Your browser doesn't support javascript.
loading
Advances and unmet needs in genetic, basic and clinical science in Alport syndrome: report from the 2015 International Workshop on Alport Syndrome.
Gross, Oliver; Kashtan, Clifford E; Rheault, Michelle N; Flinter, Frances; Savige, Judith; Miner, Jeffrey H; Torra, Roser; Ars, Elisabet; Deltas, Constantinos; Savva, Isavella; Perin, Laura; Renieri, Alessandra; Ariani, Francesca; Mari, Francesca; Baigent, Colin; Judge, Parminder; Knebelman, Bertrand; Heidet, Laurence; Lagas, Sharon; Blatt, Dave; Ding, Jie; Zhang, Yanqin; Gale, Daniel P; Prunotto, Marco; Xue, Yong; Schachter, Asher D; Morton, Lori C G; Blem, Jacqui; Huang, Michael; Liu, Shiguang; Vallee, Sebastien; Renault, Daniel; Schifter, Julia; Skelding, Jules; Gear, Susie; Friede, Tim; Turner, A Neil; Lennon, Rachel.
Afiliação
  • Gross O; Clinic of Nephrology and Rheumatology, University Medicine Goettingen, Goettingen, Germany.
  • Kashtan CE; Department of Pediatrics, University of Minnesota Medical School, Minneapolis, MN, USA.
  • Rheault MN; Department of Pediatrics, University of Minnesota Medical School, Minneapolis, MN, USA.
  • Flinter F; Department of Clinical Genetics, Guy's and St Thomas' NHS Foundation Trust, London, UK.
  • Savige J; Melbourne Health, The University of Melbourne, Parkville, VIC, Australia.
  • Miner JH; Division of Nephrology, Washington University School of Medicine, St Louis, MO, USA.
  • Torra R; Inherited Kidney Diseases, Nephrology Department, Fundació Puigvert, IIB Sant Pau, Universitat Autònoma de Barcelona and REDINREN, Barcelona, Spain.
  • Ars E; Inherited Kidney Diseases, Nephrology Department, Fundació Puigvert, IIB Sant Pau, Universitat Autònoma de Barcelona and REDINREN, Barcelona, Spain.
  • Deltas C; Molecular Medicine Research Center, Department of Biological Sciences, University of Cyprus, Nicosia, Cyprus.
  • Savva I; Molecular Medicine Research Center, Department of Biological Sciences, University of Cyprus, Nicosia, Cyprus.
  • Perin L; University of Southern California, Children's Hospital Los Angeles, Los Angeles, CA, USA.
  • Renieri A; Medical Genetics Unit, University of Siena, Siena, Italy.
  • Ariani F; Genetica Medica, Azienda Ospedaliera Universitaria Senese, Siena, Italy.
  • Mari F; Medical Genetics Unit, University of Siena, Siena, Italy.
  • Baigent C; Genetica Medica, Azienda Ospedaliera Universitaria Senese, Siena, Italy.
  • Judge P; Medical Genetics Unit, University of Siena, Siena, Italy.
  • Knebelman B; Genetica Medica, Azienda Ospedaliera Universitaria Senese, Siena, Italy.
  • Heidet L; Clinical Trial Service Unit and Epidemiological Studies Unit, Nuffield Department of Population Health, University of Oxford, Oxford, UK.
  • Lagas S; Clinical Trial Service Unit and Epidemiological Studies Unit, Nuffield Department of Population Health, University of Oxford, Oxford, UK.
  • Blatt D; Division de Néphrologie, Hôpital Necker, Assistance Publique-Hôpitaux de Paris, Paris, France.
  • Ding J; Université Paris Descartes, Paris, France.
  • Zhang Y; Centre de Référence des Maladies Rénales Héréditaires de l'Enfant et de l'Adulte (MARHEA) Service de Néphrologie Pédiatrique, Clinique Maurice Lamy, Hôpital Necker-Enfants Malades, Paris, France.
  • Gale DP; Alport Syndrome Foundation, Phoenix, AZ, USA.
  • Prunotto M; Alport Foundation of Australia, Valentine, NSW, Australia.
  • Xue Y; Pediatric Department, Peking University First Hospital, Beijing, China.
  • Schachter AD; Pediatric Department, Peking University First Hospital, Beijing, China.
  • Morton LCG; University College London-Centre for Nephrology, London, UK.
  • Blem J; Roche Innovation Center Basel, F. Hoffmann-La Roche Ltd, Roche Pharma Research & Early Development, Basel, Switzerland.
  • Huang M; Rare Disease Group-Therapeutic Area, Global Clinical Development, Sanofi Genzyme, Naarden, The Netherlands.
  • Liu S; New Indications Discovery Unit, Translational Medicine, Novartis Institutes for BioMedical Research, Cambridge, MA, USA.
  • Vallee S; Cardiovascular Research, Fibrosis Research, Regeneron Pharmaceuticals, Tarrytown, NY, USA.
  • Renault D; Clinical Development, Regulus Therapeutics, San Diego, CA, USA.
  • Schifter J; Clinical Development, Regulus Therapeutics, San Diego, CA, USA.
  • Skelding J; Department of Rare Diseases, Sanofi-Genzyme R&D Center, Framingham, MA, USA.
  • Gear S; Discovery Biology, Shire, Lexington, MA, USA.
  • Friede T; Association for Information and Research on Genetic Renal Diseases (AIRG)-France, Paris, France.
  • Turner AN; Federation of European Associations of patients affected by Genetic Renal Diseases, FEDERG, Brussels, Belgium.
  • Lennon R; Alport Israel, Israel.
Nephrol Dial Transplant ; 32(6): 916-924, 2017 Jun 01.
Article em En | MEDLINE | ID: mdl-27190345
Assuntos
Palavras-chave
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Nefrite Hereditária Tipo de estudo: Guideline / Screening_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Nefrite Hereditária Tipo de estudo: Guideline / Screening_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article