Human Genome Epidemiology Literature Finder
Records 1 - 9 (of 9 Records) |
Query Trace: Neurofibromatosis 1 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 |
Head and neck paragangliomas in von Hippel-Lindau disease and multiple endocrine neoplasia type 2. The Journal of clinical endocrinology and metabolism 2009 Jun 94 (6): 1938-44. Boedeker Carsten C, Erlic Zoran, Richard Stéphane, Kontny Udo, Gimenez-Roqueplo Anne-Paule, Cascon Alberto, Robledo Mercedes, de Campos José M, van Nederveen Francien H, de Krijger Ronald R, Burnichon Nelly, Gaal José, Walter Martin A, Reschke Kirsten, Wiech Thorsten, Weber Johannes, Rückauer Klaus, Plouin Pierre Francois, Darrouzet Vincent, Giraud Sophie, Eng Charis, Neumann Hartmut P |
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 |
Germinal mutations of RET, SDHB, SDHD, and VHL genes in patients with apparently sporadic pheochromocytomas and paragangliomas. Endokrynologia Polska 0 61 (1): 43-8. Krawczyk Aleksandra, Hasse-Lazar Kornelia, Pawlaczek Agnieszka, Szpak-Ulczok Sylwia, Krajewska Jolanta, Paliczka-Cie?lak Ewa, Jurecka-Lubieniecka Beata, Roskosz Józef, Chmielik Ewa, Ziaja Jacek, Cierpka Lech, Peczkowska Mariola, Preibisz Aleksander, Januszewicz Andrzej, Otto Maciej, Jarzab Barba |
Genetic status determines F-FDG uptake in pheochromocytoma/paraganglioma. Journal of medical imaging and radiation oncology 2017 Dec 61 (6): 745-752. Tiwari Ankita, Shah Nalini, Sarathi Vijaya, Malhotra Gaurav, Bakshi Ganesh, Prakash Gagan, Khadilkar Kranti, Pandit Reshma, Lila Anurag, Bandgar Tush |
Genotype-phenotype correlation in paediatric pheochromocytoma and paraganglioma: a single centre experience from India. Journal of pediatric endocrinology & metabolism : JPEM 2017 Apr . Khadilkar Kranti, Sarathi Vijaya, Kasaliwal Rajeev, Pandit Reshma, Goroshi Manjunath, Shivane Vyankatesh, Lila Anurag, Bandgar Tushar, Shah Nalini |
Pheochromocytoma recurrence in hereditary disease: does a cortical-sparing technique increase recurrence rate? Surgery 2022 10 173 (1): 26-34. Shirali Aditya S, Clemente-Gutierrez Uriel, Huang Bernice L, Lui Michael S, Chiang Yi-Ju, Jimenez Camilo, Fisher Sarah B, Graham Paul H, Lee Jeffrey E, Grubbs Elizabeth G, Perrier Nancy |
NF1 Gene Inactivation Acts as Tumor Driver in RET/RAS Negative Medullary Thyroid Carcinomas. European journal of endocrinology 2023 5 . Raffaele Ciampi, Teresa Ramone, Cristina Romei, Roberta Casalini, Antonio Matrone, Alessandro Prete, Carla Gambale, Simone Paolo Minardi, Giovanni Caparezza, Marco Alessandro Pierotti, Liborio Torregrossa, Clara Ugolini, Gabriele Materazzi, Rossella Elis |
Not Only RET but NF1 and Chromosomal Instability Are Seen in Young Patients with Sporadic Medullary Thyroid Carcinoma. Journal of the Endocrine Society 2024 4 8 (6): bvae059. Luciana Audi Castroneves, Flavia Regina Rotea Mangone, Antonio Marcondes Lerario, Ana Maria da Cunha Mercante, Rafael Loch Batista, Luciana Rodrigues Carvalho Barros, Carla Vaz Ferreira, Evelin Cavalcante Farias, Felipe Augusto Brasileiro Vanderlei, Ana Luiza Maia, Maria Aparecida Nagai, Alexander Augusto Lima Jorge, Ana Oliveira Ho |
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- Page last updated:May 06, 2024
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