Cremers CW - Search Results

1

SDHAF2 mutations in familial and sporadic paraganglioma and phaeochromocytoma.

Bayley JP, Kunst HP, Cascon A, Sampietro ML, Gaal J, Korpershoek E, Hinojar-Gutierrez A, Timmers HJ, Hoefsloot LH, Hermsen MA, Suárez C, Hussain AK, Vriends AH, Hes FJ, Jansen JC, Tops CM, Corssmit EP, de Knijff P, Lenders JW, Cremers CW, Devilee P, Dinjens WN, de Krijger RR, Robledo M. Bayley JP, et al. Among authors: cremers cw. Lancet Oncol. 2010 Apr;11(4):366-72. doi: 10.1016/S1470-2045(10)70007-3. Epub 2010 Jan 11. Lancet Oncol. 2010. PMID: 20071235

2

SDHAF2 (PGL2-SDH5) and hereditary head and neck paraganglioma.

Kunst HP, Rutten MH, de Mönnink JP, Hoefsloot LH, Timmers HJ, Marres HA, Jansen JC, Kremer H, Bayley JP, Cremers CW. Kunst HP, et al. Among authors: cremers cw. Clin Cancer Res. 2011 Jan 15;17(2):247-54. doi: 10.1158/1078-0432.CCR-10-0420. Epub 2011 Jan 11. Clin Cancer Res. 2011. PMID: 21224366 Free article.

3

Proximal symphalangism, hyperopia, conductive hearing impairment, and the NOG gene: 2 new mutations.

Thomeer HG, Admiraal RJ, Hoefsloot L, Kunst HP, Cremers CW. Thomeer HG, et al. Among authors: cremers cw. Otol Neurotol. 2011 Jun;32(4):632-8. doi: 10.1097/MAO.0b013e318211fada. Otol Neurotol. 2011. PMID: 21358557

4

Hearing loss and connexin 26.

Kemperman MH, Hoefsloot LH, Cremers CW. Kemperman MH, et al. Among authors: cremers cw. J R Soc Med. 2002 Apr;95(4):171-7. doi: 10.1177/014107680209500403. J R Soc Med. 2002. PMID: 11934905 Free PMC article. Review. No abstract available.

5

Hensen EF, Goeman JJ, Oosting J, Van der Mey AG, Hogendoorn PC, Cremers CW, Devilee P, Cornelisse CJ. Hensen EF, et al. Among authors: cremers cw. BMC Med Genomics. 2009 May 11;2:25. doi: 10.1186/1755-8794-2-25. BMC Med Genomics. 2009. PMID: 19432956 Free PMC article.

6

Clinical report on the L95P mutation in a Dutch family with paraganglioma.

Cremers CW, De Mönnink JP, Arts N, Joosten FB, Kremer H, Hoefsloot L. Cremers CW, et al. Otol Neurotol. 2002 Sep;23(5):755-9. doi: 10.1097/00129492-200209000-00024. Otol Neurotol. 2002. PMID: 12218630

7

Clinical characteristics of a Dutch DFNA9 family with a novel COCH mutation, G87W.

Pauw RJ, Collin RW, Huygen PL, Hoefsloot LH, Kremer H, Cremers CW. Pauw RJ, et al. Among authors: cremers cw. Audiol Neurootol. 2007;12(2):77-84. doi: 10.1159/000097794. Epub 2006 Dec 6. Audiol Neurootol. 2007. PMID: 17264471

8

Phenotypes of two Dutch DFNA3 families with mutations in GJB2.

Weegerink NJ, Pennings RJ, Huygen PL, Hoefsloot LH, Cremers CW, Kunst HP. Weegerink NJ, et al. Among authors: cremers cw. Ann Otol Rhinol Laryngol. 2011 Mar;120(3):191-7. doi: 10.1177/000348941112000308. Ann Otol Rhinol Laryngol. 2011. PMID: 21510145

9

Congenital stapes ankylosis associated with another ossicular chain anomaly: surgical results in 30 ears.

Thomeer HG, Kunst HP, Cremers CW. Thomeer HG, et al. Among authors: cremers cw. Arch Otolaryngol Head Neck Surg. 2011 Sep;137(9):935-41. doi: 10.1001/archoto.2011.137. Arch Otolaryngol Head Neck Surg. 2011. PMID: 21930985

10

SDH5, a gene required for flavination of succinate dehydrogenase, is mutated in paraganglioma.

Hao HX, Khalimonchuk O, Schraders M, Dephoure N, Bayley JP, Kunst H, Devilee P, Cremers CW, Schiffman JD, Bentz BG, Gygi SP, Winge DR, Kremer H, Rutter J. Hao HX, et al. Among authors: cremers cw. Science. 2009 Aug 28;325(5944):1139-42. doi: 10.1126/science.1175689. Epub 2009 Jul 23. Science. 2009. PMID: 19628817 Free PMC article.

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