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Distribution and severity of weakness among patients with polymyositis, dermatomyositis and juvenile dermatomyositis

Rheumatology (Oxford, England), 2009-02, Vol.48 (2), p.134-139

2009

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A case of necrotizing myopathy with proximal weakness and cardiomyopathy

Neurology, 2012-05, Vol.78 (19), p.1527-1532

2012

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Enzyme replacement therapy in the mouse model of Pompe disease

Molecular genetics and metabolism, 2003-09, Vol.80 (1), p.159-169

2003

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Conditional tissue-specific expression of the acid α-glucosidase (GAA) gene in the GAA knockout mice : implications for therapy

Human molecular genetics, 2001-09, Vol.10 (19), p.2039-2047

2001

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The idiopathic inflammatory myopathies: spectrum of MR imaging findings

Radiographics, 1995-05, Vol.15 (3), p.563-574

1995

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The Role of Autoantibodies in Autoimmune Disease

Annual review of immunology, 1993, Vol.11 (1), p.79-104

1993

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γδ T cell receptor gene expression by muscle‐infiltrating lymphocytes in the idiopathic inflammatory myopathies

Clinical and experimental immunology, 2008-06, Vol.100 (3), p.519-528

2008

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Current concepts in the idiopathic inflammatory myopathies: polymyositis, dermatomyositis, and related disorders

Annals of internal medicine, 1989-07, Vol.111 (2), p.143

1989

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Controlled Trial of Plasma Exchange and Leukapheresis in Polymyositis and Dermatomyositis

The New England journal of medicine, 1992-05, Vol.326 (21), p.1380-1384

1992

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Drug therapy of the idiopathic inflammatory myopathies: predictors of response to prednisone, azathioprine, and methotrexate and a comparison of their efficacy

The American journal of medicine, 1993-04, Vol.94 (4), p.379-387

1993

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Costimulatory Markers in Muscle of Patients with Idiopathic Inflammatory Myopathies and in Cultured Muscle Cells

Clinical immunology (Orlando, Fla.), 1999-08, Vol.92 (2), p.161-169

1999

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Role of autophagy in the pathogenesis of Pompe disease

Acta myologica, 2007-07, Vol.26 (1), p.45-48

2007

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Polymyositis: an overdiagnosed entity

Neurology, 2004-07, Vol.63 (2), p.402; author reply 403-403

2004

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Leaky splicing mutation in the acid maltase gene is associated with delayed onset of glycogenosis type II

American journal of human genetics, 1995-04, Vol.56 (4), p.887-897

1995

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Viruses in idiopathic inflammatory myopathies: absence of candidate viral genomes in muscle

The Lancet (British edition), 1992-05, Vol.339 (8803), p.1192-1195

1992

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Common mutations in the phosphofructokinase-M gene in Ashkenazi Jewish patients with glycogenesis. VII: And their population frequency

American journal of human genetics, 1994-08, Vol.55 (2), p.305-313

1994

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The Role of an Autoantigen, Histidyl-tRNA Synthetase, in the Induction and Maintenance of Autoimmunity

Proceedings of the National Academy of Sciences - PNAS, 1990-12, Vol.87 (24), p.9933-9937

1990

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Therapy of lupus nephritis. Controlled trial of prednisone and cytotoxic drugs

The New England journal of medicine, 1986-03, Vol.314 (10), p.614

1986

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The African Origin of the Common Mutation in African American Patients with Glycogen-Storage Disease Type II

American journal of human genetics, 1998-04, Vol.62 (4), p.991-994

1998

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Identification and characterization of a tissue-specific silencer element in the first intron of the human acid maltase gene

Human genetics, 2001-08, Vol.109 (2), p.186-190

2001

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A pilot study: use of fludarabine for refractory dermatomyositis and polymyositis, and examination of endpoint measures

Journal of rheumatology, 1999-02, Vol.26 (2), p.352

1999

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Predominant TCR-alpha beta variable and joining gene expression by muscle-infiltrating lymphocytes in the idiopathic inflammatory myopathies

The Journal of immunology (1950), 1994-03, Vol.152 (5), p.2569-2576

1994

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Glycogenosis type VII (Tarui disease) in a Swedish family : Two novel mutations in muscle phosphofructokinase gene (PFK-M) resulting in intron retentions

American journal of human genetics, 1996-07, Vol.59 (1), p.59-65

1996

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A new approach to the classification of idiopathic inflammatory myopathy: myositis-specific autoantibodies define useful homogeneous patient groups

Medicine (Baltimore), 1991-11, Vol.70 (6), p.360-374

1991

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Origin and regulation of a disease-specific autoantibody response: antigenic epitopes, spectrotype stability, and isotype restriction of anti-Jo-1 autoantibodies

The Journal of clinical investigation, 1990-02, Vol.85 (2), p.468-475

1990

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Distribution and severity of weakness among patients with polymyositis, dermatomyositis and juvenile dermatomyositis

A case of necrotizing myopathy with proximal weakness and cardiomyopathy

Enzyme replacement therapy in the mouse model of Pompe disease

Conditional tissue-specific expression of the acid α-glucosidase (GAA) gene in the GAA knockout mice : implications for therapy

The idiopathic inflammatory myopathies: spectrum of MR imaging findings

The Role of Autoantibodies in Autoimmune Disease

γδ T cell receptor gene expression by muscle‐infiltrating lymphocytes in the idiopathic inflammatory myopathies

Current concepts in the idiopathic inflammatory myopathies: polymyositis, dermatomyositis, and related disorders

Controlled Trial of Plasma Exchange and Leukapheresis in Polymyositis and Dermatomyositis

Drug therapy of the idiopathic inflammatory myopathies: predictors of response to prednisone, azathioprine, and methotrexate and a comparison of their efficacy

Costimulatory Markers in Muscle of Patients with Idiopathic Inflammatory Myopathies and in Cultured Muscle Cells

Role of autophagy in the pathogenesis of Pompe disease

Polymyositis: an overdiagnosed entity

Leaky splicing mutation in the acid maltase gene is associated with delayed onset of glycogenosis type II

Viruses in idiopathic inflammatory myopathies: absence of candidate viral genomes in muscle

Common mutations in the phosphofructokinase-M gene in Ashkenazi Jewish patients with glycogenesis. VII: And their population frequency

The Role of an Autoantigen, Histidyl-tRNA Synthetase, in the Induction and Maintenance of Autoimmunity

Therapy of lupus nephritis. Controlled trial of prednisone and cytotoxic drugs

The African Origin of the Common Mutation in African American Patients with Glycogen-Storage Disease Type II

Identification and characterization of a tissue-specific silencer element in the first intron of the human acid maltase gene

A pilot study: use of fludarabine for refractory dermatomyositis and polymyositis, and examination of endpoint measures

Predominant TCR-alpha beta variable and joining gene expression by muscle-infiltrating lymphocytes in the idiopathic inflammatory myopathies

Glycogenosis type VII (Tarui disease) in a Swedish family : Two novel mutations in muscle phosphofructokinase gene (PFK-M) resulting in intron retentions

A new approach to the classification of idiopathic inflammatory myopathy: myositis-specific autoantibodies define useful homogeneous patient groups

Origin and regulation of a disease-specific autoantibody response: antigenic epitopes, spectrotype stability, and isotype restriction of anti-Jo-1 autoantibodies

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