Works matching AU Parra, Alejandro

Results: 132
    1
    2

    Risk Categories in COVID-19 Based on Degrees of Inflammation: Data on More Than 17,000 Patients from the Spanish SEMI-COVID-19 Registry.

    Published in:
    Journal of Clinical Medicine, 2021, v. 10, n. 10, p. 2214, doi. 10.3390/jcm10102214
    By:
    • Rubio-Rivas, Manuel;
    • Corbella, Xavier;
    • Formiga, Francesc;
    • Menéndez Fernández, Estela;
    • Martín Escalante, María Dolores;
    • Baños Fernández, Isolina;
    • Arnalich Fernández, Francisco;
    • Del Corral-Beamonte, Esther;
    • Lalueza, Antonio;
    • Parra Virto, Alejandro;
    • Roy Vallejo, Emilia;
    • Loureiro-Amigo, José;
    • Álvarez Suárez, Ana María;
    • Abadía-Otero, Jesica;
    • Navarro De La Chica, María;
    • Estévez González, Raquel;
    • Hernández Milián, Almudena;
    • Areses Manrique, María;
    • Blázquez Encinar, Julio César;
    • González Noya, Amara
    Publication type:
    Article
    3
    4
    5
    6
    7
    8
    9

    Phenotypic spectrum and tumor risk in Simpson‐Golabi‐Behmel syndrome: Case series and comprehensive literature review.

    Published in:
    American Journal of Medical Genetics. Part A, 2024, v. 194, n. 12, p. 1, doi. 10.1002/ajmg.a.63840
    By:
    • Nisbet, Alex F.;
    • Viswanathan, Aravind;
    • George, Andrew M.;
    • Arias, Pedro;
    • Klein, Steven D.;
    • Nevado, Julian;
    • Parra, Alejandro;
    • Pascual, Patricia;
    • Romeo, Dominic J.;
    • Tenorio‐Castaño, Jair;
    • Taylor, Jesse A.;
    • Zackai, Elaine H.;
    • Lapunzina, Pablo;
    • Kalish, Jennifer M.
    Publication type:
    Article
    10

    Reduction of Sulfonylimines with Raney Nickel.

    Published in:
    Synthetic Communications, 2013, v. 43, n. 2, p. 198, doi. 10.1080/00397911.2011.594974
    By:
    • Ruano, JoséLuis García;
    • Fernández-Salas, JoséA.;
    • Maestro, M.Carmen;
    • Parra, Alejandro
    Publication type:
    Article
    11
    12
    13
    14

    AMOTL1‐Associated Multiple Congenital Anomalies (Craniofaciocardiohepatic Syndrome, CFCHS): A Novel Clinical Spectrum Including Craniofacial, Heart and Liver Abnormalities.

    Published in:
    Clinical Genetics, 2025, v. 107, n. 2, p. 234, doi. 10.1111/cge.14644
    By:
    • Gallego‐Zazo, Natalia;
    • Tenorio‐Castano, Jair;
    • Parra, Alejandro;
    • Nevado, Julián;
    • Cazalla, Mario;
    • Lucas‐Castro, Elsa;
    • Heath, Karen E.;
    • Palomares, María;
    • Soengas, Emma;
    • Lledín, M. Dolores;
    • Larrea, Emily;
    • Olveira, Antonio;
    • Morte, Beatriz;
    • Carracedo, Ángel;
    • Lapunzina, Pablo
    Publication type:
    Article
    15

    Non‐immune hydrops fetalis is associated with bi‐allelic pathogenic variants in the MYB Binding Protein 1a (MYBBP1A) gene.

    Published in:
    Clinical Genetics, 2024, v. 106, n. 6, p. 713, doi. 10.1111/cge.14601
    By:
    • Tenorio‐Castano, Jair;
    • Mansilla Aparicio, Elena;
    • García Santiago, Fe Amalia;
    • Klotz, Cherise M.;
    • Regojo, Rita María;
    • Anguita, Estefanía;
    • Ryan, Erin;
    • Juusola, Jane;
    • Herrero, Beatriz;
    • Arias, Pedro;
    • Parra, Alejandro;
    • Pascual, Patricia;
    • Gallego, Natalia;
    • Cazalla, Mario;
    • Rodriguez‐González, Roberto;
    • Antolín, Eugenia;
    • Nevado, Julián;
    • Ruiz‐Perez, Víctor L.;
    • Lapunzina, Pablo
    Publication type:
    Article
    16

    Identification of copy‐number variants in patients with overgrowth disorders.

    Published in:
    Clinical Genetics, 2024, v. 106, n. 5, p. 614, doi. 10.1111/cge.14596
    By:
    • Parra, Alejandro;
    • Tenorio‐Castano, Jair;
    • Nevado, Julián;
    • Cazalla, Mario;
    • Miranda‐Alcaraz, Lucía;
    • Gallego‐Zazo, Natalia;
    • Silván, Cristina;
    • Arias, Pedro;
    • Pozo‐Román, Jesús;
    • Ballesta‐Martínez, María Juliana;
    • Guillén‐Navarro, Encarna;
    • Arroyo, Ignacio;
    • Lotersztein, Vanesa;
    • Cosentino, Viviana;
    • González‐Meneses, Antonio;
    • Galán, Enrique;
    • Rosell, Jordi;
    • Ramos, Feliciano;
    • Plasencia, Antonio;
    • Rosa, Alberto L.
    Publication type:
    Article
    17

    Genetic and phenotypic findings in 34 novel Spanish patients with DDX3X neurodevelopmental disorder.

    Published in:
    Clinical Genetics, 2024, v. 105, n. 2, p. 140, doi. 10.1111/cge.14440
    By:
    • Parra, Alejandro;
    • Pascual, Patricia;
    • Cazalla, Mario;
    • Arias, Pedro;
    • Gallego‐Zazo, Natalia;
    • San‐Martín, Esteban A.;
    • Silván, Cristina;
    • Santos‐Simarro, Fernando;
    • Plasencia, Antonio;
    • Rosa, Alberto L.;
    • Blanquer, Aleixandre;
    • Garcı'a‐Alix, Alfredo;
    • Santana, Alfredo;
    • Delicado, Alicia;
    • Alonso, Almudena;
    • Rodriguez, Amaya;
    • Sanchis, Amparo;
    • Moreno, Ana;
    • Gar‐cía, Ana Patiño;
    • Vega, Ana
    Publication type:
    Article
    18
    19
    20
    21
    22
    23
    24
    25
    26
    27
    28
    29
    30
    31
    32
    33

    Clinical Heterogeneity and Different Phenotypes in Patients with SETD2 Variants: 18 New Patients and Review of the Literature.

    Published in:
    Genes, 2023, v. 14, n. 6, p. 1179, doi. 10.3390/genes14061179
    By:
    • Parra, Alejandro;
    • Rabin, Rachel;
    • Pappas, John;
    • Pascual, Patricia;
    • Cazalla, Mario;
    • Arias, Pedro;
    • Gallego-Zazo, Natalia;
    • Santana, Alfredo;
    • Arroyo, Ignacio;
    • Artigas, Mercè;
    • Pachajoa, Harry;
    • Alanay, Yasemin;
    • Akgun-Dogan, Ozlem;
    • Ruaud, Lyse;
    • Couque, Nathalie;
    • Levy, Jonathan;
    • Porras-Hurtado, Gloria Liliana;
    • Santos-Simarro, Fernando;
    • Ballesta-Martinez, Maria Juliana;
    • Guillén-Navarro, Encarna
    Publication type:
    Article
    34
    35
    36
    37
    38
    39
    40
    41
    42
    43
    44
    45
    46
    47
    48
    49
    50