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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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Coenzyme Q10 deficiency and isolated myopathy

Neurology, 2006-01, Vol.66 (2), p.253-255

2006

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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.2402-2404

2004

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Outcome and effect of pregnancy in myotonic dystrophy type 2

Neurology, 2006-02, Vol.66 (4), p.579-580

2006

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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.368-370

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.232-240

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

Neurology, 2001-12, Vol.57 (12), p.2273-2277

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

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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.744-749

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

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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

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Tenascin in denervated human muscle

Journal of the neurological sciences, 1996-08, Vol.139 (2), p.203-209

1996

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Lipid lowering drug and other toxic myopathies

Der Internist (Berlin), 2005-11, Vol.46 (11), p.1198

2005

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Mutations in CAV3 cause mechanical hyperirritability of skeletal muscle in rippling muscle disease

Nature genetics, 2001-07, Vol.28 (3), p.218-219

2001

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

Coenzyme Q10 deficiency and isolated myopathy

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

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

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

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

Tenascin in denervated human muscle

Lipid lowering drug and other toxic myopathies

Mutations in CAV3 cause mechanical hyperirritability of skeletal muscle in rippling muscle disease

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