Results 121 to 130 of about 233,367 (176)

Outcomes of Pediatric and Adolescent Girls with Malignant Ovarian Germ Cell Tumors after Chemotherapy and Surgery: A Single Institutional Experience. [PDF]

J Cancer Allied Spec
Ali N, Wali RM, Rashid A, Inayat N, Zainab M, Ali S, Zahra Gillani ST, Shaheen N.   +7 more
europepmc   +1 more source

Comparative Molecular and Genetic Landscape of Gonadal Germ Cell Tumors: Insights from Testicular and Ovarian Neoplasms. [PDF]

Cancers (Basel)
Parteni DE, Tîrnovanu MC, Țarcă E, Belu A, Jehac A, Lozneanu L, Giusca SE, Ungureanu C, Morosan E, Cojocaru E.   +9 more
europepmc   +1 more source

[Ovarian dysgerminoma].

Revista chilena de obstetricia y ginecologia, 1977
openaire   +1 more source

Radiotherapy of ovarian dysgerminoma.

European journal of gynaecological oncology, 1982
L, Pirtoli, L, Cionini
openaire   +1 more source

Imaging of Gynecological Disease (6): Clinical and Ultrasound Characteristics of Ovarian Dysgerminoma

Ultrasound in Obstetrics and Gynecology, 2011
Objectives To describe the clinical history and ultrasound findings in patients with ovarian dysgerminoma. Methods This was a retrospective study of patients with a histological diagnosis of ovarian dysgerminoma who had undergone preoperative ultrasound ...
Stefano Guerriero, Dirk Timmerman, Lil Valentin   +2 more
exaly   +5 more sources

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Ovarian Dysgerminoma

Journal of Computer Assisted Tomography, 1994
We determined the MR and CT appearance of ovarian dysgerminoma and correlated our findings with the pathologic features.CT and MR findings of three patients with ovarian dysgerminoma were retrospectively reviewed and compared with the pathologic findings.The tumors were divided into lobules by septa that were hypointense or isointense on T2-weighted ...
Y O, Tanaka, Y, Kurosaki, M, Nishida, N, Michishita, K, Kuramoto, Y, Itai, T, Kubo   +6 more
openaire   +4 more sources

Ovarian dysgerminoma

International Journal of Gynecological Cancer, 2022
Anas Mohamed, Ahlam Ali, Faiza M Younis
openaire   +3 more sources

Ovarian dysgerminoma and Apert syndrome

Pediatric Blood & Cancer, 2008
AbstractApert syndrome is an autosomal dominant disorder that results from gain‐of‐function mutations in the FGFR2 gene. FGFR2 also has been shown to be amplified in stomach and breast cancers. We report the case of a 13‐year‐old female with Apert syndrome who developed an ovarian dysgerminoma.
Cécile, Rouzier, Christine, Soler, Paul, Hofman, Caroline, Brennetot, Eric, Bieth, Florence, Pedeutour   +5 more
openaire   +2 more sources