Rezultati - M Prieur

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  1. 1
    Beneficial Effects of One-Year Growth Hormone Administration to Children with Juvenile Chronic Arthritis on Chronic Steroid Therapy. I. Effects on Growth Velocity and Body Composition<sup>1</sup>

    Beneficial Effects of One-Year Growth Hormone Administration to Children with Juvenile Chronic Arthritis on Chronic Steroid Therapy. I. Effects on Growth Velocity and Body Composit... od Guy Touati, A. M. Prieur, J. Ruiz, M. Noël, P Czernichow

    Izdano 1998
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  2. 2
    CD44 contributes to T cell activation.

    CD44 contributes to T cell activation. od Stéphane Huet, Hervé Groux, Bernard Caillou, H. Valentin, A. M. Prieur, Anne Bernard

    Izdano 1989
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  3. 3
    Critical role of the D21S55 region on chromosome 21 in the pathogenesis of Down syndrome.

    Critical role of the D21S55 region on chromosome 21 in the pathogenesis of Down syndrome. od Zohra Rahmani, Jean‐Louis Blouin, N. Créau-Goldberg, Paul C. Watkins, J. F. Mattéi, M Poissonnier, M Prieur, Zoubida Chettouh, Annie Nicole, Alain Aurias

    Izdano 1989
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  4. 4
    New Natural Inactivating Mutations of the Follicle-Stimulating Hormone Receptor: Correlations between Receptor Function and Phenotype

    New Natural Inactivating Mutations of the Follicle-Stimulating Hormone Receptor: Correlations between Receptor Function and Phenotype od Philippe Touraine, Isabelle Beau, A. Gougeon, Geri Méduri, Agnès Desroches, C. Pichard, Mirabelle Detoeuf, Bernard‐Jean Paniel, M Prieur, J.R. Zorn, Edwin Milgröm, F Kuttenn, Micheline Misrahi

    Izdano 1999
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  5. 5
    Classification of Human Chromosome 21 Gene-Expression Variations in Down Syndrome: Impact on Disease Phenotypes

    Classification of Human Chromosome 21 Gene-Expression Variations in Down Syndrome: Impact on Disease Phenotypes od Emilie Ait‐Yahya, Julie Aubert, Luce Dauphinot, Isabelle Rivals, M Prieur, G. Golfier, Jean Rossier, L. Personnaz, Nicole Créau, Henri Bléhaut, Stéphane Robin, Jean‐Maurice Delabar, Marie‐Claude Potier

    Izdano 2007
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  6. 6
    Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders

    Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders od M-L Jacquemont, Damien Sanlaville, Richard Redon, O Raoul, Valérie Cormier‐Daire, Stanislas Lyonnet, Jeanne Amiel, M Le Merrer, D. Héron, M‐C De Blois, M Prieur, Michel Vekemans, N P Carter, A Munnich, Laurence Colleaux, Anne Philippe

    Izdano 2006
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  7. 7
    Favourable outcome in 135 children with juvenile systemic sclerosis: results of a multi‐national survey

    Favourable outcome in 135 children with juvenile systemic sclerosis: results of a multi‐national survey od Ivan Foeldvari, M. Zhavania, Nina Birdi, Rubén Cuttica, Oliveira Sf, P. B. Dent, Renate Elborgh, Fabio Falcini, Gerd Ganser, H. J. Girschick, R. Häfner, Rik Joos, W. Kuis, P. Pelkonen, A. M. Prieur, K Rostropowicz-Denisiewicz, Ricardo Russo, A Savolainen, A. Siamopoulou‐Mayridou, Francesco Zulian

    Izdano 2000
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  8. 8
    Proxy‐reported health‐related quality of life of patients with juvenile idiopathic arthritis: The pediatric rheumatology international trials organization multinational quality of life cohort study

    Proxy‐reported health‐related quality of life of patients with juvenile idiopathic arthritis: The pediatric rheumatology international trials organization multinational quality of... od Sheila Oliveira, Angelo Ravelli, Angela Pistorio, E Castell, Clara Malattia, A M Prieur, Claudia Saad‐Magalhães, Kevin Murray, Sang‐Cheol Bae, Rik Joos, Ivan Foeldvari, Carolina Duarte‐Salazar, Nico Wulffraat, Pekka Lahdenne, Pavla Doležalová, Jaime de Inocencio Arocena, F Kanakoudi-Tsakalidou, Michaël Hofer, И. П. Никишина, Huri Özdoğan, Philip J. Hashkes, Jeanne M. Landgraf, Alberto Martini, Nicolino Ruperto

    Izdano 2007
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  9. 9
    Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study.

    Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study. od A K Ryan, Judith A. Goodship, David I. Wilson, N. Philip, A. Lévy, H. Seidel, Simone Schuffenhauer, H Oechsler, B. H. Belohradsky, M Prieur, Alain Aurias, F. Lucy Raymond, Jill Clayton‐Smith, Eli Hatchwell, C McKeown, F. A. Beemer, Bruno Dallapiccola, Giuseppe Novelli, J A Hurst, Jaakko Ignatius, Andrew Green, R M Winter, L A Brueton, Karen Brøndum‐Nielsen, Peter Scambler

    Izdano 1997
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