Alders MY - Search Results

1

International point prevalence study of Intensive Care Unit transfusion practices-Pilot study in the Netherlands.

de Bruin S, Alders MY, van Bruggen R, de Korte D, Scheeren TWL, Bakker J, Aubron C, Feldheiser A, Meier J, Cecconi M, Vlaar APJ; Cardiovascular Dynamics Section and Transfusion Task Force of the ESICM; Collaborators. de Bruin S, et al. Among authors: alders my. Transfus Clin Biol. 2019 Nov;26(4):202-208. doi: 10.1016/j.tracli.2019.09.002. Epub 2019 Sep 26. Transfus Clin Biol. 2019. PMID: 31635996

2

Etiology of mental retardation in children referred to a tertiary care center: a prospective study.

van Karnebeek CD, Scheper FY, Abeling NG, Alders M, Barth PG, Hoovers JM, Koevoets C, Wanders RJ, Hennekam RC. van Karnebeek CD, et al. Am J Ment Retard. 2005 Jul;110(4):253-67. doi: 10.1352/0895-8017(2005)110[253:EOMRIC]2.0.CO;2. Am J Ment Retard. 2005. PMID: 15941363

3

Active cascade screening in primary inherited arrhythmia syndromes: does it lead to prophylactic treatment?

Hofman N, Tan HL, Alders M, van Langen IM, Wilde AA. Hofman N, et al. J Am Coll Cardiol. 2010 Jun 8;55(23):2570-6. doi: 10.1016/j.jacc.2009.12.063. J Am Coll Cardiol. 2010. PMID: 20513597 Free article.

4

Identifying underlying medical causes of pediatric obesity: Results of a systematic diagnostic approach in a pediatric obesity center.

Kleinendorst L, Abawi O, van der Voorn B, Jongejan MHTM, Brandsma AE, Visser JA, van Rossum EFC, van der Zwaag B, Alders M, Boon EMJ, van Haelst MM, van den Akker ELT. Kleinendorst L, et al. PLoS One. 2020 May 8;15(5):e0232990. doi: 10.1371/journal.pone.0232990. eCollection 2020. PLoS One. 2020. PMID: 32384097 Free PMC article.

5

A locus for hereditary capillary malformations mapped on chromosome 5q.

Breugem CC, Alders M, Salieb-Beugelaar GB, Mannens MM, Van der Horst CM, Hennekam RC. Breugem CC, et al. Hum Genet. 2002 Apr;110(4):343-7. doi: 10.1007/s00439-002-0700-z. Epub 2002 Mar 2. Hum Genet. 2002. PMID: 11941483

6

Congenital aplastic anemia caused by mutations in the SBDS gene: a rare presentation of Shwachman-Diamond syndrome.

Kuijpers TW, Nannenberg E, Alders M, Bredius R, Hennekam RC. Kuijpers TW, et al. Pediatrics. 2004 Sep;114(3):e387-91. doi: 10.1542/peds.2003-0651-F. Pediatrics. 2004. PMID: 15342903

7

Mutations in CCBE1 cause generalized lymph vessel dysplasia in humans.

Alders M, Hogan BM, Gjini E, Salehi F, Al-Gazali L, Hennekam EA, Holmberg EE, Mannens MM, Mulder MF, Offerhaus GJ, Prescott TE, Schroor EJ, Verheij JB, Witte M, Zwijnenburg PJ, Vikkula M, Schulte-Merker S, Hennekam RC. Alders M, et al. Nat Genet. 2009 Dec;41(12):1272-4. doi: 10.1038/ng.484. Nat Genet. 2009. PMID: 19935664

8

Phenotypic variability in a family with capillary malformations caused by a mutation in the RASA1 gene.

de Wijn RS, Oduber CE, Breugem CC, Alders M, Hennekam RC, van der Horst CM. de Wijn RS, et al. Eur J Med Genet. 2012 Mar;55(3):191-5. doi: 10.1016/j.ejmg.2012.01.009. Epub 2012 Jan 28. Eur J Med Genet. 2012. PMID: 22342634

9

PTEN hamartoma tumor syndrome and Gorham-Stout phenomenon.

Hopman SM, Van Rijn RR, Eng C, Bras J, Alders M, van der Horst CM, Hennekam RC, Merks JH. Hopman SM, et al. Am J Med Genet A. 2012 Jul;158A(7):1719-23. doi: 10.1002/ajmg.a.35406. Epub 2012 May 24. Am J Med Genet A. 2012. PMID: 22628360

10

Intellectual disability and hemizygous GPD2 mutation.

Barge-Schaapveld DQ, Ofman R, Knegt AC, Alders M, Höhne W, Kemp S, Hennekam RC. Barge-Schaapveld DQ, et al. Am J Med Genet A. 2013 May;161A(5):1044-50. doi: 10.1002/ajmg.a.35873. Epub 2013 Mar 29. Am J Med Genet A. 2013. PMID: 23554088

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