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

Claude Bendavid

Showing results (11-20 of 69) with videos related to

Pageof 7
Sort By:
European Journal of Obstetrics, Gynecology, and Reproductive Biology|December 5, 2017
Serial hCG and progesterone levels to predict early pregnancy outcomes in pregnancies of uncertain viability: A prospective studyClaire Puget, Yolaine Joueidi, Estelle Bauville, et al.
Studies in Health Technology and Informatics|August 23, 2024
Monitoring Variability of Laboratory Results in a Clinical Data Warehouse Using Automatic DashboardMorgane Pierre-Jean, Dalila Rabhi, Denis Delamarre, et al.
European Thyroid Journal|February 25, 2026
Newborn Screening for Congenital Hypothyroidism in France: A Study of Current Professional PracticesMaelle Quenet, Stéphanie Leroux, Claude Bendavid, et al.
Human Genetics|September 15, 2004
FISH diagnosis of the common 57-kb deletion in CTNS causing cystinosisClaude Bendavid, Robert Kleta, Robert Long, et al.
Joint Bone Spine|April 3, 2020
Performance of a new rapid diagnostic test the lactate/glucose ratio of synovial fluid for the diagnosis of septic arthritisOlivia Berthoud, Guillaume Coiffier, Jean-David Albert, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|January 28, 2010
Genetic counseling and "molecular" prenatal diagnosis of holoprosencephaly (HPE)Sandra Mercier, Christèle Dubourg, Marion Belleguic, et al.
BMC Medical Genetics|January 18, 2006
Factor VII deficiency and developmental abnormalities in a patient with partial monosomy of 13q and trisomy of 16p: case report and review of the literatureBrian P Brooks, Jeanne M Meck, Bassem R Haddad, et al.
Clinics and Research in Hepatology and Gastroenterology|March 18, 2015
Portable hemoglobinometer is a reliable technology for the follow-up of venesections tolerance in hemochromatosisMaxime Pawlowski, Fanny Latute, Edouard Bardou-Jacquet, et al.
Clinical Chemistry and Laboratory Medicine|August 8, 2025
A novel corrective model based on red blood cells indices and haemolysis index enables accurate unhaemolysed potassium determination in haemolysed samples - Hemokalc projectCharles R Lefèvre, Bérénice Vigier, Mathilde Favalelli, et al.
Clinical Biochemistry|August 19, 2015
Histamine quantification in human plasma using high resolution accurate mass LC-MS technologyMathieu Laurichesse, Thomas Gicquel, Caroline Moreau, et al.
Pageof 7

Showing results (11-20 of 69) with videos related to

Sort By:
Pageof 7
European Journal of Obstetrics, Gynecology, and Reproductive Biology|December 5, 2017
Serial hCG and progesterone levels to predict early pregnancy outcomes in pregnancies of uncertain viability: A prospective studyClaire Puget, Yolaine Joueidi, Estelle Bauville, et al.
Studies in Health Technology and Informatics|August 23, 2024
Monitoring Variability of Laboratory Results in a Clinical Data Warehouse Using Automatic DashboardMorgane Pierre-Jean, Dalila Rabhi, Denis Delamarre, et al.
European Thyroid Journal|February 25, 2026
Newborn Screening for Congenital Hypothyroidism in France: A Study of Current Professional PracticesMaelle Quenet, Stéphanie Leroux, Claude Bendavid, et al.
Human Genetics|September 15, 2004
FISH diagnosis of the common 57-kb deletion in CTNS causing cystinosisClaude Bendavid, Robert Kleta, Robert Long, et al.
Joint Bone Spine|April 3, 2020
Performance of a new rapid diagnostic test the lactate/glucose ratio of synovial fluid for the diagnosis of septic arthritisOlivia Berthoud, Guillaume Coiffier, Jean-David Albert, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|January 28, 2010
Genetic counseling and "molecular" prenatal diagnosis of holoprosencephaly (HPE)Sandra Mercier, Christèle Dubourg, Marion Belleguic, et al.
BMC Medical Genetics|January 18, 2006
Factor VII deficiency and developmental abnormalities in a patient with partial monosomy of 13q and trisomy of 16p: case report and review of the literatureBrian P Brooks, Jeanne M Meck, Bassem R Haddad, et al.
Clinics and Research in Hepatology and Gastroenterology|March 18, 2015
Portable hemoglobinometer is a reliable technology for the follow-up of venesections tolerance in hemochromatosisMaxime Pawlowski, Fanny Latute, Edouard Bardou-Jacquet, et al.
Clinical Chemistry and Laboratory Medicine|August 8, 2025
A novel corrective model based on red blood cells indices and haemolysis index enables accurate unhaemolysed potassium determination in haemolysed samples - Hemokalc projectCharles R Lefèvre, Bérénice Vigier, Mathilde Favalelli, et al.
Clinical Biochemistry|August 19, 2015
Histamine quantification in human plasma using high resolution accurate mass LC-MS technologyMathieu Laurichesse, Thomas Gicquel, Caroline Moreau, et al.
Pageof 7