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Blood, ISSN 1528-0020, 2016, Volume 127, Issue 7, pp. 869 - 881
Journal Article
The American Journal of Surgical Pathology, ISSN 0147-5185, 11/2018, Volume 42, Issue 11, pp. 1429 - 1444
Central nervous system (CNS)-type tumors and tumor-like proliferations arising in the gynecologic tract and pelvis are rare... 
SURGERY | gynecologic tract | pelvis | CENTRAL NEUROCYTOMA | BROAD LIGAMENT | PATHOLOGY | NEUROECTODERMAL TUMORS | MYXOPAPILLARY EPENDYMOMA | BRAIN-TUMORS | central type primitive neuroectodermal tumor | EXTRASPINAL EPENDYMOMA | central nervous system tumors | OVARIAN EPENDYMOMA | MATURE CYSTIC TERATOMA | PILOCYTIC ASTROCYTOMA | OF-THE-LITERATURE | Immunohistochemistry | Oligonucleotide Array Sequence Analysis | Humans | Middle Aged | Neoplasms, Neuroepithelial - pathology | Young Adult | Pelvic Neoplasms - therapy | Neoplasm Grading | Time Factors | Neoplasms, Neuroepithelial - genetics | Adult | Female | Child | Central Nervous System Neoplasms - chemistry | Genital Neoplasms, Female - genetics | Pelvic Neoplasms - pathology | Chromosome Deletion | Pelvic Neoplasms - chemistry | Genetic Predisposition to Disease | Biomarkers, Tumor - analysis | Central Nervous System Neoplasms - genetics | Pelvic Neoplasms - genetics | Risk Factors | Neoplasm Recurrence, Local | Genital Neoplasms, Female - chemistry | Central Nervous System Neoplasms - therapy | In Situ Hybridization, Fluorescence | Neoplasms, Neuroepithelial - therapy | Central Nervous System Neoplasms - pathology | Phenotype | Genital Neoplasms, Female - therapy | Neoplasms, Neuroepithelial - chemistry | Progression-Free Survival | Adolescent | Aged | Biomarkers, Tumor - genetics | Polymorphism, Single Nucleotide | Mutation | Genital Neoplasms, Female - pathology | Pathology, Gynecological | Genetic aspects | Diagnosis | Pelvis | Identification and classification | Health aspects | Tumors | Index Medicus
Journal Article
Journal of investigative dermatology, ISSN 0022-202X, 2013, Volume 133, Issue 9, pp. 2229 - 2236
... clear. We hypothesized that a single postzygotic mutation in NRAS could be responsible for multiple CMN in the same individual, as well as for melanocytic and nonmelanocytic central nervous system (CNS) lesions... 
MC1R | VARIANTS | RAS | BRAF MUTATIONS | HIGH-FREQUENCY | PHENOTYPE | NEUROLOGICALLY ASYMPTOMATIC CHILDREN | ASSOCIATION | REGISTRY | MOSAICISM | DERMATOLOGY | Meningeal Neoplasms - epidemiology | Prevalence | Nevus, Pigmented - epidemiology | Humans | Child, Preschool | Male | Neurocutaneous Syndromes - congenital | Meningioma - genetics | Mutation, Missense - genetics | Loss of Heterozygosity - genetics | Hamartoma - pathology | Young Adult | Hamartoma - genetics | Nevus, Pigmented - genetics | Meningioma - epidemiology | Zygote | Female | Genetic Predisposition to Disease - epidemiology | Neurocutaneous Syndromes - epidemiology | Child | Melanosis - epidemiology | Melanosis - genetics | Neurocutaneous Syndromes - genetics | Genetic Predisposition to Disease - genetics | Meningeal Neoplasms - genetics | Membrane Proteins - genetics | Central Nervous System Neoplasms - genetics | Risk Factors | Hamartoma - epidemiology | Central Nervous System Neoplasms - epidemiology | Melanosis - congenital | Skin Neoplasms - epidemiology | Nevus, Pigmented - congenital | Magnetic Resonance Imaging | Meningioma - pathology | Central Nervous System Neoplasms - pathology | GTP Phosphohydrolases - genetics | Skin Neoplasms - congenital | Skin Neoplasms - genetics | Adolescent | Mosaicism | Meningeal Neoplasms - pathology | Index Medicus | Original
Journal Article
2012, Biomedical & nanomedical technologies, ISBN 9780791860038, viii, 99
eBook
The Journal of pathology, ISSN 0022-3417, 2014, Volume 232, Issue 1, pp. 23 - 31
Journal Article
Nature communications, ISSN 2041-1723, 2013, Volume 4, Issue 1, p. 2166
Isocitrate dehydrogenase (IDH) genes 1 and 2 are frequently mutated in acute myeloid leukaemia (AML), low-grade glioma, cholangiocarcinoma (CC) and... 
METHYLATION | 5-METHYLCYTOSINE | DNA | GLIOMA | MULTIDISCIPLINARY SCIENCES | MECHANISMS | RETINOIC ACID RECEPTORS | MUTATIONS | Neoplasms - metabolism | Humans | Leukemia, Myeloid, Acute - metabolism | Gene Expression Regulation, Neoplastic | Cholangiocarcinoma - metabolism | Bone Neoplasms - pathology | Receptors, Retinoic Acid - genetics | Bone Neoplasms - metabolism | Glioma - metabolism | DNA-Binding Proteins - metabolism | Glioma - genetics | DNA Methylation | Neoplasms - genetics | Glioma - pathology | Trans-Activators - genetics | Chondrosarcoma - genetics | Chondrosarcoma - pathology | Bone Neoplasms - genetics | Bile Duct Neoplasms - genetics | Proto-Oncogene Proteins - metabolism | Central Nervous System Neoplasms - metabolism | Bile Duct Neoplasms - metabolism | Signal Transduction | Leukemia, Myeloid, Acute - pathology | Central Nervous System Neoplasms - genetics | Isocitrate Dehydrogenase - genetics | Proto-Oncogene Proteins - genetics | Receptors, Retinoic Acid - metabolism | DNA-Binding Proteins - genetics | Central Nervous System Neoplasms - pathology | Cholangiocarcinoma - pathology | Chondrosarcoma - metabolism | Cholangiocarcinoma - genetics | Isocitrate Dehydrogenase - metabolism | Trans-Activators - metabolism | Glutarates - metabolism | Bile Duct Neoplasms - pathology | Mutation | Neoplasms - pathology | Leukemia, Myeloid, Acute - genetics
Journal Article
International Journal of Gynecological Cancer, ISSN 1048-891X, 09/2015, Volume 25, Issue 7, pp. 1232 - 1238
OBJECTIVESTo estimate the frequency of hereditary breast and ovarian cancer (HBOC) in women with central nervous system... 
Hereditary breast and ovarian cancer | Central nervous system metastasis | Ovarian cancer | IMPROVED SURVIVAL | BRCA1 | CHEMOTHERAPY | FEATURES | OBSTETRICS & GYNECOLOGY | WOMEN | ONCOLOGY | MUTATIONS | CARCINOMA | BRAIN | Genetic Testing | Prognosis | Follow-Up Studies | Adenocarcinoma, Mucinous - pathology | Endometrial Neoplasms - mortality | Adenocarcinoma, Clear Cell - mortality | Humans | Middle Aged | Spinal Cord Neoplasms - secondary | Ovarian Neoplasms - pathology | Cystadenocarcinoma, Serous - genetics | Ovarian Neoplasms - mortality | Cystadenocarcinoma, Serous - pathology | Ovarian Neoplasms - genetics | Brain Neoplasms - secondary | Endometrial Neoplasms - genetics | Cystadenocarcinoma, Serous - therapy | Adult | Female | Brain Neoplasms - mortality | Adenocarcinoma, Mucinous - therapy | Spinal Cord Neoplasms - genetics | Spinal Cord Neoplasms - therapy | Genetic Predisposition to Disease | Neoplasm Invasiveness | Brain Neoplasms - genetics | Survival Rate | Lymphatic Metastasis | Mutation - genetics | Adenocarcinoma, Mucinous - mortality | Spinal Cord Neoplasms - mortality | Adenocarcinoma, Clear Cell - therapy | Brain Neoplasms - therapy | Cystadenocarcinoma, Serous - mortality | Endometrial Neoplasms - therapy | Ovarian Neoplasms - therapy | Endometrial Neoplasms - pathology | Adenocarcinoma, Clear Cell - pathology | Aged | Adenocarcinoma, Mucinous - genetics | Neoplasm Staging | Adenocarcinoma, Clear Cell - genetics
Journal Article
Nature communications, ISSN 2041-1723, 2015, Volume 6, Issue 1, p. 8839
Journal Article
Science (American Association for the Advancement of Science), ISSN 1095-9203, 2011, Volume 333, Issue 6041, pp. 425 - 425
Journal Article
Journal of Neuro-Oncology, ISSN 0167-594X, 5/2016, Volume 127, Issue 3, pp. 435 - 444
Journal Article
Clinical Cancer Research, ISSN 1078-0432, 12/2010, Volume 16, Issue 23, pp. 5873 - 5882
Journal Article
by Capper, David and Jones, David T. W and Sill, Martin and Hovestadt, Volker and Schrimpf, Daniel and Sturm, Dominik and Koelsche, Christian and Sahm, Felix and Chavez, Lukas and Reuss, David E and Kratz, Annekathrin and Wefers, Annika K and Huang, Kristin and Pajtler, Kristian W and Schweizer, Leonille and Stichel, Damian and Olar, Adriana and Engel, Nils W and Lindenberg, Kerstin and Harter, Patrick N and Braczynski, Anne K and Plate, Karl H and Dohmen, Hildegard and Garvalov, Boyan K and Coras, Roland and Hölsken, Annett and Hewer, Ekkehard and Bewerunge-Hudler, Melanie and Schick, Matthias and Fischer, Roger and Beschorner, Rudi and Schittenhelm, Jens and Staszewski, Ori and Wani, Khalida and Varlet, Pascale and Pages, Melanie and Temming, Petra and Lohmann, Dietmar and Selt, Florian and Witt, Hendrik and Milde, Till and Witt, Olaf and Aronica, Eleonora and Giangaspero, Felice and Rushing, Elisabeth and Scheurlen, Wolfram and Geisenberger, Christoph and Rodriguez, Fausto J and Becker, Albert and Preusser, Matthias and Haberler, Christine and Bjerkvig, Rolf and Cryan, Jane and Farrell, Michael and Deckert, Martina and Hench, Jürgen and Frank, Stephan and Serrano, Jonathan and Kannan, Kasthuri and Tsirigos, Aristotelis and Brück, Wolfgang and Hofer, Silvia and Brehmer, Stefanie and Seiz-Rosenhagen, Marcel and Hänggi, Daniel and Hans, Volkmar and Rozsnoki, Stephanie and Hansford, Jordan R and Kohlhof, Patricia and Kristensen, Bjarne W and Lechner, Matt and Lopes, Beatriz and Mawrin, Christian and Ketter, Ralf and Kulozik, Andreas and Khatib, Ziad and Heppner, Frank and Koch, Arend and Jouvet, Anne and Keohane, Catherine and Mühleisen, Helmut and Mueller, Wolf and Pohl, Ute and Prinz, Marco and Benner, Axel and Zapatka, Marc and Gottardo, Nicholas G and Driever, Pablo Hernáiz and Kramm, Christof M and Müller, Hermann L and Rutkowski, Stefan and von Hoff, Katja and Frühwald, Michael C and Gnekow, Astrid and Fleischhack, Gudrun and Tippelt, Stephan and Calaminus, Gabriele and Monoranu, Camelia-Maria and Perry, Arie and Jones, Chris and ...
Nature (London), ISSN 1476-4687, 2018, Volume 555, Issue 7697, pp. 469 - 474
Journal Article