Hasil Pencarian - Gigliola Di Matteo

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  1. 1
    Immunological Aspects of X-Linked Chronic Granulomatous Disease Female Carriers

    Immunological Aspects of X-Linked Chronic Granulomatous Disease Female Carriers oleh Maria Chiriaco, Irene Salfa, Giorgiana Madalina Ursu, Cristina Cifaldi, Silvia Di Cesare, Paolo Rossi, Gigliola Di Matteo, Andrea Finocchi

    Diterbitkan 2021-06-01
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  2. 2
    Case Report: Hodgkin Lymphoma and Refractory Systemic Lupus Erythematosus Unveil Activated Phosphoinositide 3-Kinase-δ Syndrome 2 in an Adult Patient

    Case Report: Hodgkin Lymphoma and Refractory Systemic Lupus Erythematosus Unveil Activated Phosphoinositide 3-Kinase-δ Syndrome 2 in an Adult Patient oleh Francesca Conti, Arianna Catelli, Cristina Cifaldi, Cristina Cifaldi, Lucia Leonardi, Rita Mulè, Marco Fusconi, Vittorio Stefoni, Maria Chiriaco, Beatrice Rivalta, Beatrice Rivalta, Silvia Di Cesare, Gioacchino Schifino, Gioacchino Schifino, Fabiana Sbrega, Gigliola Di Matteo, Gigliola Di Matteo, Simona Ferrari, Caterina Cancrini, Andrea Pession

    Diterbitkan 2021-07-01
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  3. 3
    Corrigendum: Case Report: Hodgkin Lymphoma and Refractory Systemic Lupus Erythematosus Unveil Activated Phosphoinositide 3-Kinase-δ Syndrome 2 in an Adult Patient

    Corrigendum: Case Report: Hodgkin Lymphoma and Refractory Systemic Lupus Erythematosus Unveil Activated Phosphoinositide 3-Kinase-δ Syndrome 2 in an Adult Patient oleh Francesca Conti, Arianna Catelli, Cristina Cifaldi, Cristina Cifaldi, Lucia Leonardi, Rita Mulè, Marco Fusconi, Vittorio Stefoni, Maria Chiriaco, Beatrice Rivalta, Beatrice Rivalta, Silvia Di Cesare, Gioacchino Schifino, Gioacchino Schifino, Fabiana Sbrega, Gigliola Di Matteo, Gigliola Di Matteo, Simona Ferrari, Caterina Cancrini, Andrea Pession

    Diterbitkan 2021-09-01
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  4. 4
    Phenotypical T Cell Differentiation Analysis: A Diagnostic and Predictive Tool in the Study of Primary Immunodeficiencies

    Phenotypical T Cell Differentiation Analysis: A Diagnostic and Predictive Tool in the Study of Primary Immunodeficiencies oleh Enrico Attardi, Enrico Attardi, Silvia Di Cesare, Silvia Di Cesare, Donato Amodio, Donato Amodio, Carmela Giancotta, Nicola Cotugno, Nicola Cotugno, Cristina Cifaldi, Maria Chiriaco, Paolo Palma, Andrea Finocchi, Andrea Finocchi, Gigliola Di Matteo, Gigliola Di Matteo, Paolo Rossi, Paolo Rossi, Caterina Cancrini, Caterina Cancrini

    Diterbitkan 2019-11-01
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  5. 5
    Case report: Neonatal-onset inflammatory bowel disease due to novel compound heterozygous mutations in DUOX2

    Case report: Neonatal-onset inflammatory bowel disease due to novel compound heterozygous mutations in DUOX2 oleh Andrea Finocchi, Andrea Finocchi, Lucia Pacillo, Lucia Pacillo, Maria Chiriaco, Gigliola Di Matteo, Gigliola Di Matteo, Paola Francalanci, Giulia Angelino, Tamara Caldaro, Beatrice Rivalta, Beatrice Rivalta, Maurice O’Mara, Suisheng Zhang, Francesca Romana Lepri, Antonio Novelli, Paola De Angelis, Ulla G. Knaus, Francesca Rea

    Diterbitkan 2023-11-01
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  6. 6
    Dysplasia of Granulocytes in a Patient with HPV Disease, Recurrent Infections, and B Lymphopenia: A Novel Variant of WHIM Syndrome?

    Dysplasia of Granulocytes in a Patient with HPV Disease, Recurrent Infections, and B Lymphopenia: A Novel Variant of WHIM Syndrome? oleh Viviana Moschese, Viviana Moschese, Giusella M. F. Moscato, Erica Giacobbi, Lucia Anemona, Silvia Di Cesare, Gigliola Di Matteo, Massimo Andreoni, Alessandro Mauriello

    Diterbitkan 2017-05-01
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  7. 7
    Case Report: Altered NK Cell Compartment and Reduced CXCR4 Chemotactic Response of B Lymphocytes in an Immunodeficient Patient With HPV-Related Disease

    Case Report: Altered NK Cell Compartment and Reduced CXCR4 Chemotactic Response of B Lymphocytes in an Immunodeficient Patient With HPV-Related Disease oleh Margherita Doria, Giusella M. F. Moscato, Silvia Di Cesare, Gigliola Di Matteo, Mayla Sgrulletti, Mayla Sgrulletti, Françoise Bachelerie, Viviana Marin-Esteban, Viviana Moschese

    Diterbitkan 2022-01-01
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  8. 8
    Novel Compound Heterozygous Mutations in IL-7 Receptor α Gene in a 15-Month-Old Girl Presenting With Thrombocytopenia, Normal T Cell Count and Maternal Engraftment

    Novel Compound Heterozygous Mutations in IL-7 Receptor α Gene in a 15-Month-Old Girl Presenting With Thrombocytopenia, Normal T Cell Count and Maternal Engraftment oleh Paola Zangari, Cristina Cifaldi, Silvia Di Cesare, Silvia Di Cesare, Gigliola Di Matteo, Gigliola Di Matteo, Maria Chiriaco, Donato Amodio, Donato Amodio, Nicola Cotugno, Nicola Cotugno, Maia De Luca, Cecilia Surace, Saverio Ladogana, Simone Gardini, Pietro Merli, Mattia Algeri, Paolo Rossi, Paolo Rossi, Paolo Palma, Caterina Cancrini, Caterina Cancrini, Andrea Finocchi, Andrea Finocchi

    Diterbitkan 2019-10-01
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  9. 9
    Case Report: Crossing a rugged road in a primary immune regulatory disorder

    Case Report: Crossing a rugged road in a primary immune regulatory disorder oleh Mayla Sgrulletti, Mayla Sgrulletti, Cristina Cifaldi, Silvia Di Cesare, Barbara Kroegler, Elisabetta Del Duca, Valentina Ferradini, Simona Graziani, Mario Bengala, Gigliola Di Matteo, Viviana Moschese

    Diterbitkan 2023-01-01
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  10. 10
    Case Report: EBV Chronic Infection and Lymphoproliferation in Four APDS Patients: The Challenge of Proper Characterization, Therapy, and Follow-Up

    Case Report: EBV Chronic Infection and Lymphoproliferation in Four APDS Patients: The Challenge of Proper Characterization, Therapy, and Follow-Up oleh Beatrice Rivalta, Beatrice Rivalta, Donato Amodio, Cinzia Milito, Maria Chiriaco, Silvia Di Cesare, Silvia Di Cesare, Carmela Giancotta, Francesca Conti, Veronica Santilli, Lucia Pacillo, Lucia Pacillo, Cristina Cifaldi, Maria Giovanna Desimio, Margherita Doria, Isabella Quinti, Rita De Vito, Gigliola Di Matteo, Gigliola Di Matteo, Andrea Finocchi, Andrea Finocchi, Paolo Palma, Paolo Palma, Antonino Trizzino, Alberto Tommasini, Alberto Tommasini, Caterina Cancrini, Caterina Cancrini

    Diterbitkan 2021-08-01
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  11. 11
    Cryptococcal Meningitis and Post-Infectious Inflammatory Response Syndrome in a Patient With X-Linked Hyper IgM Syndrome: A Case Report and Review of the Literature

    Cryptococcal Meningitis and Post-Infectious Inflammatory Response Syndrome in a Patient With X-Linked Hyper IgM Syndrome: A Case Report and Review of the Literature oleh Lorenza Romani, Peter Richard Williamson, Silvia Di Cesare, Gigliola Di Matteo, Maia De Luca, Rita Carsetti, Lorenzo Figà-Talamanca, Caterina Cancrini, Caterina Cancrini, Paolo Rossi, Paolo Rossi, Andrea Finocchi, Andrea Finocchi

    Diterbitkan 2021-07-01
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  12. 12
    NATURAL HISTORY OF RALD: A 20 YEAR FOLLOW-UP OF A NRAS MUTATED PATIENT EXCLUDING A MALIGNANT PROGRESSION

    NATURAL HISTORY OF RALD: A 20 YEAR FOLLOW-UP OF A NRAS MUTATED PATIENT EXCLUDING A MALIGNANT PROGRESSION oleh Enrico Attardi, Beatrice Rivalta, Cristina Cifaldi, Vittorio Rosti, Lucia Pacillo, Hajro Hajrullaj, Silvia Di Cesare, Matteo Luciani, Federica Barzaghi, Andrea Finocchi, Gigliola Di Matteo, Alessandro Aiuti, Franco Locatelli, Maria Teresa Voso, Giuseppe Palumbo, Caterina Cancrini

    Diterbitkan 2023-12-01
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  13. 13
    Novel X-Linked Inhibitor of Apoptosis Mutation in Very Early-Onset Inflammatory Bowel Disease Child Successfully Treated with HLA-Haploidentical Hemapoietic Stem Cells Transplant after Removal of αβ+ T and B Cells

    Novel X-Linked Inhibitor of Apoptosis Mutation in Very Early-Onset Inflammatory Bowel Disease Child Successfully Treated with HLA-Haploidentical Hemapoietic Stem Cells Transplant a... oleh Cristina Cifaldi, Maria Chiriaco, Gigliola Di Matteo, Silvia Di Cesare, Scarselli Alessia, Paola De Angelis, Francesca Rea, Giulia Angelino, Maria Pastore, Valentina Ferradini, Daria Pagliara, Caterina Cancrini, Caterina Cancrini, Paolo Rossi, Paolo Rossi, Alice Bertaina, Andrea Finocchi, Andrea Finocchi

    Diterbitkan 2017-12-01
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  14. 14
    Clinical, Immunological, and Molecular Features of Typical and Atypical Severe Combined Immunodeficiency: Report of the Italian Primary Immunodeficiency Network

    Clinical, Immunological, and Molecular Features of Typical and Atypical Severe Combined Immunodeficiency: Report of the Italian Primary Immunodeficiency Network oleh Emilia Cirillo, Caterina Cancrini, Caterina Cancrini, Chiara Azzari, Silvana Martino, Baldassarre Martire, Andrea Pession, Alberto Tommasini, Samuele Naviglio, Andrea Finocchi, Andrea Finocchi, Rita Consolini, Paolo Pierani, Irene D'Alba, Maria Caterina Putti, Antonio Marzollo, Giuliana Giardino, Rosaria Prencipe, Federica Esposito, Fiorentino Grasso, Alessia Scarselli, Alessia Scarselli, Gigliola Di Matteo, Gigliola Di Matteo, Enrico Attardi, Silvia Ricci, Davide Montin, Fernando Specchia, Federica Barzaghi, Maria Pia Cicalese, Giuseppe Quaremba, Vassilios Lougaris, Silvia Giliani, Franco Locatelli, Paolo Rossi, Paolo Rossi, Alessandro Aiuti, Raffaele Badolato, Alessandro Plebani, Claudio Pignata

    Diterbitkan 2019-08-01
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  15. 15
    Humoral and Cellular Response Following Vaccination With the BNT162b2 mRNA COVID-19 Vaccine in Patients Affected by Primary Immunodeficiencies

    Humoral and Cellular Response Following Vaccination With the BNT162b2 mRNA COVID-19 Vaccine in Patients Affected by Primary Immunodeficiencies oleh Donato Amodio, Alessandra Ruggiero, Alessandra Ruggiero, Mayla Sgrulletti, Mayla Sgrulletti, Mayla Sgrulletti, Chiara Pighi, Nicola Cotugno, Nicola Cotugno, Chiara Medri, Elena Morrocchi, Luna Colagrossi, Cristina Russo, Salvatore Zaffina, Gigliola Di Matteo, Gigliola Di Matteo, Cristina Cifaldi, Silvia Di Cesare, Silvia Di Cesare, Beatrice Rivalta, Beatrice Rivalta, Beatrice Rivalta, Lucia Pacillo, Lucia Pacillo, Lucia Pacillo, Veronica Santilli, Carmela Giancotta, Emma Concetta Manno, Marta Ciofi Degli Atti, Massimiliano Raponi, Paolo Rossi, Paolo Rossi, Andrea Finocchi, Andrea Finocchi, Caterina Cancrini, Caterina Cancrini, Carlo Federico Perno, Carlo Federico Perno, Viviana Moschese, Viviana Moschese, Viviana Moschese, Paolo Palma, Paolo Palma

    Diterbitkan 2021-10-01
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  16. 16
    Radiosensitivity in patients affected by ARPC1B deficiency: a new disease trait?

    Radiosensitivity in patients affected by ARPC1B deficiency: a new disease trait? oleh Maria Chiriaco, Giorgiana Madalina Ursu, Giorgiana Madalina Ursu, Donato Amodio, Nicola Cotugno, Nicola Cotugno, Stefano Volpi, Francesco Berardinelli, Francesco Berardinelli, Simone Pizzi, Cristina Cifaldi, Matteo Zoccolillo, Matteo Zoccolillo, Ignazia Prigione, Silvia Di Cesare, Silvia Di Cesare, Carmela Giancotta, Elisa Anastasio, Beatrice Rivalta, Beatrice Rivalta, Lucia Pacillo, Lucia Pacillo, Paola Zangari, Alessandro G. Fiocchi, Andrea Diociaiuti, Alessandro Bruselles, Francesca Pantaleoni, Andrea Ciolfi, Valentina D’Oria, Giuseppe Palumbo, Giuseppe Palumbo, Marco Gattorno, Maya El Hachem, Jean-Pierre de Villartay, Andrea Finocchi, Andrea Finocchi, Paolo Palma, Paolo Palma, Paolo Rossi, Paolo Rossi, Paolo Rossi, Marco Tartaglia, Alessandro Aiuti, Alessandro Aiuti, Alessandro Aiuti, Antonio Antoccia, Gigliola Di Matteo, Gigliola Di Matteo, Caterina Cancrini, Caterina Cancrini

    Diterbitkan 2022-07-01
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  17. 17
    First Case of Patient With Two Homozygous Mutations in MYD88 and CARD9 Genes Presenting With Pyogenic Bacterial Infections, Elevated IgE, and Persistent EBV Viremia

    First Case of Patient With Two Homozygous Mutations in MYD88 and CARD9 Genes Presenting With Pyogenic Bacterial Infections, Elevated IgE, and Persistent EBV Viremia oleh Maria Chiriaco, Gigliola Di Matteo, Francesca Conti, Davide Petricone, Maia De Luca, Silvia Di Cesare, Cristina Cifaldi, Rita De Vito, Matteo Zoccolillo, Matteo Zoccolillo, Jessica Serafinelli, Noemi Poerio, Maurizio Fraziano, Immacolata Brigida, Fabio Cardinale, Paolo Rossi, Paolo Rossi, Alessandro Aiuti, Alessandro Aiuti, Alessandro Aiuti, Caterina Cancrini, Caterina Cancrini, Andrea Finocchi, Andrea Finocchi

    Diterbitkan 2019-02-01
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  18. 18
    Targeted NGS Platforms for Genetic Screening and Gene Discovery in Primary Immunodeficiencies

    Targeted NGS Platforms for Genetic Screening and Gene Discovery in Primary Immunodeficiencies oleh Cristina Cifaldi, Immacolata Brigida, Federica Barzaghi, Federica Barzaghi, Federica Barzaghi, Matteo Zoccolillo, Matteo Zoccolillo, Valentina Ferradini, Davide Petricone, Maria Pia Cicalese, Maria Pia Cicalese, Maria Pia Cicalese, Dejan Lazarevic, Davide Cittaro, Maryam Omrani, Enrico Attardi, Francesca Conti, Alessia Scarselli, Maria Chiriaco, Silvia Di Cesare, Francesco Licciardi, Montin Davide, Francesca Ferrua, Francesca Ferrua, Francesca Ferrua, Clementina Canessa, Clementina Canessa, Claudio Pignata, Silvia Giliani, Simona Ferrari, Georgia Fousteri, Graziano Barera, Pietro Merli, Paolo Palma, Simone Cesaro, Marco Gattorno, Antonio Trizzino, Viviana Moschese, Viviana Moschese, Loredana Chini, Loredana Chini, Anna Villa, Anna Villa, Chiara Azzari, Chiara Azzari, Andrea Finocchi, Andrea Finocchi, Franco Locatelli, Paolo Rossi, Paolo Rossi, Federica Sangiuolo, Alessandro Aiuti, Alessandro Aiuti, Alessandro Aiuti, Caterina Cancrini, Caterina Cancrini, Gigliola Di Matteo, Gigliola Di Matteo

    Diterbitkan 2019-04-01
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  19. 19
    Corrigendum: Targeted NGS Platforms for Genetic Screening and Gene Discovery in Primary Immunodeficiencies

    Corrigendum: Targeted NGS Platforms for Genetic Screening and Gene Discovery in Primary Immunodeficiencies oleh Cristina Cifaldi, Immacolata Brigida, Federica Barzaghi, Federica Barzaghi, Federica Barzaghi, Matteo Zoccolillo, Matteo Zoccolillo, Valentina Ferradini, Davide Petricone, Maria Pia Cicalese, Maria Pia Cicalese, Maria Pia Cicalese, Dejan Lazarevic, Davide Cittaro, Maryam Omrani, Enrico Attardi, Francesca Conti, Alessia Scarselli, Maria Chiriaco, Silvia Di Cesare, Francesco Licciardi, Montin Davide, Francesca Ferrua, Francesca Ferrua, Francesca Ferrua, Clementina Canessa, Clementina Canessa, Claudio Pignata, Silvia Giliani, Simona Ferrari, Georgia Fousteri, Graziano Barera, Pietro Merli, Paolo Palma, Simone Cesaro, Marco Gattorno, Antonio Trizzino, Viviana Moschese, Viviana Moschese, Loredana Chini, Loredana Chini, Anna Villa, Anna Villa, Chiara Azzari, Chiara Azzari, Andrea Finocchi, Andrea Finocchi, Franco Locatelli, Paolo Rossi, Paolo Rossi, Federica Sangiuolo, Alessandro Aiuti, Alessandro Aiuti, Alessandro Aiuti, Caterina Cancrini, Caterina Cancrini, Gigliola Di Matteo, Gigliola Di Matteo

    Diterbitkan 2019-05-01
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  20. 20
    Corrigendum: Natural Killer Cells from Patients with Recombinase-Activating Gene and Non-Homologous End Joining Gene Defects Comprise a Higher Frequency of CD56bright NKG2A+++ Cells, and Yet Display Increased Degranulation and Higher Perforin Content

    Corrigendum: Natural Killer Cells from Patients with Recombinase-Activating Gene and Non-Homologous End Joining Gene Defects Comprise a Higher Frequency of CD56bright NKG2A+++ Cell... oleh Kerry Dobbs, Giovanna Tabellini, Enrica Calzoni, Ornella Patrizi, Paula Martinez, Silvia Clara Giliani, Daniele Moratto, Waleed Al-Herz, Caterina Cancrini, Caterina Cancrini, Morton Cowan, Jacob Bleesing, Claire Booth, David Buchbinder, Siobhan O. Burns, Siobhan O. Burns, Talal A. Chatila, Janet Chou, Vanessa Daza-Cajigal, Lisa M. Ott de Bruin, Maite Teresa de la Morena, Gigliola Di Matteo, Gigliola Di Matteo, Andrea Finocchi, Andrea Finocchi, Raif Geha, Rakesh K. Goyal, Anthony Hayward, Steven Holland, Chiung-Hui Huang, Maria G. Kanariou, Alejandra King, Blanka Kaplan, Anastasiya Kleva, Taco W. Kuijpers, Bee Wah Lee, Vassilios Lougaris, Michel Massaad, Isabelle Meyts, Megan Morsheimer, Benedicte Neven, Sung-Yun Pai, Nima Parvaneh, Nima Parvaneh, Alessandro Plebani, Susan Prockop, Ismail Reisli, Jian Yi Soh, Raz Somech, Troy R. Torgerson, Yae-Jean Kim, Jolan E. Walter, Andrew R. Gennery, Andrew R. Gennery, Sevgi Keles, John P. Manis, Emanuela Marcenaro, Alessandro Moretta, Silvia Parolini, Luigi D. Notarangelo

    Diterbitkan 2017-10-01
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