檢索結果 - Caillaud, C

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  1. 1
    Microcephaly, microphthalmia, congenital cataract, optic atrophy, short stature, hypotonia, severe psychomotor retardation, and cerebral malformations: a second family with micro syndrome or a new syndrome?

    Microcephaly, microphthalmia, congenital cataract, optic atrophy, short stature, hypotonia, severe psychomotor retardation, and cerebral malformations: a second family with micro s... 由 Megarbane, A, Choueiri, R, Bleik, J, Mezzina, M, Caillaud, C

    出版 1999
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  2. 2
    Moderate- and high-intensity exhaustive exercise in the heat induce a similar increase in monocyte Hsp72

    Moderate- and high-intensity exhaustive exercise in the heat induce a similar increase in monocyte Hsp72 由 Périard, J. D., Ruell, P. A., Thompson, M. W., Caillaud, C.

    出版 2015
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  3. 3
    Exhaustive screening of the acid beta-glucosidase gene, by fluorescence-assisted mismatch analysis using universal primers: mutation profile and genotype/phenotype correlations in Gaucher disease.

    Exhaustive screening of the acid beta-glucosidase gene, by fluorescence-assisted mismatch analysis using universal primers: mutation profile and genotype/phenotype correlations in... 由 Germain, D P, Puech, J P, Caillaud, C, Kahn, A, Poenaru, L

    出版 1998
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  4. 4
    Effect of endurance training on lung function: a one year study

    Effect of endurance training on lung function: a one year study 由 Kippelen, P, Caillaud, C, Robert, E, Connes, P, Godard, P, Prefaut, C

    出版 2005
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  5. 5
    Molecular genetics of phenylketonuria in Mediterranean countries: a mutation associated with partial phenylalanine hydroxylase deficiency.

    Molecular genetics of phenylketonuria in Mediterranean countries: a mutation associated with partial phenylalanine hydroxylase deficiency. 由 Lyonnet, S, Caillaud, C, Rey, F, Berthelon, M, Frézal, J, Rey, J, Munnich, A

    出版 1989
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  6. 6
    Single-strand conformation polymorphism for detection of mutations and base substitutions in phenylketonuria.

    Single-strand conformation polymorphism for detection of mutations and base substitutions in phenylketonuria. 由 Labrune, P, Melle, D, Rey, F, Berthelon, M, Caillaud, C, Rey, J, Munnich, A, Lyonnet, S

    出版 1991
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  7. 7
    Response of bone metabolism related hormones to a single session of strenuous exercise in active elderly subjects

    Response of bone metabolism related hormones to a single session of strenuous exercise in active elderly subjects 由 Maimoun, L, Simar, D, Malatesta, D, Caillaud, C, Peruchon, E, Couret, I, Rossi, M, Mariano-Goulart, D

    出版 2005
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  8. 8
    Gaucher disease: the origins of the Ashkenazi Jewish N370S and 84GG acid beta-glucosidase mutations.

    Gaucher disease: the origins of the Ashkenazi Jewish N370S and 84GG acid beta-glucosidase mutations. 由 Diaz, G A, Gelb, B D, Risch, N, Nygaard, T G, Frisch, A, Cohen, I J, Miranda, C S, Amaral, O, Maire, I, Poenaru, L, Caillaud, C, Weizberg, M, Mistry, P, Desnick, R J

    出版 2000
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  9. 9
    Long-term neurologic and cardiac correction by intrathecal gene therapy in Pompe disease

    Long-term neurologic and cardiac correction by intrathecal gene therapy in Pompe disease 由 Hordeaux, J., Dubreil, L., Robveille, C., Deniaud, J., Pascal, Q., Dequéant, B., Pailloux, J., Lagalice, L., Ledevin, M., Babarit, C., Costiou, P., Jamme, F., Fusellier, M., Mallem, Y., Ciron, C., Huchet, C., Caillaud, C., Colle, M-A

    出版 2017
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