Works matching AU Guzman, Celina

Results: 11
    1

    Exploring Disorders of Gut–Brain Interaction in Schoolchildren and Adolescents with Autism.

    Published in:
    Life (2075-1729), 2025, v. 15, n. 6, p. 912, doi. 10.3390/life15060912
    By:
    • Velasco-Benítez, Carlos Alberto;
    • Rojas-Cerón, Christian Andrés;
    • Ortiz-Rivera, Claudia Jimena;
    • Velasco-Suárez, Daniela Alejandra;
    • Juvinao-Quintero, María Carolina;
    • Zubiri, Cecilia Elena;
    • Fernández, Julián Martín;
    • Bigliardi, Román;
    • Zosi, Anabella;
    • Chanis Águila, Ricardo A.;
    • Guzmán Acevedo, Celina;
    • Reynoso Zarzosa, Fátima Azereth;
    • Zablah Cordova, Roberto Arturo
    Publication type:
    Article
    2
    3

    Corrigendum: Deficiency of UBR1, a ubiquitin ligase of the N-end rule pathway, causes pancreatic dysfunction, malformations and mental retardation (Johanson-Blizzard syndrome).

    Published in:
    2006
    By:
    • Zenker, Martin;
    • Mayerle, Julia;
    • Lerch, Markus M;
    • Tagariello, Andreas;
    • Zerres, Klaus;
    • Durie, Peter R;
    • Beier, Matthias;
    • Hülskamp, Georg;
    • Guzman, Celina;
    • Rehder, Helga;
    • Beemer, Frits A;
    • Hamel, Ben;
    • Vanlieferinghen, Philippe;
    • Gershoni-Baruch, Ruth;
    • Vieira, Marta W;
    • Dumic, Miroslav;
    • Auslender, Ron;
    • Gil-da-Silva-Lopes, Vera L;
    • Steinlicht, Simone;
    • Rauh, Manfred
    Publication type:
    Correction Notice
    4

    Deficiency of UBR1, a ubiquitin ligase of the N-end rule pathway, causes pancreatic dysfunction, malformations and mental retardation (Johanson-Blizzard syndrome).

    Published in:
    Nature Genetics, 2005, v. 37, n. 12, p. 1345, doi. 10.1038/ng1681
    By:
    • Zenker, Martin;
    • Mayerle, Julia;
    • Lerch, Markus M.;
    • Tagariello, Andreas;
    • Zerres, Klaus;
    • Durie, Peter R.;
    • Beier, Matthias;
    • Hülskamp, Georg;
    • Guzman, Celina;
    • Rehder, Helga;
    • Beemer, Frits A.;
    • Hamel, Ben;
    • Vanlieferinghen, Philippe;
    • Gershoni-Baruch, Ruth;
    • Vieira, Marta W.;
    • Dumic, Miroslav;
    • Auslender, Ron;
    • Gil-da-Silva-Lopes, Vera L.;
    • Steinlicht, Simone;
    • Rauh, Manfred
    Publication type:
    Article
    5
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    8

    Oblique facial clefts in Johanson-Blizzard syndrome.

    Published in:
    American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 6, p. 1495, doi. 10.1002/ajmg.a.37630
    By:
    • Corona‐Rivera, Jorge Román;
    • Zapata‐Aldana, Eugenio;
    • Bobadilla‐Morales, Lucina;
    • Corona‐Rivera, Alfredo;
    • Peña‐Padilla, Christian;
    • Solis‐Hernández, Elizabeth;
    • Guzmán, Celina;
    • Richmond, Erick;
    • Zahl, Christian;
    • Zenker, Martin;
    • Sukalo, Maja
    Publication type:
    Article
    9
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    11

    Mutations in the Human UBR1 Gene and the Associated Phenotypic Spectrum.

    Published in:
    Human Mutation, 2014, v. 35, n. 5, p. 521, doi. 10.1002/humu.22538
    By:
    • Sukalo, Maja;
    • Fiedler, Ariane;
    • Guzmán, Celina;
    • Spranger, Stephanie;
    • Addor, Marie ‐ Claude;
    • Mcheik, Jiad N.;
    • Oltra Benavent, Manuel;
    • Cobben, Jan M.;
    • Gillis, Lynette A.;
    • Shealy, Amy G.;
    • Deshpande, Charu;
    • Bozorgmehr, Bita;
    • Everman, David B.;
    • Stattin, Eva ‐ Lena;
    • Liebelt, Jan;
    • Keller, Klaus ‐ Michael;
    • Bertola, Débora Romeo;
    • Karnebeek, Clara D.M.;
    • Bergmann, Carsten;
    • Liu, Zhifeng
    Publication type:
    Article