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P de Lonlay

Showing results (71-80 of 131) with videos related to

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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 De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 9, 2003
[Failure to thrive and intestinal diseases in congenital disorders of glycosylation]M Zentilin Boyer, P de Lonlay, N Seta, et al.
Molecular Genetics and Metabolism|April 28, 2009
The first founder DGUOK mutation associated with hepatocerebral mitochondrial DNA depletion syndromeN Brahimi, M Jambou, E Sarzi, et al.
Journal of Inherited Metabolic Disease|June 10, 2006
Methylmalonic and propionic acidurias: management without or with a few supplements of specific amino acid mixtureG Touati, V Valayannopoulos, K Mention, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 28, 2015
Two new cases of serine deficiency disorders treated with l-serineA Brassier, V Valayannopoulos, N Bahi-Buisson, et al.
Journal of Medical Genetics|December 20, 2003
Recurrent de novo mitochondrial DNA mutations in respiratory chain deficiencyS Lebon, M Chol, P Benit, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|February 17, 2015
Early and late complications after liver transplantation for propionic acidemia in children: a two centers studyF Charbit-Henrion, F Lacaille, P McKiernan, et al.
Neuropediatrics|March 17, 2006
Molar tooth sign and superior vermian dysplasia: a radiological, clinical, and genetic studyS Romano, N Boddaert, I Desguerre, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 4, 2005
[Congenital hyperinsulinism in newborn and infant]I Giurgea, M-J Ribeiro, N Boddaert, et al.
The Journal of Clinical Investigation|October 14, 1998
Paternal mutation of the sulfonylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasiaV Verkarre, J C Fournet, P de Lonlay, et al.
Pageof 14

Showing results (71-80 of 131) with videos related to

Sort By:
Pageof 14
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 De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 9, 2003
[Failure to thrive and intestinal diseases in congenital disorders of glycosylation]M Zentilin Boyer, P de Lonlay, N Seta, et al.
Molecular Genetics and Metabolism|April 28, 2009
The first founder DGUOK mutation associated with hepatocerebral mitochondrial DNA depletion syndromeN Brahimi, M Jambou, E Sarzi, et al.
Journal of Inherited Metabolic Disease|June 10, 2006
Methylmalonic and propionic acidurias: management without or with a few supplements of specific amino acid mixtureG Touati, V Valayannopoulos, K Mention, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 28, 2015
Two new cases of serine deficiency disorders treated with l-serineA Brassier, V Valayannopoulos, N Bahi-Buisson, et al.
Journal of Medical Genetics|December 20, 2003
Recurrent de novo mitochondrial DNA mutations in respiratory chain deficiencyS Lebon, M Chol, P Benit, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|February 17, 2015
Early and late complications after liver transplantation for propionic acidemia in children: a two centers studyF Charbit-Henrion, F Lacaille, P McKiernan, et al.
Neuropediatrics|March 17, 2006
Molar tooth sign and superior vermian dysplasia: a radiological, clinical, and genetic studyS Romano, N Boddaert, I Desguerre, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 4, 2005
[Congenital hyperinsulinism in newborn and infant]I Giurgea, M-J Ribeiro, N Boddaert, et al.
The Journal of Clinical Investigation|October 14, 1998
Paternal mutation of the sulfonylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasiaV Verkarre, J C Fournet, P de Lonlay, et al.
Pageof 14