Terms: = Thyroid cancer AND SDHC, CYBL, 6391, ENSG00000143252, SDH3, PGL3, QPS1, CYB560
24 results:
1. Observational study of population genomic screening for variants associated with endocrine tumor syndromes in a large, healthcare-based cohort.
Savatt JM; Ortiz NM; Thone GM; McDonald WS; Kelly MA; Berry ASF; Alvi MM; Hallquist MLG; Malinowski J; Purdy NC; Williams MS; Sturm AC; Buchanan AH
BMC Med; 2022 Jun; 20(1):205. PubMed ID: 35668420
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2. Long Noncoding RNA LOC554202 Predicts a Poor Prognosis and Correlates with Immune Infiltration in thyroid cancer.
Chen C; Qin L; Xiao MF
Comput Math Methods Med; 2022; 2022():3585626. PubMed ID: 35265169
[TBL] [Abstract] [Full Text] [Related]
3. Over expression of CDK4 and MDM2 in a patient with recurrent ALK-negative mediastinal inflammatory myofibroblastic tumor: A case report.
Hou TC; Wu PS; Huang WY; Yang YT; Tan KT; Liu SH; Chen YJ; Chen SJ; Su YW
Medicine (Baltimore); 2020 Mar; 99(12):e19577. PubMed ID: 32195970
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4. Tracheal paraganglioma presenting as stridor in a pediatric patient, case report and literature review.
Dimachkieh AL; Dobbie A; Olson DR; Lovell MA; Prager JD
Int J Pediatr Otorhinolaryngol; 2018 Apr; 107():145-149. PubMed ID: 29501297
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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. The Influence of Patient Age on thyroid Nodule Formation, Multinodularity, and thyroid cancer Risk.
Kwong N; Medici M; Angell TE; Liu X; Marqusee E; Cibas ES; Krane JF; Barletta JA; Kim MI; Larsen PR; Alexander EK
J Clin Endocrinol Metab; 2015 Dec; 100(12):4434-40. PubMed ID: 26465395
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7. 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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8. Germline and somatic SDHx alterations in apparently sporadic differentiated thyroid cancer.
Ni Y; Seballos S; Ganapathi S; Gurin D; Fletcher B; Ngeow J; Nagy R; Kloos RT; Ringel MD; LaFramboise T; Eng C
Endocr Relat Cancer; 2015 Apr; 22(2):121-30. PubMed ID: 25694510
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9. 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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10. Unusual case of Cowden-like syndrome, neck paraganglioma, and pituitary adenoma.
Efstathiadou ZA; Sapranidis M; Anagnostis P; Kita MD
Head Neck; 2014 Jan; 36(1):E12-6. PubMed ID: 23804288
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11. 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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12. Genetic and clinical characteristics of head and neck paragangliomas in a Chinese population.
Zheng X; Wei S; Yu Y; Xia T; Zhao J; Gao S; Li Y; Gao M
Laryngoscope; 2012 Aug; 122(8):1761-6. PubMed ID: 22566157
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13. [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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14. Head and neck paragangliomas: Report of 175 patients (1989-2010).
Papaspyrou K; Mewes T; Rossmann H; Fottner C; Schneider-Raetzke B; Bartsch O; Schreckenberger M; Lackner KJ; Amedee RG; Mann WJ
Head Neck; 2012 May; 34(5):632-7. PubMed ID: 21692132
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15. Hereditary paragangliomas.
Raygada M; Pasini B; Stratakis CA
Adv Otorhinolaryngol; 2011; 70():99-106. PubMed ID: 21358191
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16. Genetics of pheochromocytomas and paragangliomas.
Opocher G; Schiavi F
Best Pract Res Clin Endocrinol Metab; 2010 Dec; 24(6):943-56. PubMed ID: 21115163
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17. Pathogenicity of DNA variants and double mutations in multiple endocrine neoplasia type 2 and von Hippel-Lindau syndrome.
Erlic Z; Hoffmann MM; Sullivan M; Franke G; Peczkowska M; Harsch I; Schott M; Gabbert HE; Valimäki M; Preuss SF; Hasse-Lazar K; Waligorski D; Robledo M; Januszewicz A; Eng C; Neumann HP
J Clin Endocrinol Metab; 2010 Jan; 95(1):308-13. PubMed ID: 19906784
[TBL] [Abstract] [Full Text] [Related]
18. Familial pheochromocytoma.
Erlic Z; Neumann HP
Hormones (Athens); 2009; 8(1):29-38. PubMed ID: 19269919
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19. 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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20. Familial nonsyndromic pheochromocytoma.
Opocher G; Schiavi F; Iacobone M; Toniato A; Sattarova S; Erlic Z; Martella M; Mian C; Merante Boschin I; Zambonin L; De Lazzari P; Murgia A; Pelizzo MR; Favia G; Mantero F
Ann N Y Acad Sci; 2006 Aug; 1073():149-55. PubMed ID: 17102081
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