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Tumor Necrosis Factor Receptor SF10A (TNFRSF10A) SNPs Correlate With Corticosteroid Response in Duchenne Muscular Dystrophy.
Passarelli, Chiara; Selvatici, Rita; Carrieri, Alberto; Di Raimo, Francesca Romana; Falzarano, Maria Sofia; Fortunato, Fernanda; Rossi, Rachele; Straub, Volker; Bushby, Katie; Reza, Mojgan; Zharaieva, Irina; D'Amico, Adele; Bertini, Enrico; Merlini, Luciano; Sabatelli, Patrizia; Borgiani, Paola; Novelli, Giuseppe; Messina, Sonia; Pane, Marika; Mercuri, Eugenio; Claustres, Mireille; Tuffery-Giraud, Sylvie; Aartsma-Rus, Annemieke; Spitali, Pietro; T'Hoen, Peter A C; Lochmüller, Hanns; Strandberg, Kristin; Al-Khalili, Cristina; Kotelnikova, Ekaterina; Lebowitz, Michael; Schwartz, Elena; Muntoni, Francesco; Scapoli, Chiara; Ferlini, Alessandra.
Afiliação
  • Passarelli C; Unit of Medical Genetics, Department of Medical Sciences, University of Ferrara, Ferrara, Italy.
  • Selvatici R; U.O.C. Laboratory of Medical Genetics, Paediatric Hospital Bambino Gesù, IRCCS, Rome, Italy.
  • Carrieri A; Unit of Medical Genetics, Department of Medical Sciences, University of Ferrara, Ferrara, Italy.
  • Di Raimo FR; Department of Life Sciences and Biotechnology, University of Ferrara, Ferrara, Italy.
  • Falzarano MS; Unit of Medical Genetics, Department of Medical Sciences, University of Ferrara, Ferrara, Italy.
  • Fortunato F; Unit of Medical Genetics, Department of Medical Sciences, University of Ferrara, Ferrara, Italy.
  • Rossi R; Unit of Medical Genetics, Department of Medical Sciences, University of Ferrara, Ferrara, Italy.
  • Straub V; Unit of Medical Genetics, Department of Medical Sciences, University of Ferrara, Ferrara, Italy.
  • Bushby K; John Walton Muscular Dystrophy Research Centre, Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom.
  • Reza M; John Walton Muscular Dystrophy Research Centre, Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom.
  • Zharaieva I; John Walton Muscular Dystrophy Research Centre, Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom.
  • D'Amico A; Dubowitz Neuromuscular Center, University College London Institute of Child Health & Great Ormond Street Hospital, London, United Kingdom.
  • Bertini E; Molecular Medicine and Unit of Neuromuscular and Neurodegenerative Diseases, Paediatric Hospital Bambino Gesù, IRCCS, Rome, Italy.
  • Merlini L; Molecular Medicine and Unit of Neuromuscular and Neurodegenerative Diseases, Paediatric Hospital Bambino Gesù, IRCCS, Rome, Italy.
  • Sabatelli P; Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy.
  • Borgiani P; IRCCS Rizzoli & Institute of Molecular Genetics, National Research Council of Italy, Bologna, Italy.
  • Novelli G; Genetics Unit, Department of Biomedicine and Prevention, University of Rome Tor Vergata, Rome, Italy.
  • Messina S; Genetics Unit, Department of Biomedicine and Prevention, University of Rome Tor Vergata, Rome, Italy.
  • Pane M; Istituto Neuromed, IRCCS, Pozzilli, Italy.
  • Mercuri E; Department of Clinical and Experimental Medicine, Nemo Sud Clinical Center, University of Messina, Messina, Italy.
  • Claustres M; Paediatric Neurology Unit, Centro Clinico Nemo, IRCCS Fondazione Policlinico A. Gemelli, Universita' Cattolica del Sacro Cuore, Rome, Italy.
  • Tuffery-Giraud S; Paediatric Neurology Unit, Centro Clinico Nemo, IRCCS Fondazione Policlinico A. Gemelli, Universita' Cattolica del Sacro Cuore, Rome, Italy.
  • Aartsma-Rus A; Laboratory of Genetics of Rare Diseases, University of Montpellier, Montpellier, France.
  • Spitali P; Laboratory of Genetics of Rare Diseases, University of Montpellier, Montpellier, France.
  • T'Hoen PAC; John Walton Muscular Dystrophy Research Centre, Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom.
  • Lochmüller H; Department of Human Genetics, Leiden University Medical Center, Leiden, Netherlands.
  • Strandberg K; Department of Human Genetics, Leiden University Medical Center, Leiden, Netherlands.
  • Al-Khalili C; Department of Human Genetics, Leiden University Medical Center, Leiden, Netherlands.
  • Kotelnikova E; Center for Molecular and Biomolecular Informatics, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, Netherlands.
  • Lebowitz M; Department of Neuropediatrics and Muscle Disorders, Faculty of Medicine, Medical Center - University of Freiburg, Freiburg, Germany.
  • Schwartz E; Centro Nacional de Análisis Genómico (CNAG-CRG), Center for Genomic Regulation, Barcelona Institute of Science and Technology (BIST), Barcelona, Spain.
  • Muntoni F; Children's Hospital of Eastern Ontario Research Institute, Ottawa, ON, Canada.
  • Scapoli C; Division of Neurology, Department of Medicine, The Ottawa Hospital, Ottawa, ON, Canada.
  • Ferlini A; Brain and Mind Research Institute, University of Ottawa, Ottawa, ON, Canada.
Front Genet ; 11: 605, 2020.
Article em En | MEDLINE | ID: mdl-32719714
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2020 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2020 Tipo de documento: Article