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Anti-signal recognition particle autoantibodies: marker of a necrotising myopathy

Annals of the rheumatic diseases, 2006-12, Vol.65 (12), p.1635-1638

2006

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Relation between muscle fiber conduction velocity and fiber size in neuromuscular disorders

Journal of applied physiology (1985), 2006-06, Vol.100 (6), p.1837-1841

2006

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Diagnostic value of MHC class I staining in idiopathic inflammatory myopathies

Journal of neurology, neurosurgery and psychiatry, 2004-01, Vol.75 (1), p.136-139

2004

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Is muscle glycogenolysis impaired in X-linked phosphorylase b kinase deficiency?

Neurology, 2008-05, Vol.70 (20), p.1876

2008

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Complex regional pain syndrome type I (RSD): pathology of skeletal muscle and peripheral nerve

Neurology, 1998-07, Vol.51 (1), p.20

1998

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Autosomal recessive oculopharyngodistal myopathy: a distinct phenotypical, histological, and genetic entity

Journal of neurology, neurosurgery and psychiatry, 2004-10, Vol.75 (10), p.1499-1501

2004

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A locus on chromosome 15q for a dominantly inherited nemaline myopathy with core‐like lesions

Brain (London, England : 1878), 2003-07, Vol.126 (7), p.1545-1551

2003

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A 4-base pair deletion in the mitochondrial cytochrome b gene associated with parkinsonism/MELAS overlap syndrome

Annals of neurology, 1999-01, Vol.45 (1), p.130-133

1999

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Primary respiratory failure in inclusion body myositis

Neurology, 2004-12, Vol.63 (11), p.2191

2004

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Skeletal muscle ultrasonography in children with a dysfunction in the oxidative phosphorylation system

Neuropediatrics, 2006-06, Vol.37 (3), p.142

2006

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Colchicine-induced neuromyopathy in a patient with chronic renal failure : the role of clarithromycin

Netherlands journal of medicine, 2008-05, Vol.66 (5), p.204-206

2008

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Distal spinal muscular atrophy as a major feature in adult-onset ataxia telangiectasia

Neurology, 2006-07, Vol.67 (2), p.346

2006

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Histology of hereditary neuralgic amyotrophy

Journal of neurology, neurosurgery and psychiatry, 2005-03, Vol.76 (3), p.445-447

2005

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Neuromuscular abnormalities in ataxia telangiectasia: a clinical, electrophysiological and muscle ultrasound study

Neuropediatrics, 2007-06, Vol.38 (3), p.117

2007

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Genetic characteristics of myoadenylate deaminase deficiency

Annals of neurology, 1998-07, Vol.44 (1), p.140-143

1998

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Cell loss and shrinkage in the nucleus basalis Meynert complex in Alzheimer's disease

Neurobiology of aging, 1990, Vol.11 (1), p.3-13

1990

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Chronic progressive external ophthalmoplegia caused by an m.4267A > G mutation in the mitochondrial tRNAIle

Journal of neurology, 2007-11, Vol.254 (11), p.1614-1615

2007

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Hypovitaminosis D-related myopathy in immigrant teenagers

Neuropediatrics, 2004-10, Vol.35 (5), p.290

2004

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Lethal infantile mitochondrial disease with isolated complex I deficiency in fibroblasts but with combined complex I and IV deficiencies in muscle

Neurology, 1996-07, Vol.47 (1), p.243

1996

Volltextzugriff (PDF)

Anti-Jo-1 positive inclusion body myositis with a marked and sustained clinical improvement after oral prednisone

Journal of neurology, neurosurgery and psychiatry, 2001-05, Vol.70 (5), p.706-706

2001

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Myositis during long-term interferon-alpha treatment

Neurology, 2000-06, Vol.54 (11), p.2186

2000

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Spinal muscular atrophy-like picture, cardiomyopathy, and cytochrome c oxidase deficiency

Neurology, 1999-01, Vol.52 (2), p.383

1999

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High myopia and congenital myopathy with partial pachygyria in cutis laxa syndrome

European journal of ophthalmology, 2006-01, Vol.16 (1), p.190-194

2006

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Symptomatic distal myopathy with cardiomyopathy due to a MYH7 mutation

Neuromuscular disorders : NMD, 2007-06, Vol.17 (6), p.490-493

2007

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A new phenotype of autosomal dominant nemaline myopathy

Neuromuscular disorders : NMD, 2002, Vol.12 (1), p.13-18

2002

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Anti-signal recognition particle autoantibodies: marker of a necrotising myopathy

Relation between muscle fiber conduction velocity and fiber size in neuromuscular disorders

Diagnostic value of MHC class I staining in idiopathic inflammatory myopathies

Is muscle glycogenolysis impaired in X-linked phosphorylase b kinase deficiency?

Complex regional pain syndrome type I (RSD): pathology of skeletal muscle and peripheral nerve

Autosomal recessive oculopharyngodistal myopathy: a distinct phenotypical, histological, and genetic entity

A locus on chromosome 15q for a dominantly inherited nemaline myopathy with core‐like lesions

A 4-base pair deletion in the mitochondrial cytochrome b gene associated with parkinsonism/MELAS overlap syndrome

Primary respiratory failure in inclusion body myositis

Skeletal muscle ultrasonography in children with a dysfunction in the oxidative phosphorylation system

Colchicine-induced neuromyopathy in a patient with chronic renal failure : the role of clarithromycin

Distal spinal muscular atrophy as a major feature in adult-onset ataxia telangiectasia

Histology of hereditary neuralgic amyotrophy

Neuromuscular abnormalities in ataxia telangiectasia: a clinical, electrophysiological and muscle ultrasound study

Genetic characteristics of myoadenylate deaminase deficiency

Cell loss and shrinkage in the nucleus basalis Meynert complex in Alzheimer's disease

Chronic progressive external ophthalmoplegia caused by an m.4267A > G mutation in the mitochondrial tRNAIle

Hypovitaminosis D-related myopathy in immigrant teenagers

Lethal infantile mitochondrial disease with isolated complex I deficiency in fibroblasts but with combined complex I and IV deficiencies in muscle

Anti-Jo-1 positive inclusion body myositis with a marked and sustained clinical improvement after oral prednisone

Myositis during long-term interferon-alpha treatment

Spinal muscular atrophy-like picture, cardiomyopathy, and cytochrome c oxidase deficiency

High myopia and congenital myopathy with partial pachygyria in cutis laxa syndrome

Symptomatic distal myopathy with cardiomyopathy due to a MYH7 mutation

A new phenotype of autosomal dominant nemaline myopathy

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