Torthaí cuardaigh - Sheila A Simpson

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  1. 1
    Predictive DNA-testing for Huntington's disease and reproductive decision making: a European collaborative study

    Predictive DNA-testing for Huntington's disease and reproductive decision making: a European collaborative study de réir Gerry Evers‐Kiebooms, Kurt Nys, Peter S. Harper, Moniek Zoeteweij, Alexandra Dürr, Gioia Jacopini, Christos Yapijakis, Sheila A Simpson

    Foilsithe / Cruthaithe 2002
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    Artigo
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  2. 2
    Genetic professionals' reports of nondisclosure of genetic risk information within families

    Genetic professionals' reports of nondisclosure of genetic risk information within families de réir Angus Clarke, Martin Richards, L Kerzin-Storrar, Jane Halliday, Mary Young, Sheila A Simpson, Katie Featherstone, Karen Forrest, Anneke Lucassen, Patrick J. Morrison, Oliver Quarrell, Helen Stewart

    Foilsithe / Cruthaithe 2005
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    Artigo
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  3. 3
    Challenges assessing clinical endpoints in early Huntington disease

    Challenges assessing clinical endpoints in early Huntington disease de réir Jane S. Paulsen, Chiachi Wang, Karen Duff, Roger A. Barker, Martha Nance, Leigh J. Beglinger, David J. Moser, Janet K. Williams, Sheila A Simpson, Douglas R. Langbehn, Daniël P. van Kammen

    Foilsithe / Cruthaithe 2010
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    Artigo
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  4. 4
    Allelic and locus heterogeneity in inherited venous malformations

    Allelic and locus heterogeneity in inherited venous malformations de réir Jennifer T. Calvert, Travis J. Riney, Christopher D. Kontos, H. Eugene, Víctor G. Prieto, Christopher R. Shea, Jonathan Berg, N. C. Nevin, Sheila A. Simpson, Krystyna A. Pasyk, Marcy C. Speer, Kevin G. Peters, Douglas A. Marchuk

    Foilsithe / Cruthaithe 1999
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    Artigo
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  5. 5
    Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export

    Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export de réir Andrea Legati, Donatella Giovannini, Gaël Nicolas, Uriel López-Sánchez, Beatriz Quintáns, João Ricardo Mendes de Oliveira, Renee Sears, Eliana Marisa Ramos, Elizabeth Spiteri, María-Jesús Sobrido, Ángel Carracedo, Cristina Castro-Fernández, Stéphanie Cubizolle, Brent L. Fogel, Cyril Goizet, Joanna C. Jen, Suppachok Kirdlarp, Anthony E. Lang, Zosia Miedzybrodzka, Witoon Mitarnun, Martin Paucar, Henry L. Paulson, Jérémie Pariente, Anne-Claire Richard, Naomi Salins, Sheila A Simpson, Pasquale Striano, Per Svenningsson, François Tison, Vivek K. Unni, Olivier Vanakker, Marja W. Wessels, Suppachok Wetchaphanphesat, Michele Yang, François Boller, Dominique Campion, Didier Hannequin, Marc Sitbon, Daniel H. Geschwind, Jean‐Luc Battini, Giovanni Coppola

    Foilsithe / Cruthaithe 2015
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  6. 6
    Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification

    Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification de réir Sandy Hsu, Renee Sears, Roberta R. Lemos, Beatriz Quintáns, Alden Huang, Elizabeth Spiteri, Lisette Nevarez, Catherine Mamah, Mayana Zatz, Kerrie D. Pierce, Janice M. Fullerton, John C. Adair, Jon Berner, Matthew Bower, Henry Brodaty, Olga Carmona, Valerija Dobričić, Brent L. Fogel, Daniel García-Estevez, Jill Goldman, John L. Goudreau, Suellen Hopfer, Milena Janković, Serge Jaumà, Joanna C. Jen, Suppachok Kirdlarp, Joerg Klepper, Vladimir Kostić, Anthony E. Lang, Agnès Linglart, Melissa K. Maisenbacher, Bala V. Manyam, Pietro Mazzoni, Z Miedzybrodzka, Witoon Mitarnun, Philip B. Mitchell, Jennifer M. Mueller, Ivana Novaković, Martin Paucar, Henry L. Paulson, Sheila A Simpson, Per Svenningsson, Paul Tuite, Jerrold L. Vitek, Suppachok Wetchaphanphesat, Charles A. Williams, Michele Yang, Peter R. Schofield, João Ricardo Mendes de Oliveira, María-Jesús Sobrido, Daniel H. Geschwind, Giovanni Coppola

    Foilsithe / Cruthaithe 2013
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