707 results on '"Vokuhl, Christian"'
Search Results
152. Bilateral testicular juvenile granulosa cell tumor: Tumor control with conservative, antihormonal therapy.
153. Endothelial cell malignancies in infants, children and adolescents : Treatment results of three Cooperative Weichteilsarkom Studiengruppe (CWS) trials and one registry
154. Kaposiform hemangioendothelioma and tufted angioma - (epi)genetic analysis including genome-wide methylation profiling
155. Is radiotherapy required in first-line treatment of stage I diffuse anaplastic Wilms tumor? A report of SIOP-RTSG, AIEOP, JWiTS, and UKCCSG
156. Malignant peripheral nerve sheath tumors in children, adolescents, and young adults : Treatment results of five Cooperative Weichteilsarkom Studiengruppe (CWS) trials and one registry
157. Is radiotherapy required in first-line treatment of stage I diffuse anaplastic Wilms tumor? A report of SIOP-RTSG, AIEOP, JWiTS, and UKCCSG
158. Age-dependent presentation and clinical course of 1465 patients aged 0 to less than 18 years with ovarian or testicular germ cell tumors; data of the MAKEI 96 protocol revisited in the light of prenatal germ cell biology
159. Renal tumors of childhood—A histopathologic pattern-based diagnostic approach
160. Pathologie der Kindertumoren
161. Erratum: Wagner, A.E., et al. SP8 Promotes an Aggressive Phenotype in Hepatoblastoma via FGF8 Activation. Cancers 2020, 12, 2294
162. The Genomic Landscape of Pediatric Renal Cell Carcinomas
163. Clinical and genetic risk factors define two risk groups of extracranial malignant rhabdoid tumours (eMRT/RTK)
164. Pathology of childhood rhabdomyosarcoma: A consensus opinion document from the Children's Oncology Group, European Paediatric Soft Tissue Sarcoma Study Group, and the Cooperative Weichteilsarkom Studiengruppe
165. A combined clinical and biological risk classification improves prediction of outcome in hepatoblastoma patients
166. HGG-34. DETECTION OF ONCOGENIC FUSION EVENTS IN SUPRATENTORIAL GLIOBLASTOMAS OF YOUNG CHILDREN
167. Diagnosis and therapy of tumors with NTRK gene fusion
168. Local Stage Dependent Necessity of Radiation Therapy in Rhabdoid Tumors of the Kidney (RTK)
169. Aggressive Hematopoietic Malignancy Characterized by Biallelic Loss of SMARCB1
170. Malignant ectomesenchymoma in children and adolescents: Report from the Cooperative Weichteilsarkom Studiengruppe (CWS)
171. Infantile myofibromatosis: Excellent prognosis but also rare fatal progressive disease. Treatment results of five Cooperative Weichteilsarkom Studiengruppe (CWS) trials and one registry.
172. Absence of BRAF mutation in pediatric and adolescent germ cell tumors indicate biological differences to adult tumors
173. First description of a giant spindle-cell myxoid tumor with an FGFR1-CAPRIN1 fusion on the back of an infant's hand
174. The impact of local control in the treatment of children with advanced infantile and adult-type fibrosarcoma: Experience of the cooperative weichteilsarkom studiengruppe (CWS)
175. SP8 Promotes an Aggressive Phenotype in Hepatoblastoma via FGF8 Activation
176. Abstract LB-216: Frequent oncogenic tyrosine kinase gene fusions in supratentorial glioblastomas of young children
177. Abstract 5420: Multiomics approach identifies the SP8-FGF8 axis as an important promoter of metastatic features in hepatoblastoma
178. High expression of IGF2-derived intronic miR-483 predicts outcome in hepatoblastoma
179. Patterns of Prior and Subsequent Neoplasms in Children and Adolescents With Soft Tissue Sarcomas
180. Immunophenotype-Genotype Correlations in Clear Cell Sarcoma of Kidney—An Evaluation of Diagnostic Ancillary Studies
181. Renal Tumors of Childhood—A Histopathologic Pattern-Based Diagnostic Approach
182. Downregulation of SFRP1 is a protumorigenic event in hepatoblastoma and correlates with beta-catenin mutations
183. Kaposiform hemangioendothelioma and tufted angioma – (epi)genetic analysis including genome-wide methylation profiling
184. Rhabdomyosarcoma diagnosed in the first year of life: Localized, metastatic, and relapsed disease. Outcome data from five trials and one registry of the Cooperative Weichteilsarkom Studiengruppe (CWS)
185. MOESM2 of Genome-wide methylation profiling and copy number analysis in atypical fibroxanthomas and pleomorphic dermal sarcomas indicate a similar molecular phenotype
186. Alveolar soft-part sarcoma: Primary metastatic disease and metastatic relapse occurring during long-term follow-up: Treatment results of four Cooperative Weichteilsarkom Studiengruppe (CWS) trials and one registry
187. Kindliche Tumoren – eine kurze Einführung zum Thema.
188. Desmoplastic small round cell tumors : Multimodality treatment and new risk factors
189. Calcifying fibrous tumor and inflammatory myofibroblastic tumor are epigenetically related : A comparative genome-wide methylation study
190. TRIM28 haploinsufficiency predisposes to Wilms tumor
191. Desmoplastic small round cell tumors: Multimodality treatment and new risk factors
192. Calcifying fibrous tumor and inflammatory myofibroblastic tumor are epigenetically related: A comparative genome-wide methylation study
193. TRIM28 haploinsufficiency predisposes to Wilms tumor
194. Desmoplastic small round cell tumors : multimodality treatment and new risk factors
195. DNA methylation profiling distinguishes Ewing-like sarcoma with EWSR1–NFATc2 fusion from Ewing sarcoma
196. Proportion of children with cancer that have an indication for genetic counseling and testing based on the cancer type irrespective of other features.
197. IL7R is associated with CNS infiltration and relapse in pediatric B-cell precursor acute lymphoblastic leukemia
198. Lymph node metastases are more frequent in paediatric appendiceal NET ≥1.5 cm but without impact on outcome – Data from the German MET studies.
199. Systemic therapy of aggressive fibromatosis in children and adolescents: Report of the Cooperative Weichteilsarkom Studiengruppe (CWS)
200. Interferon beta induces apoptosis in nasopharyngeal carcinoma cells via the TRAIL-signaling pathway
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