Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

C Acquaviva

Showing results (51-60 of 58) with videos related to

Pageof 6
Sort By:
You have reached the last page of results.This site can display upto 58 results.
Cell|December 15, 2000
Evolutionary implications of the frequent horizontal transfer of mismatch repair genesE Denamur, G Lecointre, P Darlu, et al.
Radiology|December 1, 1994
Intervertebral disk vacuum phenomenon secondary to vertebral collapse: prevalence and significanceP F Lafforgue, C J Chagnaud, L M Daver, et al.
Revue Neurologique|October 16, 2018
Myopathy with MTCYB mutation mimicking Multiple Acyl-CoA Dehydrogenase DeficiencyE Kaphan, H Bou Ali, M Gastaldi, et al.
Revue Neurologique|April 4, 2016
Multiple acyl-CoA dehydrogenase deficiency (MADD) as a cause of late-onset treatable metabolic diseaseA Béhin, C Acquaviva-Bourdain, S Souvannanorath, et al.
Molecular Genetics and Metabolism|May 10, 2011
Comprehensive cDNA study and quantitative analysis of mutant HADHA and HADHB transcripts in a French cohort of 52 patients with mitochondrial trifunctional protein deficiencyA Boutron, C Acquaviva, C Vianey-Saban, et al.
Molecular Genetics and Metabolism|June 2, 2007
Equine biochemical multiple acyl-CoA dehydrogenase deficiency (MADD) as a cause of rhabdomyolysisC M Westermann, M G M de Sain-van der Velden, J H van der Kolk, et al.
JIMD Reports|February 23, 2016
Pilot Experience with an External Quality Assurance Scheme for Acylcarnitines in Plasma/SerumP Ruiz Sala, G Ruijter, C Acquaviva, et al.
Leukemia|March 8, 2012
The EuroChimerism concept for a standardized approach to chimerism analysis after allogeneic stem cell transplantationT Lion, F Watzinger, S Preuner, et al.
Pageof 6

Showing results (51-60 of 58) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 58 results.
Cell|December 15, 2000
Evolutionary implications of the frequent horizontal transfer of mismatch repair genesE Denamur, G Lecointre, P Darlu, et al.
Radiology|December 1, 1994
Intervertebral disk vacuum phenomenon secondary to vertebral collapse: prevalence and significanceP F Lafforgue, C J Chagnaud, L M Daver, et al.
Revue Neurologique|October 16, 2018
Myopathy with MTCYB mutation mimicking Multiple Acyl-CoA Dehydrogenase DeficiencyE Kaphan, H Bou Ali, M Gastaldi, et al.
Revue Neurologique|April 4, 2016
Multiple acyl-CoA dehydrogenase deficiency (MADD) as a cause of late-onset treatable metabolic diseaseA Béhin, C Acquaviva-Bourdain, S Souvannanorath, et al.
Molecular Genetics and Metabolism|May 10, 2011
Comprehensive cDNA study and quantitative analysis of mutant HADHA and HADHB transcripts in a French cohort of 52 patients with mitochondrial trifunctional protein deficiencyA Boutron, C Acquaviva, C Vianey-Saban, et al.
Molecular Genetics and Metabolism|June 2, 2007
Equine biochemical multiple acyl-CoA dehydrogenase deficiency (MADD) as a cause of rhabdomyolysisC M Westermann, M G M de Sain-van der Velden, J H van der Kolk, et al.
JIMD Reports|February 23, 2016
Pilot Experience with an External Quality Assurance Scheme for Acylcarnitines in Plasma/SerumP Ruiz Sala, G Ruijter, C Acquaviva, et al.
Leukemia|March 8, 2012
The EuroChimerism concept for a standardized approach to chimerism analysis after allogeneic stem cell transplantationT Lion, F Watzinger, S Preuner, et al.
Pageof 6