Germ-line deletion involving the INK4 locus in familial proneness to melanoma and nervous system tumors von BAHUAU, M, VIDAUD, D, CAILLE, B, VIDAUD, M, JENKINS, R. B, BIECHE, I, KIMMEL, D. W, ASSOULINE, B, SMITH, J. S, ALDERETE, B, CAYUELA, J.-M, HARPEY, J.-P

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TERATOGENICITY OF PYRIMETHAMINE von Harpey, Jean-Paul, Darbois, Yves, Lefèbvre, Gilles

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Mycoplasma pneumoniae postinfectious encephalomyelitis with bilateral striatal necrosis von Brandel, Jean-Philippe, Vidailhet, Marie, Noseda, Geneviéve, Harpey, Jean-Paul, Agid, Yves

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FATTY ACID β-OXIDATION DEFECTS AND SUDDEN INFANT DEATH von Harpey, Jean-Paul, Charpentier, Christiane, Paturneau-Jouas, Marion

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Ubiquinone concentration in control chorionic villi and fetal liver von Charpentier, Christiane, Chadefaux, Bernadette, Aupetit, Joelle, Harpey, Jean-Paul

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The Molecular Basis of Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency in Compound Heterozygous Patients: Is There Correlation between Genotype and Phenotype? von Andresen, Brage Storstein, Bross, Peter, Udvari, Szabolcs, Kirk, Jean, Gray, George, Kmoch, Stanislav, Chamoles, Nestor, Knudsen, Inga, Winter, Vibeke, Wilcken, Bridget, Yokota, Ichiro, Hart, Kimberly, Packman, Seymour, Harpey, Jean Paul, Saudubray, Jean Marie, Hale, Daniel E., Bolund, Lars, Kølvraa, Steen, Gregersen, Niels

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Homocystinuria caused by 5,10-methylenetetrahydrofolate reductase deficiency: a case in an infant responding to methionine, folinic acid, pyridoxine, and vitamin B12 therapy von Harpey, J P, Rosenblatt, D S, Cooper, B A, Le Moël, G, Roy, C, Lafourcade, J

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Secondary metabolic defects in spinal muscular atrophy type II von Harpey, Jean-Paul, Charpentier, Christiane, Paturneau-Jouas, Marion, Renault, Francis, Romero, Norma, Fardeau, Michel

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Sudden infant death syndrome and multiple acyl-coenzyme A dehydrogenase deficiency, ethylmalonic-adipic aciduria, or systemic carnitine deficiency von Harpey, Jean-Paul, Charpentier, Christiane, Coudé, Marie, Divry, Priscille, Paturneau-Jouas, Marion

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METHYLENE-BLUE FOR RIBOFLAVIN-UNRESPONSIVE GLUTARICACIDURIA TYPE II von Harpey, Jean-Paul, Charpentier, Christiane, Coudé, Marie

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PYRIMETHAMINE IN PREGNANCY von Harpey, Jean-Paul

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Early diagnosis of Maroteaux-Lamy syndrome in two patients with accelerated growth and advanced bone maturation von HERON, Delphine, BAUMANN, Clarisse, BENICHOU, Jean Jacques, HARPEY, Jean Paul, LE MERRER, Martine

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SUDDEN INFANT DEATH SYNDROME AND INHERITED DISORDERS OF FAT METABOLISM von Harpey, Jean-Paul, Charpentier, Christiane, Paturneau-Jouas, Marion

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CUTIS LAXA AND LOW SERUM ZINC AFTER ANTENATAL EXPOSURE TO PENICILLAMINE von Harpey, Jean-Paul, Jaudon, Marie-Chantel, Clavel, Jean-Pierre, Galli, André, Darbois, Yves

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ACUTE FATTY LIVER OF PREGNANCY von Harpey, Jean-Paul, Charpentier, Christiane

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Investigations on an animal model for a tentative explanation of increased urinary ethylmalonic acid in patients with glutaric aciduria type II treated with riboflavin von Charpentier, Christiane, Coude, Marie, Harpey, Jean-Paul, Saudubray, Jean-Marie

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Epstein-Barr virus and infantile papular acrodermatitis von Harpey, Jean-Paul, Lenoir, Gilbert

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Follow-up in a child with 5,10-methylenetetrahydrofolate reductase deficiency von Harpey, Jean-Paul, Le Moël, Giséle, Zittoun, Jacqueline

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PCR based mutation screening of the laminin α2 chain gene (LAMA2) : application to prenatal diagnosis and search for founder effects in congenital muscular dystrophy von GUICHENEY, P, VIGNIER, N, TOPALOGLU, H, MORA, M, HARPEY, J.-P, HAENGGELI, C.-A, BAROIS, A, HAINQUE, B, SCHWARTZ, K, TOME, F. M. S, FARDEAU, M, TRYGGVASON, K, XU ZHANG, YI HE, CRUAUD, C, FREY, V, HELBLING-LECLERC, A, RICHARD, P, ESTOURNET, B, MERLINI, L

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Recurrent meiotic nondisjunction of maternal chromosome 15 in a sibship von Harpey, Jean-Paul, Heron, Delphine, Prudent, Muriel, Lesourd, Sylvie, Henry, Isabelle, Royer-Legrain, Ghislaine, Munnich, Arnold, Bonnefont, Jean-Paul

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