Human Genome Epidemiology Literature Finder
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Records 1 - 17 (of 17 Records) |
| Query Trace: Neoplasms and SDHD[original query] |
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| Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations. JAMA 2004 Aug 292 (8): 943-51. Neumann Hartmut P H, Pawlu Christian, Peczkowska Mariola, Bausch Birke, McWhinney Sarah R, Muresan Mihaela, Buchta Mary, Franke Gerlind, Klisch Joachim, Bley Thorsten A, Hoegerle Stefan, Boedeker Carsten C, Opocher Giuseppe, Schipper Jörg, Januszewicz Andrzej, Eng Charis, |
| Succinate dehydrogenase D variants do not constitute a risk factor for developing C cell hyperplasia or sporadic medullary thyroid carcinoma. The Journal of clinical endocrinology and metabolism 2005 Apr 90 (4): 2127-30. Cascon Alberto, Cebrian Arancha, Pollan Marina, Ruiz-Llorente Sergio, Montero-Conde Cristina, Leton Rocio, Gutierrez Ruth, Lesueur Fabienne, Milne Roger L, Gonzalez-Albarran Olga, Lucas-Morante Tomas, Benitez Javier, Ponder Bruce A J, Robledo Merced |
| 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 |
| Germline mutations and variants in the succinate dehydrogenase genes in Cowden and Cowden-like syndromes. American journal of human genetics 2008 Aug 83 (2): 261-8. Ni Ying, Zbuk Kevin M, Sadler Tammy, Patocs Attila, Lobo Glenn, Edelman Emily, Platzer Petra, Orloff Mohammed S, Waite Kristin A, Eng Char |
| An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective analysis. The Lancet. Oncology 2009 Aug 10 (8): 764-71. van Nederveen Francien H, Gaal José, Favier Judith, Korpershoek Esther, Oldenburg Rogier A, de Bruyn Elly M C A, Sleddens Hein F B M, Derkx Pieter, Rivière Julie, Dannenberg Hilde, Petri Bart-Jeroen, Komminoth Paul, Pacak Karel, Hop Wim C J, Pollard Patrick J, Mannelli Massimo, Bayley Jean-Pierre, Perren Aurel, Niemann Stephan, Verhofstad Albert A, de Bruïne Adriaan P, Maher Eamonn R, Tissier Frédérique, Méatchi Tchao, Badoual Cécile, Bertherat Jérôme, Amar Laurence, Alataki Despoina, Van Marck Eric, Ferrau Francesco, François Jerney, de Herder Wouter W, Peeters Mark-Paul F M Vrancken, van Linge Anne, Lenders Jacques W M, Gimenez-Roqueplo Anne-Paule, de Krijger Ronald R, Dinjens Winand N |
| SDHAF2 mutations in familial and sporadic paraganglioma and phaeochromocytoma. The Lancet. Oncology 2010 Apr 11 (4): 366-72. Bayley Jean-Pierre, Kunst Henricus P M, Cascon Alberto, Sampietro Maria Lourdes, Gaal José, Korpershoek Esther, Hinojar-Gutierrez Adolfo, Timmers Henri J L M, Hoefsloot Lies H, Hermsen Mario A, Suárez Carlos, Hussain A Karim, Vriends Annette H J T, Hes Frederik J, Jansen Jeroen C, Tops Carli M, Corssmit Eleonora P, de Knijff Peter, Lenders Jacques W M, Cremers Cor W R J, Devilee Peter, Dinjens Winand N M, de Krijger Ronald R, Robledo Merced |
| Prevalence of germline mutations in patients with pheochromocytoma or abdominal paraganglioma and sporadic presentation: a population-based study in Western Sweden. World journal of surgery 2012 Jun 36 (6): 1389-94. Muth Andreas, Abel Frida, Jansson Svante, Nilsson Ola, Ahlman Håkan, Wängberg |
| Testing new susceptibility genes in the cohort of apparently sporadic phaeochromocytoma/paraganglioma patients with clinical characteristics of hereditary syndromes. Clinical endocrinology 2013 Dec 79 (6): 817-23. P?czkowska Mariola, Kowalska Aldona, Sygut Jacek, Waligórski Dariusz, Malinoc Angelica, Janaszek-Sitkowska Hanna, Prejbisz Aleksander, Januszewicz Andrzej, Neumann Hartmut P |
| Genetic testing in head and neck paraganglioma: who, what, and why? Journal of neurological surgery. Part B, Skull base 2013 Aug 74 (4): 236-40. Sridhara Shankar K, Yener Murat, Hanna Ehab Y, Rich Thereasa, Jimenez Camilo, Kupferman Michael |
| Polymorphisms in Genes of Tricarboxylic Acid Cycle Key Enzymes Are Associated with Early Recurrence of Hepatocellular Carcinoma. PloS one 2015 10 (4): e0124471. Wan Shaogui, Wu Yousheng, Zhou Xingchun, Chen Yibing, An Jiaze, Yu Xiaohe, Zhang Huiqing, Yang Hushan, Xing Jinlia |
| Profiling of somatic mutations in phaeochromocytoma and paraganglioma by targeted next generation sequencing analysis. International journal of endocrinology 2015 2015 138573. Luchetti Andrea, Walsh Diana, Rodger Fay, Clark Graeme, Martin Tom, Irving Richard, Sanna Mario, Yao Masahiro, Robledo Mercedes, Neumann Hartmut P H, Woodward Emma R, Latif Farida, Abbs Stephen, Martin Howard, Maher Eamonn |
| Familiar Papillary Thyroid Carcinoma in a Large Brazilian Family Is Not Associated with Succinate Dehydrogenase Defects. European thyroid journal 2016 Jul 5 (2): 94-9. Accordi Elen Dias, Xekouki Paraskevi, Azevedo Bruna, de Alexandre Rodrigo Bertollo, Frasson Carla, Gantzel Siliane Marie, Papadakis Georgios Z, Angelousi Anna, Stratakis Constantine A, Sotomaior Vanessa Santos, Faucz Fabio |
| 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 |
| Clinical relevance of screening checklists for detecting cancer predisposition syndromes in Asian childhood tumours. NPJ genomic medicine 2018 11 3 30. Chan Sock Hoai, Chew Winston, Ishak Nur Diana Binte, Lim Weng Khong, Li Shao-Tzu, Tan Sheng Hui, Teo Jing Xian, Shaw Tarryn, Chang Kenneth, Chen Yong, Iyer Prasad, Tan Enrica Ee Kar, Seng Michaela Su-Fern, Chan Mei Yoke, Tan Ah Moy, Low Sharon Yin Yee, Soh Shui Yen, Loh Amos Hong Pheng, Ngeow Joan |
| 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 |
| A long noncoding RNA-microRNA expression signature predicts metastatic signature in pheochromocytomas and paragangliomas. Endocrine 2021 9 75 (1): 244-253. Ghosal Suman, Zhu Boqun, Huynh Thanh-Truc, Meuter Leah, Jha Abhishek, Talvacchio Sara, Knue Marianne, Patel Mayank, Prodanov Tamara, Das Shaoli, Zeiger Martha A, Nilubol Naris, Shankavaram Uma T, Taieb David, Pacak Kar |
| 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 |
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