Vaandrager JM - Search Results

1

Postnatal onset of craniosynostosis in a case of Saethre-Chotzen syndrome.

de Heer IM, Hoogeboom J, Vermeij-Keers C, de Klein A, Vaandrager JM. de Heer IM, et al. Among authors: vaandrager jm. J Craniofac Surg. 2004 Nov;15(6):1048-52. doi: 10.1097/00001665-200411000-00034. J Craniofac Surg. 2004. PMID: 15547403

2

Clinical and genetic analysis of patients with Saethre-Chotzen syndrome.

de Heer IM, de Klein A, van den Ouweland AM, Vermeij-Keers C, Wouters CH, Vaandrager JM, Hovius SE, Hoogeboom JM. de Heer IM, et al. Among authors: vaandrager jm. Plast Reconstr Surg. 2005 Jun;115(7):1894-902; discussion 1903-5. doi: 10.1097/01.prs.0000165278.72168.51. Plast Reconstr Surg. 2005. PMID: 15923834

3

Crouzon syndrome: phenotypic signs and symptoms of the postnatally expressed subtype.

Hoefkens MF, Vermeij-Keers C, Vaandrager JM. Hoefkens MF, et al. Among authors: vaandrager jm. J Craniofac Surg. 2004 Mar;15(2):233-40; discussion 241-2. doi: 10.1097/00001665-200403000-00013. J Craniofac Surg. 2004. PMID: 15167238

4

Apoptotic cell death during normal embryogenesis of the coronal suture: early detection of apoptosis in mice using annexin V.

Bourez RL, Mathijssen IM, Vaandrager JM, Vermeij-Keers C. Bourez RL, et al. Among authors: vaandrager jm. J Craniofac Surg. 1997 Nov;8(6):441-5. doi: 10.1097/00001665-199711000-00002. J Craniofac Surg. 1997. PMID: 9477828

5

The role of bone centers in the pathogenesis of craniosynostosis: an embryologic approach using CT measurements in isolated craniosynostosis and Apert and Crouzon syndromes.

Mathijssen IM, Vaandrager JM, van der Meulen JC, Pieterman H, Zonneveld FW, Kreiborg S, Vermeij-Keers C. Mathijssen IM, et al. Among authors: vaandrager jm. Plast Reconstr Surg. 1996 Jul;98(1):17-26. doi: 10.1097/00006534-199607000-00004. Plast Reconstr Surg. 1996. PMID: 8657773

6

Tracing craniosynostosis to its developmental stage through bone center displacement.

Mathijssen IM, van Splunder J, Vermeij-Keers C, Pieterman H, de Jong TH, Mooney MP, Vaandrager JM. Mathijssen IM, et al. Among authors: vaandrager jm. J Craniofac Genet Dev Biol. 1999 Apr-Jun;19(2):57-63. J Craniofac Genet Dev Biol. 1999. PMID: 10416148 Clinical Trial.

7

FGF-4 or FGF-2 administration induces apoptosis, collagen type I expression, and mineralization in the developing coronal suture.

Mathijssen IM, van Leeuwen H, Vermeij-Keers C, Vaandrager JM. Mathijssen IM, et al. Among authors: vaandrager jm. J Craniofac Surg. 2001 Jul;12(4):399-400. doi: 10.1097/00001665-200107000-00019. J Craniofac Surg. 2001. PMID: 11482628 No abstract available.

8

Deletion of the TWIST gene in a large five-generation family.

De Heer IM, Hoogeboom AJ, Eussen HJ, Vaandrager JM, De Klein A. De Heer IM, et al. Among authors: vaandrager jm. Clin Genet. 2004 May;65(5):396-9. doi: 10.1111/j.0009-9163.2004.00244.x. Clin Genet. 2004. PMID: 15099347

9

The frontosphenoidal suture: fetal development and phenotype of its synostosis.

Mathijssen IM, van der Meulen JJ, van Adrichem LN, Vaandrager JM, van der Hulst RR, Lequin MH, Vermeij-Keers C. Mathijssen IM, et al. Among authors: vaandrager jm. Pediatr Radiol. 2008 Apr;38(4):431-7. doi: 10.1007/s00247-008-0750-z. Epub 2008 Jan 26. Pediatr Radiol. 2008. PMID: 18224314

10

Symmetry and morbidity assessment of unilateral complete cleft lip nose corrected with or without primary nasal correction.

Brussé CA, Van der Werff JF, Stevens HP, Vermeij-Keers C, Prahl-Andersen B, Van der Meulen JC, Vaandrager JM. Brussé CA, et al. Among authors: vaandrager jm. Cleft Palate Craniofac J. 1999 Jul;36(4):361-6. doi: 10.1597/1545-1569_1999_036_0361_samaou_2.3.co_2. Cleft Palate Craniofac J. 1999. PMID: 10426604

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