C. D. Jonghe

发表

Pathogenic APP mutations near the γ-secretase cleavage site differentially affect Aβ secretion and APP C-terminal fragment stability

B. Strooper, C. Broeckhoven, S. Serneels, 2001 .

Behavioral Disturbances without Amyloid Deposits in Mice Overexpressing Human Amyloid Precursor Protein with Flemish (A692G) or Dutch (E693Q) Mutation

C. Broeckhoven, P. Cras, F. Checler, 2000, Neurobiology of Disease.

Flemish and Dutch Mutations in Amyloid β Precursor Protein Have Different Effects on Amyloid β Secretion

C. Broeckhoven, S. Younkin, L. Hendriks, 1998, Neurobiology of Disease.

CHAPTER 5.6 Identification and functional analysis of genes and genetic risk factors in Alzheimer's disease

C. Broeckhoven, C. Jonghe, C. D. Jonghe, 1999 .

Immunoreactivity of Presenilin-1 and Tau in Alzheimer's Disease Brain

C. Broeckhoven, L. Hendriks, P. Cras, 1998, Experimental 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.

Nonfibrillar diffuse amyloid deposition due to a gamma(42)-secretase site mutation points to an essential role for N-truncated A beta(42) in Alzheimer's disease.

H. Vanderstichele, B. Strooper, B. de Strooper, 2000, Human molecular genetics.

Evidence That Aβ42 Plasma Levels in Presenilin-1 Mutation Carriers Do not Allow for Prediction of Their Clinical Phenotype

H. Vanderstichele, C. Broeckhoven, L. Hendriks, 1999, Neurobiology of Disease.

Presentation of amyloidosis in carriers of the codon 692 mutation in the amyloid precursor protein gene (APP692).

A. Hofman, C. Broeckhoven, C. V. van Duijn, 2000, Brain : a journal 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.