Hasil Pencarian - Luca Bosco

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  1. 1
    Il povero e il teatro

    Il povero e il teatro oleh Luca Bosco

    Diterbitkan 2013-06-01
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  2. 2
    Animal Models as a Tool to Design Therapeutical Strategies for CMT-like Hereditary Neuropathies

    Animal Models as a Tool to Design Therapeutical Strategies for CMT-like Hereditary Neuropathies oleh Luca Bosco, Yuri Matteo Falzone, Stefano Carlo Previtali

    Diterbitkan 2021-09-01
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  3. 3
    Agrochemical Contamination of Honey and Bee Bread Collected in the Piedmont Region, Italy

    Agrochemical Contamination of Honey and Bee Bread Collected in the Piedmont Region, Italy oleh Marco Bergero, Luca Bosco, Alessandra Giacomelli, Giovanni Angelozzi, Monia Perugini, Carmine Merola

    Diterbitkan 2021-07-01
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  4. 4
    Novel Splicing Mutation in <i>MTM1</i> Leading to Two Abnormal Transcripts Causes Severe Myotubular Myopathy

    Novel Splicing Mutation in <i>MTM1</i> Leading to Two Abnormal Transcripts Causes Severe Myotubular Myopathy oleh Luca Bosco, Daniela Leone, Laura Costa Comellas, Mauro Monforte, Marika Pane, Eugenio Mercuri, Enrico Bertini, Adele D’Amico, Fabiana Fattori

    Diterbitkan 2022-09-01
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  5. 5
    “Build Your Village”—Conducting the Village Test on Cognitively Impaired Patients: A First Journey into Alzheimerland

    “Build Your Village”—Conducting the Village Test on Cognitively Impaired Patients: A First Journey into Alzheimerland oleh Michelangelo Stanzani-Maserati, Maddalena De Matteis, Luca Bosco, Flavia Baccari, Corrado Zenesini, Micaela Mitolo, Chiara La Morgia, Roberto Gallassi, Sabina Capellari

    Diterbitkan 2024-05-01
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  6. 6
    Diagnostic Yield of a Targeted Next-Generation Sequencing Gene Panel for Pediatric-Onset Movement Disorders: A 3-Year Cohort Study

    Diagnostic Yield of a Targeted Next-Generation Sequencing Gene Panel for Pediatric-Onset Movement Disorders: A 3-Year Cohort Study oleh Federica Graziola, Federica Graziola, Giacomo Garone, Giacomo Garone, Fabrizia Stregapede, Fabrizia Stregapede, Luca Bosco, Federico Vigevano, Paolo Curatolo, Enrico Bertini, Lorena Travaglini, Alessandro Capuano

    Diterbitkan 2019-10-01
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  7. 7
    Hepatobiliary disease in XLMTM: a common comorbidity with potential impact on treatment strategies

    Hepatobiliary disease in XLMTM: a common comorbidity with potential impact on treatment strategies oleh Adele D’Amico, Antonella Longo, Fabiana Fattori, Michele Tosi, Luca Bosco, Maria Beatrice Chiarini Testa, Giovanna Paglietti, Claudio Cherchi, Adelina Carlesi, Irene Mizzoni, Enrico Bertini

    Diterbitkan 2021-10-01
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  8. 8
    Correction to: Hepatobiliary disease in XLMTM: a common comorbidity with potential impact on treatment strategies

    Correction to: Hepatobiliary disease in XLMTM: a common comorbidity with potential impact on treatment strategies oleh Adele D’Amico, Antonella Longo, Fabiana Fattori, Michele Tosi, Luca Bosco, Maria Beatrice Chiarini Testa, Maria Giovanna Paglietti, Claudio Cherchi, Adelina Carlesi, Irene Mizzoni, Enrico Bertini

    Diterbitkan 2022-01-01
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  9. 9
    Novel <em>KCND3</em> Variant Underlying Nonprogressive Congenital Ataxia or SCA19/22 Disrupt K<sub>V</sub>4.3 Protein Expression and K+ Currents with Variable Effects on Channel Properties

    Novel <em>KCND3</em> Variant Underlying Nonprogressive Congenital Ataxia or SCA19/22 Disrupt K<sub>V</sub>4.3 Protein Expression and K+ Currents with Variable Effects on Channel Pr... oleh Ginevra Zanni, Cheng-Tsung Hsiao, Ssu-Ju Fu, Chih-Yung Tang, Alessandro Capuano, Luca Bosco, Federica Graziola, Emanuele Bellacchio, Serenella Servidei, Guido Primiano, Bing-Wen Soong, Chung-Jiuan Jeng

    Diterbitkan 2021-05-01
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  10. 10
    Muscle hypertrophy following acquired neurogenic injury: systematic review and analysis of existing literature

    Muscle hypertrophy following acquired neurogenic injury: systematic review and analysis of existing literature oleh Camilla MM Strano, Luca Bosco, Christian Laurini, Giacomo Sferruzza, Carla Butera, Yuri M. Falzone, Benedetta Sorrenti, Adele Ratti, Laura Tufano, Luca Leonardi, Gloria Merlonghi, Stefania Morino, Simonetta Gerevini, Ubaldo Del Carro, Matteo Garibaldi, Massimo Filippi, Stefano C Previtali

    Diterbitkan 2024-08-01
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  11. 11
    SNUPN deficiency causes a recessive muscular dystrophy due to RNA mis-splicing and ECM dysregulation

    SNUPN deficiency causes a recessive muscular dystrophy due to RNA mis-splicing and ECM dysregulation oleh Marwan Nashabat, Nasrinsadat Nabavizadeh, Hilal Pırıl Saraçoğlu, Burak Sarıbaş, Şahin Avcı, Esra Börklü, Emmanuel Beillard, Elanur Yılmaz, Seyide Ecesu Uygur, Cavit Kerem Kayhan, Luca Bosco, Zeynep Bengi Eren, Katharina Steindl, Manuela Friederike Richter, Guney Bademci, Anita Rauch, Zohreh Fattahi, Maria Lucia Valentino, Anne M. Connolly, Angela Bahr, Laura Viola, Anke Katharina Bergmann, Maria Eugenia Rocha, LeShon Peart, Derly Liseth Castro-Rojas, Eva Bültmann, Suliman Khan, Miriam Liliana Giarrana, Raluca Ioana Teleanu, Joanna Michelle Gonzalez, Antonella Pini, Ines Sophie Schädlich, Katharina Vill, Melanie Brugger, Stephan Zuchner, Andreia Pinto, Sandra Donkervoort, Stephanie Ann Bivona, Anca Riza, Undiagnosed Diseases Network, Ioana Streata, Dieter Gläser, Carolina Baquero-Montoya, Natalia Garcia-Restrepo, Urania Kotzaeridou, Theresa Brunet, Diana Anamaria Epure, Aida Bertoli-Avella, Ariana Kariminejad, Mustafa Tekin, Sandra von Hardenberg, Carsten G. Bönnemann, Georg M. Stettner, Ginevra Zanni, Hülya Kayserili, Zehra Piraye Oflazer, Nathalie Escande-Beillard

    Diterbitkan 2024-02-01
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