Works matching AU Morena, Maria

Results: 67
    1

    Dissecting the transcriptional program of phosphomannomutase 2-deficient cells: Lymphoblastoide B cell lines as a valuable model for congenital disorders of glycosylation studies.

    Published in:
    Glycobiology, 2022, v. 32, n. 2, p. 84, doi. 10.1093/glycob/cwab087
    By:
    • Parrado, Antonio;
    • Rubio, Gonzalo;
    • Serrano, Mercedes;
    • Morena-Barrio, María Eugenia De la;
    • Ibáñez-Micó, Salvador;
    • Ruiz-Lafuente, Natalia;
    • Schwartz-Albiez, Reinhard;
    • Esteve-Solé, Ana;
    • Alsina, Laia;
    • Corral, Javier;
    • Hernández-Caselles, Trinidad
    Publication type:
    Article
    2
    3

    Multirefractory primary immune thrombocytopenia; targeting the decreased sialic acid content.

    Published in:
    Platelets, 2019, v. 30, n. 6, p. 743, doi. 10.1080/09537104.2018.1513476
    By:
    • Revilla, Nuria;
    • Corral, Javier;
    • Miñano, Antonia;
    • Mingot-Castellano, Maria Eva;
    • Campos, Rosa Maria;
    • Velasco, Francisco;
    • Gonzalez, Nicolas;
    • Galvez, Eva;
    • Berrueco, Ruben;
    • Fuentes, Inmaculada;
    • Gonzalez-Lopez, Tomas Jose;
    • de la Morena-Barrio, Maria Eugenia;
    • Gonzalez-Porras, Jose Ramon;
    • Vicente, Vicente;
    • Lozano, Maria Luisa
    Publication type:
    Article
    4
    5
    6
    7
    8
    9
    10
    11

    High penetrance of inferior vena cava system atresia in severe thrombophilia caused by homozygous antithrombin Budapest 3 variant: Description of a new syndrome.

    Published in:
    American Journal of Hematology, 2021, v. 96, n. 11, p. 1363, doi. 10.1002/ajh.26304
    By:
    • de la Morena‐Barrio, María E.;
    • Gindele, Réka;
    • Bravo‐Pérez, Carlos;
    • Ilonczai, Péter;
    • Zuazu, Isabel;
    • Speker, Marianna;
    • Oláh, Zsolt;
    • Rodríguez‐Sevilla, Juan J.;
    • Entrena, Laura;
    • Infante, Maria S.;
    • de la Morena‐Barrio, Belén;
    • García, José M.;
    • Schlammadinger, Ágota;
    • Cifuentes‐Riquelme, Rosa;
    • Mora‐Casado, Asunción;
    • Miñano, Antonia;
    • Padilla, Jose;
    • Vicente, Vicente;
    • Corral, Javier;
    • Bereczky, Zsuzsanna
    Publication type:
    Article
    12

    A novel genetic variant in PTGS1 affects N‐glycosylation of cyclooxygenase‐1 causing a dominant‐negative effect on platelet function and bleeding diathesis.

    Published in:
    American Journal of Hematology, 2021, v. 96, n. 3, p. E83, doi. 10.1002/ajh.26076
    By:
    • Palma‐Barqueros, Verónica;
    • Crescente, Marilena;
    • Morena, María Eugenia;
    • Chan, Melissa V.;
    • Almarza, Elena;
    • Revilla, Nuria;
    • Bohdan, Natalia;
    • Miñano, Antonia;
    • Padilla, José;
    • Allan, Harriet E.;
    • Maffucci, Tania;
    • Edin, Matthew L.;
    • Zeldin, Darryl C.;
    • Mesa‐Nuñez, Cristina;
    • Damian, Carlos;
    • Marín‐Quilez, Ana;
    • Benito, Rocío;
    • Martínez‐Martínez, Irene;
    • Bermejo, Nuria;
    • Casas‐Aviles, Ignacio
    Publication type:
    Article
    13
    14

    Intervención en la crisis COVID-19 del equipo de Psicología Clínica de la Interconsulta del IPS Gregorio Marañón.

    Published in:
    Clínica Contemporánea: Revista de Diagnóstico Psicológico, Psicoterapia y Salud, 2020, v. 11, n. 3, p. N.PAG, doi. 10.5093/cc2020a17
    By:
    • Cuellar, Marisa García-Ontiveros;
    • Rufrancos, Begoña Arbulo;
    • Caño, María Mallo;
    • Aragón, María Mayoral;
    • Ramírez, María García;
    • Hermosilla, Muriel;
    • Ortiz, Silvia Holguera;
    • Ruiz, Javier Martín;
    • Fernández, Tania Delgado;
    • Sebastián, Susana Sanz;
    • Morena, María Ángeles Ureña;
    • Agudo, Fátima Valencia;
    • Martínez, Alejandro Parages;
    • Colino, Francisco Duque
    Publication type:
    Article
    15
    16
    17

    Correction to: Clinical Practice Guidelines for the Immunological Management of Chromosome 22q11.2 Deletion Syndrome and Other Defects in Thymic Development.

    Published in:
    2024
    By:
    • Mustillo, Peter J.;
    • Sullivan, Kathleen E.;
    • Chinn, Ivan K.;
    • Notarangelo, Luigi D.;
    • Haddad, Elie;
    • Davies, E. Graham;
    • de la Morena, Maria Teresa;
    • Hartog, Nicholas;
    • Yu, Joyce E.;
    • Hernandez-Trujillo, Vivian P.;
    • Ip, Winnie;
    • Franco, Jose;
    • Gambineri, Eleonora;
    • Hickey, Scott E.;
    • Varga, Elizabeth;
    • Markert, M. Louise
    Publication type:
    Correction Notice
    18
    19
    20
    21
    22
    23
    24
    25
    26

    Factor XI in Carriers of Antiphospholipid Antibodies: Elevated Levels Associated with Symptomatic Thrombotic Cases, While Low Levels Linked to Asymptomatic Cases.

    Published in:
    International Journal of Molecular Sciences, 2023, v. 24, n. 22, p. 16270, doi. 10.3390/ijms242216270
    By:
    • Pagán-Escribano, Javier;
    • Corral, Javier;
    • Miñano, Antonia;
    • Padilla, José;
    • Roldán, Vanessa;
    • Hernández-Vidal, María Julia;
    • Lozano, Jesús;
    • de la Morena-Barrio, Isabel;
    • Vicente, Vicente;
    • Lozano, María Luisa;
    • Herranz, María Teresa;
    • de la Morena-Barrio, María Eugenia
    Publication type:
    Article
    27
    28

    N-Glycosylation as a Tool to Study Antithrombin Secretion, Conformation, and Function.

    Published in:
    International Journal of Molecular Sciences, 2021, v. 22, n. 2, p. 516, doi. 10.3390/ijms22020516
    By:
    • Águila, Sonia;
    • Noto, Rosina;
    • Luengo-Gil, Ginés;
    • Espín, Salvador;
    • Bohdan, Nataliya;
    • de la Morena-Barrio, María Eugenia;
    • Peñas, Julia;
    • Rodenas, Maria Carmen;
    • Vicente, Vicente;
    • Corral, Javier;
    • Manno, Mauro;
    • Martínez-Martínez, Irene
    Publication type:
    Article
    29
    30

    Scalable production of tissue-like vascularized liver organoids from human PSCs.

    Published in:
    Experimental & Molecular Medicine EMM, 2023, v. 55, n. 9, p. 2005, doi. 10.1038/s12276-023-01074-1
    By:
    • Harrison, Sean P.;
    • Siller, Richard;
    • Tanaka, Yoshiaki;
    • Chollet, Maria Eugenia;
    • de la Morena-Barrio, María Eugenia;
    • Xiang, Yangfei;
    • Patterson, Benjamin;
    • Andersen, Elisabeth;
    • Bravo-Pérez, Carlos;
    • Kempf, Henning;
    • Åsrud, Kathrine S.;
    • Lunov, Oleg;
    • Dejneka, Alexandr;
    • Mowinckel, Marie-Christine;
    • Stavik, Benedicte;
    • Sandset, Per Morten;
    • Melum, Espen;
    • Baumgarten, Saphira;
    • Bonanini, Flavio;
    • Kurek, Dorota
    Publication type:
    Article
    31
    32
    33
    34
    35
    36
    37
    38

    GPI-anchor and GPI-anchored protein expression in PMM2-CDG patients.

    Published in:
    Orphanet Journal of Rare Diseases, 2013, v. 8, n. 1, p. 1, doi. 10.1186/1750-1172-8-170
    By:
    • Morena-Barrio, Maria E de la;
    • Hernández-Caselles, Trinidad;
    • Corral, Javier;
    • García-López, Roberto;
    • Martínez-Martínez, Irene;
    • Pérez-Dueñas, Belen;
    • Altisent, Carmen;
    • Sevivas, Teresa;
    • Kristensen, Soren R.;
    • Guillén-Navarro, Encarna;
    • Miñano, Antonia;
    • Vicente, Vicente;
    • Jaeken, Jaak;
    • Lozano, Maria L.
    Publication type:
    Article
    39

    GPI-anchor and GPI-anchored protein expression in PMM2-CDG patients.

    Published in:
    2013
    By:
    • de la Morena-Barrio, Maria E;
    • Hernández-Caselles, Trinidad;
    • Corral, Javier;
    • García-López, Roberto;
    • Martínez-Martínez, Irene;
    • Pérez-Dueñas, Belen;
    • Altisent, Carmen;
    • Sevivas, Teresa;
    • Kristensen, Soren R;
    • Guillén-Navarro, Encarna;
    • Miñano, Antonia;
    • Vicente, Vicente;
    • Jaeken, Jaak;
    • Lozano, Maria L
    Publication type:
    journal article
    40

    International clinical guidelines for the management of phosphomannomutase 2‐congenital disorders of glycosylation: Diagnosis, treatment and follow up.

    Published in:
    Journal of Inherited Metabolic Disease, 2019, v. 42, n. 1, p. 5, doi. 10.1002/jimd.12024
    By:
    • Altassan, Ruqaiah;
    • Péanne, Romain;
    • Jaeken, Jaak;
    • Barone, Rita;
    • Bidet, Muad;
    • Borgel, Delphine;
    • Brasil, Sandra;
    • Cassiman, David;
    • Cechova, Anna;
    • Coman, David;
    • Corral, Javier;
    • Correia, Joana;
    • de la Morena‐Barrio, María Eugenia;
    • de Lonlay, Pascale;
    • Dos Reis, Vanessa;
    • Ferreira, Carlos R;
    • Fiumara, Agata;
    • Francisco, Rita;
    • Freeze, Hudson;
    • Funke, Simone
    Publication type:
    Article
    41
    42
    43

    Clinical Practice Guidelines for the Immunological Management of Chromosome 22q11.2 Deletion Syndrome and Other Defects in Thymic Development.

    Published in:
    Journal of Clinical Immunology, 2023, v. 43, n. 2, p. 247, doi. 10.1007/s10875-022-01418-y
    By:
    • Mustillo, Peter J.;
    • Sullivan, Kathleen E.;
    • Chinn, Ivan K.;
    • Notarangelo, Luigi D.;
    • Haddad, Elie;
    • Davies, E. Graham;
    • de la Morena, Maria Teresa;
    • Hartog, Nicholas;
    • Yu, Joyce E.;
    • Hernandez-Trujillo, Vivian P.;
    • Ip, Winnie;
    • Franco, Jose;
    • Gambineri, Eleonora;
    • Hickey, Scott E.;
    • Varga, Elizabeth;
    • Markert, M. Louise
    Publication type:
    Article
    44

    ICON: The Early Diagnosis of Congenital Immunodeficiencies.

    Published in:
    Journal of Clinical Immunology, 2014, v. 34, n. 4, p. 398, doi. 10.1007/s10875-014-0003-x
    By:
    • Routes, John;
    • Abinun, Mario;
    • Al-Herz, Waleed;
    • Bustamante, Jacinta;
    • Condino-Neto, Antonio;
    • Morena, Maria;
    • Etzioni, Amos;
    • Gambineri, Eleonora;
    • Haddad, Elie;
    • Kobrynski, Lisa;
    • Deist, Francoise;
    • Nonoyama, Shigeaki;
    • Oliveira, Joao;
    • Perez, Elena;
    • Picard, Capucine;
    • Rezaei, Nima;
    • Sleasman, John;
    • Sullivan, Kathleen;
    • Torgerson, Troy
    Publication type:
    Article
    45
    46

    Congenital antithrombin deficiency in patients with splanchnic vein thrombosis.

    Published in:
    Liver International, 2020, v. 40, n. 5, p. 1168, doi. 10.1111/liv.14342
    By:
    • Baiges, Anna;
    • Morena‐Barrio, María Eugenia;
    • Turon, Fanny;
    • Miñano, Antonia;
    • Alberto Ferrusquía, Jose;
    • Magaz, Marta;
    • Reverter, Juan Carlos;
    • Vicente, Vicente;
    • Hernández‐Gea, Virginia;
    • Corral, Javier;
    • García‐Pagán, Juan Carlos
    Publication type:
    Article
    47
    48
    49
    50

    Identification of the first large intronic deletion responsible of type I antithrombin deficiency not detected by routine molecular diagnostic methods.

    Published in:
    British Journal of Haematology, 2019, v. 186, n. 4, p. e82, doi. 10.1111/bjh.15913
    By:
    • De la Morena‐Barrio, Belén;
    • Borràs, Nina;
    • Rodríguez‐Alén, Agustín;
    • Morena‐Barrio, María E.;
    • García‐Hernández, Juan L.;
    • Padilla, José;
    • Bravo‐Pérez, Carlos;
    • Miñano, Antonia;
    • Rollón, Noelia;
    • Corral, Javier;
    • Vidal, Francisco;
    • Vicente, Vicente
    Publication type:
    Article