Works matching AU Morgan, Anna


Results: 79
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    Acquired Aprosodia in Children.

    Published in:
    Journal of Child Neurology, 1990, v. 5, n. 1, p. 19, doi. 10.1177/088307389000500104
    By:
    • Bell, William L.;
    • Davis, Diana L.;
    • Morgan-Fisher, Anna;
    • Ross, Elliott D.
    Publication type:
    Article
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    Puzzling Out the Genetic Architecture of Endometriosis: Whole-Exome Sequencing and Novel Candidate Gene Identification in a Deeply Clinically Characterised Cohort.

    Published in:
    Biomedicines, 2023, v. 11, n. 8, p. 2122, doi. 10.3390/biomedicines11082122
    By:
    • Santin, Aurora;
    • Spedicati, Beatrice;
    • Morgan, Anna;
    • Lenarduzzi, Stefania;
    • Tesolin, Paola;
    • Nardone, Giuseppe Giovanni;
    • Mazzà, Daniela;
    • Di Lorenzo, Giovanni;
    • Romano, Federico;
    • Buonomo, Francesca;
    • Mangogna, Alessandro;
    • Concas, Maria Pina;
    • Zito, Gabriella;
    • Ricci, Giuseppe;
    • Girotto, Giorgia
    Publication type:
    Article
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    Variants in USP48 encoding ubiquitin hydrolase are associated with autosomal dominant non-syndromic hereditary hearing loss.

    Published in:
    Human Molecular Genetics, 2021, v. 30, n. 19, p. 1785, doi. 10.1093/hmg/ddab145
    By:
    • Bassani, Sissy;
    • Beelen, Edward van;
    • Rossel, Mireille;
    • Voisin, Norine;
    • Morgan, Anna;
    • Arribat, Yoan;
    • Chatron, Nicolas;
    • Chrast, Jacqueline;
    • Cocca, Massimiliano;
    • Delprat, Benjamin;
    • Faletra, Flavio;
    • Giannuzzi, Giuliana;
    • Guex, Nicolas;
    • Machavoine, Roxane;
    • Pradervand, Sylvain;
    • Smits, Jeroen J;
    • Kamp, Jiddeke M van de;
    • Ziegler, Alban;
    • Amati, Francesca;
    • Marlin, Sandrine
    Publication type:
    Article
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    Post-entry Internationalization Dynamics.

    Published in:
    International Small Business Journal: Researching Entrepreneurship, 2009, v. 27, n. 1, p. 71, doi. 10.1177/0266242608098347
    By:
    • Morgan-Thomas, Anna;
    • Jones, Marian V.
    Publication type:
    Article
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    Mutations in PLS1, encoding fimbrin, cause autosomal dominant nonsyndromic hearing loss.

    Published in:
    Human Mutation, 2019, v. 40, n. 12, p. 2286, doi. 10.1002/humu.23891
    By:
    • Morgan, Anna;
    • Koboldt, Daniel C.;
    • Barrie, Elizabeth S.;
    • Crist, Erin R.;
    • García García, Gema;
    • Mezzavilla, Massimo;
    • Faletra, Flavio;
    • Mihalic Mosher, Theresa;
    • Wilson, Richard K.;
    • Blanchet, Catherine;
    • Manickam, Kandamurugu;
    • Roux, Anne‐Francoise;
    • Gasparini, Paolo;
    • Dell'Orco, Daniele;
    • Girotto, Giorgia
    Publication type:
    Article
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    Ask the experts.

    Published in:
    Nursing Older People, 2006, v. 18, n. 7, p. 10, doi. 10.7748/nop.18.7.10.s12
    By:
    • Morgan, Anna;
    • Barker, Wendy;
    • Frazer, Aileen;
    • Hayes, Nicky;
    • Nazarko, Linda;
    • Jackson, Jill
    Publication type:
    Article
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    Ask the experts.

    Published in:
    Nursing Older People, 2005, v. 17, n. 3, p. 14
    By:
    • Hayes, Nicky;
    • Webster, Jonathan;
    • Nazarko, Linda;
    • Lewis, Dianne;
    • Morgan, Anna;
    • Mansfield, Sally
    Publication type:
    Article
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    Uncovering a Novel Pathogenic Mechanism of BCS1L in Mitochondrial Disorders: Insights from Functional Studies on the c.38A>G Variant.

    Published in:
    International Journal of Molecular Sciences, 2025, v. 26, n. 8, p. 3670, doi. 10.3390/ijms26083670
    By:
    • Capaci, Valeria;
    • Zupin, Luisa;
    • Magistrati, Martina;
    • Bonati, Maria Teresa;
    • Celsi, Fulvio;
    • Marrone, Irene;
    • Baldo, Francesco;
    • Ura, Blendi;
    • Spedicati, Beatrice;
    • Morgan, Anna;
    • Bruno, Irene;
    • Zeviani, Massimo;
    • Dallabona, Cristina;
    • Girotto, Giorgia;
    • Magnolato, Andrea
    Publication type:
    Article