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

D Cheillan

Showing results (11-20 of 22) with videos related to

Pageof 3
Sort By:
Journal of Inherited Metabolic Disease|April 8, 2006
Genetic heterogeneity of the GLDC gene in 28 unrelated patients with glycine encephalopathyC Conter, M O Rolland, D Cheillan, et al.
Journal of Medical Genetics|April 5, 2005
Clinical, morphological, and molecular aspects of sialic acid storage disease manifesting in uteroR Froissart, D Cheillan, R Bouvier, et al.
Annales De Biologie Clinique|June 23, 1999
[A surprising aglycorrachia! A case of neurocysticercosis]D Cheillan, J Bancel, C Tiliket, et al.
Journal of Inherited Metabolic Disease|January 26, 2006
False-positive results in neonatal screening for cystic fibrosis based on a three-stage protocol (IRT/DNA/IRT): Should we adjust IRT cut-off to ethnic origin?D Cheillan, M Vercherat, F Chevalier-Porst, et al.
Diabetes & Metabolism|April 15, 2019
Large triglyceride-rich lipoproteins from fasting patients with type 2 diabetes activate plateletsM M Boulet, D Cheillan, M Di Filippo, et al.
Neuromuscular Disorders : NMD|June 18, 2013
Creatine deficiency syndrome. A treatable myopathy due to arginine-glycine amidinotransferase (AGAT) deficiencyS Nouioua, D Cheillan, S Zaouidi, et al.
Neurology|November 15, 2006
High frequency of creatine deficiency syndromes in patients with unexplained mental retardationL Lion-François, D Cheillan, G Pitelet, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 17, 2012
[Medium-chain acyl-CoA-dehydrogenase (MCAD) deficiency: French consensus for neonatal screening, diagnosis, and management]F Feillet, H Ogier, D Cheillan, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 30, 2022
Neonatal screening for congenital hypothyroidism: Time to lower the TSH threshold in FranceL Levaillant, F Huet, P Bretones, et al.
Beneficial Microbes|May 13, 2026
Gut commensal Bacteroides faecichinchillae, a potential novel candidate of next-generation probiotics targeting type 2 diabetesM Godet, E Delmas, C Gérard, et al.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
Journal of Inherited Metabolic Disease|April 8, 2006
Genetic heterogeneity of the GLDC gene in 28 unrelated patients with glycine encephalopathyC Conter, M O Rolland, D Cheillan, et al.
Journal of Medical Genetics|April 5, 2005
Clinical, morphological, and molecular aspects of sialic acid storage disease manifesting in uteroR Froissart, D Cheillan, R Bouvier, et al.
Annales De Biologie Clinique|June 23, 1999
[A surprising aglycorrachia! A case of neurocysticercosis]D Cheillan, J Bancel, C Tiliket, et al.
Journal of Inherited Metabolic Disease|January 26, 2006
False-positive results in neonatal screening for cystic fibrosis based on a three-stage protocol (IRT/DNA/IRT): Should we adjust IRT cut-off to ethnic origin?D Cheillan, M Vercherat, F Chevalier-Porst, et al.
Diabetes & Metabolism|April 15, 2019
Large triglyceride-rich lipoproteins from fasting patients with type 2 diabetes activate plateletsM M Boulet, D Cheillan, M Di Filippo, et al.
Neuromuscular Disorders : NMD|June 18, 2013
Creatine deficiency syndrome. A treatable myopathy due to arginine-glycine amidinotransferase (AGAT) deficiencyS Nouioua, D Cheillan, S Zaouidi, et al.
Neurology|November 15, 2006
High frequency of creatine deficiency syndromes in patients with unexplained mental retardationL Lion-François, D Cheillan, G Pitelet, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 17, 2012
[Medium-chain acyl-CoA-dehydrogenase (MCAD) deficiency: French consensus for neonatal screening, diagnosis, and management]F Feillet, H Ogier, D Cheillan, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 30, 2022
Neonatal screening for congenital hypothyroidism: Time to lower the TSH threshold in FranceL Levaillant, F Huet, P Bretones, et al.
Beneficial Microbes|May 13, 2026
Gut commensal Bacteroides faecichinchillae, a potential novel candidate of next-generation probiotics targeting type 2 diabetesM Godet, E Delmas, C Gérard, et al.
Pageof 3