UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 147

Sortiert nach

104-week efficacy and safety of cipaglucosidase alfa plus miglustat in adults with late-onset Pompe disease: a phase III open-label extension study (ATB200-07)

Journal of neurology, 2024-05, Vol.271 (5), p.2810-2823

2024

Link zum Volltext

Verfügbarkeit prüfen

169th ENMC International Workshop Rare Structural Congenital Myopathies 6–8 November 2009, Naarden, The Netherlands

Neuromuscular disorders : NMD, 2011-05, Vol.21 (5), p.363-374

2011

Link zum Volltext

Verfügbarkeit prüfen

246th ENMC International Workshop: Protein aggregate myopathies 24–26 May 2019, Hoofddorp, The Netherlands

Neuromuscular disorders : NMD, 2021-02, Vol.31 (2), p.158-166

2021

Link zum Volltext

Verfügbarkeit prüfen

Acute but transient neurological deterioration revealing adult polyglucosan body disease

Journal of the neurological sciences, 2013-01, Vol.324 (1), p.179-182

2013

Link zum Volltext

Verfügbarkeit prüfen

Anterior interosseous mononeuropathy associated with HEV infection

Neurology : neuroimmunology & neuroinflammation, 2018-03, Vol.5 (2), p.e429-e429

2018

Link zum Volltext

Verfügbarkeit prüfen

Anti-RuvBL1/2 autoantibodies in patients with systemic sclerosis or idiopathic inflammatory myopathy and a nuclear speckled pattern

Annals of the rheumatic diseases, 2022-05, Vol.81 (5), p.742

2022

Link zum Volltext

Verfügbarkeit prüfen

Attention to 3-D Shape, 3-D Motion, and Texture in 3-D Structure from Motion Displays

Journal of cognitive neuroscience, 2004-05, Vol.16 (4), p.665-682

2004

Link zum Volltext

Verfügbarkeit prüfen

Author Response: Prospective Natural History Study in 24 Adult Patients With LGMDR12 Over 2 Years of Follow-up: Quantitative MRI and Clinical Outcome Measures

Neurology, 2023-02, Vol.100 (7), p.354

2023

Link zum Volltext

Verfügbarkeit prüfen

Automated MRI quantification of volumetric per-muscle fat fractions in the proximal leg of patients with muscular dystrophies

Frontiers in neurology, 2023-05, Vol.14, p.1200727-1200727

2023

Link zum Volltext

Verfügbarkeit prüfen

Autosomal dominant spinal muscular atrophy with lower extremity predominance: A recognizable phenotype of BICD2 mutations

Muscle & Nerve, 2016, Vol.54 (3), p.496-500

2016

Link zum Volltext

Verfügbarkeit prüfen

Autosomal dominant spinal muscular atrophy with lower extremity predominance: A recognizable phenotype of BICD2 mutations

Muscle & nerve, 2016-09, Vol.54 (3), p.496-500

2016

Link zum Volltext

Verfügbarkeit prüfen

Autosomal dominant spinal muscular atrophy with lower extremity predominance: A recognizable phenotype of BICD2 mutations

Muscle & nerve, 2016, Vol.54 (3), p.496-500

2016

Link zum Volltext

Verfügbarkeit prüfen

Autosomal recessive demyelinating or axonal Charcot–Marie–Tooth neuropathy

Peripheral nerve disorders, 2014, p.85-101

2014

Link zum Volltext

Verfügbarkeit prüfen

Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2

Annals of neurology, 2006-02, Vol.59 (2), p.276-281

2006

Link zum Volltext

Verfügbarkeit prüfen

Biochemical and clinical biomarkers in adult SMA 3–4 patients treated with nusinersen for 22 months

Annals of clinical and translational neurology, 2022-08, Vol.9 (8), p.1241-1251

2022

Link zum Volltext

Verfügbarkeit prüfen

Chaperone Proteins

Muscle Disease, 2013, p.246-251

2013

Link zum Volltext

Verfügbarkeit prüfen

Chronic levetiracetam treatment early in life decreases epileptiform events in young GAERS, but does not prevent the expression of spike and wave discharges during adulthood

Seizure (London, England), 2005-09, Vol.14 (6), p.403-411

2005

Link zum Volltext

Verfügbarkeit prüfen

Clinical and biometrical 12-month follow-up in patients after reconstruction of the sural nerve biopsy defect by the collagen-based nerve guide Neuromaix

European journal of medical research, 2017-09, Vol.22 (1), p.34-34, Article 34

2017

Link zum Volltext

Verfügbarkeit prüfen

Clinical and muscle MRI features in a family with tubular aggregate myopathy and novel STIM1 mutation

Neuromuscular disorders : NMD, 2020, Vol.30 (9), p.709-718

2020

Link zum Volltext

Verfügbarkeit prüfen

Clinical and muscle MRI features in a family with tubular aggregate myopathy and novel STIM1 mutation

Neuromuscular disorders : NMD, 2020-09, Vol.30 (9), p.709-718

2020

Link zum Volltext

Verfügbarkeit prüfen

Clinical outcome in 19 French and Spanish patients with valosin-containing protein myopathy associated with Paget’s disease of bone and frontotemporal dementia

Neuromuscular disorders : NMD, 2009-05, Vol.19 (5), p.316-323

2009

Link zum Volltext

Verfügbarkeit prüfen

Clinical spectrum of the anti-GQ1b antibody syndrome: a case series of eight patients

Acta neurologica Belgica, 2019-03, Vol.119 (1), p.29-36

2019

Link zum Volltext

Verfügbarkeit prüfen

Color Discrimination Involves Ventral and Dorsal Stream Visual Areas

Cerebral cortex (New York, N.Y. 1991), 2004-07, Vol.14 (7), p.803-822

2004

Link zum Volltext

Verfügbarkeit prüfen

Comparison of elevated phosphorylated neurofilament heavy chains in serum and cerebrospinal fluid of patients with amyotrophic lateral sclerosis

Journal of neurology, neurosurgery and psychiatry, 2018-04, Vol.89 (4), p.367

2018

Link zum Volltext

Verfügbarkeit prüfen

Confirmation that abnormal desmin accumulation and migration are due to a desmin gene mutation in a familial cardiomyopathy and distal myopathy

Neuromuscular disorders : NMD, 2009-11, Vol.19 (11), p.802-802

2009

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 147

Suche als RSS-Feed

Aktive Filter

Zeitschrift / SerieBrain

PublikationsformBücher

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(132)
Mit Volltextzugriff
(133)

Publikationsform

Sprache

Englisch
(147)
Japanisch
(26)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(2)
... seit 90 Tagen
(4)

Menü

Weitere Dienste

Einstellungen

104-week efficacy and safety of cipaglucosidase alfa plus miglustat in adults with late-onset Pompe disease: a phase III open-label extension study (ATB200-07)

169th ENMC International Workshop Rare Structural Congenital Myopathies 6–8 November 2009, Naarden, The Netherlands

246th ENMC International Workshop: Protein aggregate myopathies 24–26 May 2019, Hoofddorp, The Netherlands

Acute but transient neurological deterioration revealing adult polyglucosan body disease

Anterior interosseous mononeuropathy associated with HEV infection

Anti-RuvBL1/2 autoantibodies in patients with systemic sclerosis or idiopathic inflammatory myopathy and a nuclear speckled pattern

Attention to 3-D Shape, 3-D Motion, and Texture in 3-D Structure from Motion Displays

Author Response: Prospective Natural History Study in 24 Adult Patients With LGMDR12 Over 2 Years of Follow-up: Quantitative MRI and Clinical Outcome Measures

Automated MRI quantification of volumetric per-muscle fat fractions in the proximal leg of patients with muscular dystrophies

Autosomal dominant spinal muscular atrophy with lower extremity predominance: A recognizable phenotype of BICD2 mutations

Autosomal dominant spinal muscular atrophy with lower extremity predominance: A recognizable phenotype of BICD2 mutations

Autosomal dominant spinal muscular atrophy with lower extremity predominance: A recognizable phenotype of BICD2 mutations

Autosomal recessive demyelinating or axonal Charcot–Marie–Tooth neuropathy

Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2

Biochemical and clinical biomarkers in adult SMA 3–4 patients treated with nusinersen for 22 months

Chaperone Proteins

Chronic levetiracetam treatment early in life decreases epileptiform events in young GAERS, but does not prevent the expression of spike and wave discharges during adulthood

Clinical and biometrical 12-month follow-up in patients after reconstruction of the sural nerve biopsy defect by the collagen-based nerve guide Neuromaix

Clinical and muscle MRI features in a family with tubular aggregate myopathy and novel STIM1 mutation

Clinical and muscle MRI features in a family with tubular aggregate myopathy and novel STIM1 mutation

Clinical outcome in 19 French and Spanish patients with valosin-containing protein myopathy associated with Paget’s disease of bone and frontotemporal dementia

Clinical spectrum of the anti-GQ1b antibody syndrome: a case series of eight patients

Color Discrimination Involves Ventral and Dorsal Stream Visual Areas

Comparison of elevated phosphorylated neurofilament heavy chains in serum and cerebrospinal fluid of patients with amyotrophic lateral sclerosis

Confirmation that abnormal desmin accumulation and migration are due to a desmin gene mutation in a familial cardiomyopathy and distal myopathy

Aktive Filter

Suchergebnisse filtern