Cremers CW - Search Results

1

The velo-cardio-facial syndrome: the otorhinolaryngeal manifestations and implications.

Vantrappen G, Rommel N, Cremers CW, Devriendt K, Frijns JP. Vantrappen G, et al. Among authors: cremers cw. Int J Pediatr Otorhinolaryngol. 1998 Oct 2;45(2):133-41. doi: 10.1016/s0165-5876(98)00067-6. Int J Pediatr Otorhinolaryngol. 1998. PMID: 9849681 Review.

2

Clinical features in 130 patients with the velo-cardio-facial syndrome. The Leuven experience.

Vantrappen G, Rommel N, Devriendt K, Cremers CW, Feenstra L, Fryns JP. Vantrappen G, et al. Among authors: cremers cw. Acta Otorhinolaryngol Belg. 2001;55(1):43-8. Acta Otorhinolaryngol Belg. 2001. PMID: 11256191

3

Velo-cardio-facial syndrome: guidelines for diagnosis, treatment and follow-up of ent manifestations.

Vantrappen G, Rommel N, Swillen A, Cremers CW, Fryns JP, Devriendt K. Vantrappen G, et al. Among authors: cremers cw. Acta Otorhinolaryngol Belg. 2003;57(2):101-6. Acta Otorhinolaryngol Belg. 2003. PMID: 12836465 Review.

4

Progressive late-onset sensorineural hearing loss and vestibular impairment with vertigo (DFNA9/COCH): longitudinal analyses in a belgian family.

Lemaire FX, Feenstra L, Huygen PL, Fransen E, Devriendt K, Van Camp G, Vantrappen G, Cremers CW, Wackym PA, Koss JC. Lemaire FX, et al. Among authors: cremers cw. Otol Neurotol. 2003 Sep;24(5):743-8. doi: 10.1097/00129492-200309000-00009. Otol Neurotol. 2003. PMID: 14501450

5

Mosaic trisomy 8 as a cause of velopharyngeal insufficiency.

Vantrappen G, Rommel N, Cremers CW, Fryns JP, Devriendt K. Vantrappen G, et al. Among authors: cremers cw. Am J Med Genet. 2002 Apr 1;108(4):337-8. doi: 10.1002/ajmg.10270. Am J Med Genet. 2002. PMID: 11920842 No abstract available.

6

Autosomal dominant isolated velopharyngeal insufficiency.

Vantrappen G, Rommel N, Wellens W, Cremers CW, Fryns JP, Devriendt K. Vantrappen G, et al. Among authors: cremers cw. Clin Genet. 2002 Jan;61(1):74-6. doi: 10.1034/j.1399-0004.2002.610115.x. Clin Genet. 2002. PMID: 11903361 No abstract available.

7

Congenital aural atresia in 18q deletion or de Grouchy syndrome.

Nuijten I, Admiraal R, Van Buggenhout G, Cremers C, Frijns JP, Smeets D, van Ravenswaaij-Arts C. Nuijten I, et al. Otol Neurotol. 2003 Nov;24(6):900-6. doi: 10.1097/00129492-200311000-00014. Otol Neurotol. 2003. PMID: 14600472

8

Hearing loss in Noonan syndrome.

Cremers CW, van der Burgt CJ. Cremers CW, et al. Int J Pediatr Otorhinolaryngol. 1992 Jan;23(1):81-4. doi: 10.1016/0165-5876(92)90082-z. Int J Pediatr Otorhinolaryngol. 1992. PMID: 1592554 Review.

9

Progressive hearing loss, hypoplasia of the cochlea and widened vestibular aqueducts are very common features in Pendred's syndrome.

Cremers CW, Admiraal RJ, Huygen PL, Bolder C, Everett LA, Joosten FB, Green ED, van Camp G, Otten BJ. Cremers CW, et al. Int J Pediatr Otorhinolaryngol. 1998 Oct 2;45(2):113-23. doi: 10.1016/s0165-5876(98)00123-2. Int J Pediatr Otorhinolaryngol. 1998. PMID: 9849679

10

The presence of a widened vestibular aqueduct and progressive sensorineural hearing loss in the branchio-oto-renal syndrome. A family study.

Stinckens C, Standaert L, Casselman JW, Huygen PL, Kumar S, Van de Wallen J, Cremers CW. Stinckens C, et al. Among authors: cremers cw. Int J Pediatr Otorhinolaryngol. 2001 Jul 2;59(3):163-72. doi: 10.1016/s0165-5876(01)00473-6. Int J Pediatr Otorhinolaryngol. 2001. PMID: 11397497

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