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D Cheillan

Showing results (1-10 of 22) with videos related to

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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 27, 2015
[How to screen for metabolic diseases?]F Labarthe, M Tardieu, D Cheillan
European Journal of Neurology|May 6, 2020
Unusual early-onset and severe adrenomyeloneuropathy in womenC Azar, D Cheillan, Y Nadjar
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 27, 2015
[The distinctive features of the Guthrie test in neonatology]M Roussey, D Cheillan, R Coutant, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 3, 2014
[Newborn screening in France: where are we going?]J Sarles, F Huet, D Cheillan, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 24, 2013
[Do we need congenital adrenal hyperplasia screening for premature infants?]F Huet, A Godefroy, D Cheillan, et al.
Annales De Biologie Clinique|June 26, 2004
[Application of tandem mass spectrometry to neonatal screening of inherited metabolic diseases: focus on present developments]D Cheillan, S Cognat, C Vianey-Saban, et al.
Annales De Biologie Clinique|September 10, 2004
[Should blood samples be drawn on heparin-anticoagulant for lipid analysis?]A Sassolas, D Cheillan, J Drai, et al.
Revue Neurologique|April 1, 2005
[Creatine deficiency syndromes]D Cheillan, S Cognat, N Vandenberghe, et al.
Journal of Inherited Metabolic Disease|April 7, 2004
CDG IIx with unusual phenotypeD Cheillan, S Cognat, C Dorche, et al.
BMC Research Notes|November 9, 2017
Management of X-linked adrenoleukodystrophy in Morocco: actual situationF Z Madani Benjelloun, Y Kriouile, D Cheillan, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 27, 2015
[How to screen for metabolic diseases?]F Labarthe, M Tardieu, D Cheillan
European Journal of Neurology|May 6, 2020
Unusual early-onset and severe adrenomyeloneuropathy in womenC Azar, D Cheillan, Y Nadjar
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 27, 2015
[The distinctive features of the Guthrie test in neonatology]M Roussey, D Cheillan, R Coutant, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 3, 2014
[Newborn screening in France: where are we going?]J Sarles, F Huet, D Cheillan, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 24, 2013
[Do we need congenital adrenal hyperplasia screening for premature infants?]F Huet, A Godefroy, D Cheillan, et al.
Annales De Biologie Clinique|June 26, 2004
[Application of tandem mass spectrometry to neonatal screening of inherited metabolic diseases: focus on present developments]D Cheillan, S Cognat, C Vianey-Saban, et al.
Annales De Biologie Clinique|September 10, 2004
[Should blood samples be drawn on heparin-anticoagulant for lipid analysis?]A Sassolas, D Cheillan, J Drai, et al.
Revue Neurologique|April 1, 2005
[Creatine deficiency syndromes]D Cheillan, S Cognat, N Vandenberghe, et al.
Journal of Inherited Metabolic Disease|April 7, 2004
CDG IIx with unusual phenotypeD Cheillan, S Cognat, C Dorche, et al.
BMC Research Notes|November 9, 2017
Management of X-linked adrenoleukodystrophy in Morocco: actual situationF Z Madani Benjelloun, Y Kriouile, D Cheillan, et al.
Pageof 3