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1. Distinct patterns of copy number alterations may predict poor outcome in central nervous system germ cell tumors

7. Genome-wide methylation profiles in primary intracranial germ cell tumors indicate a primordial germ cell origin for germinomas

12. Recurrent neomorphic mutations of MTOR in central nervous system and testicular germ cell tumors may be targeted for therapy

14. Human chorionic gonadotropin is expressed virtually in all intracranial germ cell tumors

16. Transcriptome and methylome analysis of CNS germ cell tumor finds its cell-of-origin in embryogenesis and reveals shared similarities with testicular counterparts

17. Prognostic factors of CNS germinomas; histopathological analyses on 114 cases from the iGCT consortium

18. BOT-3 Prognostic Factors of CNS Germ Cell Tumors; Molecular and Histopathological Analyses on 154 Cases from the iGCT Consortium

19. PEDT-5 Problem for the guideline of CNS germ cell tumors

20. Mutually exclusive mutations of KIT and RAS are associated with KIT mRNA expression and chromosomal instability in primary intracranial pure germinomas

21. The Japan Society for Neuro-Oncology guideline on the diagnosis and treatment of central nervous system germ cell tumors

33. Low tumor cell content predicts favorable prognosis in germinoma patients

36. GCT-52. TRANSCRIPTOME OF CENTRAL NERVOUS SYSTEM GERM CELL TUMOR REVEALS ITS PATHOGENESIS AND CONTRASTS WITH TESTICULAR COUNTERPARTS IN INTEGRATED OMICS ANALYSIS

37. MBCL-48. OUTCOMES OF TREATMENT BASED ON THE ST. JUDE MEDULLOBLASTOMA-96 REGIMEN FOR JAPANESE CHILDREN WITH MEDULLOBLASTOMA

38. GCT-59. EPIDEMIOLOGY OF PEDIATRIC INTRA-CRANIAL GERM CELL TUMORS: COMPARING THE INCIDENCE OF INTRA-CRANIAL GERM CELL TUMORS IN THE NATIVE JAPANESE POPULATION AND IMMIGRANT JAPANESE POPULATIONS ABROAD

40. Japan Society for Neuro-Oncology guideline on the diagnosis and treatment of central nervous system germ cell tumors.

42. Relapse patterns and treatment outcomes of recurrent central nervous germ cell tumors (CNS-GCTS)

45. PEDT-02 DIAGNOSIS, TREATMENT AND CLINICAL OUTCOME OF ATYPICAL BRAINSTEM TUMOUR IN CHILDHOOD

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