Human Genome Epidemiology Literature Finder
Records 1 - 19 (of 19 Records) |
Query Trace: Neuroendocrine Tumors and VHL[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 |
Isocitrate dehydrogenase mutations are rare in pheochromocytomas and paragangliomas. The Journal of clinical endocrinology and metabolism 2010 Mar 95 (3): 1274-8. Gaal José, Burnichon Nelly, Korpershoek Esther, Roncelin Isabelle, Bertherat Jérôme, Plouin Pierre-François, de Krijger Ronald R, Gimenez-Roqueplo Anne-Paule, Dinjens Winand N |
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 |
Association of urinary bladder paragangliomas with germline mutations in the SDHB and VHL genes. Urologic oncology 2015 Apr 33 (4): 167.e13-20. Martucci Victoria L, Lorenzo Zarina G, Weintraub Michael, del Rivero Jaydira, Ling Alexander, Merino Maria, Siddiqui Minhaj, Shuch Brian, Vourganti Srinivas, Linehan W Marston, Agarwal Piyush K, Pacak Kar |
Identification of the BRAF V600E mutation in gastroenteropancreatic neuroendocrine tumors. Oncotarget 2015 Dec . Park Charny, Ha Sang Yun, Kim Seung Tae, Kim Hee Cheol, Heo Jin Seok, Park Young Suk, Lauwers Gregory, Lee Jeeyun, Kim Kyoung-M |
Genes involved in angiogenesis and mTOR pathways are frequently mutated in Asian patients with pancreatic neuroendocrine tumors. International journal of biological sciences 2016 12 (12): 1523-1532. Chou Wen-Chi, Lin Po-Han, Yeh Yi-Chen, Shyr Yi-Ming, Fang Wen-Liang, Wang Shin-E, Liu Chun-Yu, Chang Peter Mu-Hsin, Chen Ming-Han, Hung Yi-Ping, Li Chung-Pin, Chao Yee, Chen Ming-Hua |
Clinical management of pheochromocytoma and paraganglioma in Singapore: missed opportunities for genetic testing. Molecular genetics & genomic medicine 2017 9 5 (5): 602-607. Chew Winston Hong Wern, Courtney Eliza, Lim Kok Hing, Li Shao Tzu, Chen Yanni, Tan Min Han, Chung Alexander, Khoo Joan, Loh Amos, Soh Shui Yen, Iyer Prasad, Loh Lih Ming, Ngeow Joan |
In silico VHL Gene Mutation Analysis and Prognosis of Pancreatic Neuroendocrine Tumors in von Hippel-Lindau Disease. The Journal of clinical endocrinology and metabolism 2018 1 103 (4): 1631-1638. Tirosh Amit, El Lakis Mustapha, Green Patience, Nockel Pavel, Patel Dhaval, Nilubol Naris, Gara Sudheer Kumar, Keutgen Xavier M, Linehan W Marston, Kebebew Electr |
New Insights Into Pheochromocytoma Surveillance of Young Patients With VHL Missense Mutations. Journal of the Endocrine Society 2019 9 3 (9): 1682-1692. Fagundes Gustavo F C, Petenuci Janaina, Lourenco Delmar M, Trarbach Ericka B, Pereira Maria Adelaide A, Correa D'Eur Joya Emilie, Hoff Ana O, Lerario Antonio M, Zerbini Maria Claudia N, Siqueira Sheila, Yamauchi Fernando, Srougi Victor, Tanno Fabio Y, Chambo Jose Luis, Latronico Ana Claudia, Mendonca Berenice B, Fragoso Maria Candida B V, Almeida Madson |
The efficacy of everolimus and sunitinib in patients with sporadic or germline mutated metastatic pancreatic neuroendocrine tumors. Journal of gastrointestinal oncology 2019 8 10 (4): 645-651. Nuñez Jose Eduardo, Donadio Mauro, Filho Duilio Rocha, Rego Juliana Florinda, Barros Milton, Formiga Maria Nirvana, Lopez Rossana, Riechelmann Rach |
Targeted next-generation sequencing of well-differentiated rectal, gastric, and appendiceal neuroendocrine tumors to identify potential targets. Human pathology 2019 Mar . Park Ha Young, Kwon Mi Jung, Kang Ho Suk, Kim Yun Joong, Kim Nan Young, Kim Min Jeong, Min Kyueng-Whan, Choi Kyung Chan, Nam Eun Sook, Cho Seong Jin, Park Hye-Rim, Min Soo Kee, Seo Jinwon, Choe Ji-Young, Lee Hye Kyu |
Real-Time Genomic Characterization of Metastatic Pancreatic Neuroendocrine Tumors Has Prognostic Implications and Identifies Potential Germline Actionability. JCO precision oncology 2019 1 2018 . Raj Nitya, Shah Ronak, Stadler Zsofia, Mukherjee Semanti, Chou Joanne, Untch Brian, Li Janet, Kelly Virginia, Saltz Leonard B, Mandelker Diana, Ladanyi Marc, Berger Michael F, Klimstra David S, Reidy-Lagunes Diane, Osoba Muyin |
Clinical presentation, genotype-phenotype correlations, and outcome of pancreatic neuroendocrine tumors in Von Hippel-Lindau syndrome. Endocrine 2021 5 74 (1): 180-187. Penitenti F, Landoni L, Scardoni M, Piredda M L, Cingarlini S, Scarpa A, D'Onofrio M, Girelli D, Davi M |
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 |
Domain landscapes of somatic NF1 mutations in pheochromocytoma and paraganglioma. Gene 2023 4 147432. Tabebi Mouna, Frikha Fakher, Volpe Massimiliano, Gimm Oliver, Söderkvist Pet |
SDHB exon 1 deletion: A recurrent germline mutation in Colombian patients with pheochromocytomas and paragangliomas. Frontiers in genetics 2023 1 13 999329. Manotas María Carolina, Rivera Ana Lucía, Gómez Ana Milena, Abisambra Patricia, Guevara Gonzalo, Medina Vilma, Tapiero Sandra, Huertas Antonio, Riaño-Moreno Julián, Mejía Juan Carlos, Gonzalez-Clavijo Angélica María, Tapiero-García Mireya, Cuéllar-Cuéllar Andrés Arturo, Fierro-Maya Luis Felipe, Sanabria-Salas María Caroli |
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- Page last updated:Apr 29, 2024
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