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150 related items for PubMed ID: 16210343

  • 1. Von Hippel-Lindau-dependent polycythemia is endemic on the island of Ischia: identification of a novel cluster.
    Perrotta S, Nobili B, Ferraro M, Migliaccio C, Borriello A, Cucciolla V, Martinelli V, Rossi F, Punzo F, Cirillo P, Parisi G, Zappia V, Rotoli B, Della Ragione F.
    Blood; 2006 Jan 15; 107(2):514-9. PubMed ID: 16210343
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  • 2. Mutations of von Hippel-Lindau tumor-suppressor gene and congenital polycythemia.
    Pastore Y, Jedlickova K, Guan Y, Liu E, Fahner J, Hasle H, Prchal JF, Prchal JT.
    Am J Hum Genet; 2003 Aug 15; 73(2):412-9. PubMed ID: 12844285
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  • 3. Congenital disorder of oxygen sensing: association of the homozygous Chuvash polycythemia VHL mutation with thrombosis and vascular abnormalities but not tumors.
    Gordeuk VR, Sergueeva AI, Miasnikova GY, Okhotin D, Voloshin Y, Choyke PL, Butman JA, Jedlickova K, Prchal JT, Polyakova LA.
    Blood; 2004 May 15; 103(10):3924-32. PubMed ID: 14726398
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  • 4. The von Hippel-Lindau Chuvash mutation promotes pulmonary hypertension and fibrosis in mice.
    Hickey MM, Richardson T, Wang T, Mosqueira M, Arguiri E, Yu H, Yu QC, Solomides CC, Morrisey EE, Khurana TS, Christofidou-Solomidou M, Simon MC.
    J Clin Invest; 2010 Mar 15; 120(3):827-39. PubMed ID: 20197624
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  • 6. The heterozygote advantage of the Chuvash polycythemia VHLR200W mutation may be protection against anemia.
    Miasnikova GY, Sergueeva AI, Nouraie M, Niu X, Okhotin DJ, Polyakova LA, Ganz T, Prchal JT, Gordeuk VR.
    Haematologica; 2011 Sep 15; 96(9):1371-4. PubMed ID: 21606165
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  • 8. Disruption of oxygen homeostasis underlies congenital Chuvash polycythemia.
    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.
    Nat Genet; 2002 Dec 15; 32(4):614-21. PubMed ID: 12415268
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  • 10. Mutations in the VHL gene in sporadic apparently congenital polycythemia.
    Pastore YD, Jelinek J, Ang S, Guan Y, Liu E, Jedlickova K, Krishnamurti L, Prchal JT.
    Blood; 2003 Feb 15; 101(4):1591-5. PubMed ID: 12393546
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  • 11. Endemic polycythemia in Russia: mutation in the VHL gene.
    Ang SO, Chen H, Gordeuk VR, Sergueeva AI, Polyakova LA, Miasnikova GY, Kralovics R, Stockton DW, Prchal JT.
    Blood Cells Mol Dis; 2002 Feb 15; 28(1):57-62. PubMed ID: 11987242
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  • 20. Chuvash-type congenital polycythemia in 4 families of Asian and Western European ancestry.
    Percy MJ, McMullin MF, Jowitt SN, Potter M, Treacy M, Watson WH, Lappin TR.
    Blood; 2003 Aug 01; 102(3):1097-9. PubMed ID: 12702509
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