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    Results: 1 to 20 of 56

    1.

    Genetic aspects of pheochromocytoma.

    Kolačkov K, Tupikowski K, Bednarek-Tupikowska G.

    Adv Clin Exp Med. 2012 Nov-Dec;21(6):821-9. Review.

    PMID:
    23457139
    [PubMed - indexed for MEDLINE]
    2.

    Immunohistochemical loss of succinate dehydrogenase subunit A (SDHA) in gastrointestinal stromal tumors (GISTs) signals SDHA germline mutation.

    Miettinen M, Killian JK, Wang ZF, Lasota J, Lau C, Jones L, Walker R, Pineda M, Zhu YJ, Kim SY, Helman L, Meltzer P.

    Am J Surg Pathol. 2013 Feb;37(2):234-40. doi: 10.1097/PAS.0b013e3182671178.

    PMID:
    23282968
    [PubMed - indexed for MEDLINE]
    3.

    Imaging work-up for screening of paraganglioma and pheochromocytoma in SDHx mutation carriers: a multicenter prospective study from the PGL.EVA Investigators.

    Gimenez-Roqueplo AP, Caumont-Prim A, Houzard C, Hignette C, Hernigou A, Halimi P, Niccoli P, Leboulleux S, Amar L, Borson-Chazot F, Cardot-Bauters C, Delemer B, Chabolle F, Coupier I, Libé R, Peitzsch M, Peyrard S, Tenenbaum F, Plouin PF, Chatellier G, Rohmer V.

    J Clin Endocrinol Metab. 2013 Jan;98(1):E162-73. doi: 10.1210/jc.2012-2975. Epub 2012 Nov 15.

    PMID:
    23162105
    [PubMed - indexed for MEDLINE]
    4.

    Succinate dehydrogenase kidney cancer: an aggressive example of the Warburg effect in cancer.

    Ricketts CJ, Shuch B, Vocke CD, Metwalli AR, Bratslavsky G, Middelton L, Yang Y, Wei MH, Pautler SE, Peterson J, Stolle CA, Zbar B, Merino MJ, Schmidt LS, Pinto PA, Srinivasan R, Pacak K, Linehan WM.

    J Urol. 2012 Dec;188(6):2063-71. doi: 10.1016/j.juro.2012.08.030. Epub 2012 Oct 18.

    PMID:
    23083876
    [PubMed - indexed for MEDLINE]
    5.

    Loss of SDHA expression identifies SDHA mutations in succinate dehydrogenase-deficient gastrointestinal stromal tumors.

    Dwight T, Benn DE, Clarkson A, Vilain R, Lipton L, Robinson BG, Clifton-Bligh RJ, Gill AJ.

    Am J Surg Pathol. 2013 Feb;37(2):226-33. doi: 10.1097/PAS.0b013e3182671155.

    PMID:
    23060355
    [PubMed - indexed for MEDLINE]
    6.

    Integrative genomics reveals frequent somatic NF1 mutations in sporadic pheochromocytomas.

    Welander J, Larsson C, Bäckdahl M, Hareni N, Sivlér T, Brauckhoff M, Söderkvist P, Gimm O.

    Hum Mol Genet. 2012 Dec 15;21(26):5406-16. doi: 10.1093/hmg/dds402. Epub 2012 Sep 24.

    PMID:
    23010473
    [PubMed - indexed for MEDLINE]
    7.

    Necessity for long-term follow-up of patients with head and neck paraganglioma and mutation in the succinate dehydrogenase genes: an index case report and literature review.

    Samji KB, Crown AL, Buxton-Thomas MS, Aylwin SJ, Schulte KM, Dizdarevic S.

    Endocr Pract. 2012 Sep-Oct;18(5):e130-4. doi: 10.4158/EP11184.CR. Review.

    PMID:
    22982783
    [PubMed - indexed for MEDLINE]
    Free Article
    8.

    Recessive germline SDHA and SDHB mutations causing leukodystrophy and isolated mitochondrial complex II deficiency.

    Alston CL, Davison JE, Meloni F, van der Westhuizen FH, He L, Hornig-Do HT, Peet AC, Gissen P, Goffrini P, Ferrero I, Wassmer E, McFarland R, Taylor RW.

    J Med Genet. 2012 Sep;49(9):569-77. doi: 10.1136/jmedgenet-2012-101146.

    PMID:
    22972948
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    9.

    Somatic NF1 inactivation is a frequent event in sporadic pheochromocytoma.

    Burnichon N, Buffet A, Parfait B, Letouzé E, Laurendeau I, Loriot C, Pasmant E, Abermil N, Valeyrie-Allanore L, Bertherat J, Amar L, Vidaud D, Favier J, Gimenez-Roqueplo AP.

    Hum Mol Genet. 2012 Dec 15;21(26):5397-405. doi: 10.1093/hmg/dds374. Epub 2012 Sep 6.

    PMID:
    22962301
    [PubMed - indexed for MEDLINE]
    10.

    Correlation of the genotype of paragangliomas and pheochromocytomas with their metabolic phenotype on 3,4-dihydroxy-6-18F-fluoro-L-phenylalanin PET.

    Rischke HC, Benz MR, Wild D, Mix M, Dumont RA, Campbell D, Seufert J, Wiech T, Rössler J, Weber WA, Neumann HP.

    J Nucl Med. 2012 Sep;53(9):1352-8. doi: 10.2967/jnumed.111.101303. Epub 2012 Jul 26.

    PMID:
    22836345
    [PubMed - indexed for MEDLINE]
    11.

    Succinate dehydrogenase-deficient tumors: diagnostic advances and clinical implications.

    Barletta JA, Hornick JL.

    Adv Anat Pathol. 2012 Jul;19(4):193-203. doi: 10.1097/PAP.0b013e31825c6bc6. Review.

    PMID:
    22692282
    [PubMed - indexed for MEDLINE]
    12.

    Carney Stratakis syndrome in a patient with SDHD mutation.

    Tenorio Jiménez C, Izatt L, Chang F, Moonim MT, Carroll PV, McGowan BM.

    Endocr Pathol. 2012 Sep;23(3):181-6. doi: 10.1007/s12022-012-9213-z. No abstract available.

    PMID:
    22638655
    [PubMed - indexed for MEDLINE]
    13.

    Over-representation of the G12S polymorphism of the SDHD gene in patients with MEN2A syndrome.

    Lendvai N, Tóth M, Valkusz Z, Bekő G, Szücs N, Csajbók E, Igaz P, Kriszt B, Kovács B, Rácz K, Patócs A.

    Clinics (Sao Paulo). 2012;67 Suppl 1:85-9.

    PMID:
    22584711
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    14.

    Head and neck paragangliomas: clinical and molecular genetic classification.

    Offergeld C, Brase C, Yaremchuk S, Mader I, Rischke HC, Gläsker S, Schmid KW, Wiech T, Preuss SF, Suárez C, Kopeć T, Patocs A, Wohllk N, Malekpour M, Boedeker CC, Neumann HP.

    Clinics (Sao Paulo). 2012;67 Suppl 1:19-28. Review.

    PMID:
    22584701
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    15.

    Somatic mutation analysis of the SDHB, SDHC, SDHD, and RET genes in the clinical assessment of sporadic and hereditary pheochromocytoma.

    Weber A, Hoffmann MM, Neumann HP, Erlic Z.

    Horm Cancer. 2012 Aug;3(4):187-92. doi: 10.1007/s12672-012-0113-y. Epub 2012 May 10.

    PMID:
    22573489
    [PubMed - indexed for MEDLINE]
    16.

    Prevalence and spectrum of SDHx mutations in pheochromocytoma and paraganglioma in patients from Belgium: an update.

    Persu A, Lannoy N, Maiter D, Mendola A, Montigny P, Oriot P, Vinck W, Garin P, Hamoir M, Vikkula M.

    Horm Metab Res. 2012 May;44(5):349-53. doi: 10.1055/s-0032-1311610. Epub 2012 May 7.

    PMID:
    22566194
    [PubMed - indexed for MEDLINE]
    17.

    Genetic and clinical characteristics of head and neck paragangliomas in a Chinese population.

    Zheng X, Wei S, Yu Y, Xia T, Zhao J, Gao S, Li Y, Gao M.

    Laryngoscope. 2012 Aug;122(8):1761-6. doi: 10.1002/lary.23360. Epub 2012 May 7.

    PMID:
    22566157
    [PubMed - indexed for MEDLINE]
    18.

    Succinate dehydrogenase (SDH) and mitochondrial driven neoplasia.

    Gill AJ.

    Pathology. 2012 Jun;44(4):285-92. doi: 10.1097/PAT.0b013e3283539932. Review.

    PMID:
    22544211
    [PubMed - indexed for MEDLINE]
    19.

    Identical germline mutations in the TMEM127 gene in two unrelated Japanese patients with bilateral pheochromocytoma.

    Takeichi N, Midorikawa S, Watanabe A, Naing BT, Tamura H, Wakakuri-Kano T, Ishizaki A, Sugihara H, Nissato S, Saito Y, Aita Y, Ishii KA, Igarashi T, Kawakami Y, Hara H, Ikeda T, Shimizu K, Suzuki S, Shimano H, Kawamoto M, Shimada T, Watanabe T, Oikawa S, Takekoshi K.

    Clin Endocrinol (Oxf). 2012 Nov;77(5):707-14. doi: 10.1111/j.1365-2265.2012.04421.x.

    PMID:
    22541004
    [PubMed - indexed for MEDLINE]
    20.

    A decade (2001-2010) of genetic testing for pheochromocytoma and paraganglioma.

    Buffet A, Venisse A, Nau V, Roncellin I, Boccio V, Le Pottier N, Boussion M, Travers C, Simian C, Burnichon N, Abermil N, Favier J, Jeunemaitre X, Gimenez-Roqueplo AP.

    Horm Metab Res. 2012 May;44(5):359-66. doi: 10.1055/s-0032-1304594. Epub 2012 Apr 19. Review.

    PMID:
    22517557
    [PubMed - indexed for MEDLINE]

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