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Epidemiology of inclusion body myositis in the Netherlands: a nationwide study

Neurology, 2000-11, Vol.55 (9), p.1385-1388

2000

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Age-related plaque morphology and C-terminal heterogeneity of amyloid β in Dutch-type hereditary cerebral hemorrhage with amyloidosis

Acta neuropathologica, 2000-04, Vol.99 (4), p.409-419

2000

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Dutch hereditary cerebral amyloid angiopathy: Structural lesions and apolipoprotein E genotype

Annals of neurology, 1997-05, Vol.41 (5), p.695-698

1997

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Frameshift proteins in autosomal dominant forms of Alzheimer disease and other tauopathies

Neurology, 2006-01, Vol.66 (2 Suppl 1), p.S86

2006

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Distribution of Inclusions in Neuronal Nuclei and Dystrophic Neurites in Huntington Disease Brain

Journal of neuropathology and experimental neurology, 1999-02, Vol.58 (2), p.129-137

1999

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Microglia in Diffuse Plaques in Hereditary Cerebral Hemorrhage with Amyloidosis (Dutch). An Immunohistochemical Study

Journal of neuropathology and experimental neurology, 1994-09, Vol.53 (5), p.483-491

1994

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Association of Vascular Amyloid β and Cells of the Mononuclear Phagocyte System in Hereditary Cerebral Hemorrhage with Amyloidosis (Dutch) and Alzheimer Disease

Journal of neuropathology and experimental neurology, 1997-03, Vol.56 (3), p.273-284

1997

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Co-localization of β/A4 and cystatin C in cortical blood vessels in Dutch, but not in Icelandic hereditary cerebral hemorrhage with amyloidosis

Acta neurologica Scandinavica, 1994-05, Vol.89 (5), p.367-371

1994

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Inclusion body myositis : Clinical features and clinical course of the disease in 64 patients

Journal of neurology, 2005-12, Vol.252 (12), p.1448-1454

2005

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Hereditary cerebral hemorrhage with amyloidosis (Dutch) : a model for congophilic plaque formation without neurofibrillary pathology

Acta neuropathologica, 1994-10, Vol.88 (4), p.371-378

1994

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Microvasculopathy is associated with the number of cerebrovascular lesions in hereditary cerebral hemorrhage with amyloidosis, Dutch type

Stroke (1970), 1998-08, Vol.29 (8), p.1588-1594

1998

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Heparan sulfate proteoglycan expression in cerebrovascular amyloid β deposits in Alzheimer's disease and hereditary cerebral hemorrhage with amyloidosis (Dutch) brains

Acta neuropathologica, 2001-12, Vol.102 (6), p.604-614

2001

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CNS involvement in primary Sjögren's syndrome: a case with a clue for the pathogenesis

Journal of neurology, 2000-01, Vol.247 (1), p.63-64

2000

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Morphology of cerebral plaque-like lesions in hereditary cerebral hemorrhage with amyloidosis (Dutch)

Acta neuropathologica, 1992-11, Vol.84 (6), p.674-679

1992

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Predominant deposition of amyloid-beta 42(43) in plaques in cases of Alzheimer's disease and hereditary cerebral hemorrhage associated with mutations in the amyloid precursor protein gene

The American journal of pathology, 1996-04, Vol.148 (4), p.1257-1266

1996

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Malignant astrocytoma following radiotherapy for craniopharyngioma

British journal of radiology, 1985-05, Vol.58 (689), p.480-482

1985

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Inclusion body myositis: its relative frequency in elderly people

Clinical neurology and neurosurgery, 1992, Vol.94, p.118-120

1992

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Associations with autoimmune disorders and HLA class I and II antigens in inclusion body myositis

Neurology, 2004-12, Vol.63 (12), p.2396-2398

2004

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'Inclusion body'-myositis

Nederlands tijdschrift voor geneeskunde, 1998-03, Vol.142 (11), p.553

1998

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Gastrointestinal dysfunction contributes to weight loss in Huntington's disease mice

Neurobiology of disease, 2011-10, Vol.44 (1), p.1-8

2011

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Lipoprotein Receptor-Related Protein-1 Mediates Amyloid-β-Mediated Cell Death of Cerebrovascular Cells

The American journal of pathology, 2007-12, Vol.171 (6), p.1989-1999

2007

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Small heat shock proteins associated with cerebral amyloid angiopathy of hereditary cerebral hemorrhage with amyloidosis (Dutch type) induce interleukin-6 secretion

Neurobiology of aging, 2009-02, Vol.30 (2), p.229-240

2009

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Comparison of weakness progression in inclusion body myositis during treatment with methotrexate or placebo

Annals of neurology, 2002-03, Vol.51 (3), p.369-372

2002

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The apolipoprotein E epsilon 4 allele does not influence the clinical expression of the amyloid precursor protein gene codon 693 or 692 mutations

Annals of neurology, 1994-09, Vol.36 (3), p.434-437

1994

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No vessel wall abnormalities in a human foetus with a NOTCH3 mutation

Acta neuropathologica, 2008-03, Vol.115 (3), p.369-370

2008

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Epidemiology of inclusion body myositis in the Netherlands: a nationwide study

Age-related plaque morphology and C-terminal heterogeneity of amyloid β in Dutch-type hereditary cerebral hemorrhage with amyloidosis

Dutch hereditary cerebral amyloid angiopathy: Structural lesions and apolipoprotein E genotype

Frameshift proteins in autosomal dominant forms of Alzheimer disease and other tauopathies

Distribution of Inclusions in Neuronal Nuclei and Dystrophic Neurites in Huntington Disease Brain

Microglia in Diffuse Plaques in Hereditary Cerebral Hemorrhage with Amyloidosis (Dutch). An Immunohistochemical Study

Association of Vascular Amyloid β and Cells of the Mononuclear Phagocyte System in Hereditary Cerebral Hemorrhage with Amyloidosis (Dutch) and Alzheimer Disease

Co-localization of β/A4 and cystatin C in cortical blood vessels in Dutch, but not in Icelandic hereditary cerebral hemorrhage with amyloidosis

Inclusion body myositis : Clinical features and clinical course of the disease in 64 patients

Hereditary cerebral hemorrhage with amyloidosis (Dutch) : a model for congophilic plaque formation without neurofibrillary pathology

Microvasculopathy is associated with the number of cerebrovascular lesions in hereditary cerebral hemorrhage with amyloidosis, Dutch type

Heparan sulfate proteoglycan expression in cerebrovascular amyloid β deposits in Alzheimer's disease and hereditary cerebral hemorrhage with amyloidosis (Dutch) brains

CNS involvement in primary Sjögren's syndrome: a case with a clue for the pathogenesis

Morphology of cerebral plaque-like lesions in hereditary cerebral hemorrhage with amyloidosis (Dutch)

Predominant deposition of amyloid-beta 42(43) in plaques in cases of Alzheimer's disease and hereditary cerebral hemorrhage associated with mutations in the amyloid precursor protein gene

Malignant astrocytoma following radiotherapy for craniopharyngioma

Inclusion body myositis: its relative frequency in elderly people

Associations with autoimmune disorders and HLA class I and II antigens in inclusion body myositis

'Inclusion body'-myositis

Gastrointestinal dysfunction contributes to weight loss in Huntington's disease mice

Lipoprotein Receptor-Related Protein-1 Mediates Amyloid-β-Mediated Cell Death of Cerebrovascular Cells

Small heat shock proteins associated with cerebral amyloid angiopathy of hereditary cerebral hemorrhage with amyloidosis (Dutch type) induce interleukin-6 secretion

Comparison of weakness progression in inclusion body myositis during treatment with methotrexate or placebo

The apolipoprotein E epsilon 4 allele does not influence the clinical expression of the amyloid precursor protein gene codon 693 or 692 mutations

No vessel wall abnormalities in a human foetus with a NOTCH3 mutation

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