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Mexiletine is an effective antimyotonia treatment in myotonic dystrophy type 1

Neurology, 2010-05, Vol.74 (18), p.1441-1448

2010

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Practice parameter: corticosteroid treatment of Duchenne dystrophy: report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society

Neurology, 2005-01, Vol.64 (1), p.13-20

2005

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Pigmentation phenotype, photosensitivity and skin neoplasms in patients with myotonic dystrophy

European journal of neurology, 2017-05, Vol.24 (5), p.713-718

2017

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Survival patterns and cancer determinants in families with myotonic dystrophy type 1

European journal of neurology, 2019-01, Vol.26 (1), p.58-65

2019

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Health supervision and anticipatory guidance in adult myotonic dystrophy type 1

Neuromuscular disorders : NMD, 2010-12, Vol.20 (12), p.847-851

2010

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Effect of prednisone on protein metabolism in Duchenne dystrophy

American journal of physiology: endocrinology and metabolism, 1995-01, Vol.268 (1), p.E67-E74

1995

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Quantitative analysis of the "warm-up" phenomenon in myotonic dystrophy type 1

Muscle & nerve, 2005-07, Vol.32 (1), p.35-42

2005

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Expansion of the myotonic dystrophy CTG repeat reduces expression of the flanking DMAHP gene

Nature genetics, 1997-08, Vol.16 (4), p.407-409

1997

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Acute effects of insulin-like growth factor I and insulin on glucose metabolism in vivo

American journal of physiology: endocrinology and metabolism, 1990-10, Vol.259 (4), p.E561-E567

1990

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Myotonic dystrophy patients have larger CTG expansions in skeletal muscle than in leukocytes

Annals of neurology, 1994-01, Vol.35 (1), p.104-107

1994

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Proximal myotonic myopathy: a new dominant disorder with myotonia, muscle weakness, and cataracts

Neurology, 1994-08, Vol.44 (8), p.1448-1448

1994

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Claude Monet's vision

The Lancet (British edition), 1997-03, Vol.349 (9053), p.734-734

1997

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Leukocyte CTG repeat length correlates with severity of myotonia in myotonic dystrophy type 1

Neurology, 2004-04, Vol.62 (7), p.1081-1089

2004

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Myotonic dystrophy with no trinucleotide repeat expansion

Annals of neurology, 1994-03, Vol.35 (3), p.269-272

1994

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Deletion and conversion in spinal muscular atrophy patients: Is there a relationship to severity?

Annals of neurology, 1997-02, Vol.41 (2), p.230-237

1997

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Proximal myotonic myopathy: a syndrome with a favourable prognosis?

Journal of the neurological sciences, 2002-01, Vol.193 (2), p.89-96

2002

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54th ENMC International Workshop: PROMM (Proximal Myotonic Myopathies) and Other Proximal Myotonic Syndromes 10–12th October 1997, Naarden, The Netherlands

Neuromuscular disorders : NMD, 1998-10, Vol.8 (7), p.508-518

1998

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Duchenne dystrophy: randomized, controlled trial of prednisone (18 months) and azathioprine (12 months)

Neurology, 1993-03, Vol.43 (3 Pt 1), p.520-520

1993

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Distribution of insulin receptor-like immunoreactivity in the rat forebrain

Neuroscience, 1989, Vol.31 (1), p.143-157

1989

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Long-term benefit from prednisone therapy in Duchenne muscular dystrophy

Neurology, 1991-12, Vol.41 (12), p.1874

1991

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Proximal myotonic myopathy: Mini-review of a recently delineated clinical disorder

Neuromuscular disorders : NMD, 1996-03, Vol.6 (2), p.87-93

Moxley, Richard T.

1996

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Carrell-Krusen Symposium Invited Lecture-1997. Myotonic disorders in childhood: diagnosis and treatment

Journal of child neurology, 1997-02, Vol.12 (2), p.116

Moxley, 3rd, R T

1997

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Hypothyroidism unmasking proximal myotonic myopathy

Neuromuscular disorders : NMD, 2000-03, Vol.10 (3), p.165-172

2000

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Abnormal Regulation of Monocyte Insulin-Binding Affinity After Glucose Ingestion in Patients with Myotonic Dystrophy

Proceedings of the National Academy of Sciences - PNAS, 1981-04, Vol.78 (4), p.2567-2571

1981

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K-40 and Dual-Energy X-ray Absorptiometry Estimates of Lean Weight Compared: Normals and Patients with Neuromuscular Disease

Annals of the New York Academy of Sciences, 2000-05, Vol.904 (1), p.111-114

2000

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Mexiletine is an effective antimyotonia treatment in myotonic dystrophy type 1

Practice parameter: corticosteroid treatment of Duchenne dystrophy: report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society

Pigmentation phenotype, photosensitivity and skin neoplasms in patients with myotonic dystrophy

Survival patterns and cancer determinants in families with myotonic dystrophy type 1

Health supervision and anticipatory guidance in adult myotonic dystrophy type 1

Effect of prednisone on protein metabolism in Duchenne dystrophy

Quantitative analysis of the "warm-up" phenomenon in myotonic dystrophy type 1

Expansion of the myotonic dystrophy CTG repeat reduces expression of the flanking DMAHP gene

Acute effects of insulin-like growth factor I and insulin on glucose metabolism in vivo

Myotonic dystrophy patients have larger CTG expansions in skeletal muscle than in leukocytes

Proximal myotonic myopathy: a new dominant disorder with myotonia, muscle weakness, and cataracts

Claude Monet's vision

Leukocyte CTG repeat length correlates with severity of myotonia in myotonic dystrophy type 1

Myotonic dystrophy with no trinucleotide repeat expansion

Deletion and conversion in spinal muscular atrophy patients: Is there a relationship to severity?

Proximal myotonic myopathy: a syndrome with a favourable prognosis?

54th ENMC International Workshop: PROMM (Proximal Myotonic Myopathies) and Other Proximal Myotonic Syndromes 10–12th October 1997, Naarden, The Netherlands

Duchenne dystrophy: randomized, controlled trial of prednisone (18 months) and azathioprine (12 months)

Distribution of insulin receptor-like immunoreactivity in the rat forebrain

Long-term benefit from prednisone therapy in Duchenne muscular dystrophy

Proximal myotonic myopathy: Mini-review of a recently delineated clinical disorder

Carrell-Krusen Symposium Invited Lecture-1997. Myotonic disorders in childhood: diagnosis and treatment

Hypothyroidism unmasking proximal myotonic myopathy

Abnormal Regulation of Monocyte Insulin-Binding Affinity After Glucose Ingestion in Patients with Myotonic Dystrophy

K-40 and Dual-Energy X-ray Absorptiometry Estimates of Lean Weight Compared: Normals and Patients with Neuromuscular Disease

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