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22. Renal cell carcinoma in a von Hippel-Lindau syndrome: when should phaeochromocytoma be anticipated? Azarisman SM, Nor Azmi K. Singapore Med J; 2007 Aug; 48(8):779-82. PubMed ID: 17657389 [Abstract] [Full Text] [Related]
23. Bilateral renal carcinoma in von Hippel-Lindau Disease. Mullin EM, White RD, Peterson LJ, Paulson DF. Urology; 1976 Nov; 8(5):475-8. PubMed ID: 982734 [Abstract] [Full Text] [Related]
24. Relation between syringomyelia and von Hippel-Lindau's disease. De Reuck J, Alva J, Roels H, vander Eecken H. Eur Neurol; 1974 Nov; 12(2):116-27. PubMed ID: 4139014 [No Abstract] [Full Text] [Related]
25. [A case of renal cell carcinoma associated with von Hippel-Lindau disease]. Matsuda J, Kawashima H, Nakatani T, Kishimoto T. Hinyokika Kiyo; 1993 Oct; 39(10):931-3. PubMed ID: 8266858 [Abstract] [Full Text] [Related]
26. Prevalence of microscopic lesions in grossly normal renal parenchyma from patients with von Hippel-Lindau disease, sporadic renal cell carcinoma and no renal disease: clinical implications. Walther MM, Lubensky IA, Venzon D, Zbar B, Linehan WM. J Urol; 1995 Dec; 154(6):2010-4; discussion 2014-5. PubMed ID: 7500446 [Abstract] [Full Text] [Related]
27. Von Hippel-Lindau disease: analysis of two families. Bilge T, Ozveren F, Senol S, Bilge S, Barut S, Karakaslar O, Aydin Y. Neurochirurgia (Stuttg); 1992 Nov; 35(6):204-6. PubMed ID: 1494415 [Abstract] [Full Text] [Related]
28. Bilateral renal cell carcinoma in von Hippel-Lindau syndrome: treatment with staged bilateral nephrectomy and hemodialysis. Fetner CD, Barilla DE, Scott T, Ballard J, Peters P. J Urol; 1977 Apr; 117(4):534-6. PubMed ID: 850326 [No Abstract] [Full Text] [Related]
29. Multifocal bilateral renal cell carcinoma and retinal angiomas in a patient with de novo von Hippel-Lindau disease: identification of a new germline mutation. Sessa A, Battini G, Meroni M, Pitingolo F, Righetti M, Ciotti P, Di Maria E, Bellone E, Ajmar F, Mandich P. J Nephrol; 2005 Apr; 18(2):209-12. PubMed ID: 15931650 [Abstract] [Full Text] [Related]
33. [A case of Von Hippel-Lindau disease: an often severe, multiorgan, hereditary phakomatosis]. Leport M, Garnier A, Massin P, D'Hermies F, Pouliquen Y. Bull Soc Ophtalmol Fr; 1989 Jan; 89(1):11-2, 15-6. PubMed ID: 2598365 [No Abstract] [Full Text] [Related]