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American Journal of Surgical Pathology, ISSN 0147-5185, 2017, Volume 41, Issue 8, pp. 1013 - 1022
Journal Article
GENES CHROMOSOMES & CANCER, ISSN 1045-2257, 04/2016, Volume 55, Issue 4, pp. 350 - 354
In schwannomatosis, germline SMARCB1 or LZTR1 mutations predispose to the development of multiple benign schwannomas. Besides these, other tumors may occur in... 
MULTIPLE MENINGIOMAS | ONCOLOGY | GENETICS & HEREDITY | INI1/SMARCB1 | NF2 | MUTATIONS | SPECTRUM
Journal Article
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, ISSN 0147-5185, 01/2012, Volume 36, Issue 1, pp. 154 - 160
Epithelioid malignant peripheral nerve sheath tumors arising in preexisting schwannomas are extremely rare. We report an unusual example occurring in a patient... 
RHABDOID TUMORS | TRANSFORMATION | SURGERY | malignant peripheral nerve sheath tumor | SMARCB1/INI1 | SOLITARY | schwannomatosis | PATHOLOGY | FAMILIAL SCHWANNOMATOSIS | SPORADIC SCHWANNOMATOSIS | INI1/SMARCB1 | SPECTRUM | DIAGNOSTIC-CRITERIA | schwannoma | NEURILEMOMA | ANGIOSARCOMA
Journal Article
Journal Article
The American Journal of Surgical Pathology, ISSN 0147-5185, 09/2015, Volume 39, Issue 9, pp. 1197 - 1205
Ovarian small cell carcinoma of the hypercalcemic type (SCCOHT)/ovarian rhabdoid tumor is a rare and highly malignant tumor that typically occurs in young... 
Rhabdoid tumor | Ovary | INI1/SMARCB1 | SMARCA4/BRG1 | Small cell carcinoma hypercalcemic type | SURGERY | SMARCB1 | FUSION | NEOPLASMS | BRG1 | PATHOLOGY | small cell carcinoma hypercalcemic type | SMARCA4 | INI1 | ovary | SARCOMAS | rhabdoid tumor | MUTATIONS | Immunohistochemistry | Predictive Value of Tests | Carcinoma, Small Cell - genetics | Nuclear Proteins - analysis | Humans | Middle Aged | Ovarian Neoplasms - pathology | Sarcoma, Ewing - pathology | Granulosa Cell Tumor - pathology | Rhabdoid Tumor - pathology | Bone Neoplasms - pathology | Ovarian Neoplasms - genetics | Young Adult | Carcinoma, Small Cell - chemistry | Sarcoma, Endometrial Stromal - pathology | Soft Tissue Neoplasms - chemistry | Melanoma - genetics | Bone Neoplasms - chemistry | Adult | Female | Bone Neoplasms - genetics | Melanoma - chemistry | Soft Tissue Neoplasms - genetics | Hypercalcemia - genetics | Diagnosis, Differential | Ovarian Neoplasms - chemistry | Sarcoma, Ewing - chemistry | Hypercalcemia - pathology | Endometrial Neoplasms - chemistry | Biomarkers, Tumor - analysis | Rhabdoid Tumor - chemistry | Hypercalcemia - metabolism | Melanoma - pathology | Sarcoma, Endometrial Stromal - chemistry | Rhabdoid Tumor - genetics | Biopsy | Adolescent | Soft Tissue Neoplasms - pathology | DNA Helicases - analysis | Endometrial Neoplasms - pathology | Granulosa Cell Tumor - chemistry | Biomarkers, Tumor - genetics | Transcription Factors - analysis | Carcinoma, Small Cell - pathology | Neoplasm Staging | Sarcoma, Ewing - genetics
Journal Article
Child's Nervous System, ISSN 0256-7040, 2/2018, Volume 34, Issue 2, pp. 367 - 371
Malignant rhabdoid tumor (MRT) is a highly aggressive childhood neoplasm and mainly presents in kidney and brain. We report the case of a patient with... 
Extradural tumor | Posterior fusion | Pediatrics | Neurosciences | Medicine & Public Health | INI1/SMARCB1/BAF47 | Neurosurgery | SURGERY | BONY INVOLVEMENT | ATYPICAL TERATOID/RHABDOID TUMOR | CERVICAL-SPINE | MUTATIONS | CLINICAL NEUROLOGY | INI1 | Usage | Chemotherapy | Research | Radiotherapy | Health aspects | Tumors | Cancer
Journal Article
Journal of Neuro-Oncology, ISSN 0167-594X, 3/2018, Volume 137, Issue 1, pp. 33 - 38
In sporadic schwannomas, inactivation of both copies of the NF2 tumor suppressor gene on 22q is common. Constitutional mutations of SMARCB1 are responsible of... 
Neurology | SMARCB1 | Medicine & Public Health | Oncology | Schwannomatosis | Neurofibromatosis type 2 | NF2 | RHABDOID TUMORS | SUPPRESSOR | PHENOTYPE | CLINICAL NEUROLOGY | INI1 | MENINGIOMAS | GENE | ONCOLOGY | INI1/SMARCB1 | NEUROFIBROMATOSIS TYPE-2 | DELETIONS | Medical colleges | Medical genetics | Missense mutation | Copy number | Schwann cells | Neurofibromin 2 | Chromosome 22 | Tumor suppressor genes | Tumorigenesis | Vestibular system | Mutation
Journal Article
Brain Pathology, ISSN 1015-6305, 07/2017, Volume 27, Issue 4, pp. 411 - 418
Journal Article
Der Pathologe, ISSN 0172-8113, 7/2017, Volume 38, Issue 4, pp. 278 - 285
Solide Kindertumoren sind extrem seltene Entitäten, die praktisch ausnahmslos in spezialisierten Zentren behandelt werden. Die Diagnose und weitere Therapie... 
Rhabdoidtumoren | Pathology | Medicine & Public Health | Neuroblastom | INI1/SMARCB1 | Neuroblastoma | Kongenitales mesoblastisches Nephrom | Congenital mesoblastic nephroma | Rhabdoid tumors | MYC-N
Journal Article
Journal Article
Journal Article
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