SMN1 gene study in three families in which ALS and spinal muscular atrophy co-exist von CORCIA, P, KHORIS, J, COURATIER, P, MAYEUX-PORTAS, V, BIETH, E, DE TOFFOL, B, AUTRET, A, MÜH, J. P, ANDRES, C, CAMU, W

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Association study with two markers of a human homeogene in infantile autism von Petit, E, Hérault, J, Martineau, J, Perrot, A, Barthélémy, C, Hameury, L, Sauvage, D, Lelord, G, Müh, J P

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Tolerance evaluation of L-asparaginase loaded in red blood cells von KRAVTZOFF, R, COLOMBAT, P, CHASSAIGNE, M, ROPARS, C, DESBOIS, I, LINASSIER, C, MUH, J. P, PHILIP, T, BLAY, J. Y, GARDENBAS, M, POUMIER-GASCHARD, P, LAMAGNERE, J. P

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Serotonin and autism: Biochemical and molecular biology features von Hérault, Josiane, Petit, Elisabeth, Martineau, Joëlle, Cherpi, Catherine, Perrot, Anne, Barthélémy, Catherine, Lelord, Gilbert, Müh, Jean Pierre

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Urinary free and conjugated catecholamines and metabolites in autistic children von BARTHELEMY, C, BRUNEAU, N, COTTET-EYMARD, J. M, DOMENECH-JOUVE, J, GARREAU, B, LELORD, G, MUH, J. P, PEYRIN, L

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Association study of the NF1 gene and autistic disorder von Mbarek, Olivier, Marouillat, Sylviane, Martineau, Joelle, Barthélémy, Catherine, Müh, Jean-Pierre, Andres, Christian

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Urinary dopamine metabolites as indicators of the responsiveness to fenfluramine treatment in children with autistic behavior von BARTHELEMY, C, BRUNEAU, N, JOUVE, J, MARTINEAU, J, MUH, J. P, LELORD, G

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High-performance liquid chromatography with electrochemical detection for the simultaneous determination of the methoxylated amines, normetanephrine, metanephrine and 3-methoxytyra... von Jouve, J., Mariotte, N., Sureau, C., Muh, J.P.

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Determination of urinary serotonin using liquid chromatography with electrochemical detection von Jouve, J., Martineau, J., Mariotte, N., Barthelemy, C., Muh, J.P., Lelord, G.

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bcl-2 evaluation in patients in long-term complete remission after bone marrow transplantation von Colombat, P, Garrigue, M A, Lamagnere, J P, Muh, J P, Linassier, C

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No mutations in the coding region of the Rett syndrome gene MECP2 in 59 autistic patients von Vourc'h, P, Bienvenu, T, Beldjord, C, Chelly, J, Barthélémy, C, Müh, J P, Andres, C

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Dopamine-beta-hydroxylase (DBH) and homovanillic acid (HVA) autistic children von GARNIER, C, COMOY, E, BARTHELEMY, C, LEDDET, I, GARREAU, B, MUH, J. P, LELORD, G

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Improved pharmacodynamics of L-asparaginase-loaded in human red blood cells von Kravtzoff, R, Desbois, I, Lamagnere, J P, Muh, J P, Valat, C, Chassaigne, M, Colombat, P, Ropars, C

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Characterization of N-glycosylated type I collagen in streptozotocin-induced diabetes von Le Pape, A, Muh, J P, Bailey, A J

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Distribution of non-enzymatically bound glucose in in vivo and in vitro glycosylated type I collagen molecules von Le Pape, Alain, Guitton, Jean-Dominique, Muh, Jean-Pierre

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Purification and characterization of ubiquitin from mammalian testis von Loir, M., Caraty, A., Lanneau, M., Menezo, Y., Muh, J.P., Sautiere, P.

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Autism and genetics: Clinical approach and association study with two markers of HRAS gene von Hérault, Josiane, Petit, Elisabeth, Martineau, Joëlle, Perrot, Anne, Lenoir, Pascal, Cherpi, Catherine, Barthélémy, Catherine, Sauvage, Dominique, Mallet, Jacques, Müh, Jean Pierre, Lelord, Gilbert

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Treatment of human spermatozoa with follicular fluid can influence lipid content and motility during in vitro capacitation von HAMAMAH, S, LANSON, M, BARTHELEMY, C, GARRIGUE, M. A, LANSAC, J, MUH, J. P, ROYERE, D

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X chromosome and infantile autism von Petit, Elisabeth, Hérault, Josiane, Raynaud, Martine, Cherpi, Catherine, Perrot, Anne, Barthélémy, Catherine, Lelord, Gilbert, Müh, Jean-Pierre

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Effects of pyridoxine and magnesium on autistic symptoms--initial observations von Lelord, G, Muh, J P, Barthelemy, C, Martineau, J, Garreau, B, Callaway, E

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