HuGE Literature Finder
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| Multiple endocrine neoplasia 2 in Cyprus: evidence for a founder effect. Journal of endocrinological investigation 2018 Oct 41 (10): 1149-1157. Fanis P, Skordis N, Frangos S, Christopoulos G, Spanou-Aristidou E, Andreou E, Manoli P, Mavrommatis M, Nicolaou S, Kleanthous M, Cariolou M A, Christophidou-Anastasiadou V, Tanteles G A, Phylactou L A, Neocleous |
| Medullary Thyroid Carcinoma: Survival Analysis and Evaluation of Mutation-Specific Immunohistochemistry in Detection of Sporadic Disease. World journal of surgery 2018 Feb . Jayakody S, Reagh J, Bullock M, Aniss A, Clifton-Bligh R, Learoyd D, Robinson B, Delbridge L, Sidhu S, Gill A J, Sywak |
| Long-Term Survivorship in Multiple Endocrine Neoplasia Type 2B Diagnosed Before and in the New Millennium. The Journal of clinical endocrinology and metabolism 2017 Oct . Raue Friedhelm, Dralle Henning, Machens Andreas, Bruckner Thomas, Frank-Raue Kar |
| Search of the p.M918T Mutation in the RET Oncogene in Mexican Adult Patients with Medullary Thyroid Carcinoma. Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association 2017 Feb . Ruiz-Garcia Erika, Vidal-Millan Silvia, Lopez-Yañez Alicia, Torres José Antonio Posada, Guadarrama-Orozco Jorge Alberto, Lino-Silva Leonardo Saul, Meneses-Garcia Abelardo, Astudillo-de la Vega Horacio, Garcia Martin Granad |
| Medullary Thyroid Carcinoma in MEN2A: ATA Moderate- or High-Risk RET Mutations Do Not Predict Disease Aggressiveness. The Journal of clinical endocrinology and metabolism 2017 05 . Voss Rachel K, Feng Lei, Lee Jeffrey E, Perrier Nancy D, Graham Paul H, Hyde Samual M, Nieves-Munoz Frances, Cabanillas Maria E, Waguespack Steven G, Cote Gilbert J., Gagel Robert F, Grubbs Elizabeth |
| M918V RET mutation causes familial medullary thyroid carcinoma: study of 8 affected kindreds. Endocrine-related cancer 2016 Dec 23 (12): 909-920. Martins-Costa M Cecília, Cunha Lucas L, Lindsey Susan C, Camacho Cleber P, Dotto Renata P, Furuzawa Gilberto K, Sousa M Sharmila A, Kasamatsu Teresa S, Kunii Ilda S, Martins Márcio M, Machado Alberto L, Martins João R M, Dias-da-Silva Magnus R, Maciel Rui M |
| The RET E616Q Variant is a Gain of Function Mutation Present in a Family with Features of Multiple Endocrine Neoplasia 2A. Endocrine pathology 2016 Oct . Grey William, Hulse Rosaline, Yakovleva Anna, Genkova Dilyana, Whitelaw Benjamin, Solomon Ellen, Diaz-Cano Salvador J, Izatt Loui |
| Medullary Thyroid Carcinoma Associated with Germline RET Mutation. Thyroid : official journal of the American Thyroid Association 2016 Sep . Xu Jian Yu, Grubbs Elizabeth G, Waguespack Steven G, Jimenez Camilo, Gagel Robert F, Sosa Julie Ann, Vassilopoulou-Sellin Rena, Dadu Ramona, Hu Mimi I, Trotter Chardria S, Jackson Michelle, Rich Thereasa A, Hyde Samuel M, Sherman Steven I, Cote Gilbert |
| [Genotype-phenotype correlations in multiple endocrine neoplasia type 2]. Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery 2016 Jul 51 (7): 538-41. Zhang X W, Wang J Y, Zhang Y B, Wan H F, Zhang B, Yan D G, Liu W S, Xu Z G, Tang P |
| A Nationwide Study of Multiple Endocrine Neoplasia Type 2A in Norway: Predictive and Prognostic Factors for the Clinical Course of Medullary Thyroid Carcinoma. Thyroid : official journal of the American Thyroid Association 2016 Jul . Opsahl Else Marie, Schlichting Ellen, Helset Kristin, Svartberg Johan, Brauckhoff Katrin, Mæhle Lovise, Engebretsen Lars Fredrik, Sigstad Eva, Grøholt Krystyna, Akslen Lars Andreas, Jørgensen Lars Hilmar, Varhaug Jan Erik, Bjøro Tri |
| Clinical significance of RET mutation screening in a pedigree of multiple endocrine neoplasia type 2A. Molecular medicine reports 2016 Jun . Ying Rongbiao, Feng J |
| Presence of the RET Cys634Tyr mutation and Gly691Ser functional polymorphism in Iranian families with multiple endocrine neoplasia type 2A. Hormones (Athens, Greece) 2016 Jan . Aghdam Maryam Nasiri, Abbaszadegan Mohammad Reza, Tafazoli JAlireza, Aslzare Mohammad, Mosavi Zohr |
| Distribution of RET Mutations and Evaluation of Treatment Approaches in Hereditary Medullary Thyroid Carcinoma in Turkey. Journal of clinical research in pediatric endocrinology 2015 Dec . Aydo?an Berna ?mge, Yüksel Ba?dagül, Tuna Mazhar Müslüm, Akkurt Kocaeli Ay?en, Ertörer Melek Eda, Ayd?n Kadriye, Güldiken Sibel, ?im?ek Yasin, Cihan Karaca Züleyha, Y?lmaz Merve, Aktürk Müjde, Anaforo?lu ?nan, Kebapç? Nur, Duran Cevdet, Ta?l?p?nar Abdullah, Kulaks?zo?lu Mustafa, Berker Dilek, Gürsoy Alptekin, Da?delen Selçuk, Erdo?an Murat Fa |
| C-Cell Neoplasia in Asymptomatic Carriers of RET Mutation in Extracellular Cysteine-Rich and Intracellular Tyrosine Kinase Domain. Human pathology 2015 Aug 46 (8): 1121-8. Abi-Raad Rita, Virk Renu K, Dinauer Catherine A, Prasad A, Morotti Raffaella A, Breuer Christopher K, Sosa Julie A, Udelsman Robert, Rivkees Scott A, Prasad Manju |
| Screening of RET gene mutations in Chinese patients with medullary thyroid carcinoma and their relatives. Familial cancer 2015 Aug . Wang Junyi, Zhang Bin, Liu Wensheng, Zhang Yongxia, Di Xuebing, Yang Yanmei, Yan Dang |
| Skewed mutational spectrum of RET proto-oncogene Exon10 in Iranian patients with medullary thyroid carcinoma. Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine 2015 Jul 36 (7): 5225-31. Zarif Yeganeh Marjan, Sheikholeslami Sara, Dehbashi Behbahani Golnoush, Farashi Samaneh, Hedayati Meh |
| Genetic screening of patients with medullary thyroid cancer in a referral center in Greece during the past two decades. European journal of endocrinology / European Federation of Endocrine Societies 2015 Apr 172 (4): 501-9. Sarika H-L, Papathoma A, Garofalaki M, Saltiki K, Pappa T, Pazaitou-Panayiotou K, Anastasiou E, Alevizaki |
| In silico analysis of RET variants in medullary thyroid cancer: from the computer to the bedside. Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery 2015 Apr 152 (4): 650-4. Heineman Thomas E, Joshi Rohan, Cohen Marc A, Kuhel William I, Kutler David |
| Exome sequencing reveals mutant genes with low penetrance involved in MEN2A-associated tumorigenesis. Endocrine-related cancer 2015 Feb 22 (1): 23-33. Cai Jie, Li Lin, Ye Lei, Jiang Xiaohua, Shen Liyun, Gao Zhibo, Fang Weiyuan, Huang Fengjiao, Su Tingwei, Zhou Yulin, Wang Weiqing, Ning Gua |
| Role of RET genetic variants in MEN2-associated pheochromocytoma. European journal of endocrinology / European Federation of Endocrine Societies 2014 Jun 170 (6): 821-8. Siqueira Débora Rodrigues, Ceolin Lucieli, Ferreira Carla Vaz, Romitti Mírian, Maia Silvana Cavalcante, Maciel Léa Maria Zanini, Maia Ana Lui |
| High penetrance of pheochromocytoma in multiple endocrine neoplasia 2 caused by germ line RET codon 634 mutation in Japanese patients. European journal of endocrinology / European Federation of Endocrine Societies 2013 May 168 (5): 683-7. Imai Tsuneo, Uchino Shinya, Okamoto Takahiro, Suzuki Shinichi, Kosugi Shinji, Kikumori Toyone, Sakurai Akihiro, |
| RET proto-oncogene genetic screening of families with multiple endocrine neoplasia type 2 optimizes diagnostic and clinical management in China. Thyroid : official journal of the American Thyroid Association 2012 Dec 22 (12): 12. Qi XP, Chen XL, Ma JM, Du ZF, Fei J, Yang CP, Cheng J, Song QZ, Han JS, Jin HY, Chen ZG, Wang JQ, Yang YP, Ying RB, Liu WT, Zhao Y, Chen CY, Jiang HL, Ke HP, Zhang XN |
| Establishing high resolution melting analysis: method validation and evaluation for c-RET proto-oncogene mutation screening. Clinical chemistry and laboratory medicine : CCLM / FESCC 2012 Jan 50 (1): 51-60. Benej Martin, Bendlova Bela, Vaclavikova Eliska, Poturnajova Marti |
| Molecular analysis of the RET proto-oncogene key exons in patients with medullary thyroid carcinoma: a comprehensive study of the Iranian population. Thyroid : official journal of the American Thyroid Association 2011 Apr 21 (4): 373-82. Alvandi Ehsan, Akrami Seyed Mohammad, Chiani Mohsen, Hedayati Mehdi, Nayer Babak Noori, Tehrani Mohammad Reza Mohajeri, Nakhjavani Manouchehr, Pedram Mehrd |
| Risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germline RET mutations located in exon 10. Human mutation 2011 Jan 32 (1): 51-8. Frank-Raue Karin, Rybicki Lisa A, Erlic Zoran, Schweizer Heiko, Winter Aurelia, Milos Ioana, Toledo Sergio P A, Toledo Rodrigo A, Tavares Marcos R, Alevizaki Maria, Mian Caterina, Siggelkow Heide, Hüfner Michael, Wohllk Nelson, Opocher Giuseppe, Dvo?áková Sárka, Bendlova Bela, Czetwertynska Ma?gorzata, Skasko El?bieta, Barontini Marta, Sanso Gabriela, Vorländer Christian, Maia Ana Luiza, Patocs Attila, Links Thera P, de Groot Jan Willem, Kerstens Michiel N, Valk Gerlof D, Miehle Konstanze, Musholt Thomas J, Biarnes Josefina, Damjanovic Svetozar, Muresan Mihaela, Wüster Christian, Fassnacht Martin, Peczkowska Mariola, Fauth Christine, Golcher Henriette, Walter Martin A, Pichl Josef, Raue Friedhelm, Eng Charis, Neumann Hartmut P H, |
| The clinical spectrum of multiple endocrine neoplasia type 2a caused by the rare intracellular RET mutation S891A. The Journal of clinical endocrinology and metabolism 2010 Sep 95 (9): E92-7. Schulte Klaus-Martin, Machens Andreas, Fugazzola Laura, McGregor Alan, Diaz-Cano Salvador, Izatt Louise, Aylwin Simon, Talat Nadia, Beck-Peccoz Paolo, Dralle Henni |
| Factors predicting outcome of total thyroidectomy in young patients with multiple endocrine neoplasia type 2: a nationwide long-term follow-up study. World journal of surgery 2010 Apr 34 (4): 852-60. Schreinemakers Jennifer M J, Vriens Menno R, Valk Gerlof D, de Groot Jan-Willem B, Plukker John T, Bax Klaas M A, Hamming Jaap F, van der Luijt Rob B, Aronson Daniel C, Borel Rinkes Inne H |
| Pathogenicity of DNA variants and double mutations in multiple endocrine neoplasia type 2 and von Hippel-Lindau syndrome. The Journal of clinical endocrinology and metabolism 2010 Jan 95 (1): 308-13. Erlic Zoran, Hoffmann Michael M, Sullivan Maren, Franke Gerlind, Peczkowska Mariola, Harsch Igor, Schott Matthias, Gabbert Helmut E, Valimäki Matti, Preuss Simon F, Hasse-Lazar Kornelia, Waligorski Dariusz, Robledo Mercedes, Januszewicz Andrzej, Eng Charis, Neumann Hartmut P |
| Clinical and genetic differences in total colonic aganglionosis in Hirschsprung's disease. Journal of pediatric surgery 2009 Oct 44 (10): 1899-903. Moore Samuel W, Zaahl Moniq |
| 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 |
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- Page last updated:Jun 22, 2022
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