Hasil Pencarian - Alessandra Renieri

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  1. 1
    Commentary: Potential Links between Hepadnavirus and Bornavirus Sequences in the Host Genome and Cancer

    Commentary: Potential Links between Hepadnavirus and Bornavirus Sequences in the Host Genome and Cancer oleh Francesco Cetta, Maria Palmieri, Alessandra Renieri, Alessandra Renieri, Elisa Frullanti

    Diterbitkan 2018-07-01
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  2. 2
    TLRs: Innate Immune Sentries against SARS-CoV-2 Infection

    TLRs: Innate Immune Sentries against SARS-CoV-2 Infection oleh Stefania Mantovani, Barbara Oliviero, Stefania Varchetta, Alessandra Renieri, Mario U. Mondelli

    Diterbitkan 2023-04-01
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  3. 3
    First Identification of a Triple Corneal Dystrophy Association: Keratoconus, Epithelial Basement Membrane Corneal Dystrophy and Fuchs' Endothelial Corneal Dystrophy

    First Identification of a Triple Corneal Dystrophy Association: Keratoconus, Epithelial Basement Membrane Corneal Dystrophy and Fuchs' Endothelial Corneal Dystrophy oleh Cosimo Mazzotta, Claudio Traversi, Frederik Raiskup, Caterina Lo Rizzo, Alessandra Renieri

    Diterbitkan 2014-09-01
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  4. 4
    Corrigendum: Spondyloocular syndrome: A novel XYLT2 variant with description of the neonatal phenotype

    Corrigendum: Spondyloocular syndrome: A novel XYLT2 variant with description of the neonatal phenotype oleh Gabriella Doddato, Gabriella Doddato, Alessandra Fabbiani, Alessandra Fabbiani, Alessandra Fabbiani, Chiara Fallerini, Chiara Fallerini, Mirella Bruttini, Mirella Bruttini, Mirella Bruttini, Theodora Hadjistilianou, Martino Landi, Caterina Coradeschi, Salvatore Grosso, Barbara Tomasini, Maria Antonietta Mencarelli, Alessandra Renieri, Alessandra Renieri, Alessandra Renieri, Francesca Ariani, Francesca Ariani, Francesca Ariani

    Diterbitkan 2023-01-01
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  5. 5
    Spondyloocular Syndrome: A Novel XYLT2 Variant with Description of the Neonatal Phenotype

    Spondyloocular Syndrome: A Novel XYLT2 Variant with Description of the Neonatal Phenotype oleh Gabriella Doddato, Gabriella Doddato, Alessandra Fabbiani, Alessandra Fabbiani, Alessandra Fabbiani, Chiara Fallerini, Chiara Fallerini, Mirella Bruttini, Mirella Bruttini, Mirella Bruttini, Theodora Hadjistilianou, Martino Landi, Caterina Coradeschi, Salvatore Grosso, Barbara Tomasini, Maria Antonietta Mencarelli, Alessandra Renieri, Alessandra Renieri, Alessandra Renieri, Francesca Ariani, Francesca Ariani, Francesca Ariani

    Diterbitkan 2021-12-01
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  6. 6
    RB1 Germline Variant Predisposing to a Rare Ovarian Germ Cell Tumor: A Case Report

    RB1 Germline Variant Predisposing to a Rare Ovarian Germ Cell Tumor: A Case Report oleh Elisa Gelli, Chiara Fallerini, Floriana Valentino, Annarita Giliberti, Francesca Castiglione, Lucrezia Laschi, Maria Palmieri, Alessandra Fabbiani, Alessandra Fabbiani, Rossella Tita, Maria Antonietta Mencarelli, Alessandra Renieri, Alessandra Renieri, Francesca Ariani, Francesca Ariani

    Diterbitkan 2020-08-01
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  7. 7
    In response to the letter to the editor by Soha Ghanian et al. re our publication “Shorter androgen receptor polyQ alleles protect against life-threatening COVID-19 disease in European males”

    In response to the letter to the editor by Soha Ghanian et al. re our publication “Shorter androgen receptor polyQ alleles protect against life-threatening COVID-19 disease in Euro... oleh Andrea M. Isidori, Marco Marcelli, Maria Grazia Castagna, Margherita Baldassarri, Francesca Fava, Alessandra Renieri

    Diterbitkan 2021-06-01
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  8. 8
    Case report: PIK3CA somatic mutation leading to Klippel Trenaunay Syndrome and multiple tumors

    Case report: PIK3CA somatic mutation leading to Klippel Trenaunay Syndrome and multiple tumors oleh Viola Bianca Serio, Viola Bianca Serio, Maria Palmieri, Maria Palmieri, Simona Innamorato, Simona Innamorato, Lorenzo Loberti, Lorenzo Loberti, Lorenzo Loberti, Chiara Fallerini, Chiara Fallerini, Francesca Ariani, Francesca Ariani, Enrica Antolini, Enrica Antolini, Jasmine Covarelli, Jasmine Covarelli, Massimo Vaghi, Massimo Vaghi, Elisa Frullanti, Elisa Frullanti, Alessandra Renieri, Alessandra Renieri, Alessandra Renieri, Anna Maria Pinto

    Diterbitkan 2023-08-01
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  9. 9
    MET is a new confirmed gene responsible for familial distal arthrogryposis

    MET is a new confirmed gene responsible for familial distal arthrogryposis oleh Debora Maffeo, Anna Carrer, Angela Rina, Loredaria Adamo, Caterina Lo Rizzo, Mirella Bruttini, Alessandra Renieri, Francesca Mari

    Diterbitkan 2024-03-01
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  10. 10
    SPTBN5, Encoding the βV-Spectrin Protein, Leads to a Syndrome of Intellectual Disability, Developmental Delay, and Seizures

    SPTBN5, Encoding the βV-Spectrin Protein, Leads to a Syndrome of Intellectual Disability, Developmental Delay, and Seizures oleh Amjad Khan, Amjad Khan, Lucia Pia Bruno, Lucia Pia Bruno, Fadhel Alomar, Muhammad Umair, Muhammad Umair, Anna Maria Pinto, Abid Ali Khan, Alamzeb Khan, Saima, Alessandra Fabbiani, Alessandra Fabbiani, Kristina Zguro, Simone Furini, Maria Antonietta Mencarelli, Alessandra Renieri, Alessandra Renieri, Alessandra Renieri, Sara Resciniti, Sara Resciniti, Karla A. Peña-Guerra, Francisco J. Guzmán-Vega, Stefan T. Arold, Stefan T. Arold, Francesca Ariani, Francesca Ariani, Francesca Ariani, Shahid Niaz Khan

    Diterbitkan 2022-06-01
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  11. 11
    Potentially Treatable Disorder Diagnosed Post Mortem by Exome Analysis in a Boy with Respiratory Distress

    Potentially Treatable Disorder Diagnosed Post Mortem by Exome Analysis in a Boy with Respiratory Distress oleh Valentina Imperatore, Maria Antonietta Mencarelli, Chiara Fallerini, Laura Bianciardi, Francesca Ariani, Simone Furini, Alessandra Renieri, Francesca Mari, Elisa Frullanti

    Diterbitkan 2016-02-01
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  12. 12
    The Medical Community’s Role in Communication Strategies during Health Crises—Perspective from European Union of Medical Specialists (UEMS)

    The Medical Community’s Role in Communication Strategies during Health Crises—Perspective from European Union of Medical Specialists (UEMS) oleh Ilia Nadareishvili, Theodore Bazas, Nicola Petrosillo, Vojko Berce, John Firth, Armando Mansilha, Mihaela Leventer, Alessandra Renieri, Mauro Zampolini, Vassilios Papalois

    Diterbitkan 2023-07-01
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  13. 13
    Author Correction: A glomerulus-on-a-chip to recapitulate the human glomerular filtration barrier

    Author Correction: A glomerulus-on-a-chip to recapitulate the human glomerular filtration barrier oleh Astgik Petrosyan, Paolo Cravedi, Valentina Villani, Andrea Angeletti, Joaquin Manrique, Alessandra Renieri, Roger E. De Filippo, Laura Perin, Stefano Da Sacco

    Diterbitkan 2019-10-01
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  14. 14
    A glomerulus-on-a-chip to recapitulate the human glomerular filtration barrier

    A glomerulus-on-a-chip to recapitulate the human glomerular filtration barrier oleh Astgik Petrosyan, Paolo Cravedi, Valentina Villani, Andrea Angeletti, Joaquin Manrique, Alessandra Renieri, Roger E. De Filippo, Laura Perin, Stefano Da Sacco

    Diterbitkan 2019-08-01
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  15. 15
    PIK3CA-CDKN2A clonal evolution in metastatic breast cancer and multiple points cell-free DNA analysis

    PIK3CA-CDKN2A clonal evolution in metastatic breast cancer and multiple points cell-free DNA analysis oleh Maria Palmieri, Margherita Baldassarri, Francesca Fava, Alessandra Fabbiani, Giuseppe Maria Campennì, Maria Antonietta Mencarelli, Rossella Tita, Stefania Marsili, Alessandra Renieri, Elisa Frullanti

    Diterbitkan 2019-10-01
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  16. 16
    An explainable model of host genetic interactions linked to COVID-19 severity

    An explainable model of host genetic interactions linked to COVID-19 severity oleh Anthony Onoja, Nicola Picchiotti, Chiara Fallerini, Margherita Baldassarri, Francesca Fava, GEN-COVID Multicenter Study, Francesca Colombo, Francesca Chiaromonte, Alessandra Renieri, Simone Furini, Francesco Raimondi

    Diterbitkan 2022-10-01
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  17. 17
    Clinical, molecular and glycophenotype insights in SLC39A8-CDG

    Clinical, molecular and glycophenotype insights in SLC39A8-CDG oleh Eleonora Bonaventura, Rita Barone, Luisa Sturiale, Rosa Pasquariello, Maria Grazia Alessandrì, Anna Maria Pinto, Alessandra Renieri, Celeste Panteghini, Barbara Garavaglia, Giovanni Cioni, Roberta Battini

    Diterbitkan 2021-07-01
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  18. 18
    X-Linked Alport Syndrome in Women: Genotype and Clinical Course in 24 Cases

    X-Linked Alport Syndrome in Women: Genotype and Clinical Course in 24 Cases oleh Antonio Mastrangelo, Marisa Giani, Elena Groppali, Pierangela Castorina, Giulia Soldà, Giulia Soldà, Michela Robusto, Chiara Fallerini, Mirella Bruttini, Alessandra Renieri, Giovanni Montini, Giovanni Montini

    Diterbitkan 2020-11-01
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  19. 19
    Hints for Genetic and Clinical Differentiation of Adult-Onset Monogenic Autoinflammatory Diseases

    Hints for Genetic and Clinical Differentiation of Adult-Onset Monogenic Autoinflammatory Diseases oleh Carla Gaggiano, Donato Rigante, Antonio Vitale, Orso Maria Lucherini, Alessandra Fabbiani, Giovanna Capozio, Chiara Marzo, Viviana Gelardi, Salvatore Grosso, Bruno Frediani, Alessandra Renieri, Luca Cantarini

    Diterbitkan 2019-01-01
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  20. 20
    JNK signaling provides a novel therapeutic target for Rett syndrome

    JNK signaling provides a novel therapeutic target for Rett syndrome oleh Clara Alice Musi, Anna Maria Castaldo, Anna Elisa Valsecchi, Sara Cimini, Noemi Morello, Riccardo Pizzo, Alessandra Renieri, Ilaria Meloni, Maurizio Bonati, Maurizio Giustetto, Tiziana Borsello

    Diterbitkan 2021-12-01
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