BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

216 related articles for article (PubMed ID: 28670912)

  • 21. Genetic mutation screening in an italian cohort of nonsyndromic pheochromocytoma/paraganglioma patients.
    Castellano M; Mori L; Giacchè M; Agliozzo E; Tosini R; Panarotto A; Cappelli C; Mulatero P; Cumetti D; Veglio F; Agabiti-Rosei E
    Ann N Y Acad Sci; 2006 Aug; 1073():156-65. PubMed ID: 17102082
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Diagnosis and management of hereditary paraganglioma syndrome due to the F933>X67 SDHD mutation.
    Marvin ML; Bradford CR; Sisson JC; Gruber SB
    Head Neck; 2009 May; 31(5):689-94. PubMed ID: 19072999
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Succinate dehydrogenase (SDH) and mitochondrial driven neoplasia.
    Gill AJ
    Pathology; 2012 Jun; 44(4):285-92. PubMed ID: 22544211
    [TBL] [Abstract][Full Text] [Related]  

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

  • 25. SDHB, SDHC, and SDHD mutation screen in sporadic and familial head and neck paragangliomas.
    Mhatre AN; Li Y; Feng L; Gasperin A; Lalwani AK
    Clin Genet; 2004 Nov; 66(5):461-6. PubMed ID: 15479192
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Clinical presentations, biochemical phenotypes, and genotype-phenotype correlations in patients with succinate dehydrogenase subunit B-associated pheochromocytomas and paragangliomas.
    Timmers HJ; Kozupa A; Eisenhofer G; Raygada M; Adams KT; Solis D; Lenders JW; Pacak K
    J Clin Endocrinol Metab; 2007 Mar; 92(3):779-86. PubMed ID: 17200167
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Uncommon case of paraganglioma syndrome in combination with malignant paraganglioma].
    Schmahl K; Atamna N; Schönijahn T; Lülsdorf P; Göller T; Jacob R
    Laryngorhinootologie; 2008 Feb; 87(2):112-7. PubMed ID: 18345539
    [TBL] [Abstract][Full Text] [Related]  

  • 28. L157X nonsense mutation of the succinate dehydrogenase subunit B gene in a Japanese patient with right paraaortic paraganglioma.
    Sato H; Kanai G; Hirabayshi K; Kajiwara H; Itoh J; Osamura RY
    Endocrine; 2010 Aug; 38(1):18-23. PubMed ID: 20960097
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Cardiac paraganglioma with a novel germline mutation of succinate dehydrogenase gene D.
    Otani N; Sugano K; Inami S; Amano H; Arikawa T; Saito S; Imai K; Ushiama M; Yoshida T; Kimura N; Toyoda S; Inoue T
    Jpn J Clin Oncol; 2017 Dec; 47(12):1193-1197. PubMed ID: 28977582
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Superiority of fluorodeoxyglucose positron emission tomography to other functional imaging techniques in the evaluation of metastatic SDHB-associated pheochromocytoma and paraganglioma.
    Timmers HJ; Kozupa A; Chen CC; Carrasquillo JA; Ling A; Eisenhofer G; Adams KT; Solis D; Lenders JW; Pacak K
    J Clin Oncol; 2007 Jun; 25(16):2262-9. PubMed ID: 17538171
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromes.
    Benn DE; Gimenez-Roqueplo AP; Reilly JR; Bertherat J; Burgess J; Byth K; Croxson M; Dahia PL; Elston M; Gimm O; Henley D; Herman P; Murday V; Niccoli-Sire P; Pasieka JL; Rohmer V; Tucker K; Jeunemaitre X; Marsh DJ; Plouin PF; Robinson BG
    J Clin Endocrinol Metab; 2006 Mar; 91(3):827-36. PubMed ID: 16317055
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Large germline deletions of mitochondrial complex II subunits SDHB and SDHD in hereditary paraganglioma.
    McWhinney SR; Pilarski RT; Forrester SR; Schneider MC; Sarquis MM; Dias EP; Eng C
    J Clin Endocrinol Metab; 2004 Nov; 89(11):5694-9. PubMed ID: 15531530
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Germline mutations and genotype-phenotype correlations in patients with apparently sporadic pheochromocytoma/paraganglioma in Korea.
    Kim JH; Seong MW; Lee KE; Choi HJ; Ku EJ; Bae JH; Park SS; Choi SH; Kim SW; Shin C; Kim SY
    Clin Genet; 2014 Nov; 86(5):482-6. PubMed ID: 24134185
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Relevance of germline mutation screening in both familial and sporadic head and neck paraganglioma for early diagnosis and clinical management.
    Hermsen MA; Sevilla MA; Llorente JL; Weiss MM; Grimbergen A; Allonca E; Garcia-Inclán C; Balbín M; Suárez C
    Cell Oncol; 2010 Jan; 32(4):275-83. PubMed ID: 20208144
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Malignant bladder pheochromocytoma with SDHB genetic mutation.
    Maeda M; Funahashi Y; Katoh M; Fujita T; Tsuruta K; Gotoh M
    Aktuelle Urol; 2013 Sep; 44(5):381-2. PubMed ID: 23807799
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Germline mutations and genotype-phenotype correlation in Asian Indian patients with pheochromocytoma and paraganglioma.
    Pandit R; Khadilkar K; Sarathi V; Kasaliwal R; Goroshi M; Khare S; Nair S; Raghavan V; Dalvi A; Hira P; Fernandes G; Sathe P; Rojekar A; Malhotra G; Bakshi G; Prakash G; Bhansali A; Walia R; Kamalanathan S; Sahoo J; Desai A; Bhagwat N; Mappa P; Rajput R; Chandrashekhar SR; Shivane V; Menon P; Lila A; Bandgar T; Shah N
    Eur J Endocrinol; 2016 Oct; 175(4):311-23. PubMed ID: 27539324
    [TBL] [Abstract][Full Text] [Related]  

  • 38. High frequency of germline succinate dehydrogenase mutations in sporadic cervical paragangliomas in northern Spain: mitochondrial succinate dehydrogenase structure-function relationships and clinical-pathological correlations.
    Lima J; Feijão T; Ferreira da Silva A; Pereira-Castro I; Fernandez-Ballester G; Máximo V; Herrero A; Serrano L; Sobrinho-Simões M; Garcia-Rostan G
    J Clin Endocrinol Metab; 2007 Dec; 92(12):4853-64. PubMed ID: 17848412
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Screening for familial paragangliomas.
    Myssiorek D; Ferlito A; Silver CE; Rodrigo JP; Baysal BE; Fagan JJ; Suárez C; Rinaldo A
    Oral Oncol; 2008 Jun; 44(6):532-7. PubMed ID: 17936061
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.