E. Bakker

发表

PRKAR1B mutation associated with a new neurodegenerative disorder with unique pathology.

J. Lebbink, A. Smit, W. Kamphorst, 2014, Brain : a journal of neurology.

Diagnostic Notch3 sequence analysis in CADASIL: Three new mutations in Dutch patients

J. Haan, J. V. van Gestel, R. Frants, 1999, Neurology.

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).

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 .

Familial Pick's disease and dementia in frontal lobe degeneration of non-Alzheimer type are not variants of prion disease.

M. Palmer, J. Hardy, A. Brun, 1994, Journal of neurology, neurosurgery, and psychiatry.

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

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

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

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

Hereditary frontotemporal dementia is linked to chromosome 17q21—q22: A genetic and clinicopathological study of three dutch families

P. Heutink, B. Oostra, C. V. van Duijn, 1997, Annals of neurology.

Cerebral microbleeds in CADASIL

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

An unusual variant of Becker muscular dystrophy

G. van Ommen, M. de Visser, P. Bolhuis, 1990, Annals 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.

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

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

Parental history of Alzheimer disease associated with lower plasma apolipoprotein E levels

W. M. van der Flier, P. Eikelenboom, R. Westendorp, 2009, Neurology.

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.

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 beta-protein precursor.

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