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Muscle atrophy in mechanically-ventilated critically ill children

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

2018

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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

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Ultrasound in the Assessment of Myopathic Disorders

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

2016

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Ultrasound of inherited vs. acquired demyelinating polyneuropathies

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

2013

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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

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Nerve ultrasound in polyneuropathies

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

2018

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

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

2009

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Electrical impedance myography for assessment of Duchenne muscular dystrophy

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

2017

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

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

2021

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Detection of peripheral nerve pathology: comparison of ultrasound and MRI

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

2013

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Quantitative muscle ultrasound detects disease progression in Duchenne muscular dystrophy

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

2017

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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

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Medical management of muscle weakness in Duchenne muscular dystrophy

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

2020

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Intramuscular blood flow quantification with power doppler ultrasonography

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

2016

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Nerve ultrasound reliability of upper limbs: Effects of examiner training

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

2018

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Minimal training is required to reliably perform quantitative ultrasound of muscle

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

2014

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Pulse oral corticosteroids in pediatric chronic inflammatory demyelinating polyneuropathy

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

2020

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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

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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

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Skeletal muscle imaging in neuromuscular disease

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

2016

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

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

2024

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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

Ultrasound of inherited vs. acquired demyelinating polyneuropathies

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

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

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

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

Detection of peripheral nerve pathology: comparison of ultrasound and MRI

Quantitative muscle ultrasound detects disease progression in Duchenne muscular dystrophy

Onasemnogene abeparvovec for presymptomatic infants with two copies of SMN2 at risk for spinal muscular atrophy type 1: the Phase III SPR1NT trial

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

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

Medical management of muscle weakness in Duchenne muscular dystrophy

Intramuscular blood flow quantification with power doppler ultrasonography

Nerve ultrasound reliability of upper limbs: Effects of examiner training

Minimal training is required to reliably perform quantitative ultrasound of muscle

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

Skeletal muscle imaging in neuromuscular disease

Practical Considerations for Delandistrogene Moxeparvovec Gene Therapy in Patients 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)

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