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Hypocretin (orexin) loss in Parkinson's disease

Brain (London, England : 1878), 2007-06, Vol.130 (6), p.1577-1585

2007

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Transmigration of beta amyloid specific heavy chain antibody fragments across the in vitro blood–brain barrier

Neuroscience, 2011-09, Vol.190, p.37-42

2011

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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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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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Lumbar disc extrusions reduce faster than bulging discs due to an active role of macrophages in sciatica

Acta neurochirurgica, 2020-01, Vol.162 (1), p.79-85

2020

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Progression and Classification of Granular Osmiophilic Material (GOM) Deposits in Functionally Characterized Human NOTCH3 Transgenic Mice

Translational stroke research, 2020-06, Vol.11 (3), p.517-527

2020

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PRKAR1B mutation associated with a new neurodegenerative disorder with unique pathology

Brain (London, England : 1878), 2014-05, Vol.137 (5), p.1361-1373

2014

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Dementia in hereditary cerebral hemorrhage with amyloidosis-Dutch type is associated with cerebral amyloid angiopathy but is independent of plaques and neurofibrillary tangles

Annals of neurology, 2001-12, Vol.50 (6), p.765-772

2001

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The Effect of Plasma From Muscle-Specific Tyrosine Kinase Myasthenia Patients on Regenerating Endplates

The American journal of pathology, 2009-10, Vol.175 (4), p.1536-1544

2009

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Carotid body tumors are not associated with an increased risk for sleep-disordered breathing

Sleep & breathing, 2014-03, Vol.18 (1), p.103-109

2014

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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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Subcortical lacunar lesions: an MR imaging finding in patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy

Radiology, 2002-09, Vol.224 (3), p.791-796

2002

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Evaluation of diagnostic NOTCH3 immunostaining in CADASIL

Acta neuropathologica, 2003-08, Vol.106 (2), p.107-111

2003

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Secondary microvascular degeneration in amyloid angiopathy of patients with hereditary cerebral hemorrhage with amyloidosis, Dutch type (HCHWA-D)

Acta neuropathologica, 1998-03, Vol.95 (3), p.235-244

1998

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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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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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Numerous and widespread α-synuclein-negative Lewy bodies in an asymptomatic patient

Acta neuropathologica, 1999-05, Vol.97 (5), p.533-539

1999

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Amyloid β precursor protein-mRNA is expressed throughout cerebral vessel walls

Brain research, 1999-05, Vol.828 (1), p.179-183

1999

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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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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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Glioblastoma causing granulocytosis by secretion of granulocyte-colony-stimulating factor

Neurology, 2000-01, Vol.54 (1), p.259-259

2000

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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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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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Toxicity of Dutch (E22Q) and flemish (A21G) mutant amyloid β proteins to human cerebral microvessel and aortic smooth muscle cells. Commentary

Stroke (1970), 2000, Vol.31 (2), p.534-538

2000

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Exocrine pancreatic insufficiency and pancreatic fibrosis due to duodenal somatostatinoma in a patient with neurofibromatosis

Pancreas, 1992, Vol.7 (1), p.98-104

1992

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Hypocretin (orexin) loss in Parkinson's disease

Transmigration of beta amyloid specific heavy chain antibody fragments across the in vitro blood–brain barrier

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

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

Lumbar disc extrusions reduce faster than bulging discs due to an active role of macrophages in sciatica

Progression and Classification of Granular Osmiophilic Material (GOM) Deposits in Functionally Characterized Human NOTCH3 Transgenic Mice

PRKAR1B mutation associated with a new neurodegenerative disorder with unique pathology

Dementia in hereditary cerebral hemorrhage with amyloidosis-Dutch type is associated with cerebral amyloid angiopathy but is independent of plaques and neurofibrillary tangles

The Effect of Plasma From Muscle-Specific Tyrosine Kinase Myasthenia Patients on Regenerating Endplates

Carotid body tumors are not associated with an increased risk for sleep-disordered breathing

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

Subcortical lacunar lesions: an MR imaging finding in patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy

Evaluation of diagnostic NOTCH3 immunostaining in CADASIL

Secondary microvascular degeneration in amyloid angiopathy of patients with hereditary cerebral hemorrhage with amyloidosis, Dutch type (HCHWA-D)

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

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

Numerous and widespread α-synuclein-negative Lewy bodies in an asymptomatic patient

Amyloid β precursor protein-mRNA is expressed throughout cerebral vessel walls

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

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

Glioblastoma causing granulocytosis by secretion of granulocyte-colony-stimulating factor

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

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

Toxicity of Dutch (E22Q) and flemish (A21G) mutant amyloid β proteins to human cerebral microvessel and aortic smooth muscle cells. Commentary

Exocrine pancreatic insufficiency and pancreatic fibrosis due to duodenal somatostatinoma in a patient with neurofibromatosis

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