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89 results
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Hereditary haemorrhagic telangiectasia: a clinical and scientific review.
Govani FS, Shovlin CL. Govani FS, et al. Among authors: shovlin cl. Eur J Hum Genet. 2009 Jul;17(7):860-71. doi: 10.1038/ejhg.2009.35. Epub 2009 Apr 1. Eur J Hum Genet. 2009. PMID: 19337313 Free PMC article. Review.
A gene for hereditary haemorrhagic telangiectasia maps to chromosome 9q3.
Shovlin CL, Hughes JM, Tuddenham EG, Temperley I, Perembelon YF, Scott J, Seidman CE, Seidman JG. Shovlin CL, et al. Nat Genet. 1994 Feb;6(2):205-9. doi: 10.1038/ng0294-205. Nat Genet. 1994. PMID: 8162076
Hereditary hemorrhagic telangiectasia.
Shovlin CL, Hughes JM. Shovlin CL, et al. N Engl J Med. 1996 Feb 1;334(5):330-1; author reply 331-2. N Engl J Med. 1996. PMID: 8532038 No abstract available.
Medical complications of pregnancy in hereditary haemorrhagic telangiectasia.
Shovlin CL, Winstock AR, Peters AM, Jackson JE, Hughes JM. Shovlin CL, et al. QJM. 1995 Dec;88(12):879-87. QJM. 1995. PMID: 8593547
Molecular defects in rare bleeding disorders: hereditary haemorrhagic telangiectasia.
Shovlin CL. Shovlin CL. Thromb Haemost. 1997 Jul;78(1):145-50. Thromb Haemost. 1997. PMID: 9198145 Review.
Characterization of endoglin and identification of novel mutations in hereditary hemorrhagic telangiectasia.
Shovlin CL, Hughes JM, Scott J, Seidman CE, Seidman JG. Shovlin CL, et al. Am J Hum Genet. 1997 Jul;61(1):68-79. doi: 10.1086/513906. Am J Hum Genet. 1997. PMID: 9245986 Free PMC article.
Glaxo/MRS Young Investigator Medal. Molecular studies on adenosine deaminase deficiency and hereditary haemorrhagic telangiectasia.
Shovlin CL. Shovlin CL. Clin Sci (Lond). 1998 Mar;94(3):207-18. doi: 10.1042/cs0940207. Clin Sci (Lond). 1998. PMID: 9616253
Hereditary haemorrhagic telangiectasia and pulmonary arteriovenous malformations: issues in clinical management and review of pathogenic mechanisms.
Shovlin CL, Letarte M. Shovlin CL, et al. Thorax. 1999 Aug;54(8):714-29. doi: 10.1136/thx.54.8.714. Thorax. 1999. PMID: 10413726 Free PMC article. Review. No abstract available.
Supermodels and disease: insights from the HHT mice.
Shovlin CL. Shovlin CL. J Clin Invest. 1999 Nov;104(10):1335-6. doi: 10.1172/JCI8730. J Clin Invest. 1999. PMID: 10562293 Free PMC article. Review. No abstract available.
Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome).
Shovlin CL, Guttmacher AE, Buscarini E, Faughnan ME, Hyland RH, Westermann CJ, Kjeldsen AD, Plauchu H. Shovlin CL, et al. Am J Med Genet. 2000 Mar 6;91(1):66-7. doi: 10.1002/(sici)1096-8628(20000306)91:1<66::aid-ajmg12>3.0.co;2-p. Am J Med Genet. 2000. PMID: 10751092
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