Sauvat F - Search Results

1

Nutritional outcome in children with severe generalized recessive dystrophic epidermolysis bullosa: a short- and long-term evaluation of gastrostomy and enteral feeding.

Colomb V, Bourdon-Lannoy E, Lambe C, Sauvat F, Hadj Rabia S, Teillac D, De Prost Y, Bodemer C. Colomb V, et al. Among authors: sauvat f. Br J Dermatol. 2012 Feb;166(2):354-61. doi: 10.1111/j.1365-2133.2011.10592.x. Br J Dermatol. 2012. PMID: 21895617

2

Outcome and long-term growth after extensive small bowel resection in the neonatal period: a survey of 87 children.

Goulet O, Baglin-Gobet S, Talbotec C, Fourcade L, Colomb V, Sauvat F, Jais JP, Michel JL, Jan D, Ricour C. Goulet O, et al. Among authors: sauvat f. Eur J Pediatr Surg. 2005 Apr;15(2):95-101. doi: 10.1055/s-2004-821214. Eur J Pediatr Surg. 2005. PMID: 15877257

3

Long-term outcome, growth and digestive function in children 2 to 18 years after intestinal transplantation.

Lacaille F, Vass N, Sauvat F, Canioni D, Colomb V, Talbotec C, De Serre NP, Salomon J, Hugot JP, Cézard JP, Révillon Y, Ruemmele FM, Goulet O. Lacaille F, et al. Among authors: sauvat f. Gut. 2008 Apr;57(4):455-61. doi: 10.1136/gut.2007.133389. Epub 2007 Dec 13. Gut. 2008. PMID: 18079282

4

Factors influencing outcome after intestinal transplantation in children.

Sauvat F, Dupic L, Caldari D, Lesage F, Cezard JP, Lacaille F, Ruemmele F, Hugot JP, Colomb V, Jan D, Hubert P, Revillon Y, Goulet O. Sauvat F, et al. Transplant Proc. 2006 Jul-Aug;38(6):1689-91. doi: 10.1016/j.transproceed.2006.05.033. Transplant Proc. 2006. PMID: 16908249

5

Is intestinal transplantation the future of children with definitive intestinal insufficiency?

Sauvat F, Fusaro F, Lacaille F, Dupic L, Bourdaud N, Colomb V, Hugot JP, Aigrain Y, Goulet O, Revillon Y. Sauvat F, et al. Eur J Pediatr Surg. 2008 Dec;18(6):368-71. doi: 10.1055/s-2008-1038928. Epub 2008 Nov 20. Eur J Pediatr Surg. 2008. PMID: 19023853

6

Results of the Paris program: ten years of pediatric intestinal transplantation.

Goulet O, Sauvat F, Ruemmele F, Caldari D, Damotte D, Cezard JP, Lacaille F, Canioni D, Hugot JP, Berebi D, Sarnacki S, Colomb V, Jan D, Aigrain Y, Revillon Y. Goulet O, et al. Among authors: sauvat f. Transplant Proc. 2005 May;37(4):1667-70. doi: 10.1016/j.transproceed.2005.03.153. Transplant Proc. 2005. PMID: 15919425 No abstract available.

7

Twenty-eight years of intestinal transplantation in Paris: experience of the oldest European center.

Lacaille F, Irtan S, Dupic L, Talbotec C, Lesage F, Colomb V, Salvi N, Moulin F, Sauvat F, Aigrain Y, Revillon Y, Goulet O, Chardot C. Lacaille F, et al. Among authors: sauvat f. Transpl Int. 2017 Feb;30(2):178-186. doi: 10.1111/tri.12894. Transpl Int. 2017. PMID: 27889929 Free article.

8

Intestinal transplantation for total intestinal aganglionosis: a series of 12 consecutive children.

Sauvat F, Grimaldi C, Lacaille F, Ruemmele F, Dupic L, Bourdaud N, Fusaro F, Colomb V, Jan D, Cezard JP, Aigrain Y, Revillon Y, Goulet O. Sauvat F, et al. J Pediatr Surg. 2008 Oct;43(10):1833-8. doi: 10.1016/j.jpedsurg.2008.03.028. J Pediatr Surg. 2008. PMID: 18926216

9

MYO5B and bile salt export pump contribute to cholestatic liver disorder in microvillous inclusion disease.

Girard M, Lacaille F, Verkarre V, Mategot R, Feldmann G, Grodet A, Sauvat F, Irtan S, Davit-Spraul A, Jacquemin E, Ruemmele F, Rainteau D, Goulet O, Colomb V, Chardot C, Henrion-Caude A, Debray D. Girard M, et al. Among authors: sauvat f. Hepatology. 2014 Jul;60(1):301-10. doi: 10.1002/hep.26974. Epub 2014 May 27. Hepatology. 2014. PMID: 24375397

10

Loss-of-function of MYO5B is the main cause of microvillus inclusion disease: 15 novel mutations and a CaCo-2 RNAi cell model.

Ruemmele FM, Müller T, Schiefermeier N, Ebner HL, Lechner S, Pfaller K, Thöni CE, Goulet O, Lacaille F, Schmitz J, Colomb V, Sauvat F, Revillon Y, Canioni D, Brousse N, de Saint-Basile G, Lefebvre J, Heinz-Erian P, Enninger A, Utermann G, Hess MW, Janecke AR, Huber LA. Ruemmele FM, et al. Among authors: sauvat f. Hum Mutat. 2010 May;31(5):544-51. doi: 10.1002/humu.21224. Hum Mutat. 2010. PMID: 20186687

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