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1 nd predispose individuals to infertility and germ cell cancer.
2 retinoic acid signals can be dissociated in germ cell cancer.
3 sease and early in the treatment of relapsed germ cell cancer.
4 lar cancer are seminoma and non-seminomatous germ-cell cancer.
5 cycles in patients with favorable-prognosis germ-cell cancer.
8 eat shock protein response of germ cells and germ cell cancer are providing increasing interest in th
9 d postpubertal factors in the development of germ cell cancer as well as increased insight into the m
10 IV- or chemically induced, increases risk of germ cell cancer by 20 to 50 times that in the general p
14 alysis, residual mass size and International Germ Cell Cancer Collaborative Group (IGCCCG) risk class
15 is issue in the context of the International Germ Cell Cancer Collaborative Group (IGCCCG) risk class
16 gnostic group according to the International Germ Cell Cancer Collaborative Group classification.
17 routine follow-up, 98% in the International Germ Cell Cancer Collaborative Group good prognosis grou
18 ata of trials according to the International Germ Cell Cancer Collaborative Group model, which has ev
19 in concentrations that matched International Germ Cell Cancer Consensus Group poor prognosis criteria
20 ents given systemic treatment for testicular germ cell cancer (GCC) are at increased risk for a secon
21 confirming a higher incidence of testicular germ cell cancer (GCC) in offspring of dizygous than in
23 factor in the exquisite chemosensitivity of germ cell cancer has been high-lighted by a report demon
28 ish observation that the rising incidence of germ cell cancer is linked to a birth cohort effect; evi
30 n on the X chromosome with susceptibility to germ cell cancer of the testis by its association with d
34 a included relapsed gonadal and extragonadal germ cell cancer unlikely to be cured by standard salvag
36 ete remissions in patients with disseminated germ cell cancer who relapse after cisplatin-etoposide-b
37 ow-up, pulmonary impairment in patients with germ cell cancer who were treated with BEP was limited.
38 ne hundred fourteen patients with metastatic germ cell cancer with elevated serum tumor markers after
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