Terms: = Endocrine gland cancer AND SDHD, PGL1, 6392, ENSG00000204370, PGL, SDH4, CBT1, O14521 AND Diagnosis
166 results:
1. Ectopic pheochromocytomas in the third trimester: A case report and literature review.
Zhao L; Chen M; Chen X; Yu L; Du SG; Gan Q; Yang WZ; Jiang C; Xiao M
Medicine (Baltimore); 2024 Feb; 103(5):e36127. PubMed ID: 38306535
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2. Pheochromocytoma and paraganglioma in children and adolescents.
Stachowicz-Stencel T; Pasikowska N; Synakiewicz A
Acta Biochim Pol; 2023 Sep; 70(3):487-493. PubMed ID: 37717273
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3. Visual analytics identifies key miRNAs for differentiating peripancreatic paraganglioma and pancreatic neuroendocrine tumors.
Enguita JM; Díaz I; García D; Cubiella T; Chiara MD; Valdés N
Front Endocrinol (Lausanne); 2023; 14():1162725. PubMed ID: 37383401
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4. Back to Biochemistry: Evaluation for and Prognostic Significance of SDH Mutations in Paragangliomas and Pheochromocytomas.
Gupta S; Erickson LA
Surg Pathol Clin; 2023 Mar; 16(1):119-129. PubMed ID: 36739159
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5. A rare case of multiple paragangliomas in the head and neck, retroperitoneum and duodenum: A case report and review of the literature.
Kawanabe S; Katabami T; Oshima R; Yanagisawa N; Sone M; Kimura N
Front Endocrinol (Lausanne); 2022; 13():1054468. PubMed ID: 36704041
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6. Low number of neurosecretory vesicles in neuroblastoma impairs massive catecholamine release and prevents hypertension.
Mühlethaler-Mottet A; Uccella S; Marchiori D; La Rosa S; Daraspe J; Balmas Bourloud K; Beck Popovic M; Eugster PJ; Grouzmann E; Abid K
Front Endocrinol (Lausanne); 2022; 13():1027856. PubMed ID: 36531507
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7. Left adrenal aldosteronism coexisting with left paraaortic paraganglioma presenting as bilateral adrenal and left paraaortic tumors- comprehensive adrenal evaluation aiding perfect management: a case report.
Hsu YC; Lee CH; Chen CY; Hung CJ
BMC Endocr Disord; 2022 Nov; 22(1):279. PubMed ID: 36371163
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8. High rates of the SDHB p.Arg46Gln pathogenic variant predisposes New Zealand Māori to phaeochromocytoma/paraganglioma.
Shand JAD; van Schalkwyk J; Beavis V; Niyagama A; Taylor S; Eagleton C
Intern Med J; 2023 Oct; 53(10):1883-1889. PubMed ID: 36346292
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9. A need to tailor surveillance based on family history: describing a highly penetrant familial paraganglioma kindred with an sdhd pathogenic variant.
Foley M; Sharma A; Garfield K; Maese L; Buchmann L; Boyle J; Kohlmann W; Jeter J; Greenberg S
Fam Cancer; 2023 Apr; 22(2):217-224. PubMed ID: 36223042
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10. Case Report: Composite pheochromocytoma with ganglioneuroma component: A report of three cases.
Araujo PB; Carvallo MS; Vidal AP; Nascimento JB; Wo JM; Naliato EO; Cunha Neto SH; Conceição FL; Fontes R; de Lima VV; Carvalho DP; Soares P; Lima J; Lourenço DM; Violante AHD
Front Endocrinol (Lausanne); 2022; 13():903085. PubMed ID: 36187102
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11. A rare case report of multifocal para-aortic and para-vesical paragangliomas.
Xiong SC; Di XP; Zhang MN; Wu K; Li X
Front Endocrinol (Lausanne); 2022; 13():946496. PubMed ID: 36004346
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12. Succinate dehydrogenase and MYC-associated factor X mutations in pituitary neuroendocrine tumours.
Loughrey PB; Roncaroli F; Healy E; Weir P; Basetti M; Casey RT; Hunter SJ; Korbonits M
Endocr Relat Cancer; 2022 Oct; 29(10):R157-R172. PubMed ID: 35938916
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13. A Case for Genetic Testing in Isolated Tympanic Paragangliomas.
Shrivastava MK; Curran JF; Sheerin F; Mohammadi BJ; Halliday D; MacKeith SAC
Otol Neurotol; 2022 Aug; 43(7):840-844. PubMed ID: 35802032
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14. Peripancreatic paraganglioma: Lesson from a round table.
Petrelli F; Fratini G; Sbrozzi-Vanni A; Giusti A; Manta R; Vignali C; Nesi G; Amorosi A; Cavazzana A; Arganini M; Ambrosio MR
World J Gastroenterol; 2022 Jun; 28(21):2396-2402. PubMed ID: 35800185
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15. Adrenocortical Tumors and Pheochromocytoma/Paraganglioma Initially Mistaken as Neuroblastoma-Experiences From the GPOH-MET Registry.
Kuhlen M; Pamporaki C; Kunstreich M; Wudy SA; Hartmann MF; Peitzsch M; Vokuhl C; Seitz G; Kreissl MC; Simon T; Hero B; Frühwald MC; Vorwerk P; Redlich A
Front Endocrinol (Lausanne); 2022; 13():918435. PubMed ID: 35784570
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16. pgl4 syndrome in a patient with synchronous paraganglioma-pheochromocytoma.
Roque JJN; Martins C; Bugalho MJGM
BMJ Case Rep; 2022 Mar; 15(3):. PubMed ID: 35351744
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17. [Recurrence and metastasis of pheochromocytoma/paraganglioma after tumor resection and clinical characteristics analysis].
Gao YJ; Cui YY; Ma XS; Wang HP; Liu J; Lou FC; Zhou T; Chen S; Lu L; Tong AL
Zhonghua Yi Xue Za Zhi; 2022 Mar; 102(10):729-734. PubMed ID: 35280017
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18. Hereditary paraganglioma presenting with atypical symptoms: Case report.
Eguchi S; Ono R; Sato T; Yada K; Umehara N; Narumi S; Ichihashi Y; Nozaki T; Kanomata N; Hasegawa T; Ozawa M; Hasegawa D
Medicine (Baltimore); 2021 Nov; 100(46):e27888. PubMed ID: 34797335
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19. Special situations in pheochromocytomas and paragangliomas: pregnancy, metastatic disease, and cyanotic congenital heart diseases.
Araujo-Castro M; Nattero Chavez L; Martínez Lorca A; Molina-Cerrillo J; Alonso-Gordoa T; Pascual-Corrales E
Clin Exp Med; 2022 Aug; 22(3):359-370. PubMed ID: 34591219
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20. A novel liquid biopsy (NETest) identifies paragangliomas and pheochromocytomas with high accuracy.
Pacak K; Kidd M; Meuter L; Modlin IM
Endocr Relat Cancer; 2021 Oct; 28(11):731-744. PubMed ID: 34515661
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