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Clinical Biochemistry
|
July 25, 2016
Validation of amino-acids measurement in dried blood spot by FIA-MS/MS for PKU management
C Bruno, D Dufour-Rainfray, F Patin, et al.
Clinical Biochemistry
|
April 4, 2017
Erratum to "Validation of amino-acids measurement in dried blood spot by FIA-MS/MS for PKU management" [Clin. Biochem. 49 (2016) 1047-1050]
C Bruno, D Dufour-Rainfray, F Patin, et al.
JIMD Reports
|
June 15, 2016
A Multiplatform Metabolomics Approach to Characterize Plasma Levels of Phenylalanine and Tyrosine in Phenylketonuria
H Blasco, C Veyrat-Durebex, M Bertrand, et al.
Clinical Biochemistry
|
March 19, 2021
Validation of plasma amino acid profile using UHPLC-mass spectrometer (QDa) as a screening method in a metabolic disorders reference centre: Performance and accreditation concerns
C Bruno, C Veyrat-Durebex, C H Lumbu Lukuntonda, 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
|
June 20, 2018
Transition from pediatric to adult care in adolescents with hereditary metabolic diseases: Specific guidelines from the French network for rare inherited metabolic diseases (G2M)
B Chabrol, P Jacquin, L Francois, et al.
Molecular Genetics and Metabolism
|
May 10, 2011
Comprehensive cDNA study and quantitative analysis of mutant HADHA and HADHB transcripts in a French cohort of 52 patients with mitochondrial trifunctional protein deficiency
A Boutron, C Acquaviva, C Vianey-Saban, et al.
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Search research articles
Search
Showing results (31-40 of 37) with videos related to
Sort By:
Page
of 4
You have reached the last page of results.
This site can display upto 37 results.
Clinical Biochemistry
|
July 25, 2016
Validation of amino-acids measurement in dried blood spot by FIA-MS/MS for PKU management
C Bruno, D Dufour-Rainfray, F Patin, et al.
Clinical Biochemistry
|
April 4, 2017
Erratum to "Validation of amino-acids measurement in dried blood spot by FIA-MS/MS for PKU management" [Clin. Biochem. 49 (2016) 1047-1050]
C Bruno, D Dufour-Rainfray, F Patin, et al.
JIMD Reports
|
June 15, 2016
A Multiplatform Metabolomics Approach to Characterize Plasma Levels of Phenylalanine and Tyrosine in Phenylketonuria
H Blasco, C Veyrat-Durebex, M Bertrand, et al.
Clinical Biochemistry
|
March 19, 2021
Validation of plasma amino acid profile using UHPLC-mass spectrometer (QDa) as a screening method in a metabolic disorders reference centre: Performance and accreditation concerns
C Bruno, C Veyrat-Durebex, C H Lumbu Lukuntonda, 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
|
June 20, 2018
Transition from pediatric to adult care in adolescents with hereditary metabolic diseases: Specific guidelines from the French network for rare inherited metabolic diseases (G2M)
B Chabrol, P Jacquin, L Francois, et al.
Molecular Genetics and Metabolism
|
May 10, 2011
Comprehensive cDNA study and quantitative analysis of mutant HADHA and HADHB transcripts in a French cohort of 52 patients with mitochondrial trifunctional protein deficiency
A Boutron, C Acquaviva, C Vianey-Saban, et al.
Page
of 4