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Adult-onset glycogen storage disease type 2: clinico-pathological phenotype revisited

Neuropathology and applied neurobiology, 2007-10, Vol.33 (5), p.544-559

2007

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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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Mutations in the acid alpha-glucosidase gene (M. Pompe) in a patient with an unusual phenotype

Neurology, 2005-01, Vol.64 (2), p.368

2005

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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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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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Missense mutations of ACTA1 cause dominant congenital myopathy with cores

Journal of medical genetics, 2004-11, Vol.41 (11), p.842-848

2004

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Creatine monohydrate in muscular dystrophies: A double-blind, placebo-controlled clinical study

Neurology, 2000-05, Vol.54 (9), p.1848

2000

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A randomized, double-blind, placebo-controlled study of the efficacy and safety of tolperisone in spasticity following cerebral stroke

European journal of neurology, 2005-06, Vol.12 (6), p.453-461

2005

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Skeletal muscle sonography: a correlative study of echogenicity and morphology

Journal of ultrasound in medicine, 1993-02, Vol.12 (2), p.73-77

1993

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Efficacy and tolerability of intravenous tropisetron in the treatment of fibromyalgia

Scandinavian journal of rheumatology, 2004-07, Vol.33 (4), p.267-270

2004

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FKRP (826C>A) frequently causes limb-girdle muscular dystrophy in German patients

Journal of medical genetics, 2004-04, Vol.41 (4), p.e50-e50

2004

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Detection of elevated Nε-carboxymethyllysine levels in muscular tissue and in serum of patients with fibromyalgia

Scandinavian journal of rheumatology, 2005-11, Vol.34 (6), p.460-463

2005

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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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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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The diagnostic process in ALS

Journal of the neurological sciences, 1999-06, Vol.165, p.S10-S13

Pongratz, D

1999

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Screening for Carnitine Palmitoyltransferase II Deficiency by Tandem Mass Spectrometry

Journal of inherited metabolic disease, 2002-02, Vol.25 (1), p.17-27

2002

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A placebo-controlled crossover trial of creatine in mitochondrial diseases

Neurology, 2000-12, Vol.55 (11), p.1748

2000

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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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Muscle and skin biopsies are a sensitive diagnostic tool in the diagnosis of CADASIL

Journal of neurology, 1999-07, Vol.246 (7), p.526-532

1999

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Fibromyalgie

Fortschritte der Neurologie, Psychiatrie, 2001, Vol.69 (4), p.189-194

2001

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Magnetic resonance imaging of skeletal muscles in idiopathic inflammatory myopathies of adults

Journal of neurology, 1994-03, Vol.241 (5), p.306-314

1994

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Efficacy and tolerability of tropisetron in primary fibromyalgia - a highly selective and competitive 5-HT3 receptor antagonist

Scandinavian journal of rheumatology, 2000, Vol.29 (113), p.49-54

Färber, T. Stratz, W. Brückle, M. Späth, D. Pongratz, J. Lautenschläger, I. Kötter, B. Zöller, H.-H. Peter, G. Neeck, R. Alten, W. Müller, L.

2000

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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

1994

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A common mutation (epsilon1267delG) in congenital myasthenic patients of Gypsy ethnic origin

Neurology, 1999-10, Vol.53 (7), p.1564

1999

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Chloroquin-induzierte Myopathie: folge einer siebenjährigen, niedrigdosierten Basistherapie bei primär-chronischer Polyarthritis

Zeitschrift für Rheumatologie, 2005-05, Vol.64 (4), p.274-276

2005

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Adult-onset glycogen storage disease type 2: clinico-pathological phenotype revisited

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

Mutations in the acid alpha-glucosidase gene (M. Pompe) in a patient with an unusual phenotype

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

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

Missense mutations of ACTA1 cause dominant congenital myopathy with cores

Creatine monohydrate in muscular dystrophies: A double-blind, placebo-controlled clinical study

A randomized, double-blind, placebo-controlled study of the efficacy and safety of tolperisone in spasticity following cerebral stroke

Skeletal muscle sonography: a correlative study of echogenicity and morphology

Efficacy and tolerability of intravenous tropisetron in the treatment of fibromyalgia

FKRP (826C>A) frequently causes limb-girdle muscular dystrophy in German patients

Detection of elevated Nε-carboxymethyllysine levels in muscular tissue and in serum of patients with fibromyalgia

Breaking the news in amyotrophic lateral sclerosis

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

The diagnostic process in ALS

Screening for Carnitine Palmitoyltransferase II Deficiency by Tandem Mass Spectrometry

A placebo-controlled crossover trial of creatine in mitochondrial diseases

Muscular ultrasound in idiopathic inflammatory myopathies of adults

Muscle and skin biopsies are a sensitive diagnostic tool in the diagnosis of CADASIL

Fibromyalgie

Magnetic resonance imaging of skeletal muscles in idiopathic inflammatory myopathies of adults

Efficacy and tolerability of tropisetron in primary fibromyalgia - a highly selective and competitive 5-HT3 receptor antagonist

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

A common mutation (epsilon1267delG) in congenital myasthenic patients of Gypsy ethnic origin

Chloroquin-induzierte Myopathie: folge einer siebenjährigen, niedrigdosierten Basistherapie bei primär-chronischer Polyarthritis

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