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Presse Medicale (Paris, France : 1983)|May 31, 1986
[Assay of anti-acetylcholine receptor antibodies in myasthenic syndromes of newborn infants]B Eymard, E Morel, J P Harpey, et al.The Journal of Pediatrics|September 1, 1983
Multiple acyl-CoA dehydrogenase deficiency occurring in pregnancy and caused by a defect in riboflavin metabolism in the mother. Study of a kindred with seven deaths in infancy: Value of riboflavin therapy in preventing this syndromeJ P Harpey, C Charpentier, S I Goodman, et al.Pediatric Neurosurgery|July 1, 1996
A male fetus with aqueductal stenosis and four accessory spleens. A case report with a tentative genetic explanationM Catala, V Aubert, S Lesourd, et al.Human Genetics|December 1, 1987
Familial deletion of Xp21.2 with glycerol kinase deficiency and congenital adrenal hypoplasiaF Marlhens, J Chelly, J C Kaplan, et al.La Revue Du Praticien|October 15, 1993
[Neurologic emergencies in acute alcoholic intoxication]B Laurent, P GarnierArchives Francaises De Pediatrie|August 1, 1977
[Hyperphenylalaninaemia with normal phenylalanine-hydroxylase activity and a deficiency of tetrahydrobiopterin and dihydropteridine reductase]F Rey, J P Harpey, R J Leeming, et al.Archives Francaises De Pediatrie|February 1, 1987
[A case of botulism in a 11-month-old infant]E Paty, L Valdes, J P Harpey, et al.Archives Francaises De Pediatrie|May 1, 1983
[Acute pseudotumoral demyelination with regressive attacks]J P Harpey, F Renault, J F Foncin, et al.Clinical Endocrinology|May 1, 1980
Clinical, cytogenetical, histological, immunological and hormonal studies in a case of true hermaphroditismC Roy, M Roger, L Boccon-Gibod, et al.Therapie|January 1, 1991
[Good practices in clinical trials. Quality control of biological trials in hospital laboratory]J P Garnier, C DreuxPageof 18