UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 78

Sortiert nach

Muscle atrophy in mechanically-ventilated critically ill children

PloS one, 2018-12, Vol.13 (12), p.e0207720-e0207720

2018

Volltextzugriff (PDF)

Nerve size in chronic inflammatory demyelinating neuropathy varies with disease activity and therapy response over time: A retrospective ultrasound study

Muscle & nerve, 2014-11, Vol.50 (5), p.733-738

2014

Volltextzugriff (PDF)

Ultrasound in the Assessment of Myopathic Disorders

Journal of clinical neurophysiology, 2016-04, Vol.33 (2), p.103-111

2016

Volltextzugriff (PDF)

Safety, Tolerability, and Efficacy of Viltolarsen in Boys With Duchenne Muscular Dystrophy Amenable to Exon 53 Skipping: A Phase 2 Randomized Clinical Trial

JAMA neurology, 2020-08, Vol.77 (8), p.982

2020

Volltextzugriff (PDF)

Ultrasound of inherited vs. acquired demyelinating polyneuropathies

Journal of neurology, 2013-12, Vol.260 (12), p.3115-3121

2013

Volltextzugriff (PDF)

Nerve ultrasound in polyneuropathies

Muscle & nerve, 2018-05, Vol.57 (5), p.716-728

2018

Volltextzugriff (PDF)

Peripheral nerve size in normals and patients with polyneuropathy: An ultrasound study

Muscle & nerve, 2009-12, Vol.40 (6), p.960-966

2009

Volltextzugriff (PDF)

Electrical impedance myography for assessment of Duchenne muscular dystrophy

Annals of neurology, 2017-05, Vol.81 (5), p.622-632

2017

Volltextzugriff (PDF)

Thrombotic Microangiopathy Following Onasemnogene Abeparvovec for Spinal Muscular Atrophy: A Case Series

The Journal of pediatrics, 2021-04, Vol.231, p.265-268

2021

Volltextzugriff (PDF)

Detection of peripheral nerve pathology: comparison of ultrasound and MRI

Neurology, 2013-04, Vol.80 (18), p.1634

2013

Volltextzugriff (PDF)

Quantitative muscle ultrasound detects disease progression in Duchenne muscular dystrophy

Annals of neurology, 2017-05, Vol.81 (5), p.633-640

2017

Volltextzugriff (PDF)

Intramuscular blood flow in Duchenne and Becker Muscular Dystrophy: Quantitative power Doppler sonography relates to disease severity

Clinical neurophysiology, 2020-01, Vol.131 (1), p.1-5

2020

Volltextzugriff (PDF)

Immune-mediated myositis following gene therapy for Duchenne muscular dystrophy: a case report

Journal of neurology, 2024-08, Vol.271 (8), p.5659-5664

2024

Volltextzugriff (PDF)

Medical management of muscle weakness in Duchenne muscular dystrophy

PloS one, 2020-10, Vol.15 (10), p.e0240687-e0240687

2020

Volltextzugriff (PDF)

Intramuscular blood flow quantification with power doppler ultrasonography

Muscle & nerve, 2016-11, Vol.54 (5), p.872-878

2016

Volltextzugriff (PDF)

Skeletal muscle imaging in neuromuscular disease

Journal of clinical neuroscience, 2016-11, Vol.33, p.1-10

2016

Volltextzugriff (PDF)

Nerve ultrasound reliability of upper limbs: Effects of examiner training

Muscle & nerve, 2018-02, Vol.57 (2), p.189-192

2018

Volltextzugriff (PDF)

Minimal training is required to reliably perform quantitative ultrasound of muscle

Muscle & nerve, 2014-07, Vol.50 (1), p.124-128

2014

Volltextzugriff (PDF)

Practical Considerations for Delandistrogene Moxeparvovec Gene Therapy in Patients With Duchenne Muscular Dystrophy

Pediatric neurology, 2024-04, Vol.153, p.11-18

2024

Volltextzugriff (PDF)

Pulse oral corticosteroids in pediatric chronic inflammatory demyelinating polyneuropathy

Muscle & nerve, 2020-12, Vol.62 (6), p.705-709

2020

Volltextzugriff (PDF)

Evaluation of rAAVrh74 gene therapy vector seroprevalence by measurement of total binding antibodies in patients with Duchenne muscular dystrophy

Therapeutic advances in neurological disorders, 2023-01, Vol.16, p.17562864221149781-17562864221149781

2023

Volltextzugriff (PDF)

Muscle ultrasound quantifies disease progression over time in infants and young boys with duchenne muscular dystrophy

Muscle & nerve, 2015-09, Vol.52 (3), p.334-338

2015

Volltextzugriff (PDF)

Delandistrogene Moxeparvovec Gene Therapy in Ambulatory Patients (Aged ≥4 to <8 Years) with Duchenne Muscular Dystrophy: 1‐Year Interim Results from Study SRP‐9001‐103 (ENDEAVOR)

Annals of neurology, 2023-11, Vol.94 (5), p.955-968

2023

Volltextzugriff (PDF)

1 – 25 von 78

Suche als RSS-Feed

Aktive Filter

KollektionOxford Journals 2020 Medicine

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(75)
Mit Volltextzugriff
(73)

Publikationsform

Artikel
(77)
Buchkapitel
(1)

Sprache

Englisch
(78)
Japanisch
(8)

Erscheinungsjahr

n.n

Thema

Science & Technology
(69)
Life Sciences & Biomedicine
(67)
Neurosciences & Neurology
(58)
Clinical Neurology
(57)
Humans
(55)
Neurosciences
(47)
Male
(44)
Child
(31)
Child, Preschool
(29)
Female
(27)
Adolescent
(25)
Ultrasound
(24)
Duchenne Muscular Dystrophy
(21)
Neurology
(19)
Children
(17)
Infant
(17)
Muscular Dystrophy
(17)
Ultrasonography
(17)
Adult
(16)
Muscle, Skeletal - Diagnostic Imaging
(16)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

Muscle atrophy in mechanically-ventilated critically ill children

Nerve size in chronic inflammatory demyelinating neuropathy varies with disease activity and therapy response over time: A retrospective ultrasound study

Ultrasound in the Assessment of Myopathic Disorders

Safety, Tolerability, and Efficacy of Viltolarsen in Boys With Duchenne Muscular Dystrophy Amenable to Exon 53 Skipping: A Phase 2 Randomized Clinical Trial

Ultrasound of inherited vs. acquired demyelinating polyneuropathies

Nerve ultrasound in polyneuropathies

Peripheral nerve size in normals and patients with polyneuropathy: An ultrasound study

Electrical impedance myography for assessment of Duchenne muscular dystrophy

Onasemnogene abeparvovec gene therapy for symptomatic infantile-onset spinal muscular atrophy in patients with two copies of SMN2 (STR1VE): an open-label, single-arm, multicentre, phase 3 trial

Thrombotic Microangiopathy Following Onasemnogene Abeparvovec for Spinal Muscular Atrophy: A Case Series

Detection of peripheral nerve pathology: comparison of ultrasound and MRI

Onasemnogene abeparvovec for presymptomatic infants with three copies of SMN2 at risk for spinal muscular atrophy: the Phase III SPR1NT trial

Quantitative muscle ultrasound detects disease progression in Duchenne muscular dystrophy

Intramuscular blood flow in Duchenne and Becker Muscular Dystrophy: Quantitative power Doppler sonography relates to disease severity

Immune-mediated myositis following gene therapy for Duchenne muscular dystrophy: a case report

Medical management of muscle weakness in Duchenne muscular dystrophy

Intramuscular blood flow quantification with power doppler ultrasonography

Skeletal muscle imaging in neuromuscular disease

Nerve ultrasound reliability of upper limbs: Effects of examiner training

Minimal training is required to reliably perform quantitative ultrasound of muscle

Practical Considerations for Delandistrogene Moxeparvovec Gene Therapy in Patients With Duchenne Muscular Dystrophy

Pulse oral corticosteroids in pediatric chronic inflammatory demyelinating polyneuropathy

Evaluation of rAAVrh74 gene therapy vector seroprevalence by measurement of total binding antibodies in patients with Duchenne muscular dystrophy

Muscle ultrasound quantifies disease progression over time in infants and young boys with duchenne muscular dystrophy

Delandistrogene Moxeparvovec Gene Therapy in Ambulatory Patients (Aged ≥4 to <8 Years) with Duchenne Muscular Dystrophy: 1‐Year Interim Results from Study SRP‐9001‐103 (ENDEAVOR)

Aktive Filter

Suchergebnisse filtern