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International Journal of Cardiology
|
September 18, 1998
Fatty acid beta-oxidation deficiency masquerading as fulminant myocarditis
P 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 deficiency
P Bénit, D Chretien, N Kadhom, et al.
Neuropediatrics
|
May 1, 1999
Respiratory chain deficiency presenting as recurrent myoglobinuria in childhood
P 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 dehydrogenase
C MacMullen, J Fang, B Y Hsu, et al.
American Journal of Medical Genetics
|
November 7, 1998
Ebstein anomaly associated with rearrangements of chromosomal region 11q
P 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 infancy
A Aynsley-Green, K Hussain, J Hall, et al.
Journal of Medical Genetics
|
January 16, 1998
Features of DiGeorge syndrome and CHARGE association in five patients
P 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 hyperinsulinism
P de Lonlay-Debeney, F Poggi-Travert, J C Fournet, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 13) with videos related to
Sort By:
Page
of 2
International Journal of Cardiology
|
September 18, 1998
Fatty acid beta-oxidation deficiency masquerading as fulminant myocarditis
P 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 deficiency
P Bénit, D Chretien, N Kadhom, et al.
Neuropediatrics
|
May 1, 1999
Respiratory chain deficiency presenting as recurrent myoglobinuria in childhood
P 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 dehydrogenase
C MacMullen, J Fang, B Y Hsu, et al.
American Journal of Medical Genetics
|
November 7, 1998
Ebstein anomaly associated with rearrangements of chromosomal region 11q
P 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 infancy
A Aynsley-Green, K Hussain, J Hall, et al.
Journal of Medical Genetics
|
January 16, 1998
Features of DiGeorge syndrome and CHARGE association in five patients
P 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 hyperinsulinism
P de Lonlay-Debeney, F Poggi-Travert, J C Fournet, et al.
Page
of 2