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Results: 1 to 20 of 28

Related Articles by Review for PubMed (Select 15521985)

1.

Mutations in endoglin and in activin receptor-like kinase 1 among Danish patients with hereditary haemorrhagic telangiectasia.

Brusgaard K, Kjeldsen AD, Poulsen L, Moss H, Vase P, Rasmussen K, Kruse TA, Hørder M.

Clin Genet. 2004 Dec;66(6):556-61.

PMID:
15521985
2.

Hereditary hemorrhagic telangiectasia: an update on clinical manifestations and diagnostic measures.

Sadick H, Sadick M, Götte K, Naim R, Riedel F, Bran G, Hörmann K.

Wien Klin Wochenschr. 2006 Mar;118(3-4):72-80. Review.

PMID:
16703249
3.

[Hereditary hemorrhagic telangiectasia].

Pérez del Molino A, Zarrabeitia R, Fernández A.

Med Clin (Barc). 2005 Apr 23;124(15):583-7. Review. Spanish.

PMID:
15860174
4.

Hereditary hemorrhagic telangiectasia: an update on transforming growth factor beta signaling in vasculogenesis and angiogenesis.

van den Driesche S, Mummery CL, Westermann CJ.

Cardiovasc Res. 2003 Apr 1;58(1):20-31. Review.

5.

Molecular defects in rare bleeding disorders: hereditary haemorrhagic telangiectasia.

Shovlin CL.

Thromb Haemost. 1997 Jul;78(1):145-50. Review.

PMID:
9198145
6.

Endoglin-deficient mice, a unique model to study hereditary hemorrhagic telangiectasia.

Bourdeau A, Faughnan ME, Letarte M.

Trends Cardiovasc Med. 2000 Oct;10(7):279-85. Review.

PMID:
11343967
7.

Genetic and molecular pathogenesis of hereditary hemorrhagic telangiectasia.

Azuma H.

J Med Invest. 2000 Aug;47(3-4):81-90. Review.

PMID:
11019486
8.

Hereditary Haemorrhagic Telangiectasia (HHT): genetic and molecular aspects.

Lenato GM, Guanti G.

Curr Pharm Des. 2006;12(10):1173-93. Review.

PMID:
16611099
9.

Genetic abnormalities in hereditary hemorrhagic telangiectasia.

Marchuk DA.

Curr Opin Hematol. 1998 Sep;5(5):332-8. Review.

PMID:
9776212
10.

The molecular genetics of hereditary hemorrhagic telangiectasia.

Marchuk DA.

Chest. 1997 Jun;111(6 Suppl):79S-82S. Review. No abstract available.

PMID:
9184539
11.

Hereditary hemorrhagic telangiectasia. Genetics, pathogenesis, clinical manifestation and management.

Stuhrmann M, El-Harith el-HA.

Saudi Med J. 2007 Jan;28(1):11-21. Review.

PMID:
17206283
12.

Hereditary haemorrhagic telangiectasia: current views on genetics and mechanisms of disease.

Abdalla SA, Letarte M.

J Med Genet. 2006 Feb;43(2):97-110. Epub 2005 May 6. Review.

13.

[Analysis of genetic mutation and modifier genes in pulmonary arterial hypertension].

Fujiwara M, Yagi H, Matsuoka R, Saji T.

Nihon Rinsho. 2008 Nov;66(11):2071-5. Review. Japanese.

PMID:
19051722
14.

Hereditary haemorrhagic telangiectasia: a clinical and scientific review.

Govani FS, Shovlin CL.

Eur J Hum Genet. 2009 Jul;17(7):860-71. doi: 10.1038/ejhg.2009.35. Epub 2009 Apr 1. Review.

15.

Pulmonary vascular manifestations of hereditary hemorrhagic telangiectasia (rendu-osler disease).

Cottin V, Dupuis-Girod S, Lesca G, Cordier JF.

Respiration. 2007;74(4):361-78. Review.

PMID:
17641482
16.

[Osler hemorrhagic telangiectasia syndrome].

Hamada J, Tanaka K.

Ryoikibetsu Shokogun Shirizu. 2000;(30 Pt 5):64-5. Review. Japanese. No abstract available.

PMID:
11057144
17.

Endoglin-mediated vascular remodeling: mechanisms underlying hereditary hemorrhagic telangiectasia.

Lebrin F, Mummery CL.

Trends Cardiovasc Med. 2008 Jan;18(1):25-32. doi: 10.1016/j.tcm.2007.11.003. Review.

PMID:
18206806
18.

[Hereditary hemorragic telangiectasia: the state of art].

Colotto M, Castellano V, Anatra GM, Borgia MC.

Clin Ter. 2007 May-Jun;158(3):253-60. Review. Italian.

PMID:
17612287
19.

[Neuroimaging of hereditary hemorrhagic telangiectasia].

Bracard S, Schmitt E, Kremer S, Anxionnat R, Picard L.

J Neuroradiol. 2005 Jun;32(3):168-73. Review. French.

PMID:
16134298
20.

Involvement of the transforming growth factor beta in the pathogenesis of hereditary hemorrhagic telangiectasia.

Jirillo E, Amati L, Suppressa P, Cirimele D, Guastamacchia E, Covelli V, Tafaro E, Sabbà C.

Curr Pharm Des. 2006;12(10):1195-200. Review.

PMID:
16611100
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