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Page 1
Respiratory chain deficiency in Alpers syndrome.
Gauthier-Villars M, Landrieu P, Cormier-Daire V, Jacquemin E, Chrétien D, Rötig A, Rustin P, Munnich A, de Lonlay P. Gauthier-Villars M, et al. Among authors: jacquemin e. Neuropediatrics. 2001 Jun;32(3):150-2. doi: 10.1055/s-2001-16614. Neuropediatrics. 2001. PMID: 11521212
Long-term outcome of pediatric liver transplantation for biliary atresia: a 10-year follow-up in a single center.
Fouquet V, Alves A, Branchereau S, Grabar S, Debray D, Jacquemin E, Devictor D, Durand P, Baujard C, Fabre M, Pariente D, Chardot C, Dousset B, Massault PP, Bernard D, Houssin D, Bernard O, Gauthier F, Soubrane O. Fouquet V, et al. Among authors: jacquemin e. Liver Transpl. 2005 Feb;11(2):152-60. doi: 10.1002/lt.20358. Liver Transpl. 2005. PMID: 15666395 Free article.
CFC1 gene involvement in biliary atresia with polysplenia syndrome.
Davit-Spraul A, Baussan C, Hermeziu B, Bernard O, Jacquemin E. Davit-Spraul A, et al. Among authors: jacquemin e. J Pediatr Gastroenterol Nutr. 2008 Jan;46(1):111-2. doi: 10.1097/01.mpg.0000304465.60788.f4. J Pediatr Gastroenterol Nutr. 2008. PMID: 18162845
258 results