BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

Terms: = Thyroid cancer AND SDHC, CYBL, 6391, ENSG00000143252, SDH3, PGL3, QPS1, CYB560 AND Diagnosis
10 results:

  • 1. 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
    [TBL] [Abstract] [Full Text] [Related]  

  • 2. 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
    [TBL] [Abstract] [Full Text] [Related]  

  • 3. 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
    [TBL] [Abstract] [Full Text] [Related]  

  • 4. 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
    [TBL] [Abstract] [Full Text] [Related]  

  • 5. 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
    [TBL] [Abstract] [Full Text] [Related]  

  • 6. 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
    [TBL] [Abstract] [Full Text] [Related]  

  • 7. [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
    [TBL] [Abstract] [Full Text] [Related]  

  • 8. Familial pheochromocytoma.
    Erlic Z; Neumann HP
    Hormones (Athens); 2009; 8(1):29-38. PubMed ID: 19269919
    [TBL] [Abstract] [Full Text] [Related]  

  • 9. 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
    [TBL] [Abstract] [Full Text] [Related]  

  • 10. [Genetics of endocrine tumours].
    Calender A; Dupasquier S; Cordier M; Zhang CX;
    Ann Pathol; 2005 Dec; 25(6):463-86. PubMed ID: 16735973
    [TBL] [Abstract] [Full Text] [Related]  


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