Snijders PJ - Search Results

1

Congenital sideroblastic anemia due to mutations in the mitochondrial HSP70 homologue HSPA9.

Schmitz-Abe K, Ciesielski SJ, Schmidt PJ, Campagna DR, Rahimov F, Schilke BA, Cuijpers M, Rieneck K, Lausen B, Linenberger ML, Sendamarai AK, Guo C, Hofmann I, Newburger PE, Matthews D, Shimamura A, Snijders PJ, Towne MC, Niemeyer CM, Watson HG, Dziegiel MH, Heeney MM, May A, Bottomley SS, Swinkels DW, Markianos K, Craig EA, Fleming MD. Schmitz-Abe K, et al. Among authors: snijders pj. Blood. 2015 Dec 17;126(25):2734-8. doi: 10.1182/blood-2015-09-659854. Epub 2015 Oct 21. Blood. 2015. PMID: 26491070 Free PMC article.

2

Hereditary sideroblastic anaemia and autosomal inheritance of erythrocyte dimorphism in a Dutch family.

van Waveren Hogervorst GD, van Roermund HP, Snijders PJ. van Waveren Hogervorst GD, et al. Among authors: snijders pj. Eur J Haematol. 1987 May;38(5):405-9. doi: 10.1111/j.1600-0609.1987.tb01436.x. Eur J Haematol. 1987. PMID: 3653362

3

Dominant hemochromatosis due to N144H mutation of SLC11A3: clinical and biological characteristics.

Njajou OT, de Jong G, Berghuis B, Vaessen N, Snijders PJ, Goossens JP, Wilson JH, Breuning MH, Oostra BA, Heutink P, Sandkuijl LA, van Duijn CM. Njajou OT, et al. Among authors: snijders pj. Blood Cells Mol Dis. 2002 Nov-Dec;29(3):439-43. doi: 10.1006/bcmd.2002.0581. Blood Cells Mol Dis. 2002. PMID: 12547233

4

Novel strategy to identify genetic risk factors for COPD severity: a genetic isolate.

van Diemen CC, Postma DS, Aulchenko YS, Snijders PJ, Oostra BA, van Duijn CM, Boezen HM. van Diemen CC, et al. Among authors: snijders pj. Eur Respir J. 2010 Apr;35(4):768-75. doi: 10.1183/09031936.00054408. Epub 2009 Sep 24. Eur Respir J. 2010. PMID: 19797132 Free article.

5

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: snijders pj. Nat Genet. 2001 Jul;28(3):213-4. doi: 10.1038/90038. Nat Genet. 2001. PMID: 11431687

6

A genome-wide search for linkage-disequilibrium with type 1 diabetes in a recent genetically isolated population from the Netherlands.

Vaessen N, Heutink P, Houwing-Duistermaat JJ, Snijders PJ, Rademaker T, Testers L, Batstra MR, Sandkuijl LA, van Duijn CM, Oostra BA. Vaessen N, et al. Among authors: snijders pj. Diabetes. 2002 Mar;51(3):856-9. doi: 10.2337/diabetes.51.3.856. Diabetes. 2002. PMID: 11872691 Free article.

7

A genome-wide search for genes involved in type 2 diabetes in a recently genetically isolated population from the Netherlands.

Aulchenko YS, Vaessen N, Heutink P, Pullen J, Snijders PJ, Hofman A, Sandkuijl LA, Houwing-Duistermaat JJ, Edwards M, Bennett S, Oostra BA, van Duijn CM. Aulchenko YS, et al. Among authors: snijders pj. Diabetes. 2003 Dec;52(12):3001-4. doi: 10.2337/diabetes.52.12.3001. Diabetes. 2003. PMID: 14633863

8

A clinical-genetic study of Parkinson's disease in a genetically isolated community.

Dekker MC, van Swieten JC, Houwing-Duistermaat JJ, Snijders PJ, Boeren E, Hofman A, Breteler MM, Heutink P, Oostra BA, van Duijn CM. Dekker MC, et al. Among authors: snijders pj. J Neurol. 2003 Sep;250(9):1056-62. doi: 10.1007/s00415-003-0151-z. J Neurol. 2003. PMID: 14504966

9

PET neuroimaging and mutations in the DJ-1 gene.

Dekker MC, Eshuis SA, Maguire RP, Veenma-van der Duijn L, Pruim J, Snijders PJ, Oostra BA, van Duijn CM, Leenders KL. Dekker MC, et al. Among authors: snijders pj. J Neural Transm (Vienna). 2004 Dec;111(12):1575-81. doi: 10.1007/s00702-004-0165-4. Epub 2004 Jun 21. J Neural Transm (Vienna). 2004. PMID: 15565491

10

Clinical features and neuroimaging of PARK7-linked parkinsonism.

Dekker M, Bonifati V, van Swieten J, Leenders N, Galjaard RJ, Snijders P, Horstink M, Heutink P, Oostra B, van Duijn C. Dekker M, et al. Mov Disord. 2003 Jul;18(7):751-7. doi: 10.1002/mds.10422. Mov Disord. 2003. PMID: 12815653

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