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SIMPSON-GOLABI-BEHMEL syndrome type 1: How placental immunohistochemistry can rapidly Predict the diagnosis.
Fiandrino, Giacomo; Arossa, Alessia; Ghirardello, Stefano; Kalantari, Silvia; Rossi, Chiara; Bonasoni, Maria Paola; Cesari, Stefania; Rizzuti, Tommaso; Giorgio, Elisa; Bassanese, Francesco; Scatigno, Annachiara Licia; Meroni, Anna; Melito, Chiara; Feltri, Monica; Longo, Stefania; Figar, Tiziana Angelica; Andorno, Annalisa; Gelli, Maria Carolina; Bertozzi, Mirko; Spinillo, Arsenio; Riccipetitoni, Giovanna; Valente, Enza Maria; Paulli, Marco; Sirchia, Fabio.
Afiliación
  • Fiandrino G; Anatomic Pathology Unit, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
  • Arossa A; Department of Obstetrics and Gynecology, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
  • Ghirardello S; Neonatal Intensive Care Unit, IRCCS San Matteo Foundation, Pavia, Italy.
  • Kalantari S; Department of Medical Sciences, University of Turin, Turin, Italy. Electronic address: silvia.kalantari@unito.it.
  • Rossi C; Anatomic Pathology Unit, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy; University of Pavia, Pavia, Italy.
  • Bonasoni MP; Pathology Unit, Azienda USL-IRCCS di Reggio Emilia, Reggio Emilia, Italy.
  • Cesari S; Anatomic Pathology Unit, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
  • Rizzuti T; Pathology Unit, Fondazione IRCCS, Cà Granda Ospedale Maggiore Policlinico, Milano, Italy.
  • Giorgio E; Department of Molecular Medicine, University of Pavia, Pavia, Italy; Medical Genetics Unit, IRCCS Mondino Foundation, Pavia, Italy.
  • Bassanese F; University of Pavia, Pavia, Italy; Department of Pediatrics, IRCCS San Matteo Foundation, Pavia, Italy.
  • Scatigno AL; Department of Obstetrics and Gynecology, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy; University of Pavia, Pavia, Italy.
  • Meroni A; Department of Obstetrics and Gynecology, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy; University of Pavia, Pavia, Italy.
  • Melito C; Department of Obstetrics and Gynecology, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy; University of Pavia, Pavia, Italy.
  • Feltri M; Anatomic Pathology Unit, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy; University of Pavia, Pavia, Italy.
  • Longo S; Neonatal Intensive Care Unit, IRCCS San Matteo Foundation, Pavia, Italy.
  • Figar TA; Neonatal Intensive Care Unit, IRCCS San Matteo Foundation, Pavia, Italy.
  • Andorno A; Division of Pathology, Department of Health Sciences, Azienda Ospedaliero-Universitaria Maggiore della Carità, Novara, Italy.
  • Gelli MC; Pathology Unit, Azienda USL-IRCCS di Reggio Emilia, Reggio Emilia, Italy.
  • Bertozzi M; Department of Clinical, Surgical, Diagnostic and Pediatric Sciences, University of Pavia, Pavia, Italy; Pediatric Surgery Unit, Department of Maternal and Child Health, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
  • Spinillo A; Department of Obstetrics and Gynecology, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy; University of Pavia, Pavia, Italy.
  • Riccipetitoni G; Department of Clinical, Surgical, Diagnostic and Pediatric Sciences, University of Pavia, Pavia, Italy; Pediatric Surgery Unit, Department of Maternal and Child Health, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
  • Valente EM; Department of Molecular Medicine, University of Pavia, Pavia, Italy; Medical Genetics Unit, IRCCS Mondino Foundation, Pavia, Italy.
  • Paulli M; Anatomic Pathology Unit, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy; Department of Molecular Medicine, University of Pavia, Pavia, Italy.
  • Sirchia F; Department of Molecular Medicine, University of Pavia, Pavia, Italy; Medical Genetics Unit, IRCCS San Matteo Foundation, Pavia, Italy.
Placenta ; 126: 119-124, 2022 08.
Article en En | MEDLINE | ID: mdl-35796063
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedades Genéticas Ligadas al Cromosoma X / Gigantismo Tipo de estudio: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Límite: Child / Female / Humans / Newborn / Pregnancy Idioma: En Revista: Placenta Año: 2022 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Países Bajos
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedades Genéticas Ligadas al Cromosoma X / Gigantismo Tipo de estudio: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Límite: Child / Female / Humans / Newborn / Pregnancy Idioma: En Revista: Placenta Año: 2022 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Países Bajos