- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1472-6874
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
Follicular dendritic cell sarcoma of the uterine cervix: a case report ; volume:20 ; number:1 ; day:17 ; month:8 ; year:2020 ; pages:1-4 ; date:12.2020
BMC women's health ; 20, Heft 1 (17.8.2020), 1-4, 12.2020
- Urheber
-
Nakamura, Takuto
Yoshihara, Masato
Tamauchi, Satoshi
Kajiyama, Hiroaki
Kikkawa, Fumitaka
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
-
10.1186/s12905-020-01045-y
- URN
-
urn:nbn:de:101:1-2020100823595723567792
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 11:04 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Nakamura, Takuto
- Yoshihara, Masato
- Tamauchi, Satoshi
- Kajiyama, Hiroaki
- Kikkawa, Fumitaka
- SpringerLink (Online service)
Ähnliche Objekte (12)
Pancreatic follicular dendritic cell sarcoma: a case report
Sarcoma of the uterine cervix: experience of a single center
Disease Response to Pazopanib in Follicular Dendritic Cell Sarcoma
Cancer of the Uterine Cervix
Clinicopathological characteristics of mediastinal follicular dendritic cell sarcoma: report of three cases
Follicular Dendritic Cell Sarcoma of the Thyroid Gland: A Rare Case Report
Endoscopic resection of an Epstein-Barr virus positive inflammatory follicular dendritic cell sarcoma
Extra-Nodal Follicular Dendritic Cell Sarcoma with Unusual Morphological Features and PDL1 Expression
NTRK-rearranged spindle cell sarcoma of the uterine cervix with a novel NUMA1::NTRK1 fusion
Completely resected follicular dendritic cell sarcoma of the posterior mediastinum: report of a case
Nodal follicular dendritic cell sarcoma with four atypical histomorphologic features: an unusual case report
Mediastinal follicular dendritic cell sarcoma: a rare, potentially under-recognized, and often misdiagnosed disease
Pancreatic follicular dendritic cell sarcoma: a case report
Sarcoma of the uterine cervix: experience of a single center
Disease Response to Pazopanib in Follicular Dendritic Cell Sarcoma
Cancer of the Uterine Cervix
Clinicopathological characteristics of mediastinal follicular dendritic cell sarcoma: report of three cases
Follicular Dendritic Cell Sarcoma of the Thyroid Gland: A Rare Case Report
Endoscopic resection of an Epstein-Barr virus positive inflammatory follicular dendritic cell sarcoma
Extra-Nodal Follicular Dendritic Cell Sarcoma with Unusual Morphological Features and PDL1 Expression
NTRK-rearranged spindle cell sarcoma of the uterine cervix with a novel NUMA1::NTRK1 fusion
Completely resected follicular dendritic cell sarcoma of the posterior mediastinum: report of a case
Nodal follicular dendritic cell sarcoma with four atypical histomorphologic features: an unusual case report
Mediastinal follicular dendritic cell sarcoma: a rare, potentially under-recognized, and often misdiagnosed disease
Pancreatic follicular dendritic cell sarcoma: a case report
Sarcoma of the uterine cervix: experience of a single center
Disease Response to Pazopanib in Follicular Dendritic Cell Sarcoma
Cancer of the Uterine Cervix
Clinicopathological characteristics of mediastinal follicular dendritic cell sarcoma: report of three cases
Follicular Dendritic Cell Sarcoma of the Thyroid Gland: A Rare Case Report
Endoscopic resection of an Epstein-Barr virus positive inflammatory follicular dendritic cell sarcoma
Extra-Nodal Follicular Dendritic Cell Sarcoma with Unusual Morphological Features and PDL1 Expression
NTRK-rearranged spindle cell sarcoma of the uterine cervix with a novel NUMA1::NTRK1 fusion
Completely resected follicular dendritic cell sarcoma of the posterior mediastinum: report of a case
Nodal follicular dendritic cell sarcoma with four atypical histomorphologic features: an unusual case report