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Late onset Pompe disease: Clinical and neurophysiological spectrum of 38 patients including long-term follow-up in 18 patients

Neuromuscular disorders : NMD, 2007-10, Vol.17 (9), p.698-706

2007

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Muscle pathology in 57 patients with myotonic dystrophy type 2

Muscle & nerve, 2004-02, Vol.29 (2), p.275-281

2004

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The long-term outcome of anti-Jo-1-positive inflammatory myopathies

Journal of neurology, 2004-07, Vol.251 (7), p.859-864

2004

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Relationship of substance P, 5-hydroxyindole acetic acid and tryptophan in serum of fibromyalgia patients

Neuroscience letters, 1999-01, Vol.259 (3), p.196-198

1999

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Mutational analysis of serotonin receptor genes: HTR3A and HTR3B in fibromyalgia patients

Clinical rheumatology, 2004-08, Vol.23 (4), p.338-344

2004

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The T102C Polymorphism of the 5-HT2A-Receptor Gene in Fibromyalgia

Neurobiology of disease, 1999-10, Vol.6 (5), p.433-439

1999

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Breaking the news in amyotrophic lateral sclerosis

Journal of the neurological sciences, 1998-10, Vol.160, p.S127-S133

1998

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Deletion of the LMNA initiator codon leading to a neurogenic variant of autosomal dominant Emery–Dreifuss muscular dystrophy

Neuromuscular disorders : NMD, 2005-01, Vol.15 (1), p.40-44

2005

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Therapeutic options in autoimmune inflammatory myopathies (dermatomyositis, polymyositis, inclusion body myositis)

Journal of neurology, 2006-09, Vol.253 Suppl 5 (S5), p.V64-v65

Pongratz, Dieter

2006

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Immunogene Myositiden

Deutsche medizinische Wochenschrift, 2006-02, Vol.131 (7), p.330-336

Pongratz, D

2006

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German open label trial of riluzole 50 mg b.i.d. in treatment of amyotrophic lateral sclerosis (ALS)

Journal of the neurological sciences, 2000-11, Vol.180 (1), p.82-85

2000

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Mutation analysis in myophosphorylase deficiency (McArdle's disease)

Annals of neurology, 1998-03, Vol.43 (3), p.326-331

1998

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Muscular ultrasound in idiopathic inflammatory myopathies of adults

Journal of the neurological sciences, 1993-05, Vol.116 (1), p.82-92

1993

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An international, randomized, double-blind, placebo-controlled, phase III trial of pregabalin monotherapy in treatment of patients with fibromyalgia

Journal of rheumatology, 2011-12, Vol.38 (12), p.2643

2011

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Polymyalgia rheumatica (arteritica)

MMW Fortschritte der Medizin, 2004-11, Vol.146 (46), p.32-34

Pongratz, D

2004

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Expression and localization of annexin VII (synexin) in muscle cells

Journal of cell science, 1995-01, Vol.108 ( Pt 1) (1), p.85-95

1995

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Scientific Aspects and Clinical Signs of Muscle Pain

Journal of musculoskeletal pain, 2004-01, Vol.12 (3-4), p.121-128

2004

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High-dose immunoglobulin therapy in sporadic inclusion body myositis : a double-blind, placebo-controlled study

Journal of neurology, 2000-01, Vol.247 (1), p.22-28

2000

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Differential expression of perforin in muscle-infiltrating T cells in polymyositis and dermatomyositis

The Journal of clinical investigation, 1996-06, Vol.97 (12), p.2905-2910

1996

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Pattern of interleukin-6 receptor complex immunoreactivity between cortical regions of rapid autopsy normal and Alzheimer's disease brain

European archives of psychiatry and clinical neuroscience, 2005-08, Vol.255 (4), p.269-278

2005

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Myocardial evidence of dystrophin mosaic in a Duchenne muscular dystrophy carrier

The Lancet (British edition), 1992-11, Vol.340 (8829), p.1235-1236

1992

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Extraocular Mitochondrial Myopathies and their Differential Diagnoses

Strabismus, 2006-01, Vol.14 (2), p.107-113

2006

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Progressive myoclonus epilepsy and mitochondrial myopathy associated with mutations in the tRNA(Ser(UCN)) gene

Annals of neurology, 1998-10, Vol.44 (4), p.635-640

1998

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Detection of humoral rejection in human cardiac allografts by assessing the capillary deposition of complement fragment C4d in endomyocardial biopsies

The Journal of heart and lung transplantation, 1999-09, Vol.18 (9), p.904-912

1999

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Decreased aminoacylation of mutant tRNAs in MELAS but not in MERRF patients

Human molecular genetics, 2000-03, Vol.9 (4), p.467-475

2000

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Late onset Pompe disease: Clinical and neurophysiological spectrum of 38 patients including long-term follow-up in 18 patients

Muscle pathology in 57 patients with myotonic dystrophy type 2

The long-term outcome of anti-Jo-1-positive inflammatory myopathies

Relationship of substance P, 5-hydroxyindole acetic acid and tryptophan in serum of fibromyalgia patients

Mutational analysis of serotonin receptor genes: HTR3A and HTR3B in fibromyalgia patients

The T102C Polymorphism of the 5-HT2A-Receptor Gene in Fibromyalgia

Breaking the news in amyotrophic lateral sclerosis

Deletion of the LMNA initiator codon leading to a neurogenic variant of autosomal dominant Emery–Dreifuss muscular dystrophy

Therapeutic options in autoimmune inflammatory myopathies (dermatomyositis, polymyositis, inclusion body myositis)

Immunogene Myositiden

German open label trial of riluzole 50 mg b.i.d. in treatment of amyotrophic lateral sclerosis (ALS)

Mutation analysis in myophosphorylase deficiency (McArdle's disease)

Muscular ultrasound in idiopathic inflammatory myopathies of adults

An international, randomized, double-blind, placebo-controlled, phase III trial of pregabalin monotherapy in treatment of patients with fibromyalgia

Polymyalgia rheumatica (arteritica)

Expression and localization of annexin VII (synexin) in muscle cells

Scientific Aspects and Clinical Signs of Muscle Pain

High-dose immunoglobulin therapy in sporadic inclusion body myositis : a double-blind, placebo-controlled study

Differential expression of perforin in muscle-infiltrating T cells in polymyositis and dermatomyositis

Pattern of interleukin-6 receptor complex immunoreactivity between cortical regions of rapid autopsy normal and Alzheimer's disease brain

Myocardial evidence of dystrophin mosaic in a Duchenne muscular dystrophy carrier

Extraocular Mitochondrial Myopathies and their Differential Diagnoses

Progressive myoclonus epilepsy and mitochondrial myopathy associated with mutations in the tRNA(Ser(UCN)) gene

Detection of humoral rejection in human cardiac allografts by assessing the capillary deposition of complement fragment C4d in endomyocardial biopsies

Decreased aminoacylation of mutant tRNAs in MELAS but not in MERRF patients

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