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J P Harpey

Showing results (11-20 of 33) with videos related to

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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.
Archives 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.
Archives Francaises De Pediatrie|December 1, 1990
[Rendu Osler disease revealed by ruptured cerebral arterial aneurysm in an infant]C Roy, G Noseda, A Arzimanoglou, et al.
Journal of Inherited Metabolic Disease|November 20, 1998
Diffuse leukodystrophy in an infant with cytochrome-c oxidase deficiencyJ P Harpey, D Heron, M Prudent, et al.
Annales D'Endocrinologie|January 1, 1980
[Clinical, cytogenetical, histological, immunological and hormonal studies in a case of true hermaphroditism (author's transl)]M Roger, C Roy, M Fellous, et al.
Pageof 4

Showing results (11-20 of 33) with videos related to

Sort By:
Pageof 4
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.
Archives 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.
Archives Francaises De Pediatrie|December 1, 1990
[Rendu Osler disease revealed by ruptured cerebral arterial aneurysm in an infant]C Roy, G Noseda, A Arzimanoglou, et al.
Journal of Inherited Metabolic Disease|November 20, 1998
Diffuse leukodystrophy in an infant with cytochrome-c oxidase deficiencyJ P Harpey, D Heron, M Prudent, et al.
Annales D'Endocrinologie|January 1, 1980
[Clinical, cytogenetical, histological, immunological and hormonal studies in a case of true hermaphroditism (author's transl)]M Roger, C Roy, M Fellous, et al.
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