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

P de Lonlay

Showing results (31-40 of 131) with videos related to

Pageof 14
Sort By:
European Journal of Pediatrics|December 3, 1998
Prevalence of the microdeletion 22q11 in newborn infants with congenital conotruncal cardiac anomaliesL Iserin, P de Lonlay, G Viot, et al.
Human Genetics|August 24, 1999
A mitochondrial cytochrome b mutation but no mutations of nuclearly encoded subunits in ubiquinol cytochrome c reductase (complex III) deficiencyI Valnot, J Kassis, D Chretien, et al.
Clinical Genetics|October 12, 1999
Scalp-ear-nipple (Finlay-Marks) syndrome: a familial case with renal involvementC Picard, S Couderc, T Skojaei, et al.
The Journal of Clinical Endocrinology and Metabolism|September 30, 2011
Morphological mosaicism of the pancreatic islets: a novel anatomopathological form of persistent hyperinsulinemic hypoglycemia of infancyC Sempoux, C Capito, C Bellanné-Chantelot, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 4, 2000
[Carbohydrate-deficient blood glycoprotein syndrome]P de Lonlay, V Cormier-Daire, S Vuillaumier-Barrot, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 1, 1996
[Monoamine decarboxylase deficiency]T Billette de Villemeur, P de Lonlay, F Poggi-Travert, et al.
Molecular Genetics and Metabolism|October 24, 2007
Variable outcome of growth hormone administration in respiratory chain deficiencyS Romano, D Samara, H Crosnier, et al.
European Heart Journal|August 26, 1998
Efficiency of metabolic screening in childhood cardiomyopathiesD Bonnet, P de Lonlay, I Gautier, et al.
Neuropediatrics|August 25, 2001
Respiratory chain deficiency in Alpers syndromeM Gauthier-Villars, P Landrieu, V Cormier-Daire, et al.
Revue Neurologique|April 8, 2020
Sensory neuronopathy as a major clinical feature of mitochondrial trifunctional protein deficiency in adultsY Nadjar, S Souvannanorath, T Maisonobe, et al.
Pageof 14

Showing results (31-40 of 131) with videos related to

Sort By:
Pageof 14
European Journal of Pediatrics|December 3, 1998
Prevalence of the microdeletion 22q11 in newborn infants with congenital conotruncal cardiac anomaliesL Iserin, P de Lonlay, G Viot, et al.
Human Genetics|August 24, 1999
A mitochondrial cytochrome b mutation but no mutations of nuclearly encoded subunits in ubiquinol cytochrome c reductase (complex III) deficiencyI Valnot, J Kassis, D Chretien, et al.
Clinical Genetics|October 12, 1999
Scalp-ear-nipple (Finlay-Marks) syndrome: a familial case with renal involvementC Picard, S Couderc, T Skojaei, et al.
The Journal of Clinical Endocrinology and Metabolism|September 30, 2011
Morphological mosaicism of the pancreatic islets: a novel anatomopathological form of persistent hyperinsulinemic hypoglycemia of infancyC Sempoux, C Capito, C Bellanné-Chantelot, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 4, 2000
[Carbohydrate-deficient blood glycoprotein syndrome]P de Lonlay, V Cormier-Daire, S Vuillaumier-Barrot, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 1, 1996
[Monoamine decarboxylase deficiency]T Billette de Villemeur, P de Lonlay, F Poggi-Travert, et al.
Molecular Genetics and Metabolism|October 24, 2007
Variable outcome of growth hormone administration in respiratory chain deficiencyS Romano, D Samara, H Crosnier, et al.
European Heart Journal|August 26, 1998
Efficiency of metabolic screening in childhood cardiomyopathiesD Bonnet, P de Lonlay, I Gautier, et al.
Neuropediatrics|August 25, 2001
Respiratory chain deficiency in Alpers syndromeM Gauthier-Villars, P Landrieu, V Cormier-Daire, et al.
Revue Neurologique|April 8, 2020
Sensory neuronopathy as a major clinical feature of mitochondrial trifunctional protein deficiency in adultsY Nadjar, S Souvannanorath, T Maisonobe, et al.
Pageof 14