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Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry.
Crotti, Lia; Spazzolini, Carla; Nyegaard, Mette; Overgaard, Michael T; Kotta, Maria-Christina; Dagradi, Federica; Sala, Luca; Aiba, Takeshi; Ayers, Mark D; Baban, Anwar; Barc, Julien; Beach, Cheyenne M; Behr, Elijah R; Bos, J Martijn; Cerrone, Marina; Covi, Peter; Cuneo, Bettina; Denjoy, Isabelle; Donner, Birgit; Elbert, Adrienne; Eliasson, Håkan; Etheridge, Susan P; Fukuyama, Megumi; Girolami, Francesca; Hamilton, Robert; Horie, Minoru; Iascone, Maria; Jiménez-Jaimez, Juan; Jensen, Henrik Kjærulf; Kannankeril, Prince J; Kaski, Juan P; Makita, Naomasa; Muñoz-Esparza, Carmen; Odland, Hans H; Ohno, Seiko; Papagiannis, John; Porretta, Alessandra Pia; Prandstetter, Christopher; Probst, Vincent; Robyns, Tomas; Rosenthal, Eric; Rosés-Noguer, Ferran; Sekarski, Nicole; Singh, Anoop; Spentzou, Georgia; Stute, Fridrike; Tfelt-Hansen, Jacob; Till, Jan; Tobert, Kathryn E; Vinocur, Jeffrey M.
Afiliação
  • Crotti L; Istituto Auxologico Italiano IRCCS, Center for Cardiac Arrhythmias of Genetic Origin and Laboratory of Cardiovascular Genetics, Via Pier Lombardo 22, 20135 Milan, Italy.
  • Spazzolini C; Department of Medicine and Surgery, University of Milano-Bicocca, Piazza dell'Ateneo Nuovo, 1, 20126 Milan, Italy.
  • Nyegaard M; Istituto Auxologico Italiano IRCCS, Center for Cardiac Arrhythmias of Genetic Origin and Laboratory of Cardiovascular Genetics, Via Pier Lombardo 22, 20135 Milan, Italy.
  • Overgaard MT; Department of Health Science and Technology, Aalborg University, Aalborg, Denmark.
  • Kotta MC; Department of Chemistry and Bioscience, Aalborg University, Aalborg, Denmark.
  • Dagradi F; Istituto Auxologico Italiano IRCCS, Center for Cardiac Arrhythmias of Genetic Origin and Laboratory of Cardiovascular Genetics, Via Pier Lombardo 22, 20135 Milan, Italy.
  • Sala L; Istituto Auxologico Italiano IRCCS, Center for Cardiac Arrhythmias of Genetic Origin and Laboratory of Cardiovascular Genetics, Via Pier Lombardo 22, 20135 Milan, Italy.
  • Aiba T; Istituto Auxologico Italiano IRCCS, Center for Cardiac Arrhythmias of Genetic Origin and Laboratory of Cardiovascular Genetics, Via Pier Lombardo 22, 20135 Milan, Italy.
  • Ayers MD; Department of Biotechnology and Biosciences, University of Milano-Bicocca, Milan, Italy.
  • Baban A; Division of Arrhythmia, National Cerebral and Cardiovascular Center, Suita, Japan.
  • Barc J; Department of Pediatrics, Division of Pediatric Cardiology, Indiana University School of Medicine, Indianapolis, IN, USA.
  • Beach CM; Member of the European Reference Network for Rare and Low Prevalence Complex Diseases of the Heart: ERN GUARD-Heart.
  • Behr ER; Pediatric Cardiology and Arrhythmia/Syncope Units, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
  • Bos JM; Université de Nantes, CHU Nantes, CNRS, INSERM, L'institut du Thorax, Nantes, France.
  • Cerrone M; Pediatric Cardiology, Yale School of Medicine, New Haven, CT, USA.
  • Covi P; Cardiology Section, Institute of Molecular and Clinical Sciences, St George's University of London and Cardiovascular Clinical Academic Group, St George's University Hospitals NHS Foundation Trust, UK.
  • Cuneo B; Departments of Cardiovascular Medicine, Pediatric and Adolescent Medicine, and Molecular Pharmacology & Experimental Therapeutics, Division of Heart Rhythm Services and Pediatric Cardiology, Windland Smith Rice Sudden Death Genomics Laboratory, Mayo Clinic, 200 First Street SW, Rochester, MN 559
  • Denjoy I; Inherited Arrhythmias Clinic, Leon H. Charney Division of Cardiology, NYU Grossmann School of Medicine, New York, NY, USA.
  • Donner B; Department of Pediatrics, University Hospital Salzburg, Paracelsus Medical University, Salzburg, Austria.
  • Elbert A; Department of Pediatrics, Section of Cardiology, University of Denver School of Medicine, Aurora, CO, USA.
  • Eliasson H; Centre de Référence Maladies Cardiaques Héréditaires Filière Cardiogen, Département de Rythmologie, Groupe Hospitalier Bichat-Claude Bernard, Paris, France.
  • Etheridge SP; Kardiologie, Universitäts-Kinderspital beider Basel (UKBB), Basel, Switzerland.
  • Fukuyama M; Department of Medical Genetics, University of British Columbia, Vancouver, BC, Canada.
  • Girolami F; Department of Women's and Children's Health, Karolinska Institutet, Stockholm, Sweden.
  • Hamilton R; Pediatric Cardiology C8:34, Karolinska University Hospital, Stockholm, Sweden.
  • Horie M; Department of Pediatrics, Division of Pediatric Cardiology, University of Utah and Primary Children's Hospital, Salt Lake City, UT, USA.
  • Iascone M; Department of Cardiovascular Medicine, Shiga University of Medical Science, Shiga, Japan.
  • Jiménez-Jaimez J; Cardiology Unit, Meyer Children's Hospital, Florence, Italy.
  • Jensen HK; Division of Cardiology, The Hospital for Sick Children (SickKids), Toronto, ON, Canada.
  • Kannankeril PJ; Department of Cardiovascular Medicine, Shiga University of Medical Science, Shiga, Japan.
  • Kaski JP; Laboratorio di Genetica Medica, ASST Papa Giovanni XXIII, Bergamo, Italy.
  • Makita N; Hospital Universitario Virgen de las Nieves, Instituto de Investigación Biosanitario IBS Granada, Spain.
  • Muñoz-Esparza C; Department of Cardiology, Department of Clinical Medicine, Aarhus University Hospital, Aarhus University, K-8200 Aarhus N, Denmark.
  • Odland HH; Department of Pediatrics, Vanderbilt University Medical Center, Nashville, TN, USA.
  • Ohno S; Centre for Paediatric Inherited and Rare Cardiovascular Disease, Institute of Cardiovascular Science, University College London, Zayed Centre for Research into Rare Disease in Childhood, London, UK.
  • Papagiannis J; Centre for Inherited Cardiovascular Diseases, Great Ormond Street Hospital, London, UK.
  • Porretta AP; National Cerebral and Cardiovascular Center, Suita, Japan.
  • Prandstetter C; Sapporo Teishinkai Hospital, Sapporo, Japan.
  • Probst V; Member of the European Reference Network for Rare and Low Prevalence Complex Diseases of the Heart: ERN GUARD-Heart.
  • Robyns T; Inherited Cardiac Disease Unit, Hospital Universitario Virgen Arrixaca, Murcia, Spain.
  • Rosenthal E; Department of Cardiology and Pediatric Cardiology, Section for Arrhythmias, Oslo University Hospital, Oslo, Norway.
  • Rosés-Noguer F; Department of Bioscience and Genetics, National Cerebral and Cardiovascular Center, Osaka, Japan.
  • Sekarski N; Pediatric and Adult Congenital Heart Disease, Onassis Cardiac Surgery Center, Athens, Greece.
  • Singh A; Unité des Troubles du Rythme, Service de Cardiologie, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland.
  • Spentzou G; Medical Faculty, Johannes Kepler University Linz, Linz, Austria.
  • Stute F; Department of Pediatric Cardiology, Kepler University Hospital, Linz, Austria.
  • Tfelt-Hansen J; Service de Cardiologie, L'institut du Thorax, CHU Nantes, Nantes, France.
  • Till J; Member of the European Reference Network for Rare and Low Prevalence Complex Diseases of the Heart: ERN GUARD-Heart.
  • Tobert KE; Department of Cardiovascular Diseases, University Hospitals Leuven, Leuven, Belgium.
  • Vinocur JM; Evelina London Children's Hospital, St Thomas' Hospital, London, UK.
Eur Heart J ; 44(35): 3357-3370, 2023 09 14.
Article em En | MEDLINE | ID: mdl-37528649
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Contexto em Saúde: 6_ODS3_enfermedades_notrasmisibles Problema de saúde: 6_cardiovascular_diseases / 6_congenital_chromosomal_anomalies Assunto principal: Síndrome do QT Longo / Calmodulina / Taquicardia Ventricular Tipo de estudo: Diagnostic_studies / Etiology_studies / Guideline / Observational_studies Limite: Child / Humans Idioma: En Revista: Eur Heart J Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Itália
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Contexto em Saúde: 6_ODS3_enfermedades_notrasmisibles Problema de saúde: 6_cardiovascular_diseases / 6_congenital_chromosomal_anomalies Assunto principal: Síndrome do QT Longo / Calmodulina / Taquicardia Ventricular Tipo de estudo: Diagnostic_studies / Etiology_studies / Guideline / Observational_studies Limite: Child / Humans Idioma: En Revista: Eur Heart J Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Itália