Chatelain P - Search Results

1

A large-scale mutation search reveals genetic heterogeneity in 3M syndrome.

Huber C, Delezoide AL, Guimiot F, Baumann C, Malan V, Le Merrer M, Da Silva DB, Bonneau D, Chatelain P, Chu C, Clark R, Cox H, Edery P, Edouard T, Fano V, Gibson K, Gillessen-Kaesbach G, Giovannucci-Uzielli ML, Graul-Neumann LM, van Hagen JM, van Hest L, Horovitz D, Melki J, Partsch CJ, Plauchu H, Rajab A, Rossi M, Sillence D, Steichen-Gersdorf E, Stewart H, Unger S, Zenker M, Munnich A, Cormier-Daire V. Huber C, et al. Among authors: chatelain p. Eur J Hum Genet. 2009 Mar;17(3):395-400. doi: 10.1038/ejhg.2008.200. Epub 2008 Oct 29. Eur J Hum Genet. 2009. PMID: 19225462 Free PMC article.

2

Acromicric dysplasia: long term outcome and evidence of autosomal dominant inheritance.

Faivre L, Le Merrer M, Baumann C, Polak M, Chatelain P, Sulmont V, Cousin J, Bost M, Cordier MP, Zackai E, Russell K, Finidori G, Pouliquen JC, Munnich A, Maroteaux P, Cormier-Daire V. Faivre L, et al. Among authors: chatelain p. J Med Genet. 2001 Nov;38(11):745-9. doi: 10.1136/jmg.38.11.745. J Med Genet. 2001. PMID: 11694546 Free PMC article.

3

Deletion of mitochondrial DNA in a case of early-onset diabetes mellitus, optic atrophy and deafness (DIDMOAD, Wolfram syndrome).

Rötig A, Cormier V, Chatelain P, Francois R, Saudubray JM, Rustin P, Munnich A. Rötig A, et al. Among authors: chatelain p. J Inherit Metab Dis. 1993;16(3):527-30. doi: 10.1007/BF00711672. J Inherit Metab Dis. 1993. PMID: 7609443 No abstract available.

4

[A familial case of Rothmund-Thomson syndrome. A case in favor of the uniqueness of the syndrome. Association with osteosarcoma].

Rebaud P, David L, Plauchu H, Chatelain P, Moulin G, François R. Rebaud P, et al. Among authors: chatelain p. Pediatrie. 1985 Sep;40(6):487-92. Pediatrie. 1985. PMID: 3869684 French.

5

Deletion of mitochondrial DNA in a case of early-onset diabetes mellitus, optic atrophy, and deafness (Wolfram syndrome, MIM 222300).

Rötig A, Cormier V, Chatelain P, Francois R, Saudubray JM, Rustin P, Munnich A. Rötig A, et al. Among authors: chatelain p. J Clin Invest. 1993 Mar;91(3):1095-8. doi: 10.1172/JCI116267. J Clin Invest. 1993. PMID: 8383698 Free PMC article.

6

Genetic and molecular analysis of familial isolated growth hormone deficiency.

Ruiz-Pacheco R, Chatelain P, Sizonenko PC, Bost M, Garandau P, Sultan C. Ruiz-Pacheco R, et al. Among authors: chatelain p. Hum Genet. 1993 Oct 1;92(3):273-81. doi: 10.1007/BF00244472. Hum Genet. 1993. PMID: 8104861

7

Follow-up of three years of treatment with growth hormone and of one post-treatment year, in children with severe growth retardation of intrauterine onset.

Job JC, Chaussain JL, Job B, Ducret JP, Maes M, Olivier M, Ponte C, Rochiccioli P, Vanderschueren-Lodeweyckx M, Chatelain P. Job JC, et al. Among authors: chatelain p. Pediatr Res. 1996 Feb;39(2):354-9. doi: 10.1203/00006450-199602000-00027. Pediatr Res. 1996. PMID: 8825812 Clinical Trial.

8

Multiple hormone resistance in short children born with intrauterine growth retardation?

Chatelain PG, Nicolino M, Claris O, Salle B, Chaussain J. Chatelain PG, et al. Horm Res. 1998;49 Suppl 2:20-2. doi: 10.1159/000053082. Horm Res. 1998. PMID: 9730667 Review.

9

Growth hormone response to a bolus injection of 1-44 growth-hormone-releasing hormone in very short children with intrauterine onset of growth failure.

Job JC, Chatelain P, Rochiccioli P, Ponte C, Olivier M, Sagnard L. Job JC, et al. Among authors: chatelain p. Horm Res. 1990;33(5):161-5. doi: 10.1159/000181502. Horm Res. 1990. PMID: 2272607

10

[Growth factors, fetal development and fetal growth deficiency].

Chatelain P, Claris O, Lapillonne A, Salle BL. Chatelain P, et al. Arch Pediatr. 1996;3 Suppl 1:184s-185s. doi: 10.1016/0929-693x(96)86035-0. Arch Pediatr. 1996. PMID: 8796010 French. No abstract available.

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