J. Haan

R. Roos, M. Bornebroek, J. Haan, 1999, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

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

R. Roos, P. Eikelenboom, A. Rozemuller, 1994, Journal of neuropathology and experimental neurology.

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

R. Roos, S. Duinen, M. Maat‐Schieman, 2004, Acta Neuropathologica.

Hereditary cerebral hemorrhage with amyloidosis — Dutch type

R. Roos, W. Luyendijk, M. Herpers, 1989, Clinical Neurology and Neurosurgery.

Hereditary cerebral hemorrhage with amyloidosis-Dutch type

B. Bloem, R. Roos, P. Algra, 2004, Neuroradiology.

Hereditary cerebral hemorrhage with amyloidosis dutch type (AβPP 693): decreased plasma amyloid-β 42 concentration

C. Broeckhoven, R. Roos, S. Younkin, 2003, Neurobiology of Disease.

Prevalence of subjective dysphagia in community residents aged over 87.

B. Bloem, R. Roos, A. Wintzen, 1990, BMJ.

Elevated Spinal Fluid Pressure as only Sign of Cerebral Venous Thrombosis

B. V. van Hilten, A. Wintzen, J. Haan, 1988, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Cerebral venous thrombosis as presenting sign of myeloproliferative disorders.

A. Wintzen, F. V. D. van der Meer, J. Caekebeke, 1988, Journal of neurology, neurosurgery, and psychiatry.

Mortality from hereditary cerebral haemorrhage with amyloidosis--Dutch type. The impact of sex, parental transmission and year of birth.

C. Broeckhoven, C. van Broeckhoven, R. Roos, 1997, Brain : a journal of neurology.

Progressive dementia, without cerebral hemorrhage, in a patient with hereditary cerebral amyloid angiopathy

R. Roos, A. Jennekens‐Schinkel, R. Roos, 1992, Clinical neurology and neurosurgery (Dutch-Flemish ed. Print).

DNA diagnosis for hereditary cerebral hemorrhage with amyloidosis (Dutch type)

C. van Broeckhoven, W. Hul, E. Bakker, 1991, American journal of human genetics.

Alzheimer's disease and hereditary cerebral hemorrhage with amyloidosis–dutch type share a decrease in cerebrospinal fluid levels of amyloid β‐protein precursor

R. Roos, S. Wagner, W. V. Van Nostrand, 1992 .

Parenchymal preamyloid and amyloid deposits in the brains of patients with hereditary cerebral hemorrhage with amyloidosis—Dutch type

F. Tagliavini, B. Frangione, J. Haan, 1990, Neuroscience Letters.

Pathological Changes in Hereditary Cerebral Hemorrhage with Amyloidosis — Dutch Type

S. Duinen, G. Bots, J. Haan, 1991 .

Amyloid beta protein precursor gene and hereditary cerebral hemorrhage with amyloidosis (Dutch).

J. Hardy, C. Broeckhoven, C. van Broeckhoven, 1990, Science.

Binding of amyloid β precursor protein to coagulation factor XIa in vivo may favour haemorrhagic stroke

R. Roos, P. A. von dem Borne, J. Meijers, 1998, Journal of Neurology.

Comparison between the Icelandic and Dutch forms of hereditary cerebral amyloid angiopathy

R. Roos, J. Haan, 1992, Clinical Neurology and Neurosurgery.

Hereditary Cerebral Hemorrhage with Amyloidosis—Dutch Type: A Congophilic Angiopathy

C. Broeckhoven, R. Roos, J. Haan, 1991 .

Alzheimer A4 peptide, gamma‐trace, leukoencephalopathy, and hereditary cerebral hemorrhage with amyloidosis–dutch type

R. Roos, J. Haan, 1991, Annals of neurology.

Dementia in hereditary cerebral hemorrhage with amyloidosis-Dutch type.

R. Roos, J. Lanser, J. Haan, 1990, Archives of neurology.

Cerebral metabolism in Alzheimer's disease

H. Weinstein, A. Hijdra, J. Haan, 1989, Neurology.

Clinical and Genetic Aspects of Hereditary Cerebral Hemorrhage with Amyloidosis Dutch Type (HCHW A-D)

R. Roos, M. Bornebroek, J. Haan, 2000 .

Cerebral infarction in hereditary spherocytosis.

J. J. van Hilten, J. C. van de Nes, A. Wintzen, 1989, Stroke.

Investigation of Gait in Elderly Subjects Over 88 Years of Age

B. Bloem, R. Roos, A. Wintzen, 1992, Journal of geriatric psychiatry and neurology.

Coexistence of Cystatin C and p Protein Immunoreactivity

R. Roos, J. Haan, 2005 .

Coexistence of cystatin C and beta protein immunoreactivity.

R. Roos, J. Haan, 1990, Stroke.

Hereditary cerebral hemorrhage with amyloidosis — Dutch type: its importance for Alzheimer research

J. Hardy, R. Roos, J. Haan, 1991, Trends in Neurosciences.

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

R. Roos, H. Vinters, S. V. van Duinen, 1998, Stroke.

Lymphocyte concanavalin A capping in hereditary cerebral haemorrhage with amyloidosis — Dutch type

R. Roos, O. Buruma, J. Haan, 1990, Journal of Neurology.

Presenilin‐I polymorphism and hereditary cerebral hemorrhage with amyloidosis, Dutch type

C. Broeckhoven, C. van Broeckhoven, M. van Buchem, 1997, Annals of neurology.

Hereditary Cerebral Hemorrhage with Amyloidosis -Dutch Type: A Study of Fibrinolysis

R. Roos, F. Leebeek, C. Kluft, 1992, Thrombosis and Haemostasis.

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

R. Roos, S. V. van Duinen, R. Natté, 2001, Annals of neurology.

Idiopathic Senile Gait Disorders Are Signs of Subclinical Disease

J. Gussekloo, A. Lagaay, B R Bloem, 2000, Journal of the American Geriatrics Society.

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

R. Roos, H. Vinters, S. V. van Duinen, 1998, Acta Neuropathologica.

The MPTP model: versatile contributions to the treatment of idiopathic Parkinson's disease

B. R. Bloem, J. W. Langston, B. Bloem, 1990, Journal of the Neurological Sciences.

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

C. Broeckhoven, C. van Broeckhoven, M. van Buchem, 1997, Annals of neurology.

White matter lesions and cognitive deterioration in presymptomatic carriers of the amyloid precursor protein gene codon 693 mutation.

M. van Buchem, R. Roos, M. Zoeteweij, 1996, Archives of neurology.

Hereditary cerebral hemorrhage with amyloidosis Dutch type (AbetaPP 693): decreased plasma amyloid-beta 42 concentration.

C. van Broeckhoven, R. Roos, S. Younkin, 2003, Neurobiology of disease.

The apolipoprotein E ε4 allele does not influence the clinical expression of the amyloid precursor protein gene codon 693 or 692 mutations

C. van Broeckhoven, C. V. van Duijn, J. V. van Swieten, 1994, Annals of neurology.

A four-generation Dutch family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), linked to chromosome 19p13

R. Ophoff, P. Scheltens, R. Frants, 1995, Clinical Neurology and Neurosurgery.

Clinical aspects of cerebral amyloid angiopathy.

R. Roos, J. Haan, M. Maat-Schieman, 1994, Dementia.

[Gait impairment in the oldest old].

B. Bloem, R. Roos, A. Wintzen, 1997, Tijdschrift voor gerontologie en geriatrie.

SPECT in the diagnosis of Alzheimer's disease and multi-infarct-dementia

E. Pauwels, R. Dunnewold, H. Weinstein, 1991, Clinical Neurology and Neurosurgery.

Cortical tissue of patients with hereditary cerebral hemorrhage with amyloidosis (Dutch) contains various extracellular matrix deposits.

R. Roos, S. V. van Duinen, J. Bruijn, 1995, Laboratory investigation; a journal of technical methods and pathology.

Hereditary Cerebral Hemorrhage with Amyloidosis- DutchType: Better Correlation of Cognitive Deterioration with Advancing Age than with Number of Focal Lesions or White Matter Hyperintensities

M. van Buchem, F. T. de Bruïne, J. Lanser, 1996, Alzheimer disease and associated disorders.

Cerebral microbleeds in CADASIL

M. Ferrari, H. V. van Houwelingen, M. van Buchem, 2001, Neurology.

Potential for imaging cerebral amyloid deposits using 123I-labelled serum amyloid P component and SPET.

R. Roos, E. Pauwels, N. Verhoeff, 1996, Nuclear medicine communications.

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: structural MR imaging changes and apolipoprotein E genotype.

M. Ferrari, M. van Buchem, M. Buchem, 2006, AJNR. American journal of neuroradiology.

Supplementary motor area activation preceding externally triggered movements

R. Roos, J. Haan, E. Bakker, 1995, Annals of neurology.

Hereditary cerebral hemorrhage with amyloidosis dutch type (AβPP 693): decreased plasma amyloid-β 42 concentration

C. Broeckhoven, R. Roos, S. Younkin, 2003, Neurobiology of Disease.

Alzheimer's disease and hereditary cerebral hemorrhage with amyloidosis-Dutch type share a decrease in cerebrospinal fluid levels of amyloid beta-protein precursor.

R. Roos, S. Wagner, W. V. Van Nostrand, 1992, Annals of neurology.

Single photon emission computed tomography in Alzheimer's disease.

E. V. van Royen, H. Weinstein, A. Hijdra, 1989, Archives of neurology.

Hereditary cerebral hemorrhage with amyloidosis-Dutch type. Clinical and computed tomographic analysis of 24 cases.

J. Haan, R. Roos, P. Algra, 1990, Archives of neurology.