检索结果 - Yitzchak Frank

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  1. 1
    Occipital-parietal encephalopathy: A new name for an old syndrome

    Occipital-parietal encephalopathy: A new name for an old syndrome 由 Steven G. Pavlakis, Yitzchak Frank, Peter Kalina, Manju Chandra, Dongfeng Lu

    出版 1997
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  2. 2
    A pilot controlled trial of insulin-like growth factor-1 in children with Phelan-McDermid syndrome

    A pilot controlled trial of insulin-like growth factor-1 in children with Phelan-McDermid syndrome 由 Alexander Kolevzon, Lauren Bush, Andrew Wang, Danielle Halpern, Yitzchak Frank, David Grodberg, Robert Rapaport, Teresa Tavassoli, William F. Chaplin, Latha Soorya, Joseph D. Buxbaum

    出版 2014
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    Artigo
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  3. 3
    FOXP1 syndrome: a review of the literature and practice parameters for medical assessment and monitoring

    FOXP1 syndrome: a review of the literature and practice parameters for medical assessment and monitoring 由 Reymundo Lozano, Catherine Gbekie, Paige M. Siper, Shubhika Srivastava, Jeffrey M. Saland, Swathi Sethuram, Lara Tang, Elodie Drapeau, Yitzchak Frank, Joseph D. Buxbaum, Alexander Kolevzon

    出版 2021
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  4. 4
    Clinical trial of insulin-like growth factor-1 in Phelan-McDermid syndrome

    Clinical trial of insulin-like growth factor-1 in Phelan-McDermid syndrome 由 Alexander Kolevzon, Michael S. Breen, Paige M. Siper, Danielle Halpern, Yitzchak Frank, Hillary Rieger, J. Weismann, M. Pilar Trelles, Bonnie Lerman, Robert Rapaport, Joseph D. Buxbaum

    出版 2022
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    Carta
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  5. 5
    Phelan-McDermid syndrome: a review of the literature and practice parameters for medical assessment and monitoring

    Phelan-McDermid syndrome: a review of the literature and practice parameters for medical assessment and monitoring 由 Alexander Kolevzon, Benjamin Angarita, Lauren Bush, A. Ting Wang, Yitzchak Frank, Amy Yang, Robert Rapaport, Jeffrey M. Saland, Shubhika Srivastava, Cristina Farrell, Lisa Edelmann, Joseph D. Buxbaum

    出版 2014
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  6. 6
    Delineation of the genetic and clinical spectrum of Phelan-McDermid syndrome caused by SHANK3 point mutations

    Delineation of the genetic and clinical spectrum of Phelan-McDermid syndrome caused by SHANK3 point mutations 由 Silvia De Rubeis, Paige M. Siper, Allison Durkin, Jordana Weissman, François Muratet, Danielle Halpern, M. Pilar Trelles, Yitzchak Frank, Reymundo Lozano, A. Ting Wang, J. Lloyd Holder, Catalina Betancur, Joseph D. Buxbaum, Alexander Kolevzon

    出版 2018
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    Artigo
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  7. 7
    Prospective investigation of autism and genotype-phenotype correlations in 22q13 deletion syndrome and SHANK3 deficiency

    Prospective investigation of autism and genotype-phenotype correlations in 22q13 deletion syndrome and SHANK3 deficiency 由 Latha Soorya, Alexander Kolevzon, Jessica Zweifach, Teresa Lim, Yuriy Dobry, Lily Schwartz, Yitzchak Frank, A. Ting Wang, Guiqing Cai, Elena Parkhomenko, Danielle Halpern, David Grodberg, Benjamin Angarita, Judith P. Willner, Amy Yang, Roberto Canitano, William F. Chaplin, Catalina Betancur, Joseph D. Buxbaum

    出版 2013
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    Artigo
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  8. 8
    Prospective investigation of FOXP1 syndrome

    Prospective investigation of FOXP1 syndrome 由 Paige M. Siper, Silvia De Rubeis, Maria del Pilar Trelles, Allison Durkin, Daniele Di Marino, François Muratet, Yitzchak Frank, Reymundo Lozano, Evan E. Eichler, Morgan Kelly, Jennifer S. Beighley, Jennifer Gerdts, Arianne S. Wallace, Heather C. Mefford, Raphael Bernier, Alexander Kolevzon, Joseph D. Buxbaum

    出版 2017
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    Artigo
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  9. 9
    Prospective and detailed behavioral phenotyping in DDX3X syndrome

    Prospective and detailed behavioral phenotyping in DDX3X syndrome 由 Lara Tang, Tess Levy, Sylvia Guillory, Danielle Halpern, Jessica Zweifach, Ivy Giserman‐Kiss, Jennifer H. Foss‐Feig, Yitzchak Frank, Reymundo Lozano, Puneet Belani, Christina Layton, Bonnie Lerman, Emanuel Frowner, Michael S. Breen, Silvia De Rubeis, Ana Kostić, Alexander Kolevzon, Joseph D. Buxbaum, Paige M. Siper, Dorothy E. Grice

    出版 2021
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    Artigo
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  10. 10
    Strong evidence for genotype–phenotype correlations in Phelan-McDermid syndrome: results from the developmental synaptopathies consortium

    Strong evidence for genotype–phenotype correlations in Phelan-McDermid syndrome: results from the developmental synaptopathies consortium 由 Tess Levy, Jennifer H. Foss‐Feig, Catalina Betancur, Paige M. Siper, María del Pilar Trelles-Thorne, Danielle Halpern, Yitzchak Frank, Reymundo Lozano, Christina Layton, Bari Britvan, Jonathan A. Bernstein, Joseph D. Buxbaum, Elizabeth Berry‐Kravis, Craig M. Powell, Siddharth Srivastava, Mustafa Şahin, Latha Soorya, Audrey Thurm, Alexander Kolevzon

    出版 2021
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