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Journal of Inherited Metabolic Disease
|
April 8, 2006
Genetic heterogeneity of the GLDC gene in 28 unrelated patients with glycine encephalopathy
C Conter, M O Rolland, D Cheillan, et al.
Journal of Medical Genetics
|
April 5, 2005
Clinical, morphological, and molecular aspects of sialic acid storage disease manifesting in utero
R Froissart, D Cheillan, R Bouvier, et al.
Annales De Biologie Clinique
|
June 23, 1999
[A surprising aglycorrachia! A case of neurocysticercosis]
D Cheillan, J Bancel, C Tiliket, et al.
Journal of Inherited Metabolic Disease
|
January 26, 2006
False-positive results in neonatal screening for cystic fibrosis based on a three-stage protocol (IRT/DNA/IRT): Should we adjust IRT cut-off to ethnic origin?
D Cheillan, M Vercherat, F Chevalier-Porst, et al.
Diabetes & Metabolism
|
April 15, 2019
Large triglyceride-rich lipoproteins from fasting patients with type 2 diabetes activate platelets
M M Boulet, D Cheillan, M Di Filippo, et al.
Neuromuscular Disorders : NMD
|
June 18, 2013
Creatine deficiency syndrome. A treatable myopathy due to arginine-glycine amidinotransferase (AGAT) deficiency
S Nouioua, D Cheillan, S Zaouidi, et al.
Neurology
|
November 15, 2006
High frequency of creatine deficiency syndromes in patients with unexplained mental retardation
L Lion-François, D Cheillan, G Pitelet, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
January 17, 2012
[Medium-chain acyl-CoA-dehydrogenase (MCAD) deficiency: French consensus for neonatal screening, diagnosis, and management]
F Feillet, H Ogier, D Cheillan, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
March 30, 2022
Neonatal screening for congenital hypothyroidism: Time to lower the TSH threshold in France
L Levaillant, F Huet, P Bretones, et al.
Beneficial Microbes
|
May 13, 2026
Gut commensal Bacteroides faecichinchillae, a potential novel candidate of next-generation probiotics targeting type 2 diabetes
M Godet, E Delmas, C Gérard, et al.
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of 3
Search research articles
Search
Showing results (11-20 of 22) with videos related to
Sort By:
Page
of 3
Journal of Inherited Metabolic Disease
|
April 8, 2006
Genetic heterogeneity of the GLDC gene in 28 unrelated patients with glycine encephalopathy
C Conter, M O Rolland, D Cheillan, et al.
Journal of Medical Genetics
|
April 5, 2005
Clinical, morphological, and molecular aspects of sialic acid storage disease manifesting in utero
R Froissart, D Cheillan, R Bouvier, et al.
Annales De Biologie Clinique
|
June 23, 1999
[A surprising aglycorrachia! A case of neurocysticercosis]
D Cheillan, J Bancel, C Tiliket, et al.
Journal of Inherited Metabolic Disease
|
January 26, 2006
False-positive results in neonatal screening for cystic fibrosis based on a three-stage protocol (IRT/DNA/IRT): Should we adjust IRT cut-off to ethnic origin?
D Cheillan, M Vercherat, F Chevalier-Porst, et al.
Diabetes & Metabolism
|
April 15, 2019
Large triglyceride-rich lipoproteins from fasting patients with type 2 diabetes activate platelets
M M Boulet, D Cheillan, M Di Filippo, et al.
Neuromuscular Disorders : NMD
|
June 18, 2013
Creatine deficiency syndrome. A treatable myopathy due to arginine-glycine amidinotransferase (AGAT) deficiency
S Nouioua, D Cheillan, S Zaouidi, et al.
Neurology
|
November 15, 2006
High frequency of creatine deficiency syndromes in patients with unexplained mental retardation
L Lion-François, D Cheillan, G Pitelet, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
January 17, 2012
[Medium-chain acyl-CoA-dehydrogenase (MCAD) deficiency: French consensus for neonatal screening, diagnosis, and management]
F Feillet, H Ogier, D Cheillan, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
March 30, 2022
Neonatal screening for congenital hypothyroidism: Time to lower the TSH threshold in France
L Levaillant, F Huet, P Bretones, et al.
Beneficial Microbes
|
May 13, 2026
Gut commensal Bacteroides faecichinchillae, a potential novel candidate of next-generation probiotics targeting type 2 diabetes
M Godet, E Delmas, C Gérard, et al.
Page
of 3