Search Results - 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... by Megarbane, A, Choueiri, R, Bleik, J, Mezzina, M, Caillaud, C

    Published 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 by Périard, J. D., Ruell, P. A., Thompson, M. W., Caillaud, C.

    Published 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... by Germain, D P, Puech, J P, Caillaud, C, Kahn, A, Poenaru, L

    Published 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 by Kippelen, P, Caillaud, C, Robert, E, Connes, P, Godard, P, Prefaut, C

    Published 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. by Lyonnet, S, Caillaud, C, Rey, F, Berthelon, M, Frézal, J, Rey, J, Munnich, A

    Published 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. by Labrune, P, Melle, D, Rey, F, Berthelon, M, Caillaud, C, Rey, J, Munnich, A, Lyonnet, S

    Published 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 by Maimoun, L, Simar, D, Malatesta, D, Caillaud, C, Peruchon, E, Couret, I, Rossi, M, Mariano-Goulart, D

    Published 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. by 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

    Published 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 by 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

    Published 2017
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