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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.
Molecular Genetics and Metabolism
|
April 7, 2009
Secondary creatine deficiency in ornithine delta-aminotransferase deficiency
V Valayannopoulos, N Boddaert, K Mention, et al.
Journal of Child Neurology
|
December 17, 2013
Acute psychosis in propionic acidemia: 2 case reports
C Dejean de la Bâtie, V Barbier, V Valayannopoulos, et al.
Pediatric Research
|
August 24, 2001
Hyperinsulinism and hyperammonemia syndrome: report of twelve unrelated patients
P De Lonlay, C Benelli, F Fouque, et al.
Journal of Inherited Metabolic Disease
|
May 4, 2005
Dominantly inherited hyperinsulinaemic hypoglycaemia
P de Lonlay, I Giurgea, C Sempoux, et al.
Molecular Genetics and Metabolism
|
August 5, 2008
Liver hepatoblastoma and multiple OXPHOS deficiency in the follow-up of a patient with methylmalonic aciduria
M A Cosson, G Touati, F Lacaille, et al.
Journal of Inherited Metabolic Disease
|
June 23, 2000
Genetic hypoglycaemia in infancy and childhood: pathophysiology and diagnosis
J M Saudubray, P de Lonlay, G Touati, et al.
The New England Journal of Medicine
|
April 15, 1999
Clinical features of 52 neonates with hyperinsulinism
P de Lonlay-Debeney, F Poggi-Travert, J C Fournet, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
January 14, 1999
[Persistent hyperinsulinemic hypoglycemia in the newborn and infants]
P de Lonlay-Debeney, J C Fournet, D Martin, et al.
Journal of Inherited Metabolic Disease
|
July 17, 1999
Recognition and management of fatty acid oxidation defects: a series of 107 patients
J M Saudubray, D Martin, P de Lonlay, et al.
Page
of 9
Search research articles
Search
Showing results (71-80 of 84) with videos related to
Sort By:
Page
of 9
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.
Molecular Genetics and Metabolism
|
April 7, 2009
Secondary creatine deficiency in ornithine delta-aminotransferase deficiency
V Valayannopoulos, N Boddaert, K Mention, et al.
Journal of Child Neurology
|
December 17, 2013
Acute psychosis in propionic acidemia: 2 case reports
C Dejean de la Bâtie, V Barbier, V Valayannopoulos, et al.
Pediatric Research
|
August 24, 2001
Hyperinsulinism and hyperammonemia syndrome: report of twelve unrelated patients
P De Lonlay, C Benelli, F Fouque, et al.
Journal of Inherited Metabolic Disease
|
May 4, 2005
Dominantly inherited hyperinsulinaemic hypoglycaemia
P de Lonlay, I Giurgea, C Sempoux, et al.
Molecular Genetics and Metabolism
|
August 5, 2008
Liver hepatoblastoma and multiple OXPHOS deficiency in the follow-up of a patient with methylmalonic aciduria
M A Cosson, G Touati, F Lacaille, et al.
Journal of Inherited Metabolic Disease
|
June 23, 2000
Genetic hypoglycaemia in infancy and childhood: pathophysiology and diagnosis
J M Saudubray, P de Lonlay, G Touati, et al.
The New England Journal of Medicine
|
April 15, 1999
Clinical features of 52 neonates with hyperinsulinism
P de Lonlay-Debeney, F Poggi-Travert, J C Fournet, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
January 14, 1999
[Persistent hyperinsulinemic hypoglycemia in the newborn and infants]
P de Lonlay-Debeney, J C Fournet, D Martin, et al.
Journal of Inherited Metabolic Disease
|
July 17, 1999
Recognition and management of fatty acid oxidation defects: a series of 107 patients
J M Saudubray, D Martin, P de Lonlay, et al.
Page
of 9