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Page 1
Objectifying Micrognathia Using Three-Dimensional Photogrammetric Analysis.
Basart H, Suttie M, Ibrahim A, Ferretti P, van der Horst CMAM, Hennekam RC, Hammond P. Basart H, et al. Among authors: van der horst cmam. J Craniofac Surg. 2018 Nov;29(8):2106-2109. doi: 10.1097/SCS.0000000000005056. J Craniofac Surg. 2018. PMID: 30320700
CONCLUSION: The 3D facial photogrammetry delineates the general facial characteristics in patients with different syndromes involving micrognathia, and can objectively estimate mandibular volume and growth, with excellent correlation with bony measurement. ...
CONCLUSION: The 3D facial photogrammetry delineates the general facial characteristics in patients with different syndromes involving …
Klippel-Trenaunay syndrome: diagnostic criteria and hypothesis on etiology.
Oduber CE, van der Horst CM, Hennekam RC. Oduber CE, et al. Among authors: van der horst cm. Ann Plast Surg. 2008 Feb;60(2):217-23. doi: 10.1097/SAP.0b013e318062abc1. Ann Plast Surg. 2008. PMID: 18216519 Review.
Klippel-Trenaunay syndrome (KTS) is a congenital malformation syndrome involving blood and lymph vessels and disturbed growth of bone and soft tissues. ...
Klippel-Trenaunay syndrome (KTS) is a congenital malformation syndrome involving blood and lymph vessels and disturbed growth …
Health-related quality of life in children with Robin sequence.
Basart H, van Oers HA, Paes EC, Breugem CC, Don Griot JP, van der Horst CM, Haverman L, Hennekam RC. Basart H, et al. Among authors: van der horst cm. Am J Med Genet A. 2017 Jan;173(1):54-61. doi: 10.1002/ajmg.a.37968. Epub 2016 Sep 20. Am J Med Genet A. 2017. PMID: 27649059
There has been differentiated between those with isolated RS and those with RS as part of a syndrome, and take various treatments into account. All RS families from an earlier described cohort were invited to participate. ...There was no major difference in HRQoL in RS chi …
There has been differentiated between those with isolated RS and those with RS as part of a syndrome, and take various treatments int …
Monozygotic twins discordant for vascular malformations and dysregulated growth.
Oduber CE, Bliek J, van der Horst CM, van Steensel MA, Hennekam RC. Oduber CE, et al. Among authors: van der horst cm. Eur J Med Genet. 2010 Jan-Feb;53(1):14-8. doi: 10.1016/j.ejmg.2009.08.004. Epub 2009 Aug 28. Eur J Med Genet. 2010. PMID: 19716450
We propose that, similarly, disturbed imprinting plays a role in the pathogenesis of VM-DG syndromes in general, and suggest the same may hold for KTS in sensu strictu or Proteus syndrome. Further studies to investigate imprinting status in VM-DG syndromes, i …
We propose that, similarly, disturbed imprinting plays a role in the pathogenesis of VM-DG syndromes in general, and suggest the same …
The persistent embryonic vein in Klippel-Trenaunay syndrome.
Oduber CE, Young-Afat DA, van der Wal AC, van Steensel MA, Hennekam RC, van der Horst CM. Oduber CE, et al. Among authors: van der horst cm. Vasc Med. 2013 Aug;18(4):185-91. doi: 10.1177/1358863X13498463. Vasc Med. 2013. PMID: 23966121
Klippel-Trenaunay syndrome (KTS) is a congenital malformation syndrome with prominent vascular anomalies. ...
Klippel-Trenaunay syndrome (KTS) is a congenital malformation syndrome with prominent vascular anomalies. ...
Frontometaphyseal dysplasia and keloid formation without FLNA mutations.
Basart H, van de Kar A, Adès L, Cho TJ, Carter E, Maas SM, Wilson LC, van der Horst CM, Wade EM, Robertson SP, Hennekam RC. Basart H, et al. Among authors: van der horst cm. Am J Med Genet A. 2015 Jun;167(6):1215-22. doi: 10.1002/ajmg.a.37044. Epub 2015 Apr 21. Am J Med Genet A. 2015. PMID: 25899317
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. Among authors: van der horst cm. 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
PTEN: hamartoma tumor syndrome (PHTS) is a group of syndromes caused by mutations in PTEN. ...
PTEN: hamartoma tumor syndrome (PHTS) is a group of syndromes caused by mutations in PTEN. ...
Etiology and pathogenesis of robin sequence in a large Dutch cohort.
Basart H, Paes EC, Maas SM, van den Boogaard MJ, van Hagen JM, Breugem CC, Cobben JM, Don Griot JP, Lachmeijer AM, Lichtenbelt KD, van Nunen DP, van der Horst CM, Hennekam RC. Basart H, et al. Among authors: van der horst cm. Am J Med Genet A. 2015 Sep;167A(9):1983-92. doi: 10.1002/ajmg.a.37154. Epub 2015 May 31. Am J Med Genet A. 2015. PMID: 26033782
Twenty-two different Mendelian disorders were diagnosed, of which Stickler syndrome was most frequent. Stratification of diagnoses according to (presumed) pathogenic mechanism in 73 non-isolated patients with reliable diagnoses showed 43.9% to have a connective tissue dysp …
Twenty-two different Mendelian disorders were diagnosed, of which Stickler syndrome was most frequent. Stratification of diagnoses ac …
Baseline Quality of Life in patients with Klippel-Trenaunay syndrome.
Oduber CE, Khemlani K, Sillevis Smitt JH, Hennekam RC, van der Horst CM. Oduber CE, et al. Among authors: van der horst cm. J Plast Reconstr Aesthet Surg. 2010 Apr;63(4):603-9. doi: 10.1016/j.bjps.2009.01.055. Epub 2009 Mar 16. J Plast Reconstr Aesthet Surg. 2010. PMID: 19289309
BACKGROUND: Klippel-Trenaunay syndrome (KTS) is a congenital group of disorders characterised by vascular malformations (capillary malformation (CM), venous malformation (VM), and lymphatic malformation (LM)) and disturbed growth regulation. ...
BACKGROUND: Klippel-Trenaunay syndrome (KTS) is a congenital group of disorders characterised by vascular malformations (capillary ma …
12 results