Dahan K - Search Results

1

Identification of de novo deletion in the factor VIII gene by MLPA technique in two girls with isolated factor VIII deficiency.

Lannoy N, Abinet I, Dahan K, Hermans C. Lannoy N, et al. Among authors: dahan k. Haemophilia. 2009 May;15(3):797-801. doi: 10.1111/j.1365-2516.2008.01974.x. Haemophilia. 2009. PMID: 19432928

2

Laryngeal signs of Ehlers Danlos syndrome in an adult: the first case reported.

Desuter G, Gardiner Q, Dahan K. Desuter G, et al. Among authors: dahan k. Otolaryngol Head Neck Surg. 2009 Sep;141(3):428-9. doi: 10.1016/j.otohns.2009.02.018. Epub 2009 Apr 16. Otolaryngol Head Neck Surg. 2009. PMID: 19716030 No abstract available.

3

Evolution of communication abilities after cochlear implantation in prelingually deaf children.

Gérard JM, Deggouj N, Hupin C, Buisson AL, Monteyne V, Lavis C, Dahan K, Gersdorff M. Gérard JM, et al. Among authors: dahan k. Int J Pediatr Otorhinolaryngol. 2010 Jun;74(6):642-8. doi: 10.1016/j.ijporl.2010.03.010. Epub 2010 Mar 26. Int J Pediatr Otorhinolaryngol. 2010. PMID: 20347162

4

[Is there a link between secondary hemochromatosis and genetics? Apropos of 2 cases].

Paris I, Dahan K, van Ypersele M, Rahier J, Michaux L, Buysschaert M. Paris I, et al. Among authors: dahan k. Acta Clin Belg. 1999 Jan-Feb;54(1):26-9. doi: 10.1080/17843286.1999.11754205. Acta Clin Belg. 1999. PMID: 10192974 French.

5

Clinical expression and insulin sensitivity in type 2 diabetic patients with heterozygous mutations for haemochromatosis.

Van Lerberghe S, Hermans MP, Dahan K, Buysschaert M. Van Lerberghe S, et al. Among authors: dahan k. Diabetes Metab. 2002 Feb;28(1):33-8. Diabetes Metab. 2002. PMID: 11938026

6

Functional classification of ATM variants in ataxia-telangiectasia patients.

Fiévet A, Bellanger D, Rieunier G, Dubois d'Enghien C, Sophie J, Calvas P, Carriere JP, Anheim M, Castrioto A, Flabeau O, Degos B, Ewenczyk C, Mahlaoui N, Touzot F, Suarez F, Hully M, Roubertie A, Aladjidi N, Tison F, Antoine-Poirel H, Dahan K, Doummar D, Nougues MC, Ioos C, Rougeot C, Masurel A, Bourjault C, Ginglinger E, Prieur F, Siri A, Bordigoni P, Nguyen K, Philippe N, Bellesme C, Demeocq F, Altuzarra C, Mathieu-Dramard M, Couderc F, Dörk T, Auger N, Parfait B, Abidallah K, Moncoutier V, Collet A, Stoppa-Lyonnet D, Stern MH. Fiévet A, et al. Among authors: dahan k. Hum Mutat. 2019 Oct;40(10):1713-1730. doi: 10.1002/humu.23778. Epub 2019 May 17. Hum Mutat. 2019. PMID: 31050087

7

Pathological splice mutations outside the invariant AG/GT splice sites of BRCA1 exon 5 increase alternative transcript levels in the 5' end of the BRCA1 gene.

Claes K, Vandesompele J, Poppe B, Dahan K, Coene I, De Paepe A, Messiaen L. Claes K, et al. Among authors: dahan k. Oncogene. 2002 Jun 13;21(26):4171-5. doi: 10.1038/sj.onc.1205520. Oncogene. 2002. PMID: 12037674

8

Rituximab in Patients With Phospholipase A2 Receptor-Associated Membranous Nephropathy and Severe CKD.

Hanset N, Esteve E, Plaisier E, Johanet C, Michel PA, Boffa JJ, Fievet P, Mesnard L, Morelle J, Ronco P, Dahan K. Hanset N, et al. Among authors: dahan k. Kidney Int Rep. 2019 Dec 20;5(3):331-338. doi: 10.1016/j.ekir.2019.12.006. eCollection 2020 Mar. Kidney Int Rep. 2019. PMID: 32154454 Free PMC article.

9

Novel COL4A1 mutations associated with HANAC syndrome: a role for the triple helical CB3[IV] domain.

Plaisier E, Chen Z, Gekeler F, Benhassine S, Dahan K, Marro B, Alamowitch S, Paques M, Ronco P. Plaisier E, et al. Among authors: dahan k. Am J Med Genet A. 2010 Oct;152A(10):2550-5. doi: 10.1002/ajmg.a.33659. Am J Med Genet A. 2010. PMID: 20818663

10

Diagnosis, management, and prognosis of HNF1B nephropathy in adulthood.

Faguer S, Decramer S, Chassaing N, Bellanné-Chantelot C, Calvas P, Beaufils S, Bessenay L, Lengelé JP, Dahan K, Ronco P, Devuyst O, Chauveau D. Faguer S, et al. Among authors: dahan k. Kidney Int. 2011 Oct;80(7):768-76. doi: 10.1038/ki.2011.225. Epub 2011 Jul 20. Kidney Int. 2011. PMID: 21775974 Free article.

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