Fayon M - Search Results

1

Splice mutation 1811+1.6kbA>G causes severe cystic fibrosis with pancreatic insufficiency: report of 11 compound heterozygous and two homozygous patients.

Reboul MP, Bieth E, Fayon M, Biteau N, Barbier R, Dromer C, Desgeorges M, Claustres M, Bremont F, Lacombe D, Iron A. Reboul MP, et al. Among authors: fayon m. J Med Genet. 2002 Nov;39(11):e73. doi: 10.1136/jmg.39.11.e73. J Med Genet. 2002. PMID: 12414835 Free PMC article. No abstract available.

2

Neonatal Noonan syndrome with a molluscoid cutaneous excess over the scalp.

Lacombe D, Taieb A, Masson P, Fayon M, Demarquez JL. Lacombe D, et al. Among authors: fayon m. Genet Couns. 1991;2(4):249-53. Genet Couns. 1991. PMID: 1799426

3

[Unusual form of Noonan syndrome: neonatal multi-organ involvement with chylothorax and nevoid Cutis verticis gyrata].

Masson P, Fayon M, Lamireau T, Llanas B, Lacombe D, Taïeb A, Demarquez JL. Masson P, et al. Among authors: fayon m. Pediatrie. 1993;48(1):59-62. Pediatrie. 1993. PMID: 8392694 French.

4

Abdominal lymphatic dysplasia and 22q11 microdeletion.

Mansir T, Lacombe D, Lamireau T, Taine L, Chateil JF, Le Bail B, Demarquez JL, Fayon M. Mansir T, et al. Among authors: fayon m. Genet Couns. 1999;10(1):67-70. Genet Couns. 1999. PMID: 10191431

5

[Etiology of chronic cough in children: analysis of 100 cases].

Brémont F, Micheau P, Le Roux P, Brouard J, Pin I, Fayon M. Brémont F, et al. Among authors: fayon m. Arch Pediatr. 2001 Aug;8 Suppl 3:645-649. doi: 10.1016/s0929-693x(01)80021-x. Arch Pediatr. 2001. PMID: 11683089 French.

6

Renal impairment in children with cystic fibrosis.

Andrieux A, Harambat J, Bui S, Nacka F, Iron A, Llanas B, Fayon M. Andrieux A, et al. Among authors: fayon m. J Cyst Fibros. 2010 Jul;9(4):263-8. doi: 10.1016/j.jcf.2010.03.006. Epub 2010 Apr 21. J Cyst Fibros. 2010. PMID: 20413352 Free article.

7

Dehydroepiandrosterone (DHEA) improves pulmonary hypertension in chronic obstructive pulmonary disease (COPD): a pilot study.

Dumas de La Roque E, Savineau JP, Metivier AC, Billes MA, Kraemer JP, Doutreleau S, Jougon J, Marthan R, Moore N, Fayon M, Baulieu EÉ, Dromer C. Dumas de La Roque E, et al. Among authors: fayon m. Ann Endocrinol (Paris). 2012 Feb;73(1):20-5. doi: 10.1016/j.ando.2011.12.005. Epub 2012 Jan 26. Ann Endocrinol (Paris). 2012. PMID: 22280813 Clinical Trial.

8

[Pulmonary inflammation in cystic fibrosis].

Bui S, Boisserie-Lacroix V, Ceccato F, Clouzeau H, Debeleix S, Fayon M. Bui S, et al. Among authors: fayon m. Arch Pediatr. 2012 May;19 Suppl 1:S8-12. doi: 10.1016/S0929-693X(12)71100-4. Arch Pediatr. 2012. PMID: 22682493 French.

9

Central venous thrombosis and thrombophilia in cystic fibrosis: A prospective study.

Munck A, Kheniche A, Alberti C, Hubert D, Martine RG, Nove-Josserand R, Pin I, Bremont F, Chiron R, Couderc L, Dalphin ML, Darviot E, Delaisi B, Dominique S, Durieu I, Fanton A, Fayon M, Gérardin M, Giniès JL, Giraut C, Grenet D, Guillot M, Huet F, Le Bourgeois M, Murris-Epin M, Ramel S, Sardet A, Sermet-Gaudelus I, Varaigne F, Wanin S, Weiss L, Hurtaud MF. Munck A, et al. Among authors: fayon m. J Cyst Fibros. 2015 Jan;14(1):97-103. doi: 10.1016/j.jcf.2014.05.015. Epub 2014 Aug 5. J Cyst Fibros. 2015. PMID: 25107684 Free article.

10

[New tools in cystic fibrosis].

Dournes G, De Boeck K, Bui S, Vermeulen F, Ramalho A, Chateil JF, Laurent F, Fayon M. Dournes G, et al. Among authors: fayon m. Arch Pediatr. 2016 Dec;23(12S):12S39-12S46. doi: 10.1016/S0929-693X(17)30061-1. Arch Pediatr. 2016. PMID: 28231892 Review. French.

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