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Pediatrics
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November 3, 2005
Long-term follow-up of neonatal mitochondrial cytopathies: a study of 57 patients
A García-Cazorla, P De Lonlay, M C Nassogne, et al.
Developmental Medicine and Child Neurology
|
August 4, 2004
Neurodevelopmental pattern of succinic semialdehyde dehydrogenase deficiency (gamma-hydroxybutyric aciduria)
A Philippe, J Deron, D Geneviève, et al.
Glycobiology
|
February 13, 2001
Defect in N-glycosylation of proteins is tissue-dependent in congenital disorders of glycosylation Ia
T Dupré, A Barnier, P de Lonlay, et al.
Nature Genetics
|
November 5, 1997
Aconitase and mitochondrial iron-sulphur protein deficiency in Friedreich ataxia
A Rötig, P de Lonlay, D Chretien, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
March 1, 2005
[Congenital hyperinsulinism of infancy: surgical treatment in 60 cases of focal form]
C Crétolle, P de Lonlay, F Sauvat, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape
|
August 12, 2025
Seizures and electroencephalographic findings in inborn errors of metabolism: Clues to differential diagnosis in the neonatal period, infancy, childhood and adolescence, and review of the literature
D Kapoor, S Sharma, A Kaminska, et al.
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.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
August 30, 2011
[Enzyme replacement therapy for lysosomal storage disorders]
V Valayannopoulos, A Brassier, A Chabli, et al.
European Journal of Pediatrics
|
February 1, 2000
Familial neonatal SIDS revealing carnitine-acylcarnitine translocase deficiency
J M Nuoffer, P de Lonlay, C Costa, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
July 27, 2010
[Diagnostic and therapeutic management of inherited metabolic diseases in emergency and intensive care unit]
P de Lonlay, V Valayannopoulos, J-B Arnoux, et al.
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of 14
Search research articles
Search
Showing results (21-30 of 131) with videos related to
Sort By:
Page
of 14
Pediatrics
|
November 3, 2005
Long-term follow-up of neonatal mitochondrial cytopathies: a study of 57 patients
A García-Cazorla, P De Lonlay, M C Nassogne, et al.
Developmental Medicine and Child Neurology
|
August 4, 2004
Neurodevelopmental pattern of succinic semialdehyde dehydrogenase deficiency (gamma-hydroxybutyric aciduria)
A Philippe, J Deron, D Geneviève, et al.
Glycobiology
|
February 13, 2001
Defect in N-glycosylation of proteins is tissue-dependent in congenital disorders of glycosylation Ia
T Dupré, A Barnier, P de Lonlay, et al.
Nature Genetics
|
November 5, 1997
Aconitase and mitochondrial iron-sulphur protein deficiency in Friedreich ataxia
A Rötig, P de Lonlay, D Chretien, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
March 1, 2005
[Congenital hyperinsulinism of infancy: surgical treatment in 60 cases of focal form]
C Crétolle, P de Lonlay, F Sauvat, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape
|
August 12, 2025
Seizures and electroencephalographic findings in inborn errors of metabolism: Clues to differential diagnosis in the neonatal period, infancy, childhood and adolescence, and review of the literature
D Kapoor, S Sharma, A Kaminska, et al.
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.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
August 30, 2011
[Enzyme replacement therapy for lysosomal storage disorders]
V Valayannopoulos, A Brassier, A Chabli, et al.
European Journal of Pediatrics
|
February 1, 2000
Familial neonatal SIDS revealing carnitine-acylcarnitine translocase deficiency
J M Nuoffer, P de Lonlay, C Costa, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
July 27, 2010
[Diagnostic and therapeutic management of inherited metabolic diseases in emergency and intensive care unit]
P de Lonlay, V Valayannopoulos, J-B Arnoux, et al.
Page
of 14