Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: Neuroendocrine Tumors and RET[original query] |
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Genetic analyses of apparently sporadic pheochromocytomas: the Rotterdam experience. Annals of the New York Academy of Sciences 2006 Aug 1073 (): 138-48. Korpershoek E, Van Nederveen F H, Dannenberg H, Petri B J, Komminoth P, Perren A, Lenders J W, Verhofstad A A, De Herder W W, De Krijger R R, Dinjens W N |
Denaturing high performance liquid chromatography detection of SDHB, SDHD, and VHL germline mutations in pheochromocytoma. The Journal of surgical research 2009 Nov 157 (1): 55-62. Meyer-Rochow Goswin Y, Smith Janine M, Richardson Anne-Louise, Marsh Deborah J, Sidhu Stan B, Robinson Bruce G, Benn Diana |
Inherited mutations in pheochromocytoma and paraganglioma: why all patients should be offered genetic testing. Annals of surgical oncology 2013 May 20 (5): 1444-50. Fishbein Lauren, Merrill Shana, Fraker Douglas L, Cohen Debbie L, Nathanson Katherine |
Activating FGFR1 Mutations in Sporadic Pheochromocytomas. World journal of surgery 2017 11 42 (2): 482-489. Welander Jenny, ?ysiak Ma?gorzata, Brauckhoff Michael, Brunaud Laurent, Söderkvist Peter, Gimm Oliv |
RET fusions in solid tumors. Cancer treatment reviews 2019 11 81 101911. Li Andrew Y, McCusker Michael G, Russo Alessandro, Scilla Katherine A, Gittens Allison, Arensmeyer Katherine, Mehra Ranee, Adamo Vincenzo, Rolfo Christi |
Pseudohypoxic pheochromocytomas and paragangliomas dominate in children. Pediatric blood & cancer 2021 3 68 (7): e28981. Redlich Antje, Pamporaki Christina, Lessel Lienhard, Frühwald Michael C, Vorwerk Peter, Kuhlen Michae |
Mutation Frequency in Main Susceptibility Genes Among Patients With Head and Neck Paragangliomas. Frontiers in genetics 2020 11 614908. Snezhkina Anastasiya V, Fedorova Maria S, Pavlov Vladislav S, Kalinin Dmitry V, Golovyuk Alexander L, Pudova Elena A, Guvatova Zulfiya G, Melnikova Nataliya V, Dmitriev Alexey A, Razmakhaev George S, Poloznikov Andrey A, Alekseeva Galina S, Kaprin Andrey D, Krasnov George S, Kudryavtseva Anna |
Sclerosing Paragangliomas: Correlations of Histological Features with Patients' Genotype and Vesicular Monoamine Transporter Expression. Head and neck pathology 2022 May . Pucci Angela, Bacca Alessandra, Barravecchia Ivana, Di Stefano Iosè, Belgio Beatrice, Lorenzini Daniele, Torregrossa Liborio, Chiacchio Serena, Congregati Caterina, Materazzi Gabriele, Ferrari Mauro, Angeloni Debora, Bernini Giampaolo, Basolo Fulv |
TNM Staging and Overall Survival in Patients with Pheochromocytoma and Sympathetic Paraganglioma. The Journal of clinical endocrinology and metabolism 2022 11 . Jimenez Camilo, Ma Junsheng, Roman Gonzalez Alejandro, Varghese Jeena, Zhang Miao, Perrier Nancy, Habra Mouhammed Amir, Graham Paul, Waguespack Steven |
[MEN for multiple endocrin neoplasms: When evokate MEN? Update 2022]. La Revue de medecine interne 2022 10 44 (1): 12-18. Duval M, Haissaguerre |
Domain landscapes of somatic NF1 mutations in pheochromocytoma and paraganglioma. Gene 2023 4 147432. Tabebi Mouna, Frikha Fakher, Volpe Massimiliano, Gimm Oliver, Söderkvist Pet |
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- Page last updated:Apr 29, 2024
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