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SPP1 genotype is a determinant of disease severity in Duchenne muscular dystrophy

Neurology, 2011-01, Vol.76 (3), p.219

2011

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Adiposity attenuates muscle quality and the adaptive response to resistance exercise in non-obese, healthy adults

International Journal of Obesity, 2011-08, Vol.35 (8), p.1095-1103

2011

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MeCP2 mutations in children with and without the phenotype of Rett syndrome

Neurology, 2001-06, Vol.56 (11), p.1486

2001

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Regenerated mdx mouse skeletal muscle shows differential mRNA expression

Journal of applied physiology (1985), 2002-08, Vol.93 (2), p.537-545

2002

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Leptin and leptin receptor genetic variants associate with habitual physical activity and the arm body composition response to resistance training

Gene, 2012-11, Vol.510 (1), p.66-70

2012

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Molecular findings in symptomatic and pre-symptomatic Alexander disease patients

Neurology, 2002-05, Vol.58 (10), p.1494

2002

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Novel mutations in collagen VI genes: expansion of the Bethlem myopathy phenotype

Neurology, 2002-02, Vol.58 (4), p.593

2002

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Indian Agarwal megalencephalic leukodystrophy with cysts is caused by a common MLC1 mutation

Neurology, 2004-03, Vol.62 (6), p.878

2004

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The glucocorticoid receptor N363S polymorphism and steroid response in Duchenne dystrophy

Journal of neurology, neurosurgery and psychiatry, 2006-10, Vol.77 (10), p.1177-1179

2006

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A new locus for hemiplegic migraine maps to chromosome 1q31

Neurology, 1997-11, Vol.49 (5), p.1231

1997

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Sensitivity and specificity of decreased CSF asialotransferrin for eIF2B-related disorder

Neurology, 2008-06, Vol.70 (23), p.2226

2008

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Molecular cloning, structure, and chromosomal localization of the human inducible nitric oxide synthase gene

The Journal of biological chemistry, 1994-03, Vol.269 (9), p.6765-6772

1994

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β-sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex

Nature genetics, 1995-11, Vol.11 (3), p.266-273

1995

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Skeletal muscle dictates the fibrinolytic state after exercise training in overweight men with characteristics of metabolic syndrome

The Journal of physiology, 2003-04, Vol.548 (2), p.401-410

2003

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Delivery of α- and β-sarcoglycan by recombinant adeno-associated virus: Efficient rescue of muscle, but differential toxicity

Human gene therapy, 2002-09, Vol.13 (13), p.1631-1646

2002

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The clinical spectrum of sarcoglycanopathies

Neurology, 1999-01, Vol.52 (1), p.176

1999

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Caveolin-3 in Muscular Dystrophy

Human molecular genetics, 1998-05, Vol.7 (5), p.871-877

1998

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Large-scale disruption of microtubule pathways in morphologically normal human spastin muscle

Neurology, 2004-04, Vol.62 (7), p.1097

2004

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Eccentric muscle challenge shows osteopontin polymorphism modulation of muscle damage

Human molecular genetics, 2014-08, Vol.23 (15), p.4043-4050

2014

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Rett Syndrome: Confirmation of X-Linked Dominant Inheritance, and Localization of the Gene to Xq28

American journal of human genetics, 1998-11, Vol.63 (5), p.1552-1557

1998

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Conversion of mdx myofibres from dystrophin-negative to -positive by injection of normal myoblasts

Nature (London), 1989-01, Vol.337 (6203), p.176-179

1989

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DNA sequence analysis for structure/function and mutation studies in Becker muscular dystrophy

Clinical genetics, 2005-07, Vol.68 (1), p.69-79

2005

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Familial Skewed X Inactivation: A Molecular Trait Associated with High Spontaneous-Abortion Rate Maps to Xq28

American journal of human genetics, 1997-07, Vol.61 (1), p.160-170

1997

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Expression Profiling in the Muscular Dystrophies: Identification of Novel Aspects of Molecular Pathophysiology

The Journal of cell biology, 2000-12, Vol.151 (6), p.1321-1336

2000

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Variability in muscle size and strength gain after unilateral resistance training

Medicine and science in sports and exercise, 2005-06, Vol.37 (6), p.964-972

2005

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