119 related articles for article (PubMed ID: 28099933)
1. Loss of maternal chromosome 11 is a signature event in SDHAF2, SDHD, and VHL-related paragangliomas, but less significant in SDHB-related paragangliomas.
Hoekstra AS; Hensen EF; Jordanova ES; Korpershoek E; van der Horst-Schrivers AN; Cornelisse C; Corssmit EP; Hes FJ; Jansen JC; Kunst HP; Timmers HJ; Bateman A; Eccles D; Bovée JV; Devilee P; Bayley JP
Oncotarget; 2017 Feb; 8(9):14525-14536. PubMed ID: 28099933
[TBL] [Abstract][Full Text] [Related]
2. Head and neck paragangliomas in von Hippel-Lindau disease and multiple endocrine neoplasia type 2.
Boedeker CC; Erlic Z; Richard S; Kontny U; Gimenez-Roqueplo AP; Cascon A; Robledo M; de Campos JM; van Nederveen FH; de Krijger RR; Burnichon N; Gaal J; Walter MA; Reschke K; Wiech T; Weber J; Rückauer K; Plouin PF; Darrouzet V; Giraud S; Eng C; Neumann HP
J Clin Endocrinol Metab; 2009 Jun; 94(6):1938-44. PubMed ID: 19336503
[TBL] [Abstract][Full Text] [Related]
3. Genotype-phenotype associations in paragangliomas of the temporal bone in a multi-ethnic cohort.
Angeli SI; Chiossone K JA; Goncalves S; Telischi FF
Acta Otolaryngol; 2023; 143(7):551-557. PubMed ID: 37354038
[TBL] [Abstract][Full Text] [Related]
4. Distortion in transmission of pathogenic SDHB- and SDHD-mutated alleles from parent to offspring.
Davidoff DF; Lim ES; Benn DE; Subramaniam Y; Dorman E; Burgess JR; Akker SA; Clifton-Bligh RJ
Endocr Relat Cancer; 2023 May; 30(5):. PubMed ID: 36786389
[TBL] [Abstract][Full Text] [Related]
5. 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
[TBL] [Abstract][Full Text] [Related]
6. Phospho-mTOR is not upregulated in metastatic SDHB paragangliomas.
Ghayee HK; Giubellino A; Click A; Kapur P; Christie A; Xie XJ; Martucci V; Shay JW; Souza RF; Pacak K
Eur J Clin Invest; 2013 Sep; 43(9):970-7. PubMed ID: 23889685
[TBL] [Abstract][Full Text] [Related]
7. The immunohistochemical, DNA methylation, and chromosomal copy number profile of cauda equina paraganglioma is distinct from extra-spinal paraganglioma.
Ramani B; Gupta R; Wu J; Barreto J; Bollen AW; Tihan T; Mummaneni PV; Ames C; Clark A; Oberheim Bush NA; Butowski N; Phillips D; King BE; Bator SM; Treynor EC; Zherebitskiy V; Quinn PS; Walker JB; Pekmezci M; Sullivan DV; Hofmann JW; Sloan EA; M Chang S; Berger MS; Solomon DA; Perry A
Acta Neuropathol; 2020 Dec; 140(6):907-917. PubMed ID: 32892244
[TBL] [Abstract][Full Text] [Related]
8. High incidence of occult familial
Guha A; Vicha A; Zelinka T; Kana M; Musil Z; Pacak K; Betka J; Chovanec M; Plzak J; Boucek J
Front Endocrinol (Lausanne); 2023; 14():1278175. PubMed ID: 38144572
[TBL] [Abstract][Full Text] [Related]
9. Ancestry-specific predisposing germline variants in cancer.
Oak N; Cherniack AD; Mashl RJ; ; Hirsch FR; Ding L; Beroukhim R; Gümüş ZH; Plon SE; Huang KL
Genome Med; 2020 May; 12(1):51. PubMed ID: 32471518
[TBL] [Abstract][Full Text] [Related]
10. A recurrent stop-codon mutation in succinate dehydrogenase subunit B gene in normal peripheral blood and childhood T-cell acute leukemia.
Baysal BE
PLoS One; 2007 May; 2(5):e436. PubMed ID: 17487275
[TBL] [Abstract][Full Text] [Related]
11. Next-generation sequencing in the clinical genetic screening of patients with pheochromocytoma and paraganglioma.
Crona J; Verdugo AD; Granberg D; Welin S; Stålberg P; Hellman P; Björklund P
Endocr Connect; 2013 Jun; 2(2):104-11. PubMed ID: 23781326
[TBL] [Abstract][Full Text] [Related]
12. Connecting molecular pathways to hereditary cancer risk syndromes.
Testa JR; Malkin D; Schiffman JD
Am Soc Clin Oncol Educ Book; 2013; ():81-90. PubMed ID: 23714463
[TBL] [Abstract][Full Text] [Related]
13. Sequence variation in human succinate dehydrogenase genes: evidence for long-term balancing selection on SDHA.
Baysal BE; Lawrence EC; Ferrell RE
BMC Biol; 2007 Mar; 5():12. PubMed ID: 17376234
[TBL] [Abstract][Full Text] [Related]
14. Three Cases of Carney-Stratakis Syndrome: A Genetically Heterogeneous Disease.
Lobato EC; Castro FF; Santana LS; Soares IC; Fagundes GFC; Almeida MQ
JCEM Case Rep; 2023 Nov; 1(6):luad139. PubMed ID: 38021081
[TBL] [Abstract][Full Text] [Related]
15. Head and Neck Paragangliomas: Overview of Institutional Experience.
Vimawala SN; Graboyes AZ; Bennett B; Bonanni M; Abbasi A; Oliphant T; Alonso-Basanta M; Rassekh C; Cohen D; Brant JA; Huan Y
Cancers (Basel); 2024 Apr; 16(8):. PubMed ID: 38672605
[TBL] [Abstract][Full Text] [Related]
16. Genealogical tree study in patients with familial paraganglioma syndrome due to SDHD mutation.
López Montalbán Á; Simón Frapolli VJ; Picón César MJ
Med Clin (Barc); 2024 Mar; 162(6):306-307. PubMed ID: 38042737
[No Abstract] [Full Text] [Related]
17. Succinate dehydrogenase mutations in head and neck paragangliomas: A systematic review and meta-analysis of individual patients' data.
Koh ES; Dabsha A; Rahouma M; Zappi K; Srinivasan Y; Hickner A; Kutler DI
Head Neck; 2024 Jan; ():. PubMed ID: 38273766
[TBL] [Abstract][Full Text] [Related]
18. Persistent Severe Hyperlactatemia and Metabolic Derangement in Lethal
Lee CH; Gundem G; Lee W; Chen YB; Cross JR; Dong Y; Redzematovic A; Mano R; Wei EY; Cheng EH; Srinivasan R; Oschwald D; Hakimi AA; Dunphy MP; Linehan WM; Papaemmanuil E; Hsieh JJ
JCO Precis Oncol; 2017 May; 1():. PubMed ID: 35172488
[TBL] [Abstract][Full Text] [Related]
19.
de Jong MAM; Corssmit EPM; Jansen JC; Potjer TP; Bayley JL; Hensen EF
Case Rep Otolaryngol; 2024; 2024():2111531. PubMed ID: 38549682
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]