Works matching AU King, Mary


Results: 303
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    What Sustainability Should Mean.

    Published in:
    Challenge (05775132), 2008, v. 51, n. 2, p. 27, doi. 10.2753/0577-5132510204
    By:
    • King, Mary C.
    Publication type:
    Article
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    Paroxysmal Movement Disorders.

    Published in:
    Frontiers in Neurology, 2021, v. 12, p. 1, doi. 10.3389/fneur.2021.659064
    By:
    • Harvey, Susan;
    • King, Mary D.;
    • Gorman, Kathleen M.
    Publication type:
    Article
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    Quality of Life After Cytoreductive Surgery and Hyperthermic Intraperitoneal Chemotherapy (CRS/HIPEC): Cancer Survivors' Perspective Through In-Depth Interviews.

    Published in:
    Annals of Surgical Oncology: An Oncology Journal for Surgeons, 2024, v. 31, n. 10, p. 7122, doi. 10.1245/s10434-024-15719-6
    By:
    • Falla-Zuniga, Luis Felipe;
    • King, Mary Caitlin;
    • Pawlikowski, Kathleen;
    • Nikiforchin, Andrei;
    • Lopez-Ramirez, Felipe;
    • Barakat, Philipp;
    • Iugai, Sergei;
    • Nieroda, Carol;
    • Gushchin, Vadim;
    • Sardi, Armando
    Publication type:
    Article
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    Response to treatment and outcomes of infantile spasms in Down syndrome.

    Published in:
    Developmental Medicine & Child Neurology, 2022, v. 64, n. 6, p. 780, doi. 10.1111/dmcn.15153
    By:
    • Harvey, Susan;
    • Allen, Nicholas M.;
    • King, Mary D.;
    • Lynch, Bryan;
    • Lynch, Sally A.;
    • O'Regan, Mary;
    • O'Rourke, Declan;
    • Shahwan, Amre;
    • Webb, David;
    • Gorman, Kathleen M.;
    • Aziz, J;
    • El Hassan, M;
    • Flynn, K;
    • Hanrahan, D;
    • Kehoe, C;
    • Leahy, C;
    • Lynch, N;
    • McHugh, JC;
    • McSweeney, N;
    • O'Mahony, E
    Publication type:
    Article
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    FBXO28 causes developmental and epileptic encephalopathy with profound intellectual disability.

    Published in:
    Epilepsia (Series 4), 2021, v. 62, n. 1, p. e13, doi. 10.1111/epi.16784
    By:
    • Schneider, Amy L.;
    • Myers, Candace T.;
    • Muir, Alison M.;
    • Calvert, Sophie;
    • Basinger, Alice;
    • Perry, M. Scott;
    • Rodan, Lance;
    • Helbig, Katherine L.;
    • Chambers, Chelsea;
    • Gorman, Kathleen M.;
    • King, Mary D.;
    • Donkervoort, Sandra;
    • Soldatos, Ariane;
    • Bönnemann, Carsten G.;
    • Spataro, Nino;
    • Gabau, Elisabeth;
    • Arellano, Montserrat;
    • Cappuccio, Gerarda;
    • Brunetti‐Pierri, Nicola;
    • Rossignol, Elsa
    Publication type:
    Article
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    The variable phenotypes of KCNQ-related epilepsy.

    Published in:
    Epilepsia (Series 4), 2014, v. 55, n. 9, p. e99, doi. 10.1111/epi.12715
    By:
    • Allen, Nicholas M.;
    • Mannion, Maria;
    • Conroy, Judith;
    • Lynch, Sally A.;
    • Shahwan, Amre;
    • Lynch, Bryan;
    • King, Mary D.
    Publication type:
    Article
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    Towards the identification of a genetic basis for Landau- Kleffner syndrome.

    Published in:
    Epilepsia (Series 4), 2014, v. 55, n. 6, p. 858, doi. 10.1111/epi.12645
    By:
    • Conroy, Judith;
    • McGettigan, Paul A.;
    • McCreary, Dara;
    • Shah, Naisha;
    • Collins, Kevin;
    • Parry‐Fielder, Bronwyn;
    • Moran, Margaret;
    • Hanrahan, Donncha;
    • Deonna, Thierry W.;
    • Korff, Christian M.;
    • Webb, David;
    • Ennis, Sean;
    • Lynch, Sally A.;
    • King, Mary D.
    Publication type:
    Article
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    Prevalence of Trachoma at Sub-District Level in Ethiopia: Determining When to Stop Mass Azithromycin Distribution.

    Published in:
    PLoS Neglected Tropical Diseases, 2014, v. 8, n. 3, p. 1, doi. 10.1371/journal.pntd.0002732
    By:
    • King, Jonathan D.;
    • Teferi, Tesfaye;
    • Cromwell, Elizabeth A.;
    • Zerihun, Mulat;
    • Ngondi, Jeremiah M.;
    • Damte, Mesele;
    • Ayalew, Frew;
    • Tadesse, Zerihun;
    • Gebre, Teshome;
    • Mulualem, Ayelign;
    • Karie, Alemu;
    • Melak, Berhanu;
    • Adugna, Mitku;
    • Gessesse, Demelash;
    • Worku, Abebe;
    • Endashaw, Tekola;
    • Admassu Ayele, Fisseha;
    • Stoller, Nicole E.;
    • King, Mary Rose A.;
    • Mosher, Aryc W.
    Publication type:
    Article
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    Prevalence of Trachoma at Sub-District Level in Ethiopia: Determining When to Stop Mass Azithromycin Distribution.

    Published in:
    PLoS Neglected Tropical Diseases, 2014, v. 8, n. 3, p. 1, doi. 10.1371/journal.pntd.0002732
    By:
    • King, Jonathan D.;
    • Teferi, Tesfaye;
    • Cromwell, Elizabeth A.;
    • Zerihun, Mulat;
    • Ngondi, Jeremiah M.;
    • Damte, Mesele;
    • Ayalew, Frew;
    • Tadesse, Zerihun;
    • Gebre, Teshome;
    • Mulualem, Ayelign;
    • Karie, Alemu;
    • Melak, Berhanu;
    • Adugna, Mitku;
    • Gessesse, Demelash;
    • Worku, Abebe;
    • Endashaw, Tekola;
    • Admassu Ayele, Fisseha;
    • Stoller, Nicole E.;
    • King, Mary Rose A.;
    • Mosher, Aryc W.
    Publication type:
    Article
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    Reduced transcript expression of genes affected by inherited and de novo CNVs in autism.

    Published in:
    European Journal of Human Genetics, 2011, v. 19, n. 6, p. 727, doi. 10.1038/ejhg.2011.24
    By:
    • Nord, Alex S.;
    • Roeb, Wendy;
    • Dickel, Diane E.;
    • Walsh, Tom;
    • Kusenda, Mary;
    • O'Connor, Kristen Lewis;
    • Malhotra, Dheeraj;
    • McCarthy, Shane E.;
    • Stray, Sunday M.;
    • Taylor, Susan M.;
    • Sebat, Jonathan;
    • King, Bryan;
    • King, Mary-Claire;
    • McClellan, Jon M.
    Publication type:
    Article
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    Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15.

    Published in:
    European Journal of Human Genetics, 2009, v. 17, n. 5, p. 554, doi. 10.1038/ejhg.2008.231
    By:
    • Doucette, Lance;
    • Merner, Nancy D.;
    • Cooke, Sandra;
    • Ives, Elizabeth;
    • Galutira, Dante;
    • Walsh, Vanessa;
    • Walsh, Tom;
    • MacLaren, Linda;
    • Cater, Tracey;
    • Fernandez, Bridget;
    • Green, Jane S.;
    • Wilcox, Edward R.;
    • Shotland, Larry;
    • Li, X. C.;
    • Lee, Ming;
    • King, Mary-Claire;
    • Young, Terry-Lynn
    Publication type:
    Article
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    Structural variation in Xq28: MECP2 duplications in 1% of patients with unexplained XLMR and in 2% of male patients with severe encephalopathy.

    Published in:
    2009
    By:
    • Lugtenberg, Dorien;
    • Kleefstra, Tjitske;
    • Oudakker, Astrid R.;
    • Nillesen, Willy M;
    • Yntema, Helger G.;
    • Tzschach, Andreas;
    • Raynaud, Martine;
    • Rating, Dietz;
    • Journel, Hubert;
    • Chelly, Jamel;
    • Goizet, Cyril;
    • Lacombe, Didier;
    • Pedespan, Jean-Michel;
    • Echenne, Bernard;
    • Tariverdian, Gholamali;
    • O'Rourke, Declan;
    • King, Mary D.;
    • Green, Andrew;
    • van Kogelenberg, Margriet;
    • Van Esch, Hilde
    Publication type:
    Correction Notice
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    Structural variation in Xq28: MECP2 duplications in 1% of patients with unexplained XLMR and in 2% of male patients with severe encephalopathy.

    Published in:
    European Journal of Human Genetics, 2009, v. 17, n. 4, p. 444, doi. 10.1038/ejhg.2008.208
    By:
    • Lugtenberg, Dorien;
    • Kleefstra, Tjitske;
    • Oudakker, Astrid R.;
    • Nillesen, Willy M.;
    • Yntema, Helger G.;
    • Tzschach, Andreas;
    • Raynaud, Martine;
    • Rating, Dietz;
    • Journel, Hubert;
    • Chelly, Jamel;
    • Goizet, Cyril;
    • Lacombe, Didier;
    • Pedespan, Jean-Michel;
    • Echenne, Bernard;
    • Tariverdian, Gholamali;
    • O'Rourke, Declan;
    • King, Mary D;
    • Green, Andrew;
    • van Kogelenberg, Margriet;
    • Van Esch, Hilde
    Publication type:
    Article
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