Guettier C - Search Results

1

Spontaneous evolution patterns of focal congenital hepatic hemangiomas: a case series of 25 patients.

Rutten C, Ladarre D, Ackermann O, Gonzales E, Guettier C, Franchi-Abella S. Rutten C, et al. Among authors: guettier c. Pediatr Radiol. 2022 May;52(6):1048-1060. doi: 10.1007/s00247-021-05277-4. Epub 2022 Feb 28. Pediatr Radiol. 2022. PMID: 35229180

2

Liver nodules after portal systemic shunt surgery for extrahepatic portal vein obstruction in children.

Guérin F, Porras J, Fabre M, Guettier C, Pariente D, Bernard O, Gauthier F. Guérin F, et al. Among authors: guettier c. J Pediatr Surg. 2009 Jul;44(7):1337-43. doi: 10.1016/j.jpedsurg.2008.11.003. J Pediatr Surg. 2009. PMID: 19573658

3

Arthrogryposis, renal dysfunction, and cholestasis syndrome caused by VIPAR mutation.

Ackermann O, Gonzales E, Keller M, Guettier C, Gissen P, Jacquemin E. Ackermann O, et al. Among authors: guettier c. J Pediatr Gastroenterol Nutr. 2014 Mar;58(3):e29-32. doi: 10.1097/MPG.0b013e318298108f. J Pediatr Gastroenterol Nutr. 2014. PMID: 23636179 No abstract available.

4

Targeted pharmacotherapy in progressive familial intrahepatic cholestasis type 2: Evidence for improvement of cholestasis with 4-phenylbutyrate.

Gonzales E, Grosse B, Schuller B, Davit-Spraul A, Conti F, Guettier C, Cassio D, Jacquemin E. Gonzales E, et al. Among authors: guettier c. Hepatology. 2015 Aug;62(2):558-66. doi: 10.1002/hep.27767. Epub 2015 Apr 8. Hepatology. 2015. PMID: 25716872

5

DCDC2 Mutations Cause Neonatal Sclerosing Cholangitis.

Girard M, Bizet AA, Lachaux A, Gonzales E, Filhol E, Collardeau-Frachon S, Jeanpierre C, Henry C, Fabre M, Viremouneix L, Galmiche L, Debray D, Bole-Feysot C, Nitschke P, Pariente D, Guettier C, Lyonnet S, Heidet L, Bertholet A, Jacquemin E, Henrion-Caude A, Saunier S. Girard M, et al. Among authors: guettier c. Hum Mutat. 2016 Oct;37(10):1025-9. doi: 10.1002/humu.23031. Epub 2016 Aug 24. Hum Mutat. 2016. PMID: 27319779

6

MYO5B mutations cause cholestasis with normal serum gamma-glutamyl transferase activity in children without microvillous inclusion disease.

Gonzales E, Taylor SA, Davit-Spraul A, Thébaut A, Thomassin N, Guettier C, Whitington PF, Jacquemin E. Gonzales E, et al. Among authors: guettier c. Hepatology. 2017 Jan;65(1):164-173. doi: 10.1002/hep.28779. Epub 2016 Oct 5. Hepatology. 2017. PMID: 27532546

7

Mutations in the novel gene FOPV are associated with familial autosomal dominant and non-familial obliterative portal venopathy.

Besmond C, Valla D, Hubert L, Poirier K, Grosse B, Guettier C, Bernard O, Gonzales E, Jacquemin E. Besmond C, et al. Among authors: guettier c. Liver Int. 2018 Feb;38(2):358-364. doi: 10.1111/liv.13547. Epub 2017 Sep 12. Liver Int. 2018. PMID: 28792652

8

Long-term outcome of liver transplantation in childhood: A study of 20-year survivors.

Martinelli J, Habes D, Majed L, Guettier C, Gonzalès E, Linglart A, Larue C, Furlan V, Pariente D, Baujard C, Branchereau S, Gauthier F, Jacquemin E, Bernard O. Martinelli J, et al. Among authors: guettier c. Am J Transplant. 2018 Jul;18(7):1680-1689. doi: 10.1111/ajt.14626. Epub 2018 Jan 12. Am J Transplant. 2018. PMID: 29247469 Free article.

9

Morphological characterization of chronic antibody-mediated rejection in ABO-identical or ABO-compatible pediatric liver graft recipients.

Dao M, Habès D, Taupin JL, Mussini C, Redon MJ, Suberbielle C, Jacquemin E, Gonzales E, Guettier C. Dao M, et al. Among authors: guettier c. Liver Transpl. 2018 Jul;24(7):897-907. doi: 10.1002/lt.25187. Liver Transpl. 2018. PMID: 29704327

10

Cholic acid for primary bile acid synthesis defects: a life-saving therapy allowing a favorable outcome in adulthood.

Gonzales E, Matarazzo L, Franchi-Abella S, Dabadie A, Cohen J, Habes D, Hillaire S, Guettier C, Taburet AM, Myara A, Jacquemin E. Gonzales E, et al. Among authors: guettier c. Orphanet J Rare Dis. 2018 Oct 29;13(1):190. doi: 10.1186/s13023-018-0920-5. Orphanet J Rare Dis. 2018. PMID: 30373615 Free PMC article.

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