Similar articles for PMID: 10735135

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1

[Von Hippel-Lindau disease: protocols for diagnosis and periodical clinical monitoring. National Von Hippel-Lindau Disease Working Group].

Hes FJ, van der Luijt RB. Hes FJ, et al. Ned Tijdschr Geneeskd. 2000 Mar 11;144(11):505-9. Ned Tijdschr Geneeskd. 2000. PMID: 10735135 Dutch.

2

[From gene to disease; Von Hippel-Lindau disease].

Hes FJ, Los M, van der Luijt RB. Hes FJ, et al. Ned Tijdschr Geneeskd. 2002 Jul 20;146(29):1364-7. Ned Tijdschr Geneeskd. 2002. PMID: 12162174 Review. Dutch.

3

Frequency of Von Hippel-Lindau germline mutations in classic and non-classic Von Hippel-Lindau disease identified by DNA sequencing, Southern blot analysis and multiplex ligation-dependent probe amplification.

Hes FJ, van der Luijt RB, Janssen AL, Zewald RA, de Jong GJ, Lenders JW, Links TP, Luyten GP, Sijmons RH, Eussen HJ, Halley DJ, Lips CJ, Pearson PL, van den Ouweland AM, Majoor-Krakauer DF. Hes FJ, et al. Clin Genet. 2007 Aug;72(2):122-9. doi: 10.1111/j.1399-0004.2007.00827.x. Clin Genet. 2007. PMID: 17661816

4

[von Hippel-Lindau hereditary tumor syndrome. Mutational analysis may improve prognosis].

Wiklund L, Nordling M, Engwall Y, Martinsson T, Szentgyörgyi E, Wahlström J. Wiklund L, et al. Lakartidningen. 1995 Mar 15;92(11):1093-6. Lakartidningen. 1995. PMID: 7700111 Swedish.

5

Juvenile renal cell carcinoma as first manifestation of von Hippel-Lindau disease.

Granata A, Sessa A, Righetti M, Cordaro S, Leone G, Figura M, Fatuzzo P, Rapisarda F, Di Maria E, Ciotti P, Mandich P, Nardo A, Ferrone M, Gallone S, Liuzzo G. Granata A, et al. J Nephrol. 2004 Mar-Apr;17(2):306-10. J Nephrol. 2004. PMID: 15293534

6

[von Hippel-Lindau syndrome: molecular diagnosis of two Lebanese families and analysis of the genotype-phenotype correlation].

Medlej-Hashim M, Leclercq A, Salem N, Moukarzel M, Merhej S, Pigny P, Megarbane A. Medlej-Hashim M, et al. J Med Liban. 2004 Jan-Mar;52(1):51-4. J Med Liban. 2004. PMID: 15881703 French.

7

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. Sessa A, et al. J Nephrol. 2005 Mar-Apr;18(2):209-12. J Nephrol. 2005. PMID: 15931650

8

Constitutional von Hippel-Lindau (VHL) gene deletions detected in VHL families by fluorescence in situ hybridization.

Pack SD, Zbar B, Pak E, Ault DO, Humphrey JS, Pham T, Hurley K, Weil RJ, Park WS, Kuzmin I, Stolle C, Glenn G, Liotta LA, Lerman MI, Klausner RD, Linehan WM, Zhuang Z. Pack SD, et al. Cancer Res. 1999 Nov 1;59(21):5560-4. Cancer Res. 1999. PMID: 10554035

9

[Von Hippel-Lindau disease].

Los M, Links TP, Lenders JW, Voest EE. Los M, et al. Ned Tijdschr Geneeskd. 2000 Mar 11;144(11):497-501. Ned Tijdschr Geneeskd. 2000. PMID: 10735133 Review. Dutch.

10

Von Hippel-Lindau disease (vHL). National clinical guideline for diagnosis and surveillance in Denmark. 3rd edition.

Binderup ML, Bisgaard ML, Harbud V, Møller HU, Gimsing S, Friis-Hansen L, Hansen Tv, Bagi P, Knigge U, Kosteljanetz M, Bøgeskov L, Thomsen C, Gerdes AM, Ousager LB, Sunde L; Danish vHL Coordination Group. Binderup ML, et al. Dan Med J. 2013 Dec;60(12):B4763. Dan Med J. 2013. PMID: 24355456 Free article.

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