Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1972 1
1975 4
1976 7
1978 1
1979 1
1980 4
1981 8
1982 1
1984 6
1985 4
1987 4
1988 7
1989 3
1990 2
1991 1
1992 3
1993 1
1994 5
1995 3
1996 1
1997 5
1998 6
1999 6
2000 7
2001 5
2002 3
2003 6
2004 8
2005 2
2006 5
2007 8
2008 8
2009 5
2010 7
2011 6
2012 11
2013 3
2014 1
2015 2
2019 1
2020 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

164 results

Results by year

Filters applied: . Clear all
Page 1
International guidelines for the diagnosis and management of hereditary haemorrhagic telangiectasia.
Faughnan ME, Palda VA, Garcia-Tsao G, Geisthoff UW, McDonald J, Proctor DD, Spears J, Brown DH, Buscarini E, Chesnutt MS, Cottin V, Ganguly A, Gossage JR, Guttmacher AE, Hyland RH, Kennedy SJ, Korzenik J, Mager JJ, Ozanne AP, Piccirillo JF, Picus D, Plauchu H, Porteous ME, Pyeritz RE, Ross DA, Sabba C, Swanson K, Terry P, Wallace MC, Westermann CJ, White RI, Young LH, Zarrabeitia R; HHT Foundation International - Guidelines Working Group. Faughnan ME, et al. Among authors: plauchu h. J Med Genet. 2011 Feb;48(2):73-87. doi: 10.1136/jmg.2009.069013. Epub 2009 Jun 23. J Med Genet. 2011. PMID: 19553198 Free article.
Toriello-Carey syndrome.
Till M, Bourgeois J, Plauchu H. Till M, et al. Among authors: plauchu h. Am J Med Genet. 1997 Jun 13;70(3):332. doi: 10.1002/(sici)1096-8628(19970613)70:3<332::aid-ajmg23>3.0.co;2-l. Am J Med Genet. 1997. PMID: 9188677 No abstract available.
[Rendu-Osler disease: clinical and molecular update].
Bailly S, Dupuis-Girod S, Plauchu H. Bailly S, et al. Among authors: plauchu h. Med Sci (Paris). 2010 Oct;26(10):855-60. doi: 10.1051/medsci/20102610855. Med Sci (Paris). 2010. PMID: 20929677 Free article. Review. French.
[Hepatic vascular malformations in Rendu-Osler disease].
Saurin JC, Dumortier J, Menard Y, Henry L, Boillot O, Plauchu H, Paliard P. Saurin JC, et al. Among authors: plauchu h. Gastroenterol Clin Biol. 2000 Jan;24(1):89-93. Gastroenterol Clin Biol. 2000. PMID: 10679590 Free article. Review. French. No abstract available.
[Ehlers-Danlos syndromes: we are all concerned].
de Wazières B, Plauchu H, Boucand MH. de Wazières B, et al. Among authors: plauchu h. Presse Med. 1998 Oct 17;27(31):1582-4. Presse Med. 1998. PMID: 9819593 French.
[Treatments of hereditary hemorrhagic telangiectasia of the nasal mucosa].
Babin E, Borsik M, Braccard S, Crampette L, Darrouzet V, Faure F, Fontanel JP, Houdart E, Jankowski R, Le Clech G, Malvezzi L, Morinière S, Perie S, Perret J, Pignat JC, Portier F, Serrano E, Plauchu H. Babin E, et al. Among authors: plauchu h. Rev Laryngol Otol Rhinol (Bord). 2005;126(1):43-8. Rev Laryngol Otol Rhinol (Bord). 2005. PMID: 16080648 French.
164 results