Terms: = Thyroid cancer AND SDHD, PGL1, 6392, ENSG00000204370, PGL, SDH4, CBT1, O14521 AND Diagnosis
19 results:
1. Non-medullary thyroid cancer Susceptibility Genes: Evidence and Disease Spectrum.
Zhou J; Singh P; Yin K; Wang J; Bao Y; Wu M; Pathak K; McKinley SK; Braun D; Lubitz CC; Hughes KS
Ann Surg Oncol; 2021 Oct; 28(11):6590-6600. PubMed ID: 33660127
[TBL] [Abstract] [Full Text] [Related]
2. Carotid Body Tumor - radiological imaging and genetic assessment.
Berger G; Łukasiewicz A; Grinevych V; Tarasów E
Pol Przegl Chir; 2020 Nov; 92(6):39-44. PubMed ID: 33408267
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3. Pycnodysostosis with novel gene mutation and sporadic medullary thyroid carcinoma: A case report.
Shi X; Huang C; Xiao F; Liu W; Zeng J; Li X
Medicine (Baltimore); 2017 Dec; 96(50):e8730. PubMed ID: 29390266
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4. ATTITUDES TOWARD GENETIC COUNSELING AND TESTING IN PATIENTS WITH INHERITED ENDOCRINOPATHIES.
Gallagher TM; Bucciarelli M; Kavalukas SL; Baker MJ; Saunders BD
Endocr Pract; 2017 Sep; 23(9):1039-1044. PubMed ID: 28613942
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5. A novel RET gene mutation in a patient with apparently sporadic pheochromocytoma.
Scollo C; Russo M; De Gregorio L; Terranova R; Mangione E; Castoro C; Squatrito S; Pellegriti G
Endocr J; 2016; 63(1):87-91. PubMed ID: 26497911
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6. Coexistence of paraganglioma/pheochromocytoma and papillary thyroid carcinoma: a four-case series analysis.
Bugalho MJ; Silva AL; Domingues R
Fam Cancer; 2015 Dec; 14(4):603-7. PubMed ID: 26071763
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7. A registry-based study of thyroid paraganglioma: histological and genetic characteristics.
von Dobschuetz E; Leijon H; Schalin-Jäntti C; Schiavi F; Brauckhoff M; Peczkowska M; Spiazzi G; Demattè S; Cecchini ME; Sartorato P; Krajewska J; Hasse-Lazar K; Roszkowska-Purska K; Taschin E; Malinoc A; Akslen LA; Arola J; Lange D; Fassina A; Pennelli G; Barbareschi M; Luettges J; Prejbisz A; Januszewicz A; Strate T; Bausch B; Castinetti F; Jarzab B; Opocher G; Eng C; Neumann HP
Endocr Relat Cancer; 2015 Apr; 22(2):191-204. PubMed ID: 25595276
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8. Genetics, diagnosis, and management of medullary thyroid carcinoma and pheochromocytoma/paraganglioma.
Moraitis AG; Martucci VL; Pacak K
Endocr Pract; 2014 Feb; 20(2):176-87. PubMed ID: 24449662
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9. Analysis of pheochromocytomas / paragangliomas from Eastern Slovakia.
Felsoci M; Lazurova I; Wagnerova H; Svajdler M
Neoplasma; 2013; 60(4):452-8. PubMed ID: 23581419
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10. Testing new susceptibility genes in the cohort of apparently sporadic phaeochromocytoma/paraganglioma patients with clinical characteristics of hereditary syndromes.
Pęczkowska M; Kowalska A; Sygut J; Waligórski D; Malinoc A; Janaszek-Sitkowska H; Prejbisz A; Januszewicz A; Neumann HP
Clin Endocrinol (Oxf); 2013 Dec; 79(6):817-23. PubMed ID: 23551045
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11. [Genetics of pheochromocytoma].
Bausch B; Malinoc A; Maruschke L; Offergeld C; Gläsker S; Rischke HC; Brauckhoff M; Boedeker CC; Neumann HP
Chirurg; 2012 Jun; 83(6):511-8. PubMed ID: 22481546
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12. Mendelian genetics of rare--and not so rare--cancers.
Eng C
Ann N Y Acad Sci; 2010 Dec; 1214():70-82. PubMed ID: 20946573
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13. diagnosis, localization and treatment of pheochromocytoma in MEN 2 syndrome.
Ilias I; Pacak K
Endocr Regul; 2009 Apr; 43(2):89-93. PubMed ID: 19856714
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14. Familial pheochromocytoma.
Erlic Z; Neumann HP
Hormones (Athens); 2009; 8(1):29-38. PubMed ID: 19269919
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15. Germline mutations in PTEN and SDHC in a woman with epithelial thyroid cancer and carotid paraganglioma.
Zbuk KM; Patocs A; Shealy A; Sylvester H; Miesfeldt S; Eng C
Nat Clin Pract Oncol; 2007 Oct; 4(10):608-12. PubMed ID: 17898811
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16. Asymptomatic bilateral adrenal pheochromocytoma in a patient with a germline V804M mutation in the RET proto-oncogene.
Recasens M; Oriola J; Fernández-Real JM; Roig J; Rodríguez-Hermosa JI; Font JA; Galofre P; López-Bermejo A; Ricart W
Clin Endocrinol (Oxf); 2007 Jul; 67(1):29-33. PubMed ID: 17466010
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17. [Genetics of endocrine tumours].
Calender A; Dupasquier S; Cordier M; Zhang CX;
Ann Pathol; 2005 Dec; 25(6):463-86. PubMed ID: 16735973
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18. Succinate dehydrogenase D variants do not constitute a risk factor for developing C cell hyperplasia or sporadic medullary thyroid carcinoma.
Cascon A; Cebrian A; Pollan M; Ruiz-Llorente S; Montero-Conde C; Leton R; Gutierrez R; Lesueur F; Milne RL; Gonzalez-Albarran O; Lucas-Morante T; Benitez J; Ponder BA; Robledo M
J Clin Endocrinol Metab; 2005 Apr; 90(4):2127-30. PubMed ID: 15623805
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19. Distinct clinical features of paraganglioma syndromes associated with SDHB and sdhd gene mutations.
Neumann HP; Pawlu C; Peczkowska M; Bausch B; McWhinney SR; Muresan M; Buchta M; Franke G; Klisch J; Bley TA; Hoegerle S; Boedeker CC; Opocher G; Schipper J; Januszewicz A; Eng C;
JAMA; 2004 Aug; 292(8):943-51. PubMed ID: 15328326
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