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Items: 6

1.

No association of the trace amine-associated receptor 6 with bipolar disorder in a northern Swedish population.

Venken T, Alaerts M, Adolfsson R, Broeckhoven CV, Del-Favero J.

Psychiatr Genet. 2006 Feb;16(1):1-2. No abstract available.

PMID:
16395122
2.

Genetic variability in the regulatory region of presenilin 1 associated with risk for Alzheimer's disease and variable expression.

Theuns J, Del-Favero J, Dermaut B, van Duijn CM, Backhovens H, Van den Broeck MV, Serneels S, Corsmit E, Van Broeckhoven CV, Cruts M.

Hum Mol Genet. 2000 Feb 12;9(3):325-31.

PMID:
10655540
3.

Hereditary motor and sensory neuropathy associated with auditory neuropathy in a Gypsy family.

Leonardis L, Zidar J, Popovič M, Timmerman V, Löfgren A, Broeckhoven CV, Butinar D.

Pflugers Arch. 2000 Jan;439(Suppl 1):r208-r210. doi: 10.1007/s004240000148.

PMID:
28176125
4.

Mutation analysis of a putative sialyltransferase gene, the SFRS2 splicing factor gene and the c-myb ET-locus in two families with hereditary neuralgic amyotrophy (HNA).

Kuhlenbaeumer G, Meuleman J, Schirmacher A, Stoegbauer F, Ringelstein EB, Wehnert M, Hoeltzenbein M, Broeckhoven CV, Timmerman V.

Ann Hum Genet. 1998 Sep;62(Pt 5):397-400.

5.

Beta-amyloid precursor protein and early-onset Alzheimer's disease.

Hendriks L, Jonghe CDXs, Cras P, Martin JJ, Broeckhoven CV.

Ciba Found Symp. 1996;199:170-80.

PMID:
8915610
6.

Screening for the beta-amyloid precursor protein mutation (APP717: Val----Ile) in extended pedigrees with early onset Alzheimer's disease.

Chartier-Harlin MC, Crawford F, Hamandi K, Mullan M, Goate A, Hardy J, Backhovens H, Martin JJ, Broeckhoven CV.

Neurosci Lett. 1991 Aug 5;129(1):134-5.

PMID:
1922963

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