Zobrazeno 1 - 10
of 1 774
pro vyhledávání: '"ALAGGIO A"'
Autor:
Virginia Di Paolo, Alessandro Paolini, Angela Galardi, Patrizia Gasparini, Loris De Cecco, Marta Colletti, Silvia Lampis, Salvatore Raieli, Cristiano De Stefanis, Evelina Miele, Ida Russo, Valentina Di Ruscio, Michela Casanova, Rita Alaggio, Andrea Masotti, Giuseppe Maria Milano, Franco Locatelli, Angela Di Giannatale
Publikováno v:
Journal of Experimental & Clinical Cancer Research, Vol 43, Iss 1, Pp 1-11 (2024)
Abstract Background Rhabdomyosarcoma (RMS) is the most common pediatric soft tissue sarcoma, with embryonal (ERMS) and alveolar (ARMS) representing the two most common histological subtypes. ARMS shows poor prognosis, being often metastatic at diagno
Externí odkaz:
https://doaj.org/article/dff12ffc5c95489591deecc318a9e227
Autor:
Giada Del Baldo, Angela Mastronuzzi, Selene Cipri, Emanuele Agolini, Marta Matraxia, Antonio Novelli, Antonella Cacchione, Annalisa Serra, Andrea Carai, Luigi Boccuto, Giovanna Stefania Colafati, Pier Luigi Di Paolo, Evelina Miele, Sabina Barresi, Rita Alaggio, Sabrina Rossi, Isabella Giovannoni
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-9 (2024)
Abstract Cancer predisposition syndromes are recognized in about 10% of pediatric malignancies with several genes specifically involved in a subset of pediatric tumors such as DICER1, in pleuropulmonary blastoma, cystic nephroma, and brain sarcomas.
Externí odkaz:
https://doaj.org/article/6e9544ccf65a442488bd95429b65a943
Autor:
Sara Patrizi, Silvia Vallese, Lucia Pedace, Claudia Nardini, Alessandra Stracuzzi, Sabina Barresi, Isabella Giovannoni, Luana Abballe, Celeste Antonacci, Ida Russo, Angela Di Giannatale, Rita Alaggio, Franco Locatelli, Giuseppe Maria Milano, Evelina Miele
Publikováno v:
Frontiers in Epigenetics and Epigenomics, Vol 2 (2024)
Ewing Sarcomas (EWS, OMIM#612219) presents a major challenge in pediatric oncology due to its aggressive nature and poor prognosis, particularly in metastatic cases. Genetic fusions involving the EWSR1 gene and ETS family transcription factors are co
Externí odkaz:
https://doaj.org/article/de3250e704584142bb010d7d8c5ba878
Autor:
Hiyama, Eiso, Hishiki, Tomoro, Yoshimura, Kenichi, Krailo, Mark, Maibach, Rudolf, Haeberle, Beate, Rangaswami, Arun, Lopez-Terrada, Dolores, Malogolowkin, Marcio H., Ansari, Marc, Alaggio, Rita, O’Neill, Allison F., Trobaugh-Lotrario, Angela D., Watanabe, Kenichiro, Schmid, Irene, Ranganathan, Sarangarajan, Tanaka, Yukichi, Inoue, Takeshi, Piao, Jin, Lin, Jason, Czauderna, Piotr, Meyers, Rebecka L., Aronson, Daniel C.
Publikováno v:
In eClinicalMedicine October 2024 76
Autor:
Maged Daruish, Francesca Ambrogio, Anna Colagrande, Andrea Marzullo, Rita Alaggio, Irma Trilli, Giuseppe Ingravallo, Gerardo Cazzato
Publikováno v:
Dermatopathology, Vol 11, Iss 1, Pp 112-123 (2024)
In recent years, particular interest has developed in molecular biology applied to the field of dermatopathology, with a focus on nevi of the Spitz spectrum. From 2014 onwards, an increasing number of papers have been published to classify, stratify,
Externí odkaz:
https://doaj.org/article/d2e0a368607240e2ac9250a83b7571fc
Autor:
Sara Patrizi, Evelina Miele, Lorenza Falcone, Silvia Vallese, Sabrina Rossi, Sabina Barresi, Isabella Giovannoni, Lucia Pedace, Claudia Nardini, Ilaria Masier, Luana Abballe, Antonella Cacchione, Ida Russo, Angela Di Giannatale, Valentina Di Ruscio, Claudia Maria Salgado, Angela Mastronuzzi, Andrea Ciolfi, Marco Tartaglia, Giuseppe Maria Milano, Franco Locatelli, Rita Alaggio
Publikováno v:
Clinical Epigenetics, Vol 16, Iss 1, Pp 1-12 (2024)
Abstract Background Malignant peripheral nerve sheath tumors (MPNSTs) account for 3–10% of pediatric sarcomas, 50% of which occur in neurofibromatosis type 1 (NF1). Sporadic MPNSTs diagnosis may be challenging due to the absence of specific markers
Externí odkaz:
https://doaj.org/article/e153def98c9c43fea6e3e57bc6160250
Autor:
Vallese, Silvia, Barresi, Sabina, Hiemcke-Jiwa, Laura, Patrizi, Sara, Kester, Lennart, Giovannoni, Isabella, Cardoni, Antonello, Pedace, Lucia, Nardini, Claudia, Tancredi, Chantal, Desideri, Martina, von Deimling, Andreas, Mura, Rosa M., Piga, Michela, Errico, Maria E., Stracuzzi, Alessandra, Alaggio, Rita, Miele, Evelina, Flucke, Uta
Publikováno v:
In Modern Pathology September 2024 37(9)
Autor:
Condorelli, Angelo Giuseppe, Nobili, Rebecca, Muglia, Anita, Scarpelli, Giorgia, Marzuolo, Elisa, De Stefanis, Cristiano, Rota, Rossella, Diociaiuti, Andrea, Alaggio, Rita, Castiglia, Daniele, Odorisio, Teresa, El Hachem, May, Zambruno, Giovanna
Publikováno v:
In Journal of Investigative Dermatology July 2024 144(7):1522-1533
Autor:
Daniela Di Carlo, Giulia Fichera, Benoit Dumont, Enrico Pozzo, Beate Timmermann, Romain Luscan, Antoine Moya-Plana, Anna Synakiewicz, Ewa Bien, Nino Jorge dos Reis Farinha, Malgorzata Krawczyk, Rita Alaggio, Apostolos Pourtsidis, Brice Fresneau, Yves Reguerre, Tal Ben-Ami, Calogero Virgone, Jelena Roganovic, Jan Godzinski, Ines B Brecht, Dominik Schneider, Andrea Ferrari, Barbara Hero, Daniel Orbach, Gianni Bisogno
Publikováno v:
EJC Paediatric Oncology, Vol 3, Iss , Pp 100136- (2024)
Olfactory neuroblastoma (ON) is a rare tumor commonly presenting between 50 and 60 years of age. In pediatric age this tumor is even rarer, with an estimated incidence of 0.1 per 100,000 children up to 15 years. It arises from the olfactory neurorepi
Externí odkaz:
https://doaj.org/article/63347801e0a243b0bc1bc645d4cb7d88
Autor:
Malgorzata A. Krawczyk, Malgorzata Styczewska, Carla Fernandez, Rita Alaggio, Jaroslaw Szydlowski, Ines B. Brecht, Daniel Orbach, Dominik T. Schneider, Jelena Roganovic, Gianni Bisogno, Calogero Virgone, Jan Godzinski, Andrea Ferrari, Nuno Jorge Farinha, Tal Ben Ami, Luca Bergamaschi, Yves Réguerre, Ewa Bien
Publikováno v:
EJC Paediatric Oncology, Vol 3, Iss , Pp 100141- (2024)
Melanotic neuroectodermal tumor of infancy (MNTI) is a very rare benign neoplasm of probable neurocristic origin. It primarily affects children in the first year of life, with the median age at diagnosis of 4.5 months (range 0–804 months). It usual
Externí odkaz:
https://doaj.org/article/8f796361f1dc4e45bfa1999b29c96f1d