HuGE Literature Finder
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| The utility of SDHB and FH immunohistochemistry in patients evaluated for hereditary paraganglioma-pheochromocytoma syndromes. Human pathology 2018 01 71 47-54. Udager Aaron M, Magers Martin J, Goerke Dayna M, Vinco Michelle L, Siddiqui Javed, Cao Xuhong, Lucas David R, Myers Jeffrey L, Chinnaiyan Arul M, McHugh Jonathan B, Giordano Thomas J, Else Tobias, Mehra Roh |
| The phenotype of SDHB germline mutation carriers: a nationwide study. European journal of endocrinology 2017 May . Niemeijer Nicolasine D, Rijken Johannes A, Eijkelenkamp Karin, van der Horst-Schrivers A N A, Kerstens Michiel N, Tops Carli M, van Berkel Anouk, Timmers Henri J, Kunst Henricus P M, Leemans C Rene, Bisschop Peter H, Dreijerink Koen Ma, van Dooren Marieke, Bayley Jean-Pierre, Pereira Alberto M, Jansen Jeroen, Hes Frederik J, Hensen Erik, Corssmit E |
| Calculating the optimal surveillance for head and neck paraganglioma in SDHB-mutation carriers. Familial cancer 2016 Aug . Eijkelenkamp Karin, Osinga Thamara E, de Jong Mirjam M, Sluiter Wim J, Dullaart Robin P F, Links Thera P, Kerstens Michiel N, van der Horst-Schrivers Anouk N |
| A registry-based study of thyroid paraganglioma: histological and genetic characteristics. Endocrine-related cancer 2015 Apr 22 (2): 191-204. von Dobschuetz Ernst, Leijon Helena, Schalin-Jäntti Camilla, Schiavi Francesca, Brauckhoff Michael, Peczkowska Mariola, Spiazzi Giovanna, Demattè Serena, Cecchini Maria Enrica, Sartorato Paola, Krajewska Jolanta, Hasse-Lazar Kornelia, Roszkowska-Purska Katarzyna, Taschin Elisa, Malinoc Angelica, Akslen Lars A, Arola Johanna, Lange Dariusz, Fassina Ambrogio, Pennelli Gianmaria, Barbareschi Mattia, Luettges Jutta, Prejbisz Aleksander, Januszewicz Andrzej, Strate Tim, Bausch Birke, Castinetti Frederic, Jarzab Barbara, Opocher Giuseppe, Eng Charis, Neumann Hartmut P |
| Germline and somatic SDHx alterations in apparently sporadic differentiated thyroid cancer. Endocrine-related cancer 2015 Apr 22 (2): 121-30. Ni Ying, Seballos Spencer, Ganapathi Shireen, Gurin Danielle, Fletcher Benjamin, Ngeow Joanne, Nagy Rebecca, Kloos Richard T, Ringel Matthew D, LaFramboise Thomas, Eng Char |
| Mutation analysis of HIF prolyl hydroxylases (PHD/EGLN) in individuals with features of phaeochromocytoma and renal cell carcinoma susceptibility. Endocrine-related cancer 2011 Feb 18 (1): 73-83. Astuti Dewi, Ricketts Christopher J, Chowdhury Rasheduzzaman, McDonough Michael A, Gentle Dean, Kirby Gail, Schlisio Susanne, Kenchappa Rajappa S, Carter Bruce D, Kaelin William G, Ratcliffe Peter J, Schofield Christopher J, Latif Farida, Maher Eamonn |
| Germline SDHB mutations and familial renal cell carcinoma. Journal of the National Cancer Institute 2008 Sep 100 (17): 1260-2. Ricketts Christopher, Woodward Emma R, Killick Pip, Morris Mark R, Astuti Dewi, Latif Farida, Maher Eamonn |
| No mutations but an increased frequency of SDHx polymorphisms in patients with sporadic and familial medullary thyroid carcinoma. Endocrine-related cancer 2005 Dec 12 (4): 1011-6. Montani M, Schmitt A M, Schmid S, Locher T, Saremaslani P, Heitz P U, Komminoth P, Perren |
| Early-onset renal cell carcinoma as a novel extraparaganglial component of SDHB-associated heritable paraganglioma. American journal of human genetics 2004 Jan 74 (1): 153-9. Vanharanta Sakari, Buchta Mary, McWhinney Sarah R, Virta Sanna K, Peçzkowska Mariola, Morrison Carl D, Lehtonen Rainer, Januszewicz Andrzej, Järvinen Heikki, Juhola Matti, Mecklin Jukka-Pekka, Pukkala Eero, Herva Riitta, Kiuru Maija, Nupponen Nina N, Aaltonen Lauri A, Neumann Hartmut P H, Eng Char |
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- Page last updated:Jun 27, 2022
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