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PMC Full-Text Search Results

Items: 8

1.
Optimal management of hereditary hemorrhagic telangiectasia
Neetika Garg, Monica Khunger, Arjun Gupta, Nilay Kumar
J Blood Med. 2014; 5: 191–206. Published online 2014 Oct 15. doi: 10.2147/JBM.S45295
PMCID:
PMC4206399
AbstractArticlePDF–350K
2.
Update on the Molecular Genetics of Vascular Anomalies
QING K. WANG
Lymphat Res Biol. Author manuscript; available in PMC 2006 Sep 28.
Published in final edited form as: Lymphat Res Biol. 2005; 3(4): 226–233. doi: 10.1089/lrb.2005.3.226
PMCID:
PMC1579841
AbstractArticlePDF–59K
3.
Biomedicine and diseases: the Klippel-Trenaunay syndrome, vascular anomalies and vascular morphogenesis
A. A. Timur, D. J. Driscoll, Q. Wang
Cell Mol Life Sci. 2005 Jul; 62(13): 1434–1447. Published online 2005 May 18. doi: 10.1007/s00018-005-4523-7
PMCID:
PMC1579804
AbstractArticlePDF–420K
4.
Somatic Activating RAS Mutations Cause Vascular Tumors Including Pyogenic Granuloma
Young H. Lim, Stephanie R. Douglas, Christine J. Ko, Richard J. Antaya, Jennifer M. McNiff, Jing Zhou, Yale Center for Genome Analysis, Keith A. Choate, Deepak Narayan
J Invest Dermatol. Author manuscript; available in PMC 2015 Dec 1.
Published in final edited form as: J Invest Dermatol. 2015 Jun; 135(6): 1698–1700. Published online 2015 Feb 19. doi: 10.1038/jid.2015.55
PMCID:
PMC4430357
ArticlePDF–1.0M
5.
Mutation affecting the proximal promoter of Endoglin as the origin of hereditary hemorrhagic telangiectasia type 1
Virginia Albiñana, Ma Paz Zafra, Jorge Colau, Roberto Zarrabeitia, Lucia Recio-Poveda, Leticia Olavarrieta, Julián Pérez-Pérez, Luisa M. Botella
BMC Med Genet. 2017; 18: 20. Published online 2017 Feb 23. doi: 10.1186/s12881-017-0380-0
PMCID:
PMC5324315
AbstractArticlePDF–812K
6.
A Review of Vascular Anomalies: Genetics and Common Syndromes
Elizabeth Killion, Kriti Mohan, Edward I. Lee
Semin Plast Surg. 2014 May; 28(2): 64–68. doi: 10.1055/s-0034-1376261
PMCID:
PMC4078216
AbstractArticlePDF–99K
7.
Heart Failure and Pulmonary Hypertension
Jordan T. Shin, Marc J. Semigran
Heart Fail Clin. Author manuscript; available in PMC 2011 Apr 1.
Published in final edited form as: Heart Fail Clin. 2010 Apr; 6(2): 215–222. doi: 10.1016/j.hfc.2009.11.007
PMCID:
PMC2847580
AbstractArticlePDF–57K
8.
BMPR2 Haploinsufficiency as the Inherited Molecular Mechanism for Primary Pulmonary Hypertension
Rajiv D Machado, Michael W. Pauciulo, Jennifer R. Thomson, Kirk B. Lane, Neil V. Morgan, Lisa Wheeler, John A. Phillips III, John Newman, Denise Williams, Nazzareno Galiè, Alessandra Manes, Keith McNeil, Magdi Yacoub, Ghada Mikhail, Paula Rogers, Paul Corris, Marc Humbert, Dian Donnai, Gunnar Martensson, Lisbeth Tranebjaerg, James E. Loyd, Richard C. Trembath, William C. Nichols
Am J Hum Genet. 2001 Jan; 68(1): 92–102. Published online 2000 Dec 12. doi: 10.1086/316947
PMCID:
PMC1234937
AbstractArticlePDF–679K

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