Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Martina Ferrata"'
Autor:
Martina Ferrata, Arno Schad, Stefanie Zimmer, Thomas J. Musholt, Katharina Bahr, Julian Kuenzel, Sven Becker, Erik Springer, Wilfried Roth, Matthias M. Weber, Christian Fottner
Publikováno v:
Frontiers in Oncology, Vol 9 (2019)
The potential of neuroendocrine neoplasms (NEN) to respond to checkpoint inhibitors is largely unknown and full of great expectations. Immunohistochemical (IHC) studies of programmed cell death ligand 1 (PD-L1) expression in the tumor microenvironmen
Externí odkaz:
https://doaj.org/article/c1d0700d969c42d1a5de48438618a00c
Autor:
Elena Guidetti, Monica Cevenini, Maria Luigia Cipollini, Martina Ferrata, Paola Tomassetti, Roberto Corinaldesi
Publikováno v:
Clinical Management Issues, Vol 6, Iss 1S, Pp 23-28 (2015)
Multiple endocrine neoplasia type 1 (MEN1) is a rare autosomal dominant endocrine disorder and is characterised by the concurrent appearance of adenomas of the parathyroid glands, neuroendocrine-enteropancreatic tumours, and pituitary adenomas, as we
Externí odkaz:
https://doaj.org/article/8069c723bfad4a558e8ada4b81602cb7
Autor:
Monica Cevenini, Elena Guidetti, Eleonora Galassi, Martina Ferrata, Paola Tomassetti, Roberto Corinaldesi
Publikováno v:
Clinical Management Issues, Vol 6, Iss 1S, Pp 11-15 (2015)
The aim of the present report is to present a possible primitive case of a neuroendocrine tumour (NET) of the liver. During a routine ultrasound examination, a 51-year-old woman was diagnosed with a lesion in the second segment of the liver, suggesti
Externí odkaz:
https://doaj.org/article/eb46f30e9ee74042a90cdcfd63cc8ebe
Autor:
Monica Cevenini, Elena Guidetti, Eleonora Galassi, Martina Ferrata, Paola Tomassetti, Roberto Corinaldesi
Publikováno v:
Clinical Management Issues, Vol 6, Iss Suppl 1, Pp 11-15 (2013)
The aim of the present report is to present a possible primitive case of a neuroendocrine tumour (NET) of the liver. During a routine ultrasound examination, a 51-year-old woman was diagnosed with a lesion in the second segment of the liver, suggesti
Externí odkaz:
https://doaj.org/article/ce1a0d0f77364b41b03d2178c1dd182c
Autor:
Elena Guidetti, Monica Cevenini, Maria Luigia Cipollini, Martina Ferrata, Paola Tomassetti, Roberto Corinaldesi
Publikováno v:
Clinical Management Issues, Vol 6, Iss Suppl 1, Pp 23-28 (2013)
Multiple endocrine neoplasia type 1 (MEN1) is a rare autosomal dominant endocrine disorder and is characterised by the concurrent appearance of adenomas of the parathyroid glands, neuroendocrine-enteropancreatic tumours, and pituitary adenomas, as we
Externí odkaz:
https://doaj.org/article/861f2445ca4b431b8c50b1b5b959b2d4
Autor:
Wilfried Roth, Martina Ferrata, Stefanie Zimmer, Thomas J. Musholt, Katharina Bahr, Matthias M. Weber, Arno Schad, Christian Fottner, Sven Becker, Julian Kuenzel, Erik Springer
Publikováno v:
Frontiers in Oncology, Vol 9 (2019)
Frontiers in Oncology
Frontiers in Oncology
The potential of neuroendocrine neoplasms (NEN) to respond to checkpoint inhibitors is largely unknown and full of great expectations. Immunohistochemical (IHC) studies of programmed cell death ligand 1 (PD-L1) expression in the tumor microenvironmen
Publikováno v:
Reviews in endocrinemetabolic disorders. 18(4)
Neuroendocrine neoplasms of the digestive system (GEP-NEN) represent a heterogeneous group of malignancies with various clinical presentation and prognosis. GEP-NENs can potentially affect all organs of the gastrointestinal tract; characteristically
Autor:
Sebastian Krug, Patrick Michl, Leonidas Apostolidis, Arno Schad, Wilfried Roth, Peter R. Galle, Christian Fottner, Dirk Jaeger, Matthias M. Weber, Martina Ferrata
Publikováno v:
Journal of Clinical Oncology. 37:4103-4103
4103 Background: High grade Neuroendocrine Neoplasias (NEN) are rare tumors with a poor prognosis and no established second line therapy when progressive after first line platinum-based chemotherapy resulting in a median overall survival (OS) of 5 mo
Autor:
Elena Guidetti, Eleonora Galassi, Roberto Corinaldesi, Paola Tomassetti, Monica Cevenini, Martina Ferrata
Publikováno v:
Clinical Management Issues, Vol 6, Iss Suppl 1, Pp 11-15 (2013)
Clinical Management Issues; Vol 6, No 1S (2012); 11-15
Clinical Management Issues, Vol 6, Iss 1S, Pp 11-15 (2015)
Clinical Management Issues; Vol 6, No 1S (2012); 11-15
Clinical Management Issues, Vol 6, Iss 1S, Pp 11-15 (2015)
The aim of the present report is to present a possible primitive case of a neuroendocrine tumour (NET) of the liver. During a routine ultrasound examination, a 51-year-old woman was diagnosed with a lesion in the second segment of the liver, suggesti
Autor:
Monica Cevenini, Martina Ferrata, Roberto Corinaldesi, Maria Luigia Cipollini, Elena Guidetti, Paola Tomassetti
Publikováno v:
Clinical Management Issues, Vol 6, Iss Suppl 1, Pp 23-28 (2013)
Clinical Management Issues, Vol 6, Iss 1S, Pp 23-28 (2015)
Clinical Management Issues, Vol 6, Iss 1S, Pp 23-28 (2015)
Multiple endocrine neoplasia type 1 (MEN1) is a rare autosomal dominant endocrine disorder and is characterised by the concurrent appearance of adenomas of the parathyroid glands, neuroendocrine-enteropancreatic tumours, and pituitary adenomas, as we