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Creatine monohydrate enhances strength and body composition in Duchenne muscular dystrophy

Neurology, 2004-05, Vol.62 (10), p.1771-1777

2004

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Spectrin repeat-containing nuclear envelope protein 2: SYNE2 presenting as a congenital myopathy: A case report

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S139-S139

2016

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P1.01 POMGnT1 enhancement for muscle–eye–brain disease

Neuromuscular disorders : NMD, 2010-10, Vol.20 (9), p.599-599

2010

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Muscle weakness in critically ill children

Neurology, 2003-12, Vol.61 (12), p.1779-1782

2003

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G.P.47

Neuromuscular disorders : NMD, 2014-10, Vol.24 (9), p.808-809

2014

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P.175 - Spectrin repeat-containing nuclear envelope protein 2: SYNE2 presenting as a congenital myopathy: A case report

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S139-S139

2016

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S.P.52 Troponin T adventures in Duchenne muscular dystrophy

Neuromuscular disorders : NMD, 2012-10, Vol.22 (9), p.884-885

2012

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Deflazacort in Duchenne muscular dystrophy: a comparison of two different protocols

Neuromuscular disorders : NMD, 2004-09, Vol.14 (8), p.476-482

2004

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G.P.48

Neuromuscular disorders : NMD, 2014-10, Vol.24 (9), p.809-809

2014

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G.P.12 Eye abnormalities in children with congenital muscular dystrophy due to mutations in FKRP

Neuromuscular disorders : NMD, 2012-10, Vol.22 (9), p.815-815

2012

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P1.7 Early death following minor trauma in Duchenne muscular dystrophy

Neuromuscular disorders : NMD, 2011-10, Vol.21 (9), p.643-643

2011

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A Source Analysis of the Late Human Auditory Evoked Potentials

Journal of cognitive neuroscience, 1989, Vol.1 (4), p.336-355

1989

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MOTOR NEURON DISORDERS AND NEUROPATHIES: EP.240 Charcot-Marie-Tooth disease, clinical and genetic features in a Canadian pediatric cohort

Neuromuscular disorders : NMD, 2021-10, Vol.31, p.S122-S122

2021

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MOTOR NEURON DISORDERS AND NEUROPATHIES

Neuromuscular disorders : NMD, 2021-10, Vol.31, p.S122

2021

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G.P.12.10 Repeat muscle biopsy in the diagnosis of cap myopathy with ACTA1 gene mutation

Neuromuscular disorders : NMD, 2009-09, Vol.19 (8), p.638-638

2009

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T.P.5.07 Long bone fractures and bone healing in boys with Duchenne muscular dystrophy treated with daily, long-term Deflazacort

Neuromuscular disorders : NMD, 2008-10, Vol.18 (9), p.825-825

2008

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SMA - CLINICAL: P.89 Scoliosis in Spinal muscular atrophy type I in the nusinersen era

Neuromuscular disorders : NMD, 2020-10, Vol.30, p.S73-S73

2020

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SMA - CLINICAL

Neuromuscular disorders : NMD, 2020-10, Vol.30, p.S73

2020

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CONGENITAL MYASTHENIC SYNDROMES AND MYASTHENIA: P.60Respiratory dysfunction in childhood myasthenia

Neuromuscular disorders : NMD, 2018-10, Vol.28, p.S48-S48

2018

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CONGENITAL MYASTHENIC SYNDROMES AND MYASTHENIA

Neuromuscular disorders : NMD, 2018-10, Vol.28, p.S48

2018

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Enterostomy tube placement in children with spinal muscular atrophy type 1

The Journal of pediatrics, 2006-12, Vol.149 (6), p.837-839

2006

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D.I.4 Patient fibroblast functional complementation studies: A valuable tool in the identification of novel Walker–Warburg syndrome disease genes

Neuromuscular disorders : NMD, 2012-10, Vol.22 (9), p.805-805

2012

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SMA – OUTCOME MEASURES AND REGISTRIES: EP.262 The Canadian neuromuscular disease registry: a national spinal muscular atrophy (SMA) registry for real world evidence

Neuromuscular disorders : NMD, 2021-10, Vol.31, p.S129-S129

2021

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G.P.1.10 Profiles of weight gain and cardiopulmonary outcomes in boys with Duchenne muscular dystrophy

Neuromuscular disorders : NMD, 2007, Vol.17 (9), p.775-775

2007

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G.P.2.06 Walker–Warburg syndrome with POMT1 mutations can be associated with cleft lip and cleft palate

Neuromuscular disorders : NMD, 2008-10, Vol.18 (9), p.736-737

2008

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Creatine monohydrate enhances strength and body composition in Duchenne muscular dystrophy

Spectrin repeat-containing nuclear envelope protein 2: SYNE2 presenting as a congenital myopathy: A case report

P1.01 POMGnT1 enhancement for muscle–eye–brain disease

Muscle weakness in critically ill children

G.P.47

P.175 - Spectrin repeat-containing nuclear envelope protein 2: SYNE2 presenting as a congenital myopathy: A case report

S.P.52 Troponin T adventures in Duchenne muscular dystrophy

Deflazacort in Duchenne muscular dystrophy: a comparison of two different protocols

G.P.48

G.P.12 Eye abnormalities in children with congenital muscular dystrophy due to mutations in FKRP

P1.7 Early death following minor trauma in Duchenne muscular dystrophy

A Source Analysis of the Late Human Auditory Evoked Potentials

MOTOR NEURON DISORDERS AND NEUROPATHIES: EP.240 Charcot-Marie-Tooth disease, clinical and genetic features in a Canadian pediatric cohort

MOTOR NEURON DISORDERS AND NEUROPATHIES

G.P.12.10 Repeat muscle biopsy in the diagnosis of cap myopathy with ACTA1 gene mutation

T.P.5.07 Long bone fractures and bone healing in boys with Duchenne muscular dystrophy treated with daily, long-term Deflazacort

SMA - CLINICAL: P.89 Scoliosis in Spinal muscular atrophy type I in the nusinersen era

SMA - CLINICAL

CONGENITAL MYASTHENIC SYNDROMES AND MYASTHENIA: P.60Respiratory dysfunction in childhood myasthenia

CONGENITAL MYASTHENIC SYNDROMES AND MYASTHENIA

Enterostomy tube placement in children with spinal muscular atrophy type 1

D.I.4 Patient fibroblast functional complementation studies: A valuable tool in the identification of novel Walker–Warburg syndrome disease genes

SMA – OUTCOME MEASURES AND REGISTRIES: EP.262 The Canadian neuromuscular disease registry: a national spinal muscular atrophy (SMA) registry for real world evidence

G.P.1.10 Profiles of weight gain and cardiopulmonary outcomes in boys with Duchenne muscular dystrophy

G.P.2.06 Walker–Warburg syndrome with POMT1 mutations can be associated with cleft lip and cleft palate

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