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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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Serum Levels of Matrix Metalloproteinases-2 and -9 and Their Tissue Inhibitors in Inflammatory Neuromuscular Disorders

European neurology, 2006-08, Vol.55 (4), p.204-208

2006

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Matrix metalloproteinases in inflammatory myopathies: enhanced immunoreactivity near atrophic myofibers

Acta neurologica Scandinavica, 2002-04, Vol.105 (4), p.309-313

2002

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Sudden cardiac death in myotonic dystrophy type 2

Neurology, 2004-12, Vol.63 (12), p.2402

2004

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Outcome and effect of pregnancy in myotonic dystrophy type 2

Neurology, 2006-02, Vol.66 (4), p.579

2006

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Cerebral hyperperfusion injury after percutaneous transluminal angioplasty of extracranial arteries

Journal of neurology, 1997-01, Vol.244 (2), p.101-104

1997

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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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Pathological consequences of VCP mutations on human striated muscle

Brain (London, England : 1878), 2007-02, Vol.130 (2), p.381-393

2007

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Brain imaging and neuropsychology in late-onset dementia due to a novel mutation (R93C) of valosin-containing protein

Clinical neuropathology, 2007-09, Vol.26 (5), p.232

2007

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Novel missense mutation in the caveolin-3 gene in a Belgian family with rippling muscle disease

Journal of neurology, neurosurgery and psychiatry, 2004-09, Vol.75 (9), p.1349-1351

2004

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Homozygosity for CCTG mutation in myotonic dystrophy type 2

Brain (London, England : 1878), 2004-08, Vol.127 (8), p.1868-1877

2004

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Autoimmune hyperthyroidism in multiple sclerosis under treatment with glatiramer acetate - a case report

European journal of neurology, 2001-03, Vol.8 (2), p.199-199

2001

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Matrix metalloproteinases MMP-2, MMP-7 and MMP-9 in denervated human muscle

Neuroreport, 1999-09, Vol.10 (13), p.2795-2797

1999

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Glykogenspeichererkrankung Typ 2 - Morbus Pompe

Aktuelle Neurologie, 2007-06, Vol.34 (5), p.283-290

Schoser, B. G. H.

2007

Volltextzugriff (PDF)

A sporadic case of rippling muscle disease caused by a de novo caveolin-3 mutation

Neurology, 2001-12, Vol.57 (12), p.2273

2001

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Mutations in mtDNA-encoded cytochrome c oxidase subunit genes causing isolated myopathy or severe encephalomyopathy

Neuromuscular disorders : NMD, 2005-12, Vol.15 (12), p.851-857

2005

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CD95-mediated apoptosis and DNA fragmentation in MS

Acta neurologica Scandinavica, 2000-11, Vol.102 (5), p.333-336

2000

Volltextzugriff (PDF)

Myotone Dystrophien - Aktueller Stand der molekularen Pathogenese

Aktuelle Neurologie, 2005-08, Vol.32 (6), p.324-330

Schoser, B. G. H.

2005

Volltextzugriff (PDF)

The impact of raised intracranial pressure on cerebral venous hemodynamics: a prospective venous transcranial Doppler ultrasonography study

Journal of neurosurgery, 1999-11, Vol.91 (5), p.744

1999

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Prediction of response to IVIg treatment in patients with lower motor neurone disorders

European journal of neurology, 2006-02, Vol.13 (2), p.135-140

2006

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Subacute onset of oculogyric crises and generalized dystonia following intranasal administration of heroin

Addiction (Abingdon, England), 1999-03, Vol.94 (3), p.431-434

1999

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Immunolocalization of leukemia inhibitory factor in normal and denervated human muscle

Neuroreport, 1998-08, Vol.9 (12), p.2843-2846

1998

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Acute overdosage and intoxication with carbidopa/levodopa can be detected in the subacute stage by measurement of 3-o-methyldopa

Journal of neurology, neurosurgery and psychiatry, 1999-07, Vol.67 (1), p.122-123a

1999

Volltextzugriff (PDF)

Partial loss of NADPH-diaphorase/nitric oxide synthase-complex in amyotrophic lateral sclerosis and human type-II myofiber atrophy

Neuroscience letters, 1997-08, Vol.231 (3), p.163-166

1997

Volltextzugriff (PDF)

Matrix metalloproteinases in inflammatory myopathies: enhanced immunoreactivity near atrophic myofibers: MMPs in inflamed muscle

Acta neurologica Scandinavica, 2002-04, Vol.105 (4), p.309-313

2002

Volltextzugriff (PDF)

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

Serum Levels of Matrix Metalloproteinases-2 and -9 and Their Tissue Inhibitors in Inflammatory Neuromuscular Disorders

Matrix metalloproteinases in inflammatory myopathies: enhanced immunoreactivity near atrophic myofibers

Sudden cardiac death in myotonic dystrophy type 2

Outcome and effect of pregnancy in myotonic dystrophy type 2

Cerebral hyperperfusion injury after percutaneous transluminal angioplasty of extracranial arteries

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

Pathological consequences of VCP mutations on human striated muscle

Brain imaging and neuropsychology in late-onset dementia due to a novel mutation (R93C) of valosin-containing protein

Novel missense mutation in the caveolin-3 gene in a Belgian family with rippling muscle disease

Homozygosity for CCTG mutation in myotonic dystrophy type 2

Autoimmune hyperthyroidism in multiple sclerosis under treatment with glatiramer acetate - a case report

Matrix metalloproteinases MMP-2, MMP-7 and MMP-9 in denervated human muscle

Glykogenspeichererkrankung Typ 2 - Morbus Pompe

A sporadic case of rippling muscle disease caused by a de novo caveolin-3 mutation

Mutations in mtDNA-encoded cytochrome c oxidase subunit genes causing isolated myopathy or severe encephalomyopathy

CD95-mediated apoptosis and DNA fragmentation in MS

Myotone Dystrophien - Aktueller Stand der molekularen Pathogenese

The impact of raised intracranial pressure on cerebral venous hemodynamics: a prospective venous transcranial Doppler ultrasonography study

Prediction of response to IVIg treatment in patients with lower motor neurone disorders

Subacute onset of oculogyric crises and generalized dystonia following intranasal administration of heroin

Immunolocalization of leukemia inhibitory factor in normal and denervated human muscle

Acute overdosage and intoxication with carbidopa/levodopa can be detected in the subacute stage by measurement of 3-o-methyldopa

Partial loss of NADPH-diaphorase/nitric oxide synthase-complex in amyotrophic lateral sclerosis and human type-II myofiber atrophy

Matrix metalloproteinases in inflammatory myopathies: enhanced immunoreactivity near atrophic myofibers: MMPs in inflamed muscle

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