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Franck Ceppa

Showing results (21-30 of 30) with videos related to

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Annals of Hepatology|September 6, 2007
MDR3 mutations associated with intrahepatic and gallbladder cholesterol cholelithiasis: an updateElvire Mbongo-Kama, Florence Harnois, Didier Mennecier, et al.
Annales De Biologie Clinique|October 23, 2014
[Rapid detection of BCHE atypical variant (p.Asp70Gly) by high resolution melting curve analysis]Isabelle Mabboux, Mélanie Dos Santos, Sébastien Courcelle, et al.
Presse Medicale (Paris, France : 1983)|July 15, 2006
[Urinary dipsticks must not be used to detect diabetes-induced incipient nephropathy]Carine Garcia, Lyse Bordier, Pascal Burnat, et al.
Gastroenterologie Clinique Et Biologique|October 11, 2007
[Acute pancreatitis after treatment by celecoxib]Didier Mennecier, Franck Ceppa, Leila Sinayoko, et al.
Annales De Biologie Clinique|April 7, 2018
[Myoglobin: still a useful biomarker in 2017?]Aurélie Servonnet, Clément Dubost, Guillaume Martin, et al.
Biochemical Pharmacology|September 30, 2014
Characterization of a novel butyrylcholinesterase point mutation (p.Ala34Val), "silent" with mivacuriumHerve Delacour, Sofya Lushchekina, Isabelle Mabboux, et al.
Military Medicine|October 31, 2019
Evaluation of Systematic Blood Testing at the Time of Recruitment to the Armed Forces: Retrospective Monocentric Study Among 726 French Army SoldiersWeniko Caré, Jessica Hénard, Jonathan Gillard, et al.
Plos One|July 24, 2014
Characterization of a novel BCHE "silent" allele: point mutation (p.Val204Asp) causes loss of activity and prolonged apnea with suxamethoniumHerve Delacour, Sofya Lushchekina, Isabelle Mabboux, et al.
The Pharmacogenomics Journal|October 7, 2020
Characterization of four BCHE mutations associated with prolonged effect of suxamethoniumXavier Brazzolotto, Sébastien Courcelle, Christophe Sauvanet, et al.
American Journal of Respiratory and Critical Care Medicine|July 22, 2006
Mutations of DNAI1 in primary ciliary dyskinesia: evidence of founder effect in a common mutationMaimoona A Zariwala, Margaret W Leigh, Franck Ceppa, et al.
Pageof 3

Showing results (21-30 of 30) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 30 results.
Annals of Hepatology|September 6, 2007
MDR3 mutations associated with intrahepatic and gallbladder cholesterol cholelithiasis: an updateElvire Mbongo-Kama, Florence Harnois, Didier Mennecier, et al.
Annales De Biologie Clinique|October 23, 2014
[Rapid detection of BCHE atypical variant (p.Asp70Gly) by high resolution melting curve analysis]Isabelle Mabboux, Mélanie Dos Santos, Sébastien Courcelle, et al.
Presse Medicale (Paris, France : 1983)|July 15, 2006
[Urinary dipsticks must not be used to detect diabetes-induced incipient nephropathy]Carine Garcia, Lyse Bordier, Pascal Burnat, et al.
Gastroenterologie Clinique Et Biologique|October 11, 2007
[Acute pancreatitis after treatment by celecoxib]Didier Mennecier, Franck Ceppa, Leila Sinayoko, et al.
Annales De Biologie Clinique|April 7, 2018
[Myoglobin: still a useful biomarker in 2017?]Aurélie Servonnet, Clément Dubost, Guillaume Martin, et al.
Biochemical Pharmacology|September 30, 2014
Characterization of a novel butyrylcholinesterase point mutation (p.Ala34Val), "silent" with mivacuriumHerve Delacour, Sofya Lushchekina, Isabelle Mabboux, et al.
Military Medicine|October 31, 2019
Evaluation of Systematic Blood Testing at the Time of Recruitment to the Armed Forces: Retrospective Monocentric Study Among 726 French Army SoldiersWeniko Caré, Jessica Hénard, Jonathan Gillard, et al.
Plos One|July 24, 2014
Characterization of a novel BCHE "silent" allele: point mutation (p.Val204Asp) causes loss of activity and prolonged apnea with suxamethoniumHerve Delacour, Sofya Lushchekina, Isabelle Mabboux, et al.
The Pharmacogenomics Journal|October 7, 2020
Characterization of four BCHE mutations associated with prolonged effect of suxamethoniumXavier Brazzolotto, Sébastien Courcelle, Christophe Sauvanet, et al.
American Journal of Respiratory and Critical Care Medicine|July 22, 2006
Mutations of DNAI1 in primary ciliary dyskinesia: evidence of founder effect in a common mutationMaimoona A Zariwala, Margaret W Leigh, Franck Ceppa, et al.
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