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178 related items for PubMed ID: 9329368
1. Functioning thoracic paraganglioma: association with Von Hippel-Lindau syndrome. Bender BU, Altehöfer C, Januszewicz A, Gärtner R, Schmidt H, Hoffmann MM, Heidemann PH, Neumann HP. J Clin Endocrinol Metab; 1997 Oct; 82(10):3356-60. PubMed ID: 9329368 [Abstract] [Full Text] [Related]
2. 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 [Abstract] [Full Text] [Related]
3. Germline mutations in the von Hippel-Lindau disease tumor suppressor gene: correlations with phenotype. Chen F, Kishida T, Yao M, Hustad T, Glavac D, Dean M, Gnarra JR, Orcutt ML, Duh FM, Glenn G. Hum Mutat; 1995 May; 5(1):66-75. PubMed ID: 7728151 [Abstract] [Full Text] [Related]
4. 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 18; 329(21):1531-8. PubMed ID: 8105382 [Abstract] [Full Text] [Related]
5. Parasympathetic paragangliomas are part of the Von Hippel-Lindau syndrome. Gaal J, van Nederveen FH, Erlic Z, Korpershoek E, Oldenburg R, Boedeker CC, Kontny U, Neumann HP, Dinjens WN, de Krijger RR. J Clin Endocrinol Metab; 2009 Nov 18; 94(11):4367-71. PubMed ID: 19808854 [Abstract] [Full Text] [Related]
6. Identification of novel SDHD mutations in patients with phaeochromocytoma and/or paraganglioma. Cascon A, Ruiz-Llorente S, Cebrian A, Telleria D, Rivero JC, Diez JJ, Lopez-Ibarra PJ, Jaunsolo MA, Benitez J, Robledo M. Eur J Hum Genet; 2002 Aug 18; 10(8):457-61. PubMed ID: 12111639 [Abstract] [Full Text] [Related]
7. Retroperitoneal paraganglioma with loss of heterozygosity of the von Hippel-Lindau gene: a case report and review of the literature. Anno M, Izawa S, Fujioka Y, Matsuzawa K, Saito K, Hikita K, Makishima K, Nosaka K, Takenaka A, Usui T, Yamamoto K. Endocr J; 2022 Sep 28; 69(9):1137-1147. PubMed ID: 35466127 [Abstract] [Full Text] [Related]
8. Pathogenicity of DNA variants and double mutations in multiple endocrine neoplasia type 2 and von Hippel-Lindau syndrome. Erlic Z, Hoffmann MM, Sullivan M, Franke G, Peczkowska M, Harsch I, Schott M, Gabbert HE, Valimäki M, Preuss SF, Hasse-Lazar K, Waligorski D, Robledo M, Januszewicz A, Eng C, Neumann HP. J Clin Endocrinol Metab; 2010 Jan 28; 95(1):308-13. PubMed ID: 19906784 [Abstract] [Full Text] [Related]
11. 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 28; 94(6):1938-44. PubMed ID: 19336503 [Abstract] [Full Text] [Related]
13. Intrathoracic and multiple abdominal pheochromocytomas in von Hippel-Lindau disease. Hoffman RW, Gardner DW, Mitchell FL. Arch Intern Med; 1982 Oct 28; 142(10):1962-4. PubMed ID: 7125783 [Abstract] [Full Text] [Related]
14. Phaeochromocytoma associated with a de novo VHL mutation as form fruste of von Hippel-Lindau disease. Frenzel S, Apel TW, Heidemann PH, Zerres K, Neumann HP, Dörr HG. Eur J Pediatr; 2001 Jul 28; 160(7):421-4. PubMed ID: 11475579 [Abstract] [Full Text] [Related]
15. Bilateral pheochromocytomas and congenital anomalies associated with a de novo germline mutation in the von Hippel-Lindau gene. Assadi F, Brackbill EL. Am J Kidney Dis; 2003 Jan 28; 41(1):E3. PubMed ID: 12500216 [Abstract] [Full Text] [Related]
16. Differences in allelic distribution of two polymorphisms in the VHL-associated gene CUL2 in pheochromocytoma patients without somatic CUL2 mutations. Duerr EM, Gimm O, Neuberg DS, Kum JB, Clifford SC, Toledo SP, Maher ER, Dahia PL, Eng C. J Clin Endocrinol Metab; 1999 Sep 28; 84(9):3207-11. PubMed ID: 10487688 [Abstract] [Full Text] [Related]
17. Pheochromocytoma and multifocal functioning paraganglioma in a 9-year-old boy with von Hippel-Lindau disease. Tröbs RB, Reichardt P, Friedrich T, Klöppel R, Bennek J. Urol Int; 2002 Sep 28; 68(4):299-301. PubMed ID: 12053037 [Abstract] [Full Text] [Related]
18. How many pathways to pheochromocytoma? Neumann HP, Hoegerle S, Manz T, Brenner K, Iliopoulos O. Semin Nephrol; 2002 Mar 28; 22(2):89-99. PubMed ID: 11891502 [Abstract] [Full Text] [Related]
19. Genetic screening for von Hippel-Lindau gene mutations in non-syndromic pheochromocytoma: low prevalence and false-positives or misdiagnosis indicate a need for caution. Eisenhofer G, Vocke CD, Elkahloun A, Huynh TT, Prodanov T, Lenders JW, Timmers HJ, Benhammou JN, Linehan WM, Pacak K. Horm Metab Res; 2012 May 28; 44(5):343-8. PubMed ID: 22438210 [Abstract] [Full Text] [Related]
20. 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 28; 90(6):3747-51. PubMed ID: 15769989 [Abstract] [Full Text] [Related] Page: [Next] [New Search]