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C Corpechot

Showing results (11-20 of 21) with videos related to

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Journal of Hepatology|October 11, 2001
Apolipoprotein E polymorphism, a marker of disease severity in primary biliary cirrhosis?C Corpechot, P Benlian, V Barbu, et al.
The American Journal of Gastroenterology|October 1, 1996
Acute renal failure associated with nonfulminant hepatitis A viral infectionJ F Cadranel, C Corpechot, V Di Martino, et al.
Gastroenterologie Clinique Et Biologique|April 27, 2010
Triple therapy with ursodeoxycholic acid, budesonide and mycophenolate mofetil in patients with features of severe primary biliary cirrhosis not responding to ursodeoxycholic acid aloneN Rabahi, Y Chrétien, F Gaouar, et al.
The American Journal of Pathology|October 9, 1999
Hepatocellular hypoxia-induced vascular endothelial growth factor expression and angiogenesis in experimental biliary cirrhosisO Rosmorduc, D Wendum, C Corpechot, et al.
Gastroenterologie Clinique Et Biologique|January 1, 1994
[Cholestatic viral hepatitis A in adults. Clinical, biological and histopathological study of 9 cases]C Corpechot, J F Cadranel, C Hoang, et al.
The American Journal of Gastroenterology|December 22, 1998
Granulocytic sarcoma of the jejunum: a rare cause of small bowel obstructionC Corpechot, M Lémann, I Brocheriou, et al.
Clinics and Research in Hepatology and Gastroenterology|March 25, 2024
Endoscopic features of low-phospholipid-associated cholelithiasis syndrome: A retrospective cohort studyG Salin, C Corpechot, S Ouazana, et al.
Lancet (London, England)|December 6, 1997
Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patientsA Joutel, K Vahedi, C Corpechot, et al.
Alimentary Pharmacology & Therapeutics|November 4, 2015
The safety and efficacy of nasobiliary drainage in the treatment of refractory cholestatic pruritus: a multicentre European studyV S Hegade, M Krawczyk, A E Kremer, et al.
Annals of the New York Academy of Sciences|November 5, 1997
Notch3 mutations in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), a mendelian condition causing stroke and vascular dementiaA Joutel, C Corpechot, A Ducros, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Journal of Hepatology|October 11, 2001
Apolipoprotein E polymorphism, a marker of disease severity in primary biliary cirrhosis?C Corpechot, P Benlian, V Barbu, et al.
The American Journal of Gastroenterology|October 1, 1996
Acute renal failure associated with nonfulminant hepatitis A viral infectionJ F Cadranel, C Corpechot, V Di Martino, et al.
Gastroenterologie Clinique Et Biologique|April 27, 2010
Triple therapy with ursodeoxycholic acid, budesonide and mycophenolate mofetil in patients with features of severe primary biliary cirrhosis not responding to ursodeoxycholic acid aloneN Rabahi, Y Chrétien, F Gaouar, et al.
The American Journal of Pathology|October 9, 1999
Hepatocellular hypoxia-induced vascular endothelial growth factor expression and angiogenesis in experimental biliary cirrhosisO Rosmorduc, D Wendum, C Corpechot, et al.
Gastroenterologie Clinique Et Biologique|January 1, 1994
[Cholestatic viral hepatitis A in adults. Clinical, biological and histopathological study of 9 cases]C Corpechot, J F Cadranel, C Hoang, et al.
The American Journal of Gastroenterology|December 22, 1998
Granulocytic sarcoma of the jejunum: a rare cause of small bowel obstructionC Corpechot, M Lémann, I Brocheriou, et al.
Clinics and Research in Hepatology and Gastroenterology|March 25, 2024
Endoscopic features of low-phospholipid-associated cholelithiasis syndrome: A retrospective cohort studyG Salin, C Corpechot, S Ouazana, et al.
Lancet (London, England)|December 6, 1997
Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patientsA Joutel, K Vahedi, C Corpechot, et al.
Alimentary Pharmacology & Therapeutics|November 4, 2015
The safety and efficacy of nasobiliary drainage in the treatment of refractory cholestatic pruritus: a multicentre European studyV S Hegade, M Krawczyk, A E Kremer, et al.
Annals of the New York Academy of Sciences|November 5, 1997
Notch3 mutations in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), a mendelian condition causing stroke and vascular dementiaA Joutel, C Corpechot, A Ducros, et al.
Pageof 3