Cavé H - Search Results

1

Neuropsychological dysfunction and developmental defects associated with genetic changes in infants with neonatal diabetes mellitus: a prospective cohort study [corrected].

Busiah K, Drunat S, Vaivre-Douret L, Bonnefond A, Simon A, Flechtner I, Gérard B, Pouvreau N, Elie C, Nimri R, De Vries L, Tubiana-Rufi N, Metz C, Bertrand AM, Nivot-Adamiak S, de Kerdanet M, Stuckens C, Jennane F, Souchon PF, Le Tallec C, Désirée C, Pereira S, Dechaume A, Robert JJ, Phillip M, Scharfmann R, Czernichow P, Froguel P, Vaxillaire M, Polak M, Cavé H; French NDM study group. Busiah K, et al. Among authors: cave h. Lancet Diabetes Endocrinol. 2013 Nov;1(3):199-207. doi: 10.1016/S2213-8587(13)70059-7. Epub 2013 Sep 6. Lancet Diabetes Endocrinol. 2013. PMID: 24622368

2

Delineation of a 6 cM commonly deleted region in childhood acute lymphoblastic leukemia on the 6q chromosomal arm.

Gérard B, Cavé H, Guidal C, Dastugue N, Vilmer E, Grandchamp B. Gérard B, et al. Among authors: cave h. Leukemia. 1997 Feb;11(2):228-32. doi: 10.1038/sj.leu.2400566. Leukemia. 1997. PMID: 9009085

3

Refinement of the 6q chromosomal region implicated in transient neonatal diabetes.

Cavé H, Polak M, Drunat S, Denamur E, Czernichow P. Cavé H, et al. Diabetes. 2000 Jan;49(1):108-13. doi: 10.2337/diabetes.49.1.108. Diabetes. 2000. PMID: 10615957

4

Glucokinase gene mutations are not a common cause of permanent neonatal diabetes in France.

Vaxillaire M, Samson C, Cavé H, Metz C, Froguel P, Polak M. Vaxillaire M, et al. Among authors: cave h. Diabetologia. 2002 Mar;45(3):454-5. doi: 10.1007/s00125-001-0741-1. Diabetologia. 2002. PMID: 11914755 No abstract available.

5

Neonatal diabetes mellitus: chromosomal analysis in transient and permanent cases.

Metz C, Cavé H, Bertrand AM, Deffert C, Gueguen-Giroux B, Czernichow P, Polak M; NDM French Study Group. Neonatal diabetes mellitus. Metz C, et al. Among authors: cave h. J Pediatr. 2002 Oct;141(4):483-9. doi: 10.1067/mpd.2002.127089. J Pediatr. 2002. PMID: 12378186 Clinical Trial.

6

Kir6.2 mutations are a common cause of permanent neonatal diabetes in a large cohort of French patients.

Vaxillaire M, Populaire C, Busiah K, Cavé H, Gloyn AL, Hattersley AT, Czernichow P, Froguel P, Polak M. Vaxillaire M, et al. Among authors: cave h. Diabetes. 2004 Oct;53(10):2719-22. doi: 10.2337/diabetes.53.10.2719. Diabetes. 2004. PMID: 15448107

7

Activating mutations in the ABCC8 gene in neonatal diabetes mellitus.

Babenko AP, Polak M, Cavé H, Busiah K, Czernichow P, Scharfmann R, Bryan J, Aguilar-Bryan L, Vaxillaire M, Froguel P. Babenko AP, et al. Among authors: cave h. N Engl J Med. 2006 Aug 3;355(5):456-66. doi: 10.1056/NEJMoa055068. N Engl J Med. 2006. PMID: 16885549 Free article.

8

Neonatal diabetes mellitus: a disease linked to multiple mechanisms.

Polak M, Cavé H. Polak M, et al. Among authors: cave h. Orphanet J Rare Dis. 2007 Mar 9;2:12. doi: 10.1186/1750-1172-2-12. Orphanet J Rare Dis. 2007. PMID: 17349054 Free PMC article. Review.

9

New ABCC8 mutations in relapsing neonatal diabetes and clinical features.

Vaxillaire M, Dechaume A, Busiah K, Cavé H, Pereira S, Scharfmann R, de Nanclares GP, Castano L, Froguel P, Polak M; SUR1-Neonatal Diabetes Study Group. Vaxillaire M, et al. Among authors: cave h. Diabetes. 2007 Jun;56(6):1737-41. doi: 10.2337/db06-1540. Epub 2007 Mar 27. Diabetes. 2007. PMID: 17389331

10

The spectrum of cardiac anomalies in Noonan syndrome as a result of mutations in the PTPN11 gene.

Sznajer Y, Keren B, Baumann C, Pereira S, Alberti C, Elion J, Cavé H, Verloes A. Sznajer Y, et al. Among authors: cave h. Pediatrics. 2007 Jun;119(6):e1325-31. doi: 10.1542/peds.2006-0211. Epub 2007 May 21. Pediatrics. 2007. PMID: 17515436

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