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Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|July 1, 1979
[Neonatal screening for congenital hypothyroidism by measuring TSH in dried blood samples. Two years experience in the method (author's transl)]M David, C Dorche, G Teyssier, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 15, 1996
Metabolic studies in twin brothers with 2-methylacetoacetyl-CoA thiolase deficiencyM Fontaine, G Briand, N Ser, et al.
Archives Francaises De Pediatrie|June 1, 1993
[Generalized epilepsy disclosing medium-chain-acyl-CoA dehydrogenase deficiency]B Chabrol, J Mancini, C Bertrand, et al.
Acta Paediatrica (Oslo, Norway : 1992)|August 7, 2002
An intestinal obstruction in an eight-month-old child suffering from mevalonic aciduriaL Nimubona, D Laloum, M O Rolland, et al.
La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris|June 3, 1982
[Partial monosomy 20q : a new syndrome. Regional assignment of the ADA locus on 20q132 (author's transl)]J Fraisse, M F Bertheas, F Frère, et al.
Rheumatology (Oxford, England)|September 7, 2007
Diagnostic value of serum immunoglobulinaemia D level in patients with a clinical suspicion of hyper IgD syndromeW Ammouri, L Cuisset, S Rouaghe, et al.
Pediatrie|January 1, 1993
[Multiple acyl-CoA dehydrogenase deficiency. Report of 2 siblings]N Guffon, C Vianey-Saban, J C Berthier, et al.
Revue De Pneumologie Clinique|January 14, 2012
[Nicardipine induced hypoxia: role of hypoxic pulmonary vasoconstriction]J Cotte, E D'Aranda, P Esnault, et al.
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