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P de Lonlay-Debeney

Showing results (1-10 of 13) with videos related to

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International Journal of Cardiology|September 18, 1998
Fatty acid beta-oxidation deficiency masquerading as fulminant myocarditisP de Lonlay-Debeney, J C Fournet, D Bonnet
Annales D'Endocrinologie|August 29, 2000
[Molecular basis of hyperinsulinisms]P de Lonlay-Debeney, J J Robert, J M Saudubray
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 8, 2001
[Hyperinsulinism]P de Lonlay-Debeney, J C Fournet, G Touati, et al.
American Journal of Human Genetics|May 12, 2001
Large-scale deletion and point mutations of the nuclear NDUFV1 and NDUFS1 genes in mitochondrial complex I deficiencyP Bénit, D Chretien, N Kadhom, et al.
Neuropediatrics|May 1, 1999
Respiratory chain deficiency presenting as recurrent myoglobinuria in childhoodP de Lonlay-Debeney, P Edery, V Cormier-Daire, et al.
The Journal of Clinical Endocrinology and Metabolism|April 12, 2001
Hyperinsulinism/hyperammonemia syndrome in children with regulatory mutations in the inhibitory guanosine triphosphate-binding domain of glutamate dehydrogenaseC MacMullen, J Fang, B Y Hsu, et al.
American Journal of Medical Genetics|November 7, 1998
Ebstein anomaly associated with rearrangements of chromosomal region 11qP de Lonlay-Debeney, M C de Blois, D Bonnet, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition|February 24, 2000
Practical management of hyperinsulinism in infancyA Aynsley-Green, K Hussain, J Hall, et al.
Journal of Medical Genetics|January 16, 1998
Features of DiGeorge syndrome and CHARGE association in five patientsP de Lonlay-Debeney, V Cormier-Daire, J Amiel, et al.
The New England Journal of Medicine|April 15, 1999
Clinical features of 52 neonates with hyperinsulinismP de Lonlay-Debeney, F Poggi-Travert, J C Fournet, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
International Journal of Cardiology|September 18, 1998
Fatty acid beta-oxidation deficiency masquerading as fulminant myocarditisP de Lonlay-Debeney, J C Fournet, D Bonnet
Annales D'Endocrinologie|August 29, 2000
[Molecular basis of hyperinsulinisms]P de Lonlay-Debeney, J J Robert, J M Saudubray
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 8, 2001
[Hyperinsulinism]P de Lonlay-Debeney, J C Fournet, G Touati, et al.
American Journal of Human Genetics|May 12, 2001
Large-scale deletion and point mutations of the nuclear NDUFV1 and NDUFS1 genes in mitochondrial complex I deficiencyP Bénit, D Chretien, N Kadhom, et al.
Neuropediatrics|May 1, 1999
Respiratory chain deficiency presenting as recurrent myoglobinuria in childhoodP de Lonlay-Debeney, P Edery, V Cormier-Daire, et al.
The Journal of Clinical Endocrinology and Metabolism|April 12, 2001
Hyperinsulinism/hyperammonemia syndrome in children with regulatory mutations in the inhibitory guanosine triphosphate-binding domain of glutamate dehydrogenaseC MacMullen, J Fang, B Y Hsu, et al.
American Journal of Medical Genetics|November 7, 1998
Ebstein anomaly associated with rearrangements of chromosomal region 11qP de Lonlay-Debeney, M C de Blois, D Bonnet, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition|February 24, 2000
Practical management of hyperinsulinism in infancyA Aynsley-Green, K Hussain, J Hall, et al.
Journal of Medical Genetics|January 16, 1998
Features of DiGeorge syndrome and CHARGE association in five patientsP de Lonlay-Debeney, V Cormier-Daire, J Amiel, et al.
The New England Journal of Medicine|April 15, 1999
Clinical features of 52 neonates with hyperinsulinismP de Lonlay-Debeney, F Poggi-Travert, J C Fournet, et al.
Pageof 2