Zespół von Hippla-Lindaua (Polish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Zespół von Hippla-Lindaua" in Polish language version.

refsWebsite

Global rank Polish rank

21nih.gov

4^th place

7^th place

3vhl.org

low place

3web.archive.org

1^st place

2oup.com

485^th place

620^th place

2vhl-europa.org

low place

2springer.com

274^th place

376^th place

1aacrjournals.org

8,869^th place

9,541^st place

1jbc.org

4,455^th place

6,144^th place

1sciencedirect.com

149^th place

235^th place

1omim.org

4,380^th place

2,468^th place

1nature.com

234^th place

204^th place

1vhlcan.ca

low place

1vhl-uk-ireland.org

low place

1vhlfrance.org

low place

1hippel-lindau.de

low place

1vhl.it

low place

1vhl-japan.org

low place

1msn.com

117^th place

278^th place

aacrjournals.org

cancerres.aacrjournals.org

Zatyka M, da Silva NF, Clifford SC, Morris MR, Wiesener MS, Eckardt KU, Houlston RS, Richards FM, Latif F, Maher ER. Identification of cyclin D1 and other novel targets for the von Hippel-Lindau tumor suppressor gene by expression array analysis and investigation of cyclin D1 genotype as a modifier in von Hippel-Lindau disease. „Cancer Res”. 62. 13, s. 3803–3811, 2002. PMID: 12097293.

hippel-lindau.de

Hippel-Lindau.de. [dostęp 2007-07-22].

jbc.org

Okuda H, Saitoh K, Hirai S, Iwai K, Takaki Y, Baba M, Minato N, Ohno S, Shuin T. The von Hippel-Lindau tumor suppressor protein mediates ubiquitination of activated atypical protein kinase C. „J Biol Chem”. 276(47):43611-7, 2001. PMID: 11574546.

msn.com

msnbc.msn.com

Hatfield-McCoy feud blamed on ‘rage’ disease. [dostęp 2007-07-26].

nature.com

Ang SO, Chen H, Hirota K, Gordeuk VR, Jelinek J, Guan Y, Liu E, Sergueeva AI, Miasnikova GY, Mole D, Maxwell PH, Stockton DW, Semenza GL, Prchal JT. Disruption of oxygen homeostasis underlies congenital Chuvash polycythemia. „Nature Genetics”. 32. 4, s. 614–621, 2002. PMID: 12415268.

nih.gov

ncbi.nlm.nih.gov

Maher ER, Iselius L, Yates JRW, Littler M, Benjamin C, Harris R, Sampson J, Williams A, Ferguson-Smith MA, Morton N. Von Hippel-Lindau disease: a genetic study. „J Med Genet”. 28, s. 443–447, 1991. PMID: 1895313.
Neumann HPH, Wiestler OD. Clustering of features of von Hippel-Lindau syndrome: evidence for a complex genetic locus. „Lancet”. 337, s. 1052–1054, 1991. PMID: 1673491.
Knudson A. Mutation and cancer: statistical study of retinoblastoma. „Proc Natl Acad Sci U S A”. 68. 4, s. 820–823, 1971. PMID: 5279523.
Sgambati MT, Stolle C, Choyke PL, Walther MM, Pack S, Linehan WM, Glenn GM. Mosaicism in von Hippel-Lindau disease: lessons from kindreds with germline mutations identified in offspring with mosaic parents. „Am J Hum Genet”. 66. 1, s. 84–91, 2000. PMID: 10631138.
Zatyka M, da Silva NF, Clifford SC, Morris MR, Wiesener MS, Eckardt KU, Houlston RS, Richards FM, Latif F, Maher ER. Identification of cyclin D1 and other novel targets for the von Hippel-Lindau tumor suppressor gene by expression array analysis and investigation of cyclin D1 genotype as a modifier in von Hippel-Lindau disease. „Cancer Res”. 62. 13, s. 3803–3811, 2002. PMID: 12097293.
Shuin, T, Yamasaki, I, Tamura, K, Okuda, H, Furihata, M, Ashida, S. Von Hippel-Lindau disease: molecular pathological basis, clinical criteria, genetic testing, clinical features of tumors and treatment. „Japanese Journal of Clinical Oncology”. 36. 6, s. 337–343, 2006. PMID: 16818478.
Okuda H, Saitoh K, Hirai S, Iwai K, Takaki Y, Baba M, Minato N, Ohno S, Shuin T. The von Hippel-Lindau tumor suppressor protein mediates ubiquitination of activated atypical protein kinase C. „J Biol Chem”. 276(47):43611-7, 2001. PMID: 11574546.
Lee S, Nakamura E, Yang H, Wei W, Linggi MS, Sajan MP, Farese RV, Freeman RS, Carter BD, Kaelin WG, Schlisio S. Neuronal apoptosis linked to EglN3 prolyl hydroxylase and familial pheochromocytoma genes: developmental culling and cancer. „Cancer Cell”. 8. 2, s. 155–167, 2005. PMID: 16098468.
Manski TJ, Heffner DK, Glenn GM, Patronas NJ, Pikus AT, Katz D, Lebovics R, Sledjeski K, Choyke PL, Zbar B, Linehan WM, Oldfield EH. Endolymphatic sac tumors: a source of morbid hearing loss in von Hippel-Lindau disease. „JAMA”. 277, s. 1461–1466, 1997. PMID: 9145719.
Erbe, RW. Cabot case. „New Eng J Med”. 298, s. 95–101, 1978. PMID: 413035.
Ang SO, Chen H, Hirota K, Gordeuk VR, Jelinek J, Guan Y, Liu E, Sergueeva AI, Miasnikova GY, Mole D, Maxwell PH, Stockton DW, Semenza GL, Prchal JT. Disruption of oxygen homeostasis underlies congenital Chuvash polycythemia. „Nature Genetics”. 32. 4, s. 614–621, 2002. PMID: 12415268.
Maher ER, Yates JR, Harries R, Benjamin C, Harris R, Moore AT, Ferguson-Smith MA. Clinical features and natural history of von Hippel-Lindau disease. „Q J Med”. 77, s. 1151–1163, 1990. PMID: 2274658.
Przez lata studentów medycyny uczono, że 10% pheochromocytoma występuje obustronnie, 10% występuje poza nadnerczami, 10% jest złośliwych i 10% związanych jest z zespołami rodzinnymi. Zobacz: Vinay Kumar, Ramzi S. Cotran, Stanley L. Robbins: Patologia Robinsa. Wrocław: Urban & Partner, 2005. ISBN 0-7216-9274-5. i Dluhy, RG. Pheochromocytoma--death of an axiom. „The New England Journal of Medicine”. 346. 19, s. 1486–1488, 9 maja. PMID: 12000821.
Brugarolas J. Renal-Cell Carcinoma – Molecular Pathways and Therapies. „New England Journal of Medicine”. 356. 2. s. 185–187. PMID: 17215538.
Choyke PL, Glenn GM, Walther MM, Patronas NJ, Linehan WM, Zbar B. von Hippel-Lindau disease: genetic, clinical, and imaging features. „Radiology”. 194. 3, s. 629–642, 1995. PMID: 7862955.
Atuk NO, Stolle C, Owen JA Jr., Vance ML. Pheochromocytoma in von Hippel-Lindau disease: clinical presentation and mutation analysis in a large, multigenerational kindred. „Clin Endocrinol Metab”. 83. 1, s. 117–120, 1998. PMID: 9435426.
Melmon KL, Rosen SW. Lindau’s disease: review of the literature and study of a large kindred. „Am J Med”. 36, s. 595–617, 1964. PMID: 14142412.
Latif, F, Tory, K, Gnarra, J, Yao, M, Duh, FM, Orcutt, ML, Stackhouse, T, Kuzmin, I, Modi, W, Geil, L, et al. Identification of the von Hippel-Lindau disease tumor suppressor gene. „Science”. 260. 5112, s. 1235, 1993. PMID: 8493574.
Brauch, H, Kishida, T, Glavac, D, Chen, F, Pausch, F, Höfler, H, Latif, F, Lerman, MI, Zbar, B, Neumann, HP. Von Hippel-Lindau (VHL) disease with pheochromocytoma in the Black Forest region of Germany: evidence for a founder effect. „Hum Genet”. 95. 5, s. 551–556, 1995. PMID: 7759077.
Hoffman, MA, Ohh, M, Yang, H, Kico, JM, Ivan, M, Kaelin, WG, Jr. von Hippel-Lindau, protein mutants linked to type 2C VHL disease preserve the ability to downregulated HIF. „Hum Molec Genet”. 10, s. 1019–1027, 2001. PMID: 11331612.

pubmedcentral.nih.gov

Sgambati MT, Stolle C, Choyke PL, Walther MM, Pack S, Linehan WM, Glenn GM. Mosaicism in von Hippel-Lindau disease: lessons from kindreds with germline mutations identified in offspring with mosaic parents. „Am J Hum Genet”. 66. 1, s. 84–91, 2000. PMID: 10631138.

omim.org

Online Mendelian Inheritance in Man. 2007. [dostęp 2007-07-26].

oup.com

academic.oup.com

Shuin, T, Yamasaki, I, Tamura, K, Okuda, H, Furihata, M, Ashida, S. Von Hippel-Lindau disease: molecular pathological basis, clinical criteria, genetic testing, clinical features of tumors and treatment. „Japanese Journal of Clinical Oncology”. 36. 6, s. 337–343, 2006. PMID: 16818478.
Hoffman, MA, Ohh, M, Yang, H, Kico, JM, Ivan, M, Kaelin, WG, Jr. von Hippel-Lindau, protein mutants linked to type 2C VHL disease preserve the ability to downregulated HIF. „Hum Molec Genet”. 10, s. 1019–1027, 2001. PMID: 11331612.

sciencedirect.com

Lee S, Nakamura E, Yang H, Wei W, Linggi MS, Sajan MP, Farese RV, Freeman RS, Carter BD, Kaelin WG, Schlisio S. Neuronal apoptosis linked to EglN3 prolyl hydroxylase and familial pheochromocytoma genes: developmental culling and cancer. „Cancer Cell”. 8. 2, s. 155–167, 2005. PMID: 16098468.

springer.com

link.springer.com

von Hippel, E. Über eine sehr seltene Erkrankung der Netzhaut. „Albrecht von Graefes Arch Ophthal”. 59, s. 83–106, 1904.
von Hippel E. Die anatomische Grundlage der von mir beschrieben „sehr seltene Erkrankung der Netzhaut”. „Albrecht von Graefes Arch Ophthal”. 79, s. 350–377, 1911.

vhl-europa.org

Polski rejestr VHL powstał w 1997 roku przy Ośrodku Nowotworów Dziedzicznych w Szczecinie VHL Polska. [dostęp 2007-07-22].
VHL Switzerland. [dostęp 2007-07-22]. [zarchiwizowane z tego adresu (2 września 2007)].

vhl-japan.org

VHL Japan. [dostęp 2007-07-22].

vhl-uk-ireland.org

VHL UK/Ireland. [dostęp 2007-07-22].

vhl.it

VHL Italia. [dostęp 2007-07-22].

vhl.org

VHL Alliance USA. [dostęp 2007-07-22].
VHL Belgie. [dostęp 2007-07-22]. [zarchiwizowane z tego adresu (2003-08-11)].
VHL Alliance USA Newsletter. [dostęp 2007-07-26]. [zarchiwizowane z tego adresu (28 września 2007)].

vhlcan.ca

VHL Canada. [dostęp 2007-07-22].

vhlfrance.org

VHL France. [dostęp 2007-07-22].

web.archive.org

VHL Belgie. [dostęp 2007-07-22]. [zarchiwizowane z tego adresu (2003-08-11)].
VHL Switzerland. [dostęp 2007-07-22]. [zarchiwizowane z tego adresu (2 września 2007)].
VHL Alliance USA Newsletter. [dostęp 2007-07-26]. [zarchiwizowane z tego adresu (28 września 2007)].