Rezultati pretrage - Giovanni Baranello

Detaljiziraj rezultate
  1. 1
    Brain, cognition, and language development in spinal muscular atrophy type 1: a scoping review

    Brain, cognition, and language development in spinal muscular atrophy type 1: a scoping review od Riccardo Masson, Chiara Brusa, Mariacristina Scoto, Giovanni Baranello

    Izdano 2021
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  2. 2
    Effect of Nusinersen on Respiratory Muscle Function in Different Subtypes of Type 1 Spinal Muscular Atrophy

    Effect of Nusinersen on Respiratory Muscle Function in Different Subtypes of Type 1 Spinal Muscular Atrophy od Antonella LoMauro, Chiara Mastella, Katia Alberti, Riccardo Masson, Andréa Aliverti, Giovanni Baranello

    Izdano 2019
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  3. 3
    Spontaneous Breathing Pattern as Respiratory Functional Outcome in Children with Spinal Muscular Atrophy (SMA)

    Spontaneous Breathing Pattern as Respiratory Functional Outcome in Children with Spinal Muscular Atrophy (SMA) od Antonella LoMauro, Andrea Aliverti, Chiara Mastella, Maria Teresa Arnoldi, Paolo Banfi, Giovanni Baranello

    Izdano 2016
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  4. 4
    Spinal Muscular Atrophy, types I and II: What are the differences in body composition and resting energy expenditure?

    Spinal Muscular Atrophy, types I and II: What are the differences in body composition and resting energy expenditure? od Simona Bertoli, Ramona De Amicis, Chiara Mastella, Giulia Pieri, Ester Giaquinto, Alberto Battezzati, Alessandro Leone, Giovanni Baranello

    Izdano 2016
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  5. 5
    Peak functional ability and age at loss of ambulation in Duchenne muscular dystrophy

    Peak functional ability and age at loss of ambulation in Duchenne muscular dystrophy od Alberto A. Zambon, Vandana Ayyar Gupta, Deborah Ridout, Adnan Y. Manzur, Giovanni Baranello, Federica Trucco, Francesco Muntoni

    Izdano 2022
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  6. 6
    Evolution of bulbar function in spinal muscular atrophy type 1 treated with nusinersen

    Evolution of bulbar function in spinal muscular atrophy type 1 treated with nusinersen od Harriet Weststrate, Georgia Stimpson, Lily Thomas, Mariacristina Scoto, Emily Johnson, Alexandra Stewart, Francesco Muntoni, Giovanni Baranello, Eleanor Conway

    Izdano 2022
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  7. 7
    Spinal presentations in children with type 1 spinal muscular atrophy on nusinersen treatment across the SMA-REACH UK network: a retrospective national observational study

    Spinal presentations in children with type 1 spinal muscular atrophy on nusinersen treatment across the SMA-REACH UK network: a retrospective national observational study od Lianne Abbott, Marion Main, Amy Wolfe, Annemarie Rohwer, Giovanni Baranello, Pinki Munot, Adnan Manzur, Francesco Muntoni, Mariacristina Scoto

    Izdano 2025
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  8. 8
    Visual Function Classification System for children with cerebral palsy: development and validation

    Visual Function Classification System for children with cerebral palsy: development and validation od Giovanni Baranello, Sabrina Signorini, Francesca Tinelli, Andrea Guzzetta, Emanuela Pagliano, Andrea Rossi, Maria Foscan, Irene Tramacere, Domenico M. Romeo, Daniela Ricci

    Izdano 2019
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  9. 9
    Prognostic Factors and Treatment‐Effect Modifiers in Spinal Muscular Atrophy

    Prognostic Factors and Treatment‐Effect Modifiers in Spinal Muscular Atrophy od Giovanni Baranello, Ksenija Gorni, Monica Daigl, Anna Kotzeva, Rachel Evans, Neil Hawkins, David A. Scott, Anadi Mahajan, Francesco Muntoni, Laurent Servais

    Izdano 2021
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  10. 10
    Dystrophin isoform deficiency and upper‐limb and respiratory function in Duchenne muscular dystrophy

    Dystrophin isoform deficiency and upper‐limb and respiratory function in Duchenne muscular dystrophy od Mary Chesshyre, Deborah Ridout, Georgia Stimpson, Valeria Ricotti, Silvana De Lucia, Erik H. Niks, Volker Straub, Teresa Gidaro, Jean‐Yves Hogrel, Giovanni Baranello, Adnan Manzur, Francesco Muntoni

    Izdano 2025
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  11. 11
    Risdiplam in Spinal Muscular Atrophy: Safety Profile and Use Through The Early Access to Medicine Scheme for the Paediatric Cohort in Great Britain

    Risdiplam in Spinal Muscular Atrophy: Safety Profile and Use Through The Early Access to Medicine Scheme for the Paediatric Cohort in Great Britain od Nikki Cornell, Anne‐Marie Childs, Elizabeth Wraige, Pinki Munot, Gautam Ambegaonkar, Gabriel Chow, Imelda Hughes, Marjorie Illingworth, Anirban Majumdar, Chiara Marini‐Bettolo, Deepak Parasuraman, Stefan Spinty, Tracey Willis, Mariacristina Scoto, Giovanni Baranello

    Izdano 2024
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  12. 12
    Circulating MyomiRs as Potential Biomarkers to Monitor Response to Nusinersen in Pediatric SMA Patients

    Circulating MyomiRs as Potential Biomarkers to Monitor Response to Nusinersen in Pediatric SMA Patients od Silvia Bonanno, Stefania Marcuzzo, Claudia Malacarne, Eleonora Giagnorio, Riccardo Masson, Riccardo Zanin, Maria Teresa Arnoldi, Francesca Andreetta, Ornella Simoncini, Anna Venerando, Cinzia Gellera, Chiara Pantaleoni, Renato Mantegazza, Pia Bernasconi, Giovanni Baranello, Lorenzo Maggi

    Izdano 2020
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  13. 13
    Risdiplam in Type 1 Spinal Muscular Atrophy

    Risdiplam in Type 1 Spinal Muscular Atrophy od Giovanni Baranello, Basil T. Darras, John Day, Nicolas Deconinck, Andrea Klein, Riccardo Masson, Eugenio Mercuri, Kristy Rose, Muna El-Khairi, Marianne Gerber, Ksenija Gorni, Omar Khwaja, H. Kletzl, R. Scalco, Timothy J. Seabrook, Paulo Fontoura, Laurent Servais

    Izdano 2021
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  14. 14
    Risdiplam-Treated Infants with Type 1 Spinal Muscular Atrophy versus Historical Controls

    Risdiplam-Treated Infants with Type 1 Spinal Muscular Atrophy versus Historical Controls od Basil T. Darras, Riccardo Masson, Maria Mazurkiewicz-Bełdzińska, Kristy Rose, Hui Xiong, Edmar Zanoteli, Giovanni Baranello, Claudio Bruno, D. Vlodavets, Yi Wang, Muna El-Khairi, Marianne Gerber, Ksenija Gorni, Omar Khwaja, H. Kletzl, R. Scalco, Paulo Fontoura, Laurent Servais

    Izdano 2021
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  15. 15
    Investigating the role of dystrophin isoform deficiency in motor function in Duchenne muscular dystrophy

    Investigating the role of dystrophin isoform deficiency in motor function in Duchenne muscular dystrophy od Mary Chesshyre, Deborah Ridout, Yasumasa Hashimoto, Yoko Ookubo, Silvia Torelli, Kate Maresh, Valeria Ricotti, Lianne Abbott, Vandana Ayyar Gupta, Marion Main, Giuliana Ferrari, Anna Kowala, Yung‐Yao Lin, Francesco Saverio Tedesco, Mariacristina Scoto, Giovanni Baranello, Adnan Manzur, Yoshitsugu Aoki, Francesco Muntoni

    Izdano 2022
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  16. 16
    Revised North Star Ambulatory Assessment for Young Boys with Duchenne Muscular Dystrophy

    Revised North Star Ambulatory Assessment for Young Boys with Duchenne Muscular Dystrophy od Eugenio Mercuri, Giorgia Coratti, Sonia Messina, Valeria Ricotti, Giovanni Baranello, Adele D’Amico, Maria Carmela Pera, Emilio Albamonte, Serena Sivo, Elena Mazzone, Maria Teresa Arnoldi, Lavinia Fanelli, Roberto De Sanctis, Domenico M. Romeo, Gian Luca Vita, Roberta Battini, Enrico Bertini, Francesco Muntoni, Marika Pane

    Izdano 2016
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  17. 17
    SMA - TREATMENT

    SMA - TREATMENT od Riccardo Masson, Odile Boespflug‐Tanguy, Basil T. Darras, John Day, Nicolas Deconinck, Andrea Klein, Maria Mazurkiewicz‐Bełdzińska, Eugenio Mercuri, K. Röse, Laurent Servais, D. Vlodavets, Hui Xiong, Edmar Zanoteli, Angela Dodman, Muna El-Khairi, Εleni Gaki, Marianne Gerber, Ksenija Gorni, Heidemarie Kletzl, Giovanni Baranello

    Izdano 2021
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  18. 18
    Two-year efficacy and safety of risdiplam in patients with type 2 or non-ambulant type 3 spinal muscular atrophy (SMA)

    Two-year efficacy and safety of risdiplam in patients with type 2 or non-ambulant type 3 spinal muscular atrophy (SMA) od Maryam Oskoui, John Day, Nicolas Deconinck, Elena Mazzone, A. Nascimento, Kayoko Saito, Carole Vuillerot, Giovanni Baranello, Nathalie Goemans, Janbernd Kirschner, Anna Kostera‐Pruszczyk, Laurent Servais, G. Papp, Ksenija Gorni, Heidemarie Kletzl, Carmen Martín, Tammy McIver, R. Scalco, Hannah Staunton, Wai Yin Yeung, Paulo Fontoura, Eugenio Mercuri

    Izdano 2023
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  19. 19
    Risdiplam in types 2 and 3 spinal muscular atrophy: A randomised, placebo‐controlled, dose‐finding trial followed by 24 months of treatment

    Risdiplam in types 2 and 3 spinal muscular atrophy: A randomised, placebo‐controlled, dose‐finding trial followed by 24 months of treatment od Eugenio Mercuri, Giovanni Baranello, Odile Boespflug‐Tanguy, Liesbeth De Waele, Nathalie Goemans, Janbernd Kirschner, Riccardo Masson, Elena Mazzone, Astrid Pechmann, Maria Carmela Pera, Carole Vuillerot, Silvia Bader‐Weder, Marianne Gerber, Ksenija Gorni, Janine Hoffart, Heidemarie Kletzl, Carmen Martín, Tammy McIver, R. Scalco, Wai Yin Yeung, Laurent Servais

    Izdano 2022
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  20. 20
    PDCD10 Gene Mutations in Multiple Cerebral Cavernous Malformations

    PDCD10 Gene Mutations in Multiple Cerebral Cavernous Malformations od Maria Sole Cigoli, Francesca Avemaria, Stefano De Benedetti, Giovanni Gesu, Lucio Giordano Accorsi, Stefano Parmigiani, Maria Franca Corona, Valeria Capra, Andrea Mosca, S. Giovannini, Francesca Notturno, Fausta Ciccocioppo, L. Volpi, Margherita Estienne, Giuseppe De Michele, Antonella Antenora, Leonilda Bilo, Antonietta Tavoni, Nelia Zamponi, Enrico Alfei, Giovanni Baranello, Daria Riva, Silvana Penco

    Izdano 2014
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