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Quoted phrase not found in phrase index: "Childhood Mixed Germ Cell Tumor"
Page 1
Childhood cerebellar tumours mirror conserved fetal transcriptional programs.
Vladoiu MC, El-Hamamy I, Donovan LK, Farooq H, Holgado BL, Sundaravadanam Y, Ramaswamy V, Hendrikse LD, Kumar S, Mack SC, Lee JJY, Fong V, Juraschka K, Przelicki D, Michealraj A, Skowron P, Luu B, Suzuki H, Morrissy AS, Cavalli FMG, Garzia L, Daniels C, Wu X, Qazi MA, Singh SK, Chan JA, Marra MA, Malkin D, Dirks P, Heisler L, Pugh T, Ng K, Notta F, Thompson EM, Kleinman CL, Joyner AL, Jabado N, Stein L, Taylor MD. Vladoiu MC, et al. Nature. 2019 Aug;572(7767):67-73. doi: 10.1038/s41586-019-1158-7. Epub 2019 May 1. Nature. 2019. PMID: 31043743 Free PMC article.
Study of the origin and development of cerebellar tumours has been hampered by the complexity and heterogeneity of cerebellar cells that change over the course of development. Here we use single-cell transcriptomics to study more than 60,000 cells from the developing mouse …
Study of the origin and development of cerebellar tumours has been hampered by the complexity and heterogeneity of cerebellar cells that cha …
Breastfeeding and risk of childhood brain tumors: a report from the Childhood Cancer and Leukemia International Consortium.
Schraw JM, Petridou ET, Bonaventure A, Dockerty JD, Karalexi M, Ntzani E, Infante-Rivard C, Clavel J, Bracci PM, McKean-Cowdin R, Roman E, Kane E, Erdmann F, Schüz J, Mueller BA, Scheurer ME. Schraw JM, et al. Cancer Causes Control. 2023 Nov;34(11):1005-1015. doi: 10.1007/s10552-023-01746-3. Epub 2023 Jul 8. Cancer Causes Control. 2023. PMID: 37421504 Free article.
PURPOSE: Studies report mixed findings regarding the association of breastfeeding with childhood brain tumors (CBT), the leading causes of cancer-related mortality in young people. ...METHODS: We pooled data on N = 2610 cases with CBT (including 697 cases with astro …
PURPOSE: Studies report mixed findings regarding the association of breastfeeding with childhood brain tumors (CBT), the leadi …
Associations between birth defects and childhood and adolescent germ cell tumors according to sex, histologic subtype, and site.
Schraw JM, Sok P, Desrosiers TA, Janitz AE, Langlois PH, Canfield MA, Frazier AL, Plon SE, Lupo PJ, Poynter JN. Schraw JM, et al. Cancer. 2023 Oct 15;129(20):3300-3308. doi: 10.1002/cncr.34906. Epub 2023 Jun 27. Cancer. 2023. PMID: 37366624
BACKGROUND: Studies have reported increased rates of birth defects among children with germ cell tumors (GCTs). However, few studies have evaluated associations by sex, type of defect, or tumor characteristics. METHODS: Birth defect-GCT associations were eval …
BACKGROUND: Studies have reported increased rates of birth defects among children with germ cell tumors (GCTs). However, few s …
Intratubular germ cell neoplasia of the testis: a brief review.
Al-Hussain T, Bakshi N, Akhtar M. Al-Hussain T, et al. Adv Anat Pathol. 2015 May;22(3):202-12. doi: 10.1097/PAP.0000000000000066. Adv Anat Pathol. 2015. PMID: 25844678 Review.
The second group consists of tumors presenting in third and fourth decade of life and include seminoma, embryonal carcinoma, yolk sac tumor, choriocarcinoma, and teratoma as well as mixed germ cell tumors. ...The level of DNA methylation general …
The second group consists of tumors presenting in third and fourth decade of life and include seminoma, embryonal carcinoma, yolk sac …
Pinealoblastomas in children.
Cuccia V, Rodríguez F, Palma F, Zuccaro G. Cuccia V, et al. Childs Nerv Syst. 2006 Jun;22(6):577-85. doi: 10.1007/s00381-006-0095-6. Epub 2006 Mar 23. Childs Nerv Syst. 2006. PMID: 16555075 Clinical Trial.
INTRODUCTION: Series of pinealoblastomas (PB) usually comprise small number of cases as this tumor type is extremely rare and occurs mainly in childhood (especially under 9 years of age). ...All children had negative serum and CSF markers and only one case had posit …
INTRODUCTION: Series of pinealoblastomas (PB) usually comprise small number of cases as this tumor type is extremely rare and occurs …
Gonadal malignancy risk and prophylactic gonadectomy in disorders of sexual development.
Abacı A, Çatlı G, Berberoğlu M. Abacı A, et al. J Pediatr Endocrinol Metab. 2015 Sep;28(9-10):1019-27. doi: 10.1515/jpem-2014-0522. J Pediatr Endocrinol Metab. 2015. PMID: 25879315 Review.
The most important clinical problems in DSD comprise physical and psychological disturbances and the risk of gonadal tumor development. Germ cell tumor risk is lowest (<5%) in patients with defects in androgene action or synthesis (such as complete …
The most important clinical problems in DSD comprise physical and psychological disturbances and the risk of gonadal tumor developmen …
Primary central nervous system germ cell tumors in children and young adults: A review of controversies in diagnostic and treatment approach.
Yeo KK, Nagabushan S, Dhall G, Abdelbaki MS. Yeo KK, et al. Neoplasia. 2023 Feb;36:100860. doi: 10.1016/j.neo.2022.100860. Epub 2022 Dec 13. Neoplasia. 2023. PMID: 36521378 Free PMC article. Review.
Primary central nervous system (CNS) germ cell tumors (GCT) are a rare heterogenous group of cancers, arising most commonly in the second decade of life. ...
Primary central nervous system (CNS) germ cell tumors (GCT) are a rare heterogenous group of cancers, arising most commonly in …
Molecular markers and potential therapeutic targets in non-WNT/non-SHH (group 3 and group 4) medulloblastomas.
Menyhárt O, Giangaspero F, Győrffy B. Menyhárt O, et al. J Hematol Oncol. 2019 Mar 15;12(1):29. doi: 10.1186/s13045-019-0712-y. J Hematol Oncol. 2019. PMID: 30876441 Free PMC article. Review.
Childhood medulloblastomas (MB) are heterogeneous and are divided into four molecular subgroups. ...Current preclinical models do not represent the full scale of group 3 and group 4 heterogeneity: all of existing group 3 cell lines are MYC-amplified and most mouse m
Childhood medulloblastomas (MB) are heterogeneous and are divided into four molecular subgroups. ...Current preclinical models do not
Chromosomal gains of 12p and 1q are not associated with inferior outcome of pediatric and adolescent germ cell tumors.
Greimelmaier K, Calaminus G, Kristiansen G, Vokuhl C, Klapper W. Greimelmaier K, et al. Pediatr Blood Cancer. 2019 Aug;66(8):e27777. doi: 10.1002/pbc.27777. Epub 2019 May 2. Pediatr Blood Cancer. 2019. PMID: 31045322
BACKGROUND: Pediatric germ cell tumors (GCT) are rare and very heterogeneous neoplasms that show a high diversity in tumor biology and histology. ...METHODS: One hundred and eighty pediatric nonseminomatous GCT, that is, mature teratomas, immature tera …
BACKGROUND: Pediatric germ cell tumors (GCT) are rare and very heterogeneous neoplasms that show a high diversity in …
Testicular malignancy in persistent Mullerian duct syndrome: Experience from an apex cancer center with review of literature.
Philips MR, Menon AR, Kumar GR, Malik K, Chandrasekaran S, Ramaswamy T, Narayanaswamy K, Raja A. Philips MR, et al. Urol Oncol. 2023 May;41(5):258.e1-258.e6. doi: 10.1016/j.urolonc.2023.02.008. Epub 2023 Apr 3. Urol Oncol. 2023. PMID: 37019765 Review.
RESULTS: Of 637 patients treated for testicular tumors during the specified time period in our institution, 4 patients had a concomitant diagnosis of PMDS. Testicular tumor was pathologically confirmed as seminoma in 3, 1 had mixed germ cell tumor
RESULTS: Of 637 patients treated for testicular tumors during the specified time period in our institution, 4 patients had a concomitant dia …
66 results