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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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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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A case of necrotizing myopathy with proximal weakness and cardiomyopathy

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

2012

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International consensus outcome measures for patients with idiopathic inflammatory myopathies. Development and initial validation of myositis activity and damage indices in patients with adult onset disease

Rheumatology (Oxford, England), 2004-01, Vol.43 (1), p.49-54

2004

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Biphasic aggregation of a perylene bisimide dye identified by exciton-vibrational spectra

Physical chemistry chemical physics : PCCP, 2016-09, Vol.18 (36), p.2511-25119

2016

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CO2 Mitigation Potential of Plug-in Hybrid Electric Vehicles larger than expected

Scientific reports, 2017-11, Vol.7 (1), p.1-6, Article 16493

2017

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Effective spin model for interband transport in a Wannier-Stark lattice system

The European physical journal. D, Atomic, molecular, and optical physics, 2011-06, Vol.63 (1), p.47-53

2011

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Systemic Correction of the Muscle Disorder Glycogen Storage Disease Type II after Hepatic Targeting of a Modified Adenovirus Vector Encoding Human Acid α -Glucosidase

Proceedings of the National Academy of Sciences - PNAS, 1999-08, Vol.96 (16), p.8861-8866

1999

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Detection and imaging of non-contractile inclusions and sarcomeric anomalies in skeletal muscle by second harmonic generation combined with two-photon excited fluorescence

Journal of structural biology, 2008-06, Vol.162 (3), p.500-508

2008

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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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Role of autophagy in the pathogenesis of Pompe disease

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

2007

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The place of autoimmunity in myositis

Autoimmunity reviews, 2004-06, Vol.3 Suppl 1, p.S36-S36

Plotz, P

2004

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A variety of cytokines and immunologically relevant surface molecules are expressed by normal human skeletal muscle cells under proinflammatory stimuli

Clinical and experimental immunology, 1998-09, Vol.113 (3), p.407-414

1998

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Modelling market diffusion of electric vehicles with real world driving data – German market and policy options

Transportation research. Part A, Policy and practice, 2015-07, Vol.77, p.95-112

2015

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P.10.21 Next-generation sequencing meets genetic diagnostics: Development of a comprehensive workflow for neuromuscular disorders

Neuromuscular disorders : NMD, 2013-10, Vol.23 (9), p.795-795

2013

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Suppression of autophagy in skeletal muscle uncovers the accumulation of ubiquitinated proteins and their potential role in muscle damage in Pompe disease

Human molecular genetics, 2008-12, Vol.17 (24), p.3897-3908

2008

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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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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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Enhanced autoantigen expression in regenerating muscle cells in idiopathic inflammatory myopathy

The Journal of experimental medicine, 2005-02, Vol.201 (4), p.591-601

2005

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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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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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The idiopathic inflammatory myopathies: spectrum of MR imaging findings

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

1995

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Surprises of genetic engineering: a possible model of polyglucosan body disease

Neurology, 2001-06, Vol.56 (12), p.1739

2001

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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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Intercellular transfer of the virally derived precursor form of acid α-glucosidase corrects the enzyme deficiency in inherited cardioskeletal myopathy pompe disease

Human gene therapy, 2001-03, Vol.12 (5), p.527-538

2001

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

Enzyme replacement therapy in the mouse model of Pompe disease

A case of necrotizing myopathy with proximal weakness and cardiomyopathy

International consensus outcome measures for patients with idiopathic inflammatory myopathies. Development and initial validation of myositis activity and damage indices in patients with adult onset disease

Biphasic aggregation of a perylene bisimide dye identified by exciton-vibrational spectra

CO2 Mitigation Potential of Plug-in Hybrid Electric Vehicles larger than expected

Effective spin model for interband transport in a Wannier-Stark lattice system

Systemic Correction of the Muscle Disorder Glycogen Storage Disease Type II after Hepatic Targeting of a Modified Adenovirus Vector Encoding Human Acid α -Glucosidase

Detection and imaging of non-contractile inclusions and sarcomeric anomalies in skeletal muscle by second harmonic generation combined with two-photon excited fluorescence

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

Role of autophagy in the pathogenesis of Pompe disease

The place of autoimmunity in myositis

A variety of cytokines and immunologically relevant surface molecules are expressed by normal human skeletal muscle cells under proinflammatory stimuli

Modelling market diffusion of electric vehicles with real world driving data – German market and policy options

P.10.21 Next-generation sequencing meets genetic diagnostics: Development of a comprehensive workflow for neuromuscular disorders

Suppression of autophagy in skeletal muscle uncovers the accumulation of ubiquitinated proteins and their potential role in muscle damage in Pompe disease

The Role of Autoantibodies in Autoimmune Disease

Controlled Trial of Plasma Exchange and Leukapheresis in Polymyositis and Dermatomyositis

Enhanced autoantigen expression in regenerating muscle cells in idiopathic inflammatory myopathy

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

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

The idiopathic inflammatory myopathies: spectrum of MR imaging findings

Surprises of genetic engineering: a possible model of polyglucosan body disease

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

Intercellular transfer of the virally derived precursor form of acid α-glucosidase corrects the enzyme deficiency in inherited cardioskeletal myopathy pompe disease

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