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Somatic USP8 mutations are frequent events in corticotroph tumor progression causing Nelson's tumor.
Pérez-Rivas, Luis G; Theodoropoulou, Marily; Puar, Troy H; Fazel, Julia; Stieg, Mareike R; Ferraù, Francesco; Assié, Guillaume; Gadelha, Monica R; Deutschbein, Timo; Fragoso, Maria C; Kusters, Benno; Saeger, Wolfgang; Honegger, Jürgen; Buchfelder, Michael; Korbonits, Márta; Bertherat, Jérôme; Stalla, Günter K; Hermus, Ad R; Beuschlein, Felix; Reincke, Martin.
Afiliação
  • Pérez-Rivas LG; Medizinische Klinik und Poliklinik IV, Ludwig-Maximilians-Universität München, Munich, Germany.
  • Theodoropoulou M; Medizinische Klinik und Poliklinik IV, Ludwig-Maximilians-Universität München, Munich, Germany.
  • Puar TH; Clinical Neuroendocrinology, Max Planck Institute of Psychiatry, Munich, Germany.
  • Fazel J; Department of Internal Medicine, Division of Endocrinology, Radboud University Medical Centre, Nijmegen, The Netherlands.
  • Stieg MR; Department of Endocrinology, Changi General Hospital, Singapore, Singapore.
  • Ferraù F; Medizinische Klinik und Poliklinik IV, Ludwig-Maximilians-Universität München, Munich, Germany.
  • Assié G; Clinical Neuroendocrinology, Max Planck Institute of Psychiatry, Munich, Germany.
  • Gadelha MR; Centre for Endocrinology, William Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, UK.
  • Deutschbein T; Department of Endocrinology, Cochin Hospital, Assistance Publique Hôpitaux de Paris; Inserm Unité 1016, Centre National de la Recherche Scientifique Unité Mixte de Recherche, Institut Cochin, Université Paris Descartes, Paris, France.
  • Fragoso MC; Division of Endocrinology, Hospital Universitário Clementino Fraga Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
  • Kusters B; Division of Endocrinology and Diabetology, Department of Internal Medicine, University Hospital Würzburg, University of Würzburg, Würzburg, Germany.
  • Saeger W; Unidade de Neuroendocrinologia, Laboratório de Hormônios e Genética Molecular/LIM42, Disciplina de Endocrinologia e Metabologia, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brasil.
  • Honegger J; Department of Pathology, Radboud University Medical Centre, Nijmegen, The Netherlands.
  • Buchfelder M; Institut für Neuropathologie der Universität Hamburg, Hamburg, Germany.
  • Korbonits M; Department of Neurosurgery, Eberhard Karls University Tübingen, Tübingen, Germany.
  • Bertherat J; Neurochirurgische Klinik, Klinikum der Universität Erlangen, Erlangen, Germany.
  • Stalla GK; Centre for Endocrinology, William Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, UK.
  • Hermus AR; Department of Endocrinology, Cochin Hospital, Assistance Publique Hôpitaux de Paris; Inserm Unité 1016, Centre National de la Recherche Scientifique Unité Mixte de Recherche, Institut Cochin, Université Paris Descartes, Paris, France.
  • Beuschlein F; Clinical Neuroendocrinology, Max Planck Institute of Psychiatry, Munich, Germany.
  • Reincke M; Department of Internal Medicine, Division of Endocrinology, Radboud University Medical Centre, Nijmegen, The Netherlands.
Eur J Endocrinol ; 178(1): 57-63, 2018 Jan.
Article em En | MEDLINE | ID: mdl-28982703

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Endopeptidases / Progressão da Doença / Ubiquitina Tiolesterase / Complexos Endossomais de Distribuição Requeridos para Transporte / Carcinogênese / Mutação / Síndrome de Nelson Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male Idioma: En Revista: Eur J Endocrinol Assunto da revista: ENDOCRINOLOGIA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Alemanha País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Endopeptidases / Progressão da Doença / Ubiquitina Tiolesterase / Complexos Endossomais de Distribuição Requeridos para Transporte / Carcinogênese / Mutação / Síndrome de Nelson Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male Idioma: En Revista: Eur J Endocrinol Assunto da revista: ENDOCRINOLOGIA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Alemanha País de publicação: Reino Unido