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Showing results (11-20 of 13) with videos related to

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La Revue De Medecine Interne|January 1, 1993
[Pulmonary pneumocystosis in immunodepression: apropos of 78 consecutive cases seen at the CHRU of Clermont-Ferrand from 1984 to 1993]H Laurichesse, M Cambon, R Conductier, 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.
Revue Neurologique|April 4, 2016
Multiple acyl-CoA dehydrogenase deficiency (MADD) as a cause of late-onset treatable metabolic diseaseA Béhin, C Acquaviva-Bourdain, S Souvannanorath, et al.
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Showing results (11-20 of 13) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 13 results.
La Revue De Medecine Interne|January 1, 1993
[Pulmonary pneumocystosis in immunodepression: apropos of 78 consecutive cases seen at the CHRU of Clermont-Ferrand from 1984 to 1993]H Laurichesse, M Cambon, R Conductier, 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.
Revue Neurologique|April 4, 2016
Multiple acyl-CoA dehydrogenase deficiency (MADD) as a cause of late-onset treatable metabolic diseaseA Béhin, C Acquaviva-Bourdain, S Souvannanorath, et al.
Pageof 2