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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2000 | 2 |
2013 | 1 |
2017 | 1 |
2024 | 0 |
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Page 1
Childhood pheochromocytoma in a survivor of central primitive neuroectodermal tumor.
Pediatr Int. 2013 Aug;55(4):e100-2. doi: 10.1111/ped.12074.
Pediatr Int. 2013.
PMID: 23910809
The former is usually benign and develops mainly in adulthood and the latter brain tumor mainly occurs in childhood and has a poor prognosis. We report a case of a 15-year-old boy who developed pheochromocytoma after more than 10 years of complete remission of central prim …
The former is usually benign and develops mainly in adulthood and the latter brain tumor mainly occurs in childhood and has a poor progno …
Ewing's family of tumors involving structures related to the central nervous system: a review.
Hadfield MG, Quezado MM, Williams RL, Luo VY.
Hadfield MG, et al.
Pediatr Dev Pathol. 2000 May-Jun;3(3):203-10. doi: 10.1007/s100249910026.
Pediatr Dev Pathol. 2000.
PMID: 10742406
Review.
We have separated the cases by skull region and spinal column level, and we discuss the attendant differences in prognosis following treatment by neurosurgery, radiation, and chemotherapy. ...We conclude that EFT involving the CNS and adjacent structures is not so rare as …
We have separated the cases by skull region and spinal column level, and we discuss the attendant differences in prognosis following …
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Two Tumors in 1: What Should be the Therapeutic Target? Pediatric Germ Cell Tumor With Somatic Malignant Transformation.
Faure Conter C, Fresneau B, Thebaud E, Bertrand A, Dijoud F, Rome A, Dumesnil C, Castex MP, Ghanem A, Orbach D.
Faure Conter C, et al.
J Pediatr Hematol Oncol. 2017 Jul;39(5):388-394. doi: 10.1097/MPH.0000000000000823.
J Pediatr Hematol Oncol. 2017.
PMID: 28375941
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Are clinical parameters valuable prognostic factors in childhood primitive neuroectodermal tumors? A multivariate analysis of 105 cases.
Michiels EM, Heikens J, Jansen MJ, Oldenburger F, Voûte T.
Michiels EM, et al.
Radiother Oncol. 2000 Mar;54(3):229-38. doi: 10.1016/s0167-8140(00)00155-9.
Radiother Oncol. 2000.
PMID: 10738081
Long-term survivors are often confronted with serious late sequelae, caused by the therapy. Therefore, prognostic markers must be identified that allow the children to be assigned to different treatment schedules according to their predicted outcome. ...CONCLUSION: …
Long-term survivors are often confronted with serious late sequelae, caused by the therapy. Therefore, prognostic markers must be ide …
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