Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 78 Records) |
Query Trace: Pheochromocytoma and RET[original query] |
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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 |
[Hereditary pheochromocytoma-associated syndromes. Part 2]. Terapevticheskii arkhiv 2017 6 87 (10): 115-119. Yukina M Yu, Troshina E A, Beltsevich D |
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 |
Update on Multiple Endocrine Neoplasia Type 2: Focus on Medullary Thyroid Carcinoma. Journal of the Endocrine Society 2018 8 2 (8): 933-943. Raue Friedhelm, Frank-Raue Kar |
A Novel RET D898Y Germline Mutation in a Patient with Pheochromocytoma. Case reports in endocrinology 2018 6 2018 8657914. Yi Jin Wook, Kang Hye In, Kim Su-Jin, Seong Chan Yong, Chai Young Jun, Choi June Young, Seong Moon-Woo, Lee Kyu Eun, Park Sung S |
Comparison of Pheochromocytoma-Specific Morbidity and Mortality Among Adults With Bilateral Pheochromocytomas Undergoing Total Adrenalectomy vs Cortical-Sparing Adrenalectomy. JAMA network open 2019 8 2 (8): e198898. Neumann Hartmut P H, Tsoy Uliana, Bancos Irina, Amodru Vincent, Walz Martin K, Tirosh Amit, Kaur Ravinder Jeet, McKenzie Travis, Qi Xiaoping, Bandgar Tushar, Petrov Roman, Yukina Marina Y, Roslyakova Anna, van der Horst-Schrivers Anouk N A, Berends Annika M A, Hoff Ana O, Castroneves Luciana Audi, Ferrara Alfonso Massimiliano, Rizzati Silvia, Mian Caterina, Dvorakova Sarka, Hasse-Lazar Kornelia, Kvachenyuk Andrey, Peczkowska Mariola, Loli Paola, Erenler Feyza, Krauss Tobias, Almeida Madson Q, Liu Longfei, Zhu Feizhou, Recasens Mònica, Wohllk Nelson, Corssmit Eleonora P M, Shafigullina Zulfiya, Calissendorff Jan, Grozinsky-Glasberg Simona, Kunavisarut Tada, Schalin-Jäntti Camilla, Castinetti Frederic, Vlcek Petr, Beltsevich Dmitry, Egorov Viacheslav I, Schiavi Francesca, Links Thera P, Lechan Ronald M, Bausch Birke, Young William F, Eng Charis, |
Clinical utility of genetic diagnosis for sporadic and hereditary medullary thyroid carcinoma. Annales d'endocrinologie 2019 5 80 (3): 187-190. Elisei Rossella, Bottici Valeria, Cappagli Virginia, Ramone Teresa, Tacito Alessia, Ciampi Raffaele, Romei Cristi |
Loss of BAP1 in Pheochromocytomas and Paragangliomas Seems Unrelated to Genetic Mutations. Endocrine pathology 2019 11 30 (4): 276-284. Maffeis Valeria, Cappellesso Rocco, Nicolè Lorenzo, Guzzardo Vincenza, Menin Chiara, Elefanti Lisa, Schiavi Francesca, Guido Maria, Fassina Ambrog |
Mutational profile and genotype/phenotype correlation of non-familial pheochromocytoma and paraganglioma. Oncotarget 2019 11 10 (57): 5919-5931. Albattal Shatha, Alswailem Meshael, Moria Yosra, Al-Hindi Hindi, Dasouki Majed, Abouelhoda Mohamed, Alkhail Hala Aba, Alsuhaibani Entissar, Alzahrani Ali |
Role of [68Ga]DOTANOC PET/computed tomography and [131I]MIBG scintigraphy in the management of patients with pheochromocytoma and paraganglioma: a prospective study. Nuclear medicine communications 2020 8 41 (10): 1047-1059. Singh Deepa, Shukla Jaya, Walia Rama, Vatsa Rakhee, Paul Nandini, Chhabra Anupriya, Nahar Uma, Singh Harmandeep, Kumar Rajender, Bhansali Anil, Rai Mittal Bhagwa |
Pheochromocytoma and Paraganglioma in Children and Adolescents: Experience of the French Society of Pediatric Oncology (SFCE). Journal of the Endocrine Society 2020 5 4 (5): bvaa039. de Tersant Marie, Généré Lucile, Freyçon Claire, Villebasse Sophie, Abbas Rachid, Barlier Anne, Bodet Damien, Corradini Nadège, Defachelles Anne-Sophie, Entz-Werle Natacha, Fouquet Cyrielle, Galmiche Louise, Gandemer Virginie, Lacour Brigitte, Mansuy Ludovic, Orbach Daniel, Pluchart Claire, Réguerre Yves, Rigaud Charlotte, Sarnacki Sabine, Sirvent Nicolas, Stephan Jean-Louis, Thebaud Estelle, Gimenez-Roqueplo Anne-Paule, Brugières Lauren |
Clinical and genetic features of pediatric PCCs/PGLs patients: a single-center experience in China. Translational andrology and urology 2020 5 9 (2): 267-275. Li Minghao, Wang Cikui, Liu Peihua, Qi Lin, Chen Xiang, Fan Benyi, Zhang Xiangyang, Zhang Bo, Xiao Qiao, Yu Anze, Liu Longf |
Genetic and Clinical Profiles of Pheochromocytoma and Paraganglioma: A Single Center Study. Frontiers in endocrinology 2020 12 11 574662. Ma Xiaosen, Li Ming, Tong Anli, Wang Fen, Cui Yunying, Zhang Xuebin, Zhang Yushi, Chen Shi, Li Yux |
Efficacy of Immunohistochemistry for SDHB in the Screening of Hereditary Pheochromocytoma-Paraganglioma. Biology 2021 8 10 (7): . Choi Hye-Ryeon, Koo Ja-Seung, Lee Cho-Rok, Lee Jan-Dee, Kang Sang-Wook, Jo Young-Seok, Chung Woong-Yo |
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 |
Germline Pathogenic Variants Identified by Targeted Next-Generation Sequencing of Susceptibility Genes in Pheochromocytoma and Paraganglioma. Journal of kidney cancer and VHL 2021 8 (1): 19-24. Yalcintepe Sinem, Gurkan Hakan, Korkmaz Fatma Nur, Demir Selma, Atli Engin, Eker Damla, Guler Hazal Sezginer, Zhuri Drenusha, Atli Emine Ikbal, Salt Semra Ayturk, Sahin Mustafa, Guldiken Sib |
Genetic and clinical aspects of paediatric pheochromocytomas and paragangliomas. Clinical endocrinology 2021 Mar . Petenuci Janaina, Guimaraes Augusto G, Fagundes Gustavo F C, Benedetti Anna Flavia F, Afonso Ana Caroline F, Pereira Maria Adelaide A, Zerbini Maria Claudia N, Siqueira Sheila, Yamauchi Fernando, Soares Silvia C, Srougi Victor, Tanno Fabio Y, Chambo Jose L, Lopes Roberto I, Denes Francisco T, Hoff Ana O, Latronico Ana Claudia, Mendonca Berenice B, Fragoso Maria Candida B V, Almeida Madson |
Case Report: A Case of Moyamoya Syndrome Associated With Multiple Endocrine Neoplasia Type 2A. Frontiers in endocrinology 2021 12 12 703410. Matano Fumihiro, Murai Yasuo, Watanabe Atsushi, Shirokane Kazutaka, Igarashi Takehito, Shimizu Kazuo, Shimada Takashi, Morita Ak |
Germline RET Leu56Met Variant Is Likely Not Causative of Multiple Endocrine Neoplasia Type 2. Frontiers in endocrinology 2021 12 12 764512. Hansen Anna Reimer, Borgwardt Line, Rasmussen Åse Krogh, Godballe Christian, Poulsen Morten Møller, Vieira Filipe G, Mathiesen Jes Sloth, Rossing Mar |
Clinical features and signaling effects of RET D631Y variant multiple endocrine neoplasia type 2 (MEN2). The Korean journal of internal medicine 2021 12 37 (2): 398-410. Lee Ji-Young, Kim Su Yeon, Jo Kwan Hoon, Mo Eun Yeong, Kim Eun Sook, Kim Hye Soo, Han Je Ho, Moon Sung-D |
Hereditary medullary thyroid carcinoma syndromes: experience from western India. Familial cancer 2021 1 20 (3): 241-251. Diwaker Chakra, Sarathi Vijaya, Jaiswal Sanjeet Kumar, Shah Ravikumar, Deshmukh Anuja, Thomas Anand Ebin, Prakash Gagan, Malhotra Gaurav, Patil Virendra, Lila Anurag, Shah Nalini, Bandgar Tush |
Medullary thyroid cancer with RET V804M mutation: more indolent than expected? Surgery 2022 9 173 (1): 260-267. Frisco Nicholas A, Gunn Alexander H, Thomas Samantha M, Stang Michael T, Scheri Randall P, Kazaure Hadiza |
Novel Germline PHD2 Variant in a Metastatic Pheochromocytoma and Chronic Myeloid Leukemia, but in the Absence of Polycythemia. Medicina (Kaunas, Lithuania) 2022 Aug 58 (8): . Provenzano Aldesia, Chetta Massimiliano, De Filpo Giuseppina, Cantini Giulia, La Barbera Andrea, Nesi Gabriella, Santi Raffaella, Martinelli Serena, Rapizzi Elena, Luconi Michaela, Maggi Mario, Mannelli Massimo, Ercolino Tonino, Canu Letiz |
A Case of I-Metaiodobenzylguanidine Scintigraphy-Negative Pheochromocytoma with a Tumor-Developing Mutation in the RET Gene. Journal of clinical medicine 2022 8 11 (15): . Kubo Haremaru, Tsurutani Yuya, Sunouchi Takashi, Hoshino Yoshitomo, Hirose Rei, Katsuragawa Sho, Kimura Noriko, Saito Jun, Nishikawa Tets |
Genetic Characteristics of Incidental Pheochromocytoma and Paraganglioma. The Journal of clinical endocrinology and metabolism 2022 Feb . Zhang Jing, Li Minghao, Pang Yingxian, Wang Cikui, Wu Jingjing, Cheng Ziyun, Li Xiaomu, Lu Zhiqiang, Liu Yujun, Guo Jianming, Chen Xiang, He Yao, Guan Xiao, Xu Xiaowen, Wang Yong, Liu Jiahao, Guo Wei, Hou Yingyong, Liu Longfei, Jiang Jingjing, Gao X |
[MEN for multiple endocrin neoplasms: When evokate MEN? Update 2022]. La Revue de medecine interne 2022 10 44 (1): 12-18. Duval M, Haissaguerre |
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 |
Germline founder variant c.1998delinsTTCT in the RET oncogene: a cohort study in 15 Belgian families. European journal of endocrinology 2023 9 189 (3): 402-408. Axelle Vuylsteke, Laurens Hannes, Hilde Brems, Koen Devis, Marleen Renard, Anne Uyttebroeck, Eric Legius, Brigitte Decallon |
Domain landscapes of somatic NF1 mutations in pheochromocytoma and paraganglioma. Gene 2023 4 147432. Tabebi Mouna, Frikha Fakher, Volpe Massimiliano, Gimm Oliver, Söderkvist Pet |
Clinical characteristics of a large familial cohort with Medullary thyroid cancer and germline Cys618Arg RET mutation in an Israeli multicenter study. Frontiers in endocrinology 2023 11 14 1268193. Rachel Chava Rosenblum, Dania Hirsch, Simona Grozinsky-Glasberg, Carlos Benbassat, Uri Yoel, Avraham Ishay, Sagit Zolotov, Gideon Bachar, Ehud Banne, Sigal Levy, Orit Twi |
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- Page last updated:Apr 16, 2024
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