BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

100 related articles for article (PubMed ID: 23822988)

  • 21. Pediatric paraganglioma: an early manifestation of an adult disease secondary to germline mutations.
    Mora J; Cascón A; Robledo M; Catala A
    Pediatr Blood Cancer; 2006 Nov; 47(6):785-9. PubMed ID: 16304664
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Pheochromocytomas and paragangliomas: implications of new insights for diagnosis and treatment].
    van der Kleij-Corssmit EP; Havekes B; Vriends AH; Jansen JC; Romijn JA
    Ned Tijdschr Geneeskd; 2008 Mar; 152(9):489-93. PubMed ID: 18389879
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Pheochromocytoma: an update on genetics and management.
    Karagiannis A; Mikhailidis DP; Athyros VG; Harsoulis F
    Endocr Relat Cancer; 2007 Dec; 14(4):935-56. PubMed ID: 18045948
    [TBL] [Abstract][Full Text] [Related]  

  • 24. New insights in the genetics of adrenocortical tumors, pheochromocytomas and paragangliomas.
    Bertherat J; Gimenez-Roqueplo AP
    Horm Metab Res; 2005 Jun; 37(6):384-90. PubMed ID: 16001332
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Familial paraganglioma syndromes.
    Chetty R
    J Clin Pathol; 2010 Jun; 63(6):488-91. PubMed ID: 20498024
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Hereditary pheochromocytoma and paraganglioma].
    Musil Z; Vícha A; Zelinka T; Turková H; Labudová T; Kohoutová M; Pacák K
    Klin Onkol; 2012; 25 Suppl():S21-6. PubMed ID: 22920202
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Uncommon clinical presentations of pheochromocytoma and paraganglioma in two different patients affected by two distinct novel VHL germline mutations.
    Ercolino T; Becherini L; Valeri A; Maiello M; Gaglianò MS; Parenti G; Ramazzotti M; Piscitelli E; Simi L; Pinzani P; Nesi G; Degl'Innocenti D; Console N; Bergamini C; Mannelli M
    Clin Endocrinol (Oxf); 2008 May; 68(5):762-8. PubMed ID: 18031321
    [TBL] [Abstract][Full Text] [Related]  

  • 28. High prevalence of SDHB mutations in head and neck paraganglioma in Belgium.
    Persu A; Hamoir M; Grégoire V; Garin P; Duvivier E; Reychler H; Chantrain G; Mortier G; Mourad M; Maiter D; Vikkula M
    J Hypertens; 2008 Jul; 26(7):1395-401. PubMed ID: 18551016
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Paragangliomas: etiology, presentation, and management.
    Joynt KE; Moslehi JJ; Baughman KL
    Cardiol Rev; 2009; 17(4):159-64. PubMed ID: 19525677
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Pheochromocytoma: diagnostic and therapeutic update.
    Oleaga A; Goñi F
    Endocrinol Nutr; 2008 May; 55(5):202-16. PubMed ID: 22967914
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Multidisciplinary practice guidelines for the diagnosis, genetic counseling and treatment of pheochromocytomas and paragangliomas.
    Garcia-Carbonero R; Matute Teresa F; Mercader-Cidoncha E; Mitjavila-Casanovas M; Robledo M; Tena I; Alvarez-Escola C; Arístegui M; Bella-Cueto MR; Ferrer-Albiach C; Hanzu FA
    Clin Transl Oncol; 2021 Oct; 23(10):1995-2019. PubMed ID: 33959901
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Diagnosis and management of tumors of the adrenal medulla.
    Ilias I; Pacak K
    Horm Metab Res; 2005 Dec; 37(12):717-21. PubMed ID: 16372223
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Genetic and molecular bases of paragangliomas].
    Núñez Lozano M; González Sarmiento R
    Acta Otorrinolaringol Esp; 2009 Feb; 60 Suppl 1():24-8. PubMed ID: 19245772
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Head and neck paragangliomas: genetic spectrum and clinical variability in 79 consecutive patients.
    Piccini V; Rapizzi E; Bacca A; Di Trapani G; Pulli R; Giachè V; Zampetti B; Lucci-Cordisco E; Canu L; Corsini E; Faggiano A; Deiana L; Carrara D; Tantardini V; Mariotti S; Ambrosio MR; Zatelli MC; Parenti G; Colao A; Pratesi C; Bernini G; Ercolino T; Mannelli M
    Endocr Relat Cancer; 2012 Apr; 19(2):149-55. PubMed ID: 22241717
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Pheochromocytomas, multiple endocrine neoplasia type 2, and von Hippel-Lindau disease.
    Neumann HP; Berger DP; Sigmund G; Blum U; Schmidt D; Parmer RJ; Volk B; Kirste G
    N Engl J Med; 1993 Nov; 329(21):1531-8. PubMed ID: 8105382
    [TBL] [Abstract][Full Text] [Related]  

  • 36. An update on the genetics of paraganglioma, pheochromocytoma, and associated hereditary syndromes.
    Gimenez-Roqueplo AP; Dahia PL; Robledo M
    Horm Metab Res; 2012 May; 44(5):328-33. PubMed ID: 22328163
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Comparative genomic hybridization reveals frequent losses of chromosomes 1p and 3q in pheochromocytomas and abdominal paragangliomas, suggesting a common genetic etiology.
    Edström E; Mahlamäki E; Nord B; Kjellman M; Karhu R; Höög A; Goncharov N; Teh BT; Bäckdahl M; Larsson C
    Am J Pathol; 2000 Feb; 156(2):651-9. PubMed ID: 10666394
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Genetic testing in pheochromocytoma: increasing importance for clinical decision making.
    Bornstein SR; Gimenez-Roqueplo AP
    Ann N Y Acad Sci; 2006 Aug; 1073():94-103. PubMed ID: 17102076
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Adrenal tumours in childhood].
    Martos-Moreno GA; Pozo-Román J; Argente J
    An Pediatr (Barc); 2013 Sep; 79(3):187.e1-187.e16. PubMed ID: 23796614
    [TBL] [Abstract][Full Text] [Related]  

  • 40. The management of head-and-neck paragangliomas.
    Capatina C; Ntali G; Karavitaki N; Grossman AB
    Endocr Relat Cancer; 2013 Oct; 20(5):R291-305. PubMed ID: 23921204
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.