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Journal Abstract Search

241 related items for PubMed ID: 17922902

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  • 23. Pheochromocytoma in a 2.75-year-old-girl with a germline von Hippel-Lindau mutation Q164R.
    Sovinz P, Urban C, Uhrig S, Stepan V, Lackner H, Schwinger W, Benesch M, Moser A, Spuller E, Speicher MR.
    Am J Med Genet A; 2010 Jul; 152A(7):1752-5. PubMed ID: 20583150
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  • 25. Discovering a novel genetic variant in 11 family members who had isolated pheochromocytoma linked to von Hippel-Lindau (VHL) syndrome, aligning with the type 2c phenotype.
    Alhawari H, Obeidat Z, Wahbeh L, Mismar A, Younis N, Jafar H, Momani M, Alsabatin N, Awidi A, Alhawari H.
    Blood Press; 2024 Dec; 33(1):2355268. PubMed ID: 38824681
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  • 26. Differential expression of erythropoietin and its receptor in von hippel-lindau-associated and multiple endocrine neoplasia type 2-associated pheochromocytomas.
    Vogel TW, Brouwers FM, Lubensky IA, Vortmeyer AO, Weil RJ, Walther MM, Oldfield EH, Linehan WM, Pacak K, Zhuang Z.
    J Clin Endocrinol Metab; 2005 Jun; 90(6):3747-51. PubMed ID: 15769989
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  • 29. von Hippel Lindau disease with colon adenocarcinoma, renal cell carcinoma and adrenal pheochromocytoma.
    Zinnamosca L, Laudisi A, Petramala L, Marinelli C, Roselli M, Vitolo D, Montesani C, Letizia C.
    Intern Med; 2013 Jun; 52(14):1599-603. PubMed ID: 23857093
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  • 31. A novel von Hippel-Lindau point mutation presents as apparently sporadic pheochromocytoma.
    Rich TA, Jonasch E, Matin S, Waguespack SG, Gombos DS, Santarpia L, Stolle C, Jimenez C.
    Cancer Invest; 2008 Jul; 26(6):642-6. PubMed ID: 18584357
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  • 32. Brain Tumor, Pheochromocytoma, and Pregnancy: A Case Report of a Cesarean Delivery in a Patient With Von Hippel-Lindau Disease.
    Burnette MS, Mann TS, Berman DJ, Nguyen TT.
    A A Pract; 2019 Oct 15; 13(8):289-291. PubMed ID: 31206381
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  • 35. Laparoscopic bilateral cortical-sparing adrenalectomy for pheochromocytoma.
    Biteman BR, Randall JA, Brody F.
    Surg Endosc; 2016 Dec 15; 30(12):5622-5623. PubMed ID: 27177950
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  • 37. Isolated familial pheochromocytoma as a variant of von Hippel-Lindau disease.
    Ritter MM, Frilling A, Crossey PA, Höppner W, Maher ER, Mulligan L, Ponder BA, Engelhardt D.
    J Clin Endocrinol Metab; 1996 Mar 15; 81(3):1035-7. PubMed ID: 8772572
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  • 39. Bilateral pheochromocytoma as first presentation of von Hippel-Lindau disease in a Chinese family.
    Tong AL, Zeng ZP, Zhou YR, Yuan T, Cao CX, Zhang J, Li M.
    Chin Med Sci J; 2009 Dec 15; 24(4):197-201. PubMed ID: 20120764
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  • 40. Abdominal visceral lesions in von Hippel-Lindau disease: incidence and clinical behavior of pancreatic and adrenal lesions at a single center.
    Delman KA, Shapiro SE, Jonasch EW, Lee JE, Curley SA, Evans DB, Perrier ND.
    World J Surg; 2006 May 15; 30(5):665-9. PubMed ID: 16617420
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