequences for targeted skipping of exon 51 during dystrophin pre-mRNA splicing in human muscle

Human gene therapy, 2007-09, Vol.18 (9), p.798-810

2007

Volltextzugriff (PDF)

Molecular mechanisms and phenotypic variation in RYR1-related congenital myopathies

Brain (London, England : 1878), 2007-08, Vol.130 (8), p.2024-2036

2007

Volltextzugriff (PDF)

Swallowing difficulties in Duchenne muscular dystrophy: Indications for feeding assessment and outcome of videofluroscopic swallow studies

European journal of paediatric neurology, 2008-05, Vol.12 (3), p.239-245

2008

Volltextzugriff (PDF)

Congenital Myasthenic Syndromes in childhood: Diagnostic and management challenges

Journal of neuroimmunology, 2008-09, Vol.201, p.6-12

2008

Volltextzugriff (PDF)

Immunohistological intensity measurements as a tool to assess sarcolemma-associated protein expression

Neuropathology and applied neurobiology, 2010-06, Vol.36 (4), p.265-274

2010

Volltextzugriff (PDF)

Management of scoliosis in Duchenne muscular dystrophy: a large 10-year retrospective study

Developmental medicine and child neurology, 2006-06, Vol.48 (6), p.513-518

2006

Volltextzugriff (PDF)

Pilot trial of albuterol in spinal muscular atrophy

Neurology, 2002-08, Vol.59 (4), p.609-610

2002

Volltextzugriff (PDF)

Predictive factors for the development of scoliosis in Duchenne muscular dystrophy

European journal of paediatric neurology, 2007-05, Vol.11 (3), p.160-166

2007

Volltextzugriff (PDF)

Cardiac tissue velocities and strain rate in the early detection of myocardial dysfunction of asymptomatic boys with Duchenne’s muscular dystrophy: relationship to clinical outcome

Heart (British Cardiac Society), 2006-06, Vol.92 (6), p.840-842

2006

Volltextzugriff (PDF)

G.P.191

Neuromuscular disorders : NMD, 2014-10, Vol.24 (9), p.867-867

2014

Volltextzugriff (PDF)

Microseismic Events Cause Significant pH Drops in Groundwater

Geophysical research letters, 2021-01, Vol.48 (2), p.n/a

2021

Volltextzugriff (PDF)

Extreme variability of skeletal and cardiac muscle involvement in patients with mutations in exon 11 of the lamin A/C gene

Muscle & nerve, 2005-05, Vol.31 (5), p.602-609

2005

Volltextzugriff (PDF)

P08 Exploring emotional impact in a proof-of-principle single-blind, controlled, two-doses escalation intramuscular study of a morpholino splice-switching oligonucleotide (AVI-4658) trial to induce dystrophin restoration in children with Duchenne muscular dystrophy

Neuromuscular disorders : NMD, 2010, Vol.20, p.S7-S7

2010

Volltextzugriff (PDF)

Collagen VI involvement in Ullrich syndrome: a clinical, genetic, and immunohistochemical study

Neurology, 2002-05, Vol.58 (9), p.1354-1359

2002

Volltextzugriff (PDF)

Expanding the phenotype of potassium channelopathy: severe neuromyotonia and skeletal deformities without prominent Episodic Ataxia

Neuromuscular disorders : NMD, 2004-10, Vol.14 (10), p.689-693

2004

Volltextzugriff (PDF)

T.P.1.09 Correlation of hand-held myometry with alternative methods of assessment of muscle strength and function in DMD patients

Neuromuscular disorders : NMD, 2008-10, Vol.18 (9), p.741-741

2008

Volltextzugriff (PDF)

Refining genotype–phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycan

Brain (London, England : 1878), 2007-10, Vol.130 (10), p.2725-2735

2007

Volltextzugriff (PDF)

P3.08 Induction of dystrophin in DMD patients by antisense oligonucleotide AVI-4658 restores the dystrophin glycoprotein complex

Neuromuscular disorders : NMD, 2010-10, Vol.20 (9), p.643-643

2010

Volltextzugriff (PDF)

G.P.12.12 Predictive factors for progressive foot deformity in non-ambulant boys with Duchenne muscular dystrophy

Neuromuscular disorders : NMD, 2008-10, Vol.18 (9), p.807-807

2008

Volltextzugriff (PDF)

Pilot trial of salbutamol in central core and multi-minicore diseases

Neuropediatrics, 2004-10, Vol.35 (5), p.262

2004

Volltextzugriff (PDF)

Congenital form of spinal muscular atrophy predominantly affecting the lower limbs: a clinical and muscle MRI study

Neuromuscular disorders : NMD, 2004-02, Vol.14 (2), p.125-129

2004

Volltextzugriff (PDF)

1 – 25 von 104

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(97)
Mit Volltextzugriff
(81)

Publikationsform

Sprache

Englisch
(101)
Deutsch
(3)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Muscle histology vs MRI in Duchenne muscular dystrophy

Update on the management of Duchenne muscular dystrophy

Natural history of Ullrich congenital muscular dystrophy

Randomized, double-blind, placebo-controlled trial of phenylbutyrate in spinal muscular atrophy

Comparative analysis of antisense oligonucleotide sequences for targeted skipping of exon 51 during dystrophin pre-mRNA splicing in human muscle

Molecular mechanisms and phenotypic variation in RYR1-related congenital myopathies

Swallowing difficulties in Duchenne muscular dystrophy: Indications for feeding assessment and outcome of videofluroscopic swallow studies

Congenital Myasthenic Syndromes in childhood: Diagnostic and management challenges

Immunohistological intensity measurements as a tool to assess sarcolemma-associated protein expression

Management of scoliosis in Duchenne muscular dystrophy: a large 10-year retrospective study

Pilot trial of albuterol in spinal muscular atrophy

Predictive factors for the development of scoliosis in Duchenne muscular dystrophy

Cardiac tissue velocities and strain rate in the early detection of myocardial dysfunction of asymptomatic boys with Duchenne’s muscular dystrophy: relationship to clinical outcome

G.P.191

Microseismic Events Cause Significant pH Drops in Groundwater

Extreme variability of skeletal and cardiac muscle involvement in patients with mutations in exon 11 of the lamin A/C gene

P08 Exploring emotional impact in a proof-of-principle single-blind, controlled, two-doses escalation intramuscular study of a morpholino splice-switching oligonucleotide (AVI-4658) trial to induce dystrophin restoration in children with Duchenne muscular dystrophy

Collagen VI involvement in Ullrich syndrome: a clinical, genetic, and immunohistochemical study

Expanding the phenotype of potassium channelopathy: severe neuromyotonia and skeletal deformities without prominent Episodic Ataxia

T.P.1.09 Correlation of hand-held myometry with alternative methods of assessment of muscle strength and function in DMD patients

Refining genotype–phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycan

P3.08 Induction of dystrophin in DMD patients by antisense oligonucleotide AVI-4658 restores the dystrophin glycoprotein complex

G.P.12.12 Predictive factors for progressive foot deformity in non-ambulant boys with Duchenne muscular dystrophy

Pilot trial of salbutamol in central core and multi-minicore diseases

Congenital form of spinal muscular atrophy predominantly affecting the lower limbs: a clinical and muscle MRI study

Suchergebnisse filtern