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DMD – CLINICAL CARE

Neuromuscular disorders : NMD, 2021-10, Vol.31, p.S80

2021

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DMD – CLINICAL CARE: EP.102 Clinical characteristics of early-onset cardiomyopathy in patients with Duchenne muscular dystrophy

Neuromuscular disorders : NMD, 2021-10, Vol.31, p.S80-S80

2021

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SMA - CLINICAL

Neuromuscular disorders : NMD, 2020-10, Vol.30, p.S71-S72

2020

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SMA - CLINICAL: P.84 Magnetic resonance imaging of muscle and motor functional changes in patients with spinal muscular atrophy treated with nusinersen

Neuromuscular disorders : NMD, 2020-10, Vol.30, p.S71-S72

2020

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P.123 A Phase I/II study of NS-089/NCNP-02, Exon 44 skipping drug, in patients with Duchenne muscular dystrophy

Neuromuscular disorders : NMD, 2022-10, Vol.32, p.S99-S100

2022

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P.373Longitudinal changes in electrophysiological findings caused by nusinersen administration in patients with spinal muscular atrophy type 2 or type 3

Neuromuscular disorders : NMD, 2019-10, Vol.29, p.S190-S190

2019

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REGISTRIES, CARE, QUALITY OF LIFE, MANAGEMENT OF NMD

Neuromuscular disorders : NMD, 2020-10, Vol.30, p.S145

2020

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REGISTRIES, CARE, QUALITY OF LIFE, MANAGEMENT OF NMD: P.337 Variability of cardiac function in patients with Duchenne muscular dystrophy experiencing sudden onset chest pain and electrocardiographic changes

Neuromuscular disorders : NMD, 2020-10, Vol.30, p.S145-S145

2020

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CONGENITAL MUSCULAR DYSTROPHIES

Neuromuscular disorders : NMD, 2021-10, Vol.31, p.S68-S69

2021

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FSHD

Neuromuscular disorders : NMD, 2021-10, Vol.31, p.S100

2021

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CONGENITAL MUSCULAR DYSTROPHIES: EP.64 Brain image phenotypes and developmental milestones in Fukuyama congenital muscular dystrophy

Neuromuscular disorders : NMD, 2021-10, Vol.31, p.S68-S69

2021

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FSHD: EP.167 Longitudinal clinical course of early-onset facioscapulohumeral muscular dystrophy

Neuromuscular disorders : NMD, 2021-10, Vol.31, p.S100-S100

2021

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DUCHENNE MUSCULAR DYSTROPHY – CLINICAL: P.29Analysis of respiratory function of Duchenne muscular dystrophy with Chilaiditi syndrome

Neuromuscular disorders : NMD, 2018-10, Vol.28, p.S39-S40

2018

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DUCHENNE MUSCULAR DYSTROPHY – CLINICAL

Neuromuscular disorders : NMD, 2018-10, Vol.28, p.S39-S40

2018

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P.230Phenotype and pathological variability in RYR1-related myopathy with compound heterozygous variants in Japan

Neuromuscular disorders : NMD, 2019-10, Vol.29, p.S133-S134

2019

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E-POSTERS – MITOCHONDRIAL / METABOLIC DISEASES –CASE REPORTS: EP.01Becker muscular dystrophy with acid α-glucosidase pseudodeficiency

Neuromuscular disorders : NMD, 2019-10, Vol.29, p.S70-S70

2019

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E-POSTERS – MITOCHONDRIAL / METABOLIC DISEASES –CASE REPORTS

Neuromuscular disorders : NMD, 2019-10, Vol.29, p.S70

2019

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FSHD / OPMD / EDMD / DMI

Neuromuscular disorders : NMD, 2018-10, Vol.28, p.S140-S141

2018

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FSHD / OPMD / EDMD / DMI: P.368Clinical characteristics of 4 patients with childhood-onset reducing body myopathy in Japan

Neuromuscular disorders : NMD, 2018-10, Vol.28, p.S140-S141

2018

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Exon 53 skipping of the dystrophin gene in patients with Duchenne muscular dystrophy by systemic administration of NS-065/NCNP-01: A phase 1, dose escalation, first-in-human study

Neuromuscular disorders : NMD, 2015-10, Vol.25, p.S261-S262

2015

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P.344Assessment of longitudinal developmental milestones in Fukuyama congenital muscular dystrophy

Neuromuscular disorders : NMD, 2019-10, Vol.29, p.S168-S168

2019

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Signal abnormalities of muscle and fascia in muscular MRI imaging at pretreatment stage in children with juvenile dermatomyositis

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S146-S146

2016

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IBIC-LG: Selectivity pattern of muscular MRI images in limb-girdle muscular dystrophy (LGMD) 2A using database of skeletal muscular images

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S99-S99

2016

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G.P.179

Neuromuscular disorders : NMD, 2014-10, Vol.24 (9), p.859-859

2014

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Quantitative analysis of muscle resonance imaging of fatty infiltration of the pelvic and lower limb muscles in Duchenne muscular dystrophy using excel based auto calculation program

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S124-S125

2017

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DMD – CLINICAL CARE

DMD – CLINICAL CARE: EP.102 Clinical characteristics of early-onset cardiomyopathy in patients with Duchenne muscular dystrophy

SMA - CLINICAL

SMA - CLINICAL: P.84 Magnetic resonance imaging of muscle and motor functional changes in patients with spinal muscular atrophy treated with nusinersen

P.123 A Phase I/II study of NS-089/NCNP-02, Exon 44 skipping drug, in patients with Duchenne muscular dystrophy

P.373Longitudinal changes in electrophysiological findings caused by nusinersen administration in patients with spinal muscular atrophy type 2 or type 3

REGISTRIES, CARE, QUALITY OF LIFE, MANAGEMENT OF NMD

REGISTRIES, CARE, QUALITY OF LIFE, MANAGEMENT OF NMD: P.337 Variability of cardiac function in patients with Duchenne muscular dystrophy experiencing sudden onset chest pain and electrocardiographic changes

CONGENITAL MUSCULAR DYSTROPHIES

FSHD

CONGENITAL MUSCULAR DYSTROPHIES: EP.64 Brain image phenotypes and developmental milestones in Fukuyama congenital muscular dystrophy

FSHD: EP.167 Longitudinal clinical course of early-onset facioscapulohumeral muscular dystrophy

DUCHENNE MUSCULAR DYSTROPHY – CLINICAL: P.29Analysis of respiratory function of Duchenne muscular dystrophy with Chilaiditi syndrome

DUCHENNE MUSCULAR DYSTROPHY – CLINICAL

P.230Phenotype and pathological variability in RYR1-related myopathy with compound heterozygous variants in Japan

E-POSTERS – MITOCHONDRIAL / METABOLIC DISEASES –CASE REPORTS: EP.01Becker muscular dystrophy with acid α-glucosidase pseudodeficiency

E-POSTERS – MITOCHONDRIAL / METABOLIC DISEASES –CASE REPORTS

FSHD / OPMD / EDMD / DMI

FSHD / OPMD / EDMD / DMI: P.368Clinical characteristics of 4 patients with childhood-onset reducing body myopathy in Japan

Exon 53 skipping of the dystrophin gene in patients with Duchenne muscular dystrophy by systemic administration of NS-065/NCNP-01: A phase 1, dose escalation, first-in-human study

P.344Assessment of longitudinal developmental milestones in Fukuyama congenital muscular dystrophy

Signal abnormalities of muscle and fascia in muscular MRI imaging at pretreatment stage in children with juvenile dermatomyositis

IBIC-LG: Selectivity pattern of muscular MRI images in limb-girdle muscular dystrophy (LGMD) 2A using database of skeletal muscular images

G.P.179

Quantitative analysis of muscle resonance imaging of fatty infiltration of the pelvic and lower limb muscles in Duchenne muscular dystrophy using excel based auto calculation program

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