Oostra BA - Search Results

1

Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17.

Hutton M, Lendon CL, Rizzu P, Baker M, Froelich S, Houlden H, Pickering-Brown S, Chakraverty S, Isaacs A, Grover A, Hackett J, Adamson J, Lincoln S, Dickson D, Davies P, Petersen RC, Stevens M, de Graaff E, Wauters E, van Baren J, Hillebrand M, Joosse M, Kwon JM, Nowotny P, Che LK, Norton J, Morris JC, Reed LA, Trojanowski J, Basun H, Lannfelt L, Neystat M, Fahn S, Dark F, Tannenberg T, Dodd PR, Hayward N, Kwok JB, Schofield PR, Andreadis A, Snowden J, Craufurd D, Neary D, Owen F, Oostra BA, Hardy J, Goate A, van Swieten J, Mann D, Lynch T, Heutink P. Hutton M, et al. Among authors: oostra ba. Nature. 1998 Jun 18;393(6686):702-5. doi: 10.1038/31508. Nature. 1998. PMID: 9641683

2

High prevalence of mutations in the microtubule-associated protein tau in a population study of frontotemporal dementia in the Netherlands.

Rizzu P, Van Swieten JC, Joosse M, Hasegawa M, Stevens M, Tibben A, Niermeijer MF, Hillebrand M, Ravid R, Oostra BA, Goedert M, van Duijn CM, Heutink P. Rizzu P, et al. Among authors: oostra ba. Am J Hum Genet. 1999 Feb;64(2):414-21. doi: 10.1086/302256. Am J Hum Genet. 1999. PMID: 9973279 Free PMC article.

3

Construction of a detailed physical and transcript map of the FTDP-17 candidate region on chromosome 17q21.

Froelich S, Houlden H, Rizzu P, Chakraverty S, Baker M, Kwon J, Nowotny P, Isaacs A, Nowotny V, Wauters E, van Baren MJ, Oostra BA, Hardy J, Lannfelt L, Goate A, Hutton M, Lendon CL, Heutink P. Froelich S, et al. Among authors: oostra ba. Genomics. 1999 Sep 1;60(2):129-36. doi: 10.1006/geno.1999.5892. Genomics. 1999. PMID: 10486204

4

Hereditary frontotemporal dementia is linked to chromosome 17q21-q22: a genetic and clinicopathological study of three Dutch families.

Heutink P, Stevens M, Rizzu P, Bakker E, Kros JM, Tibben A, Niermeijer MF, van Duijn CM, Oostra BA, van Swieten JC. Heutink P, et al. Among authors: oostra ba. Ann Neurol. 1997 Feb;41(2):150-9. doi: 10.1002/ana.410410205. Ann Neurol. 1997. PMID: 9029063

5

Characterization and localization of the FMR-1 gene product associated with fragile X syndrome.

Verheij C, Bakker CE, de Graaff E, Keulemans J, Willemsen R, Verkerk AJ, Galjaard H, Reuser AJ, Hoogeveen AT, Oostra BA. Verheij C, et al. Among authors: oostra ba. Nature. 1993 Jun 24;363(6431):722-4. doi: 10.1038/363722a0. Nature. 1993. PMID: 8515814

6

A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis.

Njajou OT, Vaessen N, Joosse M, Berghuis B, van Dongen JW, Breuning MH, Snijders PJ, Rutten WP, Sandkuijl LA, Oostra BA, van Duijn CM, Heutink P. Njajou OT, et al. Among authors: oostra ba. Nat Genet. 2001 Jul;28(3):213-4. doi: 10.1038/90038. Nat Genet. 2001. PMID: 11431687

7

Familial aggregation in frontotemporal dementia.

Stevens M, van Duijn CM, Kamphorst W, de Knijff P, Heutink P, van Gool WA, Scheltens P, Ravid R, Oostra BA, Niermeijer MF, van Swieten JC. Stevens M, et al. Among authors: oostra ba. Neurology. 1998 Jun;50(6):1541-5. doi: 10.1212/wnl.50.6.1541. Neurology. 1998. PMID: 9633692

8

Characterization of the full fragile X syndrome mutation in fetal gametes.

Malter HE, Iber JC, Willemsen R, de Graaff E, Tarleton JC, Leisti J, Warren ST, Oostra BA. Malter HE, et al. Among authors: oostra ba. Nat Genet. 1997 Feb;15(2):165-9. doi: 10.1038/ng0297-165. Nat Genet. 1997. PMID: 9020841

9

A point mutation in the FMR-1 gene associated with fragile X mental retardation.

De Boulle K, Verkerk AJ, Reyniers E, Vits L, Hendrickx J, Van Roy B, Van den Bos F, de Graaff E, Oostra BA, Willems PJ. De Boulle K, et al. Among authors: oostra ba. Nat Genet. 1993 Jan;3(1):31-5. doi: 10.1038/ng0193-31. Nat Genet. 1993. PMID: 8490650

10

Apolipoprotein E gene and sporadic frontal lobe dementia.

Stevens M, van Duijn CM, de Knijff P, van Broeckhoven C, Heutink P, Oostra BA, Niermeijer MF, van Swieten JC. Stevens M, et al. Among authors: oostra ba. Neurology. 1997 Jun;48(6):1526-9. doi: 10.1212/wnl.48.6.1526. Neurology. 1997. PMID: 9191760

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