Cerebrovascular disease in children under 16 years of age in the city of Dijon, France: A study of incidence and clinical features from 1985 to 1993 von Giroud, Maurice, Lemesle, Martine, Gouyon, Jean-Bernard, Nivelon, Jean-Louis, Milan, Chantal, Dumas, Raymond

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Vitamin A deficiency and nocturnal vision in teenagers with cystic fibrosis von HUET, F, SEMAMA, D, MAINGUENEAU, C, CHARAVEL, A, NIVELON, J.-L

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Long-term results of GH therapy in GH-deficient children treated before 1 year of age von HUET, F, CAREL, J.-C, NIVELON, J.-L, CHAUSSAIN, J.-L

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Rattrapage statural des enfants ayant un déficit en hormone de croissance traités dès la première année de vie von Huet, F, Carel, JC, Nivelon, JL, Chaussain, JL

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Hemiballismus revealing multiple sclerosis in an infant von GIROUD, M, SEMAMA, D, PRADEAUX, L, GOUYON, J. B, DUMAS, R, NIVELON, J. L

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New autosomal recessive chondrodysplasia--pseudohermaphrodism syndrome von Nivelon, A, Nivelon, J L, Mabille, J P, Maroteaux, P, Feldman, J P, Douvier, S, Aymé, S

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Conservative management of cerebellar hematomas in neonates von Gouyon, J.B., Alison, M., Nivelon, J-L.

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Dandy-Walker Malformation Associated With Occipital Meningocele and Cardiac Anomalies: A Rare Complex Embryologic Defect von Sautreaux, Jean Louis, Giroud, Maurice, Dauvergne, Michel, Nivelon, Jean Louis, Thierry, André

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Use of microcomputer for self-evaluation in pediatric practice von Gouyon, J B, Alison, M, Nivelon, J L, Dusserre, L

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Late thalamic atrophy in infarction of the middle cerebral artery territory in neonates: a prospective clinical and radiological study in four children von GIROUD, M, FAYOLLE, H, MARTIN, D, BAUDOIN, N, ANDRE, N, GOUYON, J. B, NIVELON, J. L, DUMAS, R

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Spectrum of phenylketonuria mutations in western Europe and north Africa, and their relation to polymorphic DNA haplotypes at the phenylalanine hydroxylase locus von Berthelon, M, Caillaud, C, Rey, F, Labrune, P, Melle, D, Feingold, J, Frézal, J, Briard, M L, Farriaux, J P, Guibaud, P

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Investigation of a specific IgM antibody test in neonatal congenital syphilis von Sepetjian, M, Tissot Guerraz, F, Monier, J C, Nivelon, J L, Thivolet, J

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Dépistage de l'hyperplasie congénitale des surrénales par déficit en 21 hydroxylase (HSC) von Nivelon, JL

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Catch-up growth in growth hormone deficit children treated with GH since the first year of life von Huet, F, Carel, J C, Nivelon, J L, Chaussain, J L

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Aérosolthérapie et mucoviscidose: Enquête nationale von Huet, F., Nivelon, JL

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Familial benign neonatal seizures: EEG, clinical, prognosis and genetic features von Giroud, M, Soichot, P, Nivelon-Chevalier, A, Gouyon, J B, Nivelon, J L, Dumas, R

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Catch-up growth in growth hormone deficit children treated with GH since the first year of life von Huet, F, Carel, J C, Nivelon, J L, Chaussain, J L

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PRENATAL DIAGNOSIS OF CONGENITAL ADRENAL HYPERPLASIA DUE TO 21-HYDROXYLASE DEFICIENCY von Morel, Y, Murena, M, Forest, M G, Carel, J C, Leger, J, Nivelon, J-L, David, M

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Familial benign neonatal seizures: EEG, clinical, prognosis and genetic features von Giroud, M, Soichot, P, Nivelon-Chevalier, A, Gouyon, J B, Nivelon, J L, Dumas, R

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STUDY OF FINAL HEIGHT IN TURNER SYNDROME(N = 216) von Rochiccioli, P, Battin, J, Bertrand, A M, Bouquier, J J, Bost, M, Chatelain, P, Colle, M, David, M, Freycon, R, Limal, J M, Malpuech, G, Mariani, R, Nivelon, J L, Pieron, M, Simonin, G, Sultan, C

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