Similar articles for PMID: 16155196

Year	Number of Results
2000	3
2001	1
2002	2
2003	2
2004	4
2005	7
2006	16
2007	6
2008	5
2009	9
2010	8
2011	12
2012	8
2013	13
2014	12
2015	9
2016	4
2017	8
2018	2
2019	2
2020	8
2021	10
2022	8
2023	2
2024	0

1

Genotype-phenotype relationship in hereditary haemorrhagic telangiectasia.

Letteboer TG, Mager JJ, Snijder RJ, Koeleman BP, Lindhout D, Ploos van Amstel JK, Westermann CJ. Letteboer TG, et al. J Med Genet. 2006 Apr;43(4):371-7. doi: 10.1136/jmg.2005.035451. Epub 2005 Sep 9. J Med Genet. 2006. PMID: 16155196 Free PMC article.

2

Hereditary hemorrhagic telangiectasia: clinical features in ENG and ALK1 mutation carriers.

Sabbà C, Pasculli G, Lenato GM, Suppressa P, Lastella P, Memeo M, Dicuonzo F, Guant G. Sabbà C, et al. J Thromb Haemost. 2007 Jun;5(6):1149-57. doi: 10.1111/j.1538-7836.2007.02531.x. J Thromb Haemost. 2007. PMID: 17388964 Free article.

3

Genotype-phenotype correlations in hereditary hemorrhagic telangiectasia: data from the French-Italian HHT network.

Lesca G, Olivieri C, Burnichon N, Pagella F, Carette MF, Gilbert-Dussardier B, Goizet C, Roume J, Rabilloud M, Saurin JC, Cottin V, Honnorat J, Coulet F, Giraud S, Calender A, Danesino C, Buscarini E, Plauchu H; French-Italian-Rendu-Osler Network. Lesca G, et al. Genet Med. 2007 Jan;9(1):14-22. doi: 10.1097/gim.0b013e31802d8373. Genet Med. 2007. PMID: 17224686 Free article.

4

Genotype-phenotype relationship for localization and age distribution of telangiectases in hereditary hemorrhagic telangiectasia.

Letteboer TG, Mager HJ, Snijder RJ, Lindhout D, Ploos van Amstel HK, Zanen P, Westermann KJ. Letteboer TG, et al. Am J Med Genet A. 2008 Nov 1;146A(21):2733-9. doi: 10.1002/ajmg.a.32243. Am J Med Genet A. 2008. PMID: 18831062

5

Genotype-phenotype correlation in hereditary hemorrhagic telangiectasia: mutations and manifestations.

Bayrak-Toydemir P, McDonald J, Markewitz B, Lewin S, Miller F, Chou LS, Gedge F, Tang W, Coon H, Mao R. Bayrak-Toydemir P, et al. Am J Med Genet A. 2006 Mar 1;140(5):463-70. doi: 10.1002/ajmg.a.31101. Am J Med Genet A. 2006. PMID: 16470787

6

Hereditary hemorrhagic telangiectasia in Japanese patients.

Komiyama M, Ishiguro T, Yamada O, Morisaki H, Morisaki T. Komiyama M, et al. J Hum Genet. 2014 Jan;59(1):37-41. doi: 10.1038/jhg.2013.113. Epub 2013 Nov 7. J Hum Genet. 2014. PMID: 24196379

7

Clinical symptoms according to genotype amongst patients with hereditary haemorrhagic telangiectasia.

Kjeldsen AD, Møller TR, Brusgaard K, Vase P, Andersen PE. Kjeldsen AD, et al. J Intern Med. 2005 Oct;258(4):349-55. doi: 10.1111/j.1365-2796.2005.01555.x. J Intern Med. 2005. PMID: 16164574 Free article.

8

Hereditary haemorrhagic telangiectasia: a questionnaire based study to delineate the different phenotypes caused by endoglin and ALK1 mutations.

Berg J, Porteous M, Reinhardt D, Gallione C, Holloway S, Umasunthar T, Lux A, McKinnon W, Marchuk D, Guttmacher A. Berg J, et al. J Med Genet. 2003 Aug;40(8):585-90. doi: 10.1136/jmg.40.8.585. J Med Genet. 2003. PMID: 12920067 Free PMC article.

9

Non-invasive CT screening for pulmonary arteriovenous malformations in children with confirmed hereditary hemorrhagic telangiectasia: Results from two pediatric centers.

Soysal N, Eyries M, Verlhac S, Escabasse V, Remus N, Tamalet A, Rioux JY, Franchi-Abella S, Vasile M, Robert S, Delestrain C, Hau I, Ducou-Le Pointe H, Soubrier F, Carette MF, Epaud R. Soysal N, et al. Pediatr Pulmonol. 2017 May;52(5):642-649. doi: 10.1002/ppul.23649. Epub 2017 Feb 6. Pediatr Pulmonol. 2017. PMID: 28165669

10

Mutation study of Spanish patients with hereditary hemorrhagic telangiectasia.

Fontalba A, Fernandez-L A, García-Alegria E, Albiñana V, Garrido-Martin EM, Blanco FJ, Zarrabeitia R, Perez-Molino A, Bernabeu-Herrero ME, Ojeda ML, Fernandez-Luna JL, Bernabeu C, Botella LM. Fontalba A, et al. BMC Med Genet. 2008 Aug 1;9:75. doi: 10.1186/1471-2350-9-75. BMC Med Genet. 2008. PMID: 18673552 Free PMC article.

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