BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

241 related articles for article (PubMed ID: 37448268)

  • 1. [Rare forms of hereditary endocrine neoplasia: co-existence of pituitary adenoma and pheochromocytoma/paraganglioma].
    Mamedova EO; Lisina DV; Belaya ZE
    Probl Endokrinol (Mosk); 2023 May; 69(2):24-30. PubMed ID: 37448268
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Pituitary adenoma with paraganglioma/pheochromocytoma (3PAs) and succinate dehydrogenase defects in humans and mice.
    Xekouki P; Szarek E; Bullova P; Giubellino A; Quezado M; Mastroyannis SA; Mastorakos P; Wassif CA; Raygada M; Rentia N; Dye L; Cougnoux A; Koziol D; Sierra Mde L; Lyssikatos C; Belyavskaya E; Malchoff C; Moline J; Eng C; Maher LJ; Pacak K; Lodish M; Stratakis CA
    J Clin Endocrinol Metab; 2015 May; 100(5):E710-9. PubMed ID: 25695889
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Germinal defects of SDHx genes in patients with isolated pituitary adenoma.
    Mougel G; Lagarde A; Albarel F; Essamet W; Luigi P; Mouly C; Vialon M; Cuny T; Castinetti F; Saveanu A; Brue T; Barlier A; Romanet P
    Eur J Endocrinol; 2020 Oct; 183(4):369-379. PubMed ID: 32621582
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Heterogeneous genetic background of the association of pheochromocytoma/paraganglioma and pituitary adenoma: results from a large patient cohort.
    Dénes J; Swords F; Rattenberry E; Stals K; Owens M; Cranston T; Xekouki P; Moran L; Kumar A; Wassif C; Fersht N; Baldeweg SE; Morris D; Lightman S; Agha A; Rees A; Grieve J; Powell M; Boguszewski CL; Dutta P; Thakker RV; Srirangalingam U; Thompson CJ; Druce M; Higham C; Davis J; Eeles R; Stevenson M; O'Sullivan B; Taniere P; Skordilis K; Gabrovska P; Barlier A; Webb SM; Aulinas A; Drake WM; Bevan JS; Preda C; Dalantaeva N; Ribeiro-Oliveira A; Garcia IT; Yordanova G; Iotova V; Evanson J; Grossman AB; Trouillas J; Ellard S; Stratakis CA; Maher ER; Roncaroli F; Korbonits M
    J Clin Endocrinol Metab; 2015 Mar; 100(3):E531-41. PubMed ID: 25494863
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 15 YEARS OF PARAGANGLIOMA: The association of pituitary adenomas and phaeochromocytomas or paragangliomas.
    O'Toole SM; Dénes J; Robledo M; Stratakis CA; Korbonits M
    Endocr Relat Cancer; 2015 Aug; 22(4):T105-22. PubMed ID: 26113600
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 3P association (3PAs): Pituitary adenoma and pheochromocytoma/paraganglioma. A heterogeneous clinical syndrome associated with different gene mutations.
    Guerrero-Pérez F; Fajardo C; Torres Vela E; Giménez-Palop O; Lisbona Gil A; Martín T; González N; Díez JJ; Iglesias P; Robledo M; Villabona C
    Eur J Intern Med; 2019 Nov; 69():14-19. PubMed ID: 31431315
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Pituitary adenoma associated with pheochromocytoma/paraganglioma: A new form of multiple endocrine neoplasia.
    Guerrero Pérez F; Lisbona Gil A; Robledo M; Iglesias P; Villabona Artero C
    Endocrinol Nutr; 2016 Nov; 63(9):506-508. PubMed ID: 27639663
    [No Abstract]   [Full Text] [Related]  

  • 8. Recent insights into the molecular pathogenesis of pheochromocytoma and paraganglioma.
    Nakamura E; Kaelin WG
    Endocr Pathol; 2006; 17(2):97-106. PubMed ID: 17159241
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The 3PAs: An Update on the Association of Pheochromocytomas, Paragangliomas, and Pituitary Tumors.
    Xekouki P; Brennand A; Whitelaw B; Pacak K; Stratakis CA
    Horm Metab Res; 2019 Jul; 51(7):419-436. PubMed ID: 30273935
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Familial SDHA mutation associated with pituitary adenoma and pheochromocytoma/paraganglioma.
    Dwight T; Mann K; Benn DE; Robinson BG; McKelvie P; Gill AJ; Winship I; Clifton-Bligh RJ
    J Clin Endocrinol Metab; 2013 Jun; 98(6):E1103-8. PubMed ID: 23633203
    [TBL] [Abstract][Full Text] [Related]  

  • 11. DIAGNOSIS of ENDOCRINE DISEASE: SDHx mutations: beyond pheochromocytomas and paragangliomas.
    Mannelli M; Canu L; Ercolino T; Rapizzi E; Martinelli S; Parenti G; De Filpo G; Nesi G
    Eur J Endocrinol; 2018 Jan; 178(1):R11-R17. PubMed ID: 28924001
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Succinate dehydrogenase (SDHx) mutations in pituitary tumors: could this be a new role for mitochondrial complex II and/or Krebs cycle defects?
    Xekouki P; Stratakis CA
    Endocr Relat Cancer; 2012 Dec; 19(6):C33-40. PubMed ID: 22889736
    [TBL] [Abstract][Full Text] [Related]  

  • 13. SDHx mutation and pituitary adenoma: can in vivo 1H-MR spectroscopy unravel the link?
    Branzoli F; Salgues B; Marjańska M; Laloi-Michelin M; Herman P; Le Collen L; Delemer B; Riancho J; Kuhn E; Jublanc C; Burnichon N; Amar L; Favier J; Gimenez-Roqueplo AP; Buffet A; Lussey-Lepoutre C
    Endocr Relat Cancer; 2023 Feb; 30(2):. PubMed ID: 36449569
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Pheochromocytoma/Paraganglioma: Review of perioperative management of blood pressure and update on genetic mutations associated with pheochromocytoma.
    Fishbein L; Orlowski R; Cohen D
    J Clin Hypertens (Greenwich); 2013 Jun; 15(6):428-34. PubMed ID: 23730992
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Carney Triad, Carney-Stratakis Syndrome, 3PAS and Other Tumors Due to SDH Deficiency.
    Pitsava G; Settas N; Faucz FR; Stratakis CA
    Front Endocrinol (Lausanne); 2021; 12():680609. PubMed ID: 34012423
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Pheochromocytoma, paragangliomas, and pituitary adenoma: An unusual association in a patient with an SDHD mutation. Case report.
    Lemelin A; Lapoirie M; Abeillon J; Lasolle H; Giraud S; Philouze P; Ceruse P; Raverot G; Vighetto A; Borson-Chazot F
    Medicine (Baltimore); 2019 Jul; 98(30):e16594. PubMed ID: 31348302
    [TBL] [Abstract][Full Text] [Related]  

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

  • 18. Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas.
    Benn DE; Croxson MS; Tucker K; Bambach CP; Richardson AL; Delbridge L; Pullan PT; Hammond J; Marsh DJ; Robinson BG
    Oncogene; 2003 Mar; 22(9):1358-64. PubMed ID: 12618761
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 15 YEARS OF PARAGANGLIOMA: Genetics and mechanism of pheochromocytoma-paraganglioma syndromes characterized by germline SDHB and SDHD mutations.
    Baysal BE; Maher ER
    Endocr Relat Cancer; 2015 Aug; 22(4):T71-82. PubMed ID: 26113606
    [TBL] [Abstract][Full Text] [Related]  

  • 20. An aggressive cabergoline-resistant, temozolomide-responsive macroprolactinoma due to a germline
    Alzahrani AS; Bin Nafisah A; Alswailem M; Moria Y; Poprawski D; Al-Hindi H; Pacak K
    Front Endocrinol (Lausanne); 2023; 14():1273093. PubMed ID: 38152133
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.