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Multiple Congenital Melanocytic Nevi and Neurocutaneous Melanosis Are Caused by Postzygotic Mutations in Codon 61 of NRAS
Kinsler, Veronica A., Thomas, Anna C., Ishida, Miho, Bulstrode, Neil W., Loughlin, Sam, Hing, Sandra, Chalker, Jane, McKenzie, Kathryn, Abu-Amero, Sayeda, Slater, Olga, Chanudet, Estelle, Palmer, Rodger, Morrogh, Deborah, Stanier, Philip, Healy, Eugene, Sebire, Neil J., Moore, Gudrun E.
Published in Journal of investigative dermatology (01.09.2013)
Published in Journal of investigative dermatology (01.09.2013)
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Exceptional aggressiveness of cerebral cavernous malformation disease associated with PDCD10 mutations
Shenkar, Robert, Shi, Changbin, Rebeiz, Tania, Stockton, Rebecca A., McDonald, David A., Mikati, Abdul Ghani, Zhang, Lingjiao, Austin, Cecilia, Akers, Amy L., Gallione, Carol J., Rorrer, Autumn, Gunel, Murat, Min, Wang, Marcondes de Souza, Jorge, Lee, Connie, Marchuk, Douglas A., Awad, Issam A.
Published in Genetics in medicine (01.03.2015)
Published in Genetics in medicine (01.03.2015)
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Pediatric spinal pilocytic astrocytomas form a distinct epigenetic subclass from pilocytic astrocytomas of other locations and diffuse leptomeningeal glioneuronal tumours
Métais, Alice, Bouchoucha, Yassine, Kergrohen, Thomas, Dangouloff-Ros, Volodia, Maynadier, Xavier, Ajlil, Yassine, Carton, Matthieu, Yacoub, Wael, Saffroy, Raphael, Figarella-Branger, Dominique, Uro-Coste, Emmanuelle, Sevely, Annick, Larrieu-Ciron, Delphine, Faisant, Maxime, Machet, Marie-Christine, Wahler, Ellen, Roux, Alexandre, Benichi, Sandro, Beccaria, Kevin, Blauwblomme, Thomas, Boddaert, Nathalie, Chrétien, Fabrice, Doz, François, Dufour, Christelle, Grill, Jacques, Debily, Marie Anne, Varlet, Pascale, Tauziède-Espariat, Arnault
Published in Acta neuropathologica (01.01.2023)
Published in Acta neuropathologica (01.01.2023)
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Clinicopathologic and Genetic Features of Primary T-cell Lymphomas of the Central Nervous System: An Analysis of 11 Cases Using Targeted Gene Sequencing
Yim, Jeemin, Koh, Jiwon, Kim, Sehui, Song, Seung Geun, Bae, Jeong Mo, Yun, Hongseok, Sung, Ji-Youn, Kim, Tae Min, Park, Sung-Hye, Jeon, Yoon Kyung
Published in The American journal of surgical pathology (01.04.2022)
Published in The American journal of surgical pathology (01.04.2022)
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Recent Advances in the Treatment of Malignant Astrocytoma
Reardon, David A., Rich, Jeremy N., Friedman, Henry S., Bigner, Darell D.
Published in Journal of clinical oncology (10.03.2006)
Published in Journal of clinical oncology (10.03.2006)
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Epithelioid solitary fibrous tumors from CNS and soft tissues: an unusual morphologic variant
Zhao, Lina, Ma, Jiajing, Ren, Jiacai, Yuan, Jingping, He, Huihua, Huang, Yabing, Yan, Honglin
Published in Diagnostic pathology (25.10.2024)
Published in Diagnostic pathology (25.10.2024)
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Loss of the Tumor Suppressor PML in Human Cancers of Multiple Histologic Origins
Gurrieri, C., Capodieci, P., Bernardi, R., Scaglioni, P. P., Nafa, K., Rush, L. J., Verbel, D. A., Cordon-Cardo, C., Pandolfi, P. P.
Published in JNCI : Journal of the National Cancer Institute (18.02.2004)
Published in JNCI : Journal of the National Cancer Institute (18.02.2004)
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Identification of an m6A RNA Methylation Regulator Risk Score Model for Prediction of Clinical Prognosis in Astrocytoma
Guo, Fangzhou, Deng, Teng, Shi, Liu, Wu, Pinghua, Yan, Jun, Ling, Guoyuan, Chen, Hainan, Huang, Qianrong, Mu, Junbo, Mo, Ligen
Published in Computational and mathematical methods in medicine (10.01.2022)
Published in Computational and mathematical methods in medicine (10.01.2022)
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A Novel MGC4607/CCM2 Gene Mutation Associated with Cerebral Spinal and Cutaneous Cavernous Angiomas
Cigoli, M. S., De Benedetti, S., Marocchi, A., Bacigaluppi, S., Primignani, P., Gesu, G., Citterio, A., Tassi, L., Mecarelli, O., Pulitano, P., Penco, S.
Published in Journal of molecular neuroscience (01.07.2015)
Published in Journal of molecular neuroscience (01.07.2015)
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Cerebral cavernous malformations associated to meningioma: High penetrance in a novel family mutated in the PDCD10 gene
Garaci, Francesco, Marsili, Luisa, Riant, Florence, Marziali, Simone, Cécillon, Michaelle, Pasquarelli, Roberto, Sangiuolo, Federica, Floris, Roberto, Novelli, Giuseppe, Tournier-Lasserve, Elisabeth, Brancati, Francesco
Published in The neuroradiology journal (01.06.2015)
Published in The neuroradiology journal (01.06.2015)
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Single nucleotide polymorphisms of matrix metallopeptidase 3 and risk of gliomas in a Chinese Han population
Fan, Weiwei, Zhou, Keke, Hu, Dezhi, Song, Xiao, Zhao, Yingjie, Chen, Hongyan, Wei, Qingyi, Chen, Gong, Shi, Jinlong, Du, Guhong, Mao, Ying, Lu, Daru, Zhou, Liangfu
Published in Molecular carcinogenesis (01.10.2012)
Published in Molecular carcinogenesis (01.10.2012)
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De Novo MGC4607 Gene Heterozygous Missense Variants in a Child with Multiple Cerebral Cavernous Malformations
Mosca, Lorena, Pileggi, Silvana, Avemaria, Francesca, Tarlarini, Claudia, Cigoli, Maria Sole, Capra, Valeria, De Marco, Patrizia, Pavanello, Marco, Marocchi, Alessandro, Penco, Silvana
Published in Journal of molecular neuroscience (01.07.2012)
Published in Journal of molecular neuroscience (01.07.2012)
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Clinical and molecular features of familial and sporadic cases of von Hippel-Lindau disease from Mexico
Chacon-Camacho, Oscar F, Rodriguez-Dennen, Fernando, Camacho-Molina, Alejandra, Rasmussen, Astrid, Alonso-Vilatela, Elisa, Zenteno, Juan C
Published in Clinical & experimental ophthalmology (01.04.2010)
Published in Clinical & experimental ophthalmology (01.04.2010)
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Angiotensin-converting enzyme insertion/deletion gene polymorphism in patients with familial multiple cerebral cavernous malformations
Altas, M., Bayrak, O.F., Cerci, A., Isık, N., Celik, M., Culha, M., Sahin, F., Elmacı, I.
Published in Journal of clinical neuroscience (01.08.2010)
Published in Journal of clinical neuroscience (01.08.2010)
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The G1359A-CNR1 gene polymorphism is associated to glioma in Spanish patients
Núñez, Mercedes, Perdomo, Sandra, Moreta, Juan, Santos-Briz, Ángel, González-Sarmiento, Rogelio
Published in Clinical & translational oncology (01.12.2010)
Published in Clinical & translational oncology (01.12.2010)
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A chromosomal region 7p11.2 transcript map: Its development and application to the study of EGFR amplicons in glioblastoma
Eley, Greg D., Reiter, Jill L., Pandita, Ajay, Park, Soyeon, Jenkins, Robert B., Maihle, Nita J., James, C. David
Published in Neuro-oncology (Charlottesville, Va.) (01.04.2002)
Published in Neuro-oncology (Charlottesville, Va.) (01.04.2002)
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