Alders M - Search Results

1

Hematologic abnormalities in Shwachman Diamond syndrome: lack of genotype-phenotype relationship.

Kuijpers TW, Alders M, Tool AT, Mellink C, Roos D, Hennekam RC. Kuijpers TW, et al. Among authors: alders m. Blood. 2005 Jul 1;106(1):356-61. doi: 10.1182/blood-2004-11-4371. Epub 2005 Mar 15. Blood. 2005. PMID: 15769891 Free article.

2

SBDS mutations and isochromosome 7q in a patient with Shwachman-Diamond syndrome: no predisposition to malignant transformation?

Mellink CH, Alders M, van der Lelie H, Hennekam RH, Kuijpers TW. Mellink CH, et al. Among authors: alders m. Cancer Genet Cytogenet. 2004 Oct 15;154(2):144-9. doi: 10.1016/j.cancergencyto.2004.02.001. Cancer Genet Cytogenet. 2004. PMID: 15474150

3

Unilateral condylar hyperplasia in hemifacial hyperplasia, is there genetic proof of overgrowth?

Nolte JW, Alders M, Karssemakers LHE, Becking AG, Hennekam RCM. Nolte JW, et al. Among authors: alders m. Int J Oral Maxillofac Surg. 2020 Nov;49(11):1464-1469. doi: 10.1016/j.ijom.2020.02.002. Epub 2020 Apr 3. Int J Oral Maxillofac Surg. 2020. PMID: 32249036

4

Molecular basis of unilateral condylar hyperplasia?

Nolte JW, Alders M, Karssemakers LHE, Becking AG, Hennekam RCM. Nolte JW, et al. Among authors: alders m. Int J Oral Maxillofac Surg. 2020 Nov;49(11):1397-1401. doi: 10.1016/j.ijom.2020.01.017. Epub 2020 May 16. Int J Oral Maxillofac Surg. 2020. PMID: 32423691

5

Dihydropyrimidine Dehydrogenase Deficiency: Metabolic Disease or Biochemical Phenotype?

Fleger M, Willomitzer J, Meinsma R, Alders M, Meijer J, Hennekam RCM, Huemer M, van Kuilenburg ABP. Fleger M, et al. Among authors: alders m. JIMD Rep. 2017;37:49-54. doi: 10.1007/8904_2017_14. Epub 2017 Mar 9. JIMD Rep. 2017. PMID: 28275972 Free PMC article.

6

Lymphedema-lymphangiectasia-mental retardation (Hennekam) syndrome: a review.

Van Balkom ID, Alders M, Allanson J, Bellini C, Frank U, De Jong G, Kolbe I, Lacombe D, Rockson S, Rowe P, Wijburg F, Hennekam RC. Van Balkom ID, et al. Among authors: alders m. Am J Med Genet. 2002 Nov 1;112(4):412-21. doi: 10.1002/ajmg.10707. Am J Med Genet. 2002. PMID: 12376947 Review.

7

Increased tumour risk for BWS patients correlates with aberrant H19 and not KCNQ1OT1 methylation: occurrence of KCNQ1OT1 hypomethylation in familial cases of BWS.

Bliek J, Maas SM, Ruijter JM, Hennekam RC, Alders M, Westerveld A, Mannens MM. Bliek J, et al. Among authors: alders m. Hum Mol Genet. 2001 Mar 1;10(5):467-76. doi: 10.1093/hmg/10.5.467. Hum Mol Genet. 2001. PMID: 11181570

8

Evaluation of Clinical Manifestations in Patients with Severe Lymphedema with and without CCBE1 Mutations.

Alders M, Mendola A, Adès L, Al Gazali L, Bellini C, Dallapiccola B, Edery P, Frank U, Hornshuh F, Huisman SA, Jagadeesh S, Kayserili H, Keng WT, Lev D, Prada CE, Sampson JR, Schmidtke J, Shashi V, van Bever Y, Van der Aa N, Verhagen JM, Verheij JB, Vikkula M, Hennekam RC. Alders M, et al. Mol Syndromol. 2013 Mar;4(3):107-13. doi: 10.1159/000342486. Epub 2012 Oct 2. Mol Syndromol. 2013. PMID: 23653581 Free PMC article.

9

Specific combinations of biallelic POLR3A variants cause Wiedemann-Rautenstrauch syndrome.

Paolacci S, Li Y, Agolini E, Bellacchio E, Arboleda-Bustos CE, Carrero D, Bertola D, Al-Gazali L, Alders M, Altmüller J, Arboleda G, Beleggia F, Bruselles A, Ciolfi A, Gillessen-Kaesbach G, Krieg T, Mohammed S, Müller C, Novelli A, Ortega J, Sandoval A, Velasco G, Yigit G, Arboleda H, Lopez-Otin C, Wollnik B, Tartaglia M, Hennekam RC. Paolacci S, et al. Among authors: alders m. J Med Genet. 2018 Dec;55(12):837-846. doi: 10.1136/jmedgenet-2018-105528. Epub 2018 Oct 15. J Med Genet. 2018. PMID: 30323018

10

The role of the epinephrine test in the diagnosis and management of children suspected of having congenital long QT syndrome.

Clur SA, Chockalingam P, Filippini LH, Widyanti AP, Van Cruijsen M, Blom NA, Alders M, Hofman N, Wilde AA. Clur SA, et al. Among authors: alders m. Pediatr Cardiol. 2010 May;31(4):462-8. doi: 10.1007/s00246-009-9603-2. Epub 2009 Dec 3. Pediatr Cardiol. 2010. PMID: 19957170 Free PMC article.

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