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Showing results (331-340 of 381) with videos related to

Pageof 39
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Tumori|October 9, 2002
Sentinel node detection with imaging probeO Schillaci, G D'Errico, R Scafè, et al.
Human Genetics|April 1, 1993
Analysis of 160 CF chromosomes: detection of a novel mutation in exon 20I Dorval, S Odent, P Jezequel, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 28, 2008
[Therapeutic education in cystic fibrosis's children: skills, objectives and guides]V David, J Iguenane, S Ravilly, et al.
Journal of Medical Genetics|May 1, 1992
Familial screening for genetic haemochromatosis by means of DNA markersJ Yaouanq, A el Kahloun, M Chorney, et al.
Gastroenterology|October 27, 1999
Insulin resistance-associated hepatic iron overloadM H Mendler, B Turlin, R Moirand, et al.
Bulletin De L'Academie Nationale De Medecine|February 1, 1993
[Molecular genetics of hemochromatosis]J Y Le Gall, V David, J Yaouanq, et al.
Health Services Insights|April 3, 2026
A Qualitative Study of a Pilot of Clinician Perspectives on the Delivery of Medicare Annual Wellness Visits for Patients with Dementia in an Academic Health Science Center in TexasHuey-Ming Tzeng, Yong-Fang Kuo, Monique R Pappadis, et al.
Minerva Cardioangiologica|April 13, 2012
Dual source CT: state of the art in the depiction of coronary arteries anatomy, anatomical variants and myocardial segmentsC N De Cecco, G Bastarrika, M Arraiza, et al.
Annales De Gastroenterologie Et D'Hepatologie|November 1, 1993
[Molecular genetics of hemochromatosis]J Y Le Gall, V David, J Yaouanq, et al.
Applied Clinical Informatics|January 15, 2016
A Framework for (Tele-) Monitoring of the Rehabilitation Progress in Stroke Patients: eHealth 2015 Special IssueH Jagos, V David, M Haller, et al.
Pageof 39

Showing results (331-340 of 381) with videos related to

Sort By:
Pageof 39
Tumori|October 9, 2002
Sentinel node detection with imaging probeO Schillaci, G D'Errico, R Scafè, et al.
Human Genetics|April 1, 1993
Analysis of 160 CF chromosomes: detection of a novel mutation in exon 20I Dorval, S Odent, P Jezequel, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 28, 2008
[Therapeutic education in cystic fibrosis's children: skills, objectives and guides]V David, J Iguenane, S Ravilly, et al.
Journal of Medical Genetics|May 1, 1992
Familial screening for genetic haemochromatosis by means of DNA markersJ Yaouanq, A el Kahloun, M Chorney, et al.
Gastroenterology|October 27, 1999
Insulin resistance-associated hepatic iron overloadM H Mendler, B Turlin, R Moirand, et al.
Bulletin De L'Academie Nationale De Medecine|February 1, 1993
[Molecular genetics of hemochromatosis]J Y Le Gall, V David, J Yaouanq, et al.
Health Services Insights|April 3, 2026
A Qualitative Study of a Pilot of Clinician Perspectives on the Delivery of Medicare Annual Wellness Visits for Patients with Dementia in an Academic Health Science Center in TexasHuey-Ming Tzeng, Yong-Fang Kuo, Monique R Pappadis, et al.
Minerva Cardioangiologica|April 13, 2012
Dual source CT: state of the art in the depiction of coronary arteries anatomy, anatomical variants and myocardial segmentsC N De Cecco, G Bastarrika, M Arraiza, et al.
Annales De Gastroenterologie Et D'Hepatologie|November 1, 1993
[Molecular genetics of hemochromatosis]J Y Le Gall, V David, J Yaouanq, et al.
Applied Clinical Informatics|January 15, 2016
A Framework for (Tele-) Monitoring of the Rehabilitation Progress in Stroke Patients: eHealth 2015 Special IssueH Jagos, V David, M Haller, et al.
Pageof 39