Vandenberghe A - Search Results

1

Evidence for allelic heterogeneity in familial early-onset Alzheimer's disease.

van Duijn CM, van Broeckhoven C, Hardy JA, Goate AM, Rossor MN, Vandenberghe A, Martin JJ, Hofman A, Mullan MJ. van Duijn CM, et al. Among authors: vandenberghe a. Br J Psychiatry. 1991 Apr;158:471-4. doi: 10.1192/bjp.158.4.471. Br J Psychiatry. 1991. PMID: 2054561

2

[Genetic coupling study using DNA markers in the familial form of Alzheimer's disease].

Vandenberghe A, Van Broeckhoven C. Vandenberghe A, et al. Acta Neurol Belg. 1989 May-Oct;89(3-4):300-1. Acta Neurol Belg. 1989. PMID: 2516981 Dutch. No abstract available.

3

[Genetic findings in degenerative dementia].

Vandenberghe A, Van Broeckhoven C. Vandenberghe A, et al. Acta Neurol Belg. 1989 May-Oct;89(3-4):194-7. Acta Neurol Belg. 1989. PMID: 2534260 Dutch. No abstract available.

4

Absence of genetic linkage of Charcot-Marie-Tooth disease (HMSN Ia) with chromosome 1 gene markers.

Raeymaekers P, De Jonghe P, Backhovens H, Wehnert A, De Winter G, Swerts L, Gheuens J, Martin JJ, Vandenberghe A, Van Broeckhoven C. Raeymaekers P, et al. Among authors: vandenberghe a. Neurology. 1989 Jun;39(6):844-6. doi: 10.1212/wnl.39.6.844. Neurology. 1989. PMID: 2725880

5

Early-onset Alzheimer's disease in 2 large Belgian families.

Martin JJ, Gheuens J, Bruyland M, Cras P, Vandenberghe A, Masters CL, Beyreuther K, Dom R, Ceuterick C, Lübke U, et al. Martin JJ, et al. Among authors: vandenberghe a. Neurology. 1991 Jan;41(1):62-8. doi: 10.1212/wnl.41.1.62. Neurology. 1991. PMID: 1985297

6

Physical mapping of chromosome 21 DNA markers in Alzheimer's disease region using somatic cell hybrids.

Van Camp G, Van Hul W, Backhovens H, Stinissen P, Wehnert A, Patterson D, Vandenberghe A, Van Broeckhoven C. Van Camp G, et al. Among authors: vandenberghe a. Somat Cell Mol Genet. 1990 May;16(3):241-9. doi: 10.1007/BF01233360. Somat Cell Mol Genet. 1990. PMID: 1972817

7

Assignment of the Charcot-Marie-Tooth neuropathy type 1 (CMT 1a) gene to 17p11.2-p12.

Timmerman V, Raeymaekers P, De Jonghe P, De Winter G, Swerts L, Jacobs K, Gheuens J, Martin JJ, Vandenberghe A, Van Broeckhoven C. Timmerman V, et al. Among authors: vandenberghe a. Am J Hum Genet. 1990 Oct;47(4):680-5. Am J Hum Genet. 1990. PMID: 2220808 Free PMC article.

8

Localization of the mutation in an extended family with Charcot-Marie-Tooth neuropathy (HMSN I).

Raeymaekers P, Timmerman V, De Jonghe P, Swerts L, Gheuens J, Martin JJ, Muylle L, De Winter G, Vandenberghe A, Van Broeckhoven C. Raeymaekers P, et al. Among authors: vandenberghe a. Am J Hum Genet. 1989 Dec;45(6):953-8. Am J Hum Genet. 1989. PMID: 2589322 Free PMC article.

9

Linkage analysis of the Duffy blood group marker with several chromosome 1 genes in an extended pedigree with Charcot-Marie-Tooth disease.

Raeymaekers P, Van Broeckhoven C, Backhovens H, Wehnert A, Muylle L, De Jonghe P, Gheuens J, Martin JJ, Vandenberghe A. Raeymaekers P, et al. Among authors: vandenberghe a. Hum Genet. 1989 Feb;81(3):231-3. doi: 10.1007/BF00278994. Hum Genet. 1989. PMID: 2921030

10

Failure of familial Alzheimer's disease to segregate with the A4-amyloid gene in several European families.

Van Broeckhoven C, Genthe AM, Vandenberghe A, Horsthemke B, Backhovens H, Raeymaekers P, Van Hul W, Wehnert A, Gheuens J, Cras P, et al. Van Broeckhoven C, et al. Among authors: vandenberghe a. Nature. 1987 Sep 10-16;329(6135):153-5. doi: 10.1038/329153a0. Nature. 1987. PMID: 3306405

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