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A retrospective study of the role of the argon laser in the management of epistaxis secondary to hereditary haemorrhagic telangiectasia

Published online by Cambridge University Press:  29 June 2007

P. A. Lennox ,
M. Harries ,
V. J. Lund  and
D. J. Howard
P. A. Lennox
Affiliation:
Institute of Laryngology and Otology, 330 Grays Inn Road, London, UK.
M. Harries
Affiliation:
Institute of Laryngology and Otology, 330 Grays Inn Road, London, UK.
V. J. Lund*
Affiliation:
Institute of Laryngology and Otology, 330 Grays Inn Road, London, UK.
D. J. Howard
Affiliation:
Institute of Laryngology and Otology, 330 Grays Inn Road, London, UK.
*
Address for correspondence: Professor Valerie J. Lund, M.S. F.R.C.S., F.R.C.S. (Ed.) Professorial Unit, Royal National Throat, Nose and Ear Hospital, 330/332 Gray's Inn Road, London WC1X 8DA.
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Type
Main Articles
Information
The Journal of Laryngology & Otology , Volume 111 , Issue 1 , January 1997 , pp. 34 - 37
Copyright
Copyright © JLO (1984) Limited 1997

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References

Gluckman, J. L., Portugal, L. G. (1994) Modified Young's procedure for refractory epistaxis due to hereditary haemorrhagic telangiectasia. Laryngoscope 104: 1174–1177.CrossRefGoogle Scholar
Hanes, F. M. (1909) Multiple haemorrhagic telangiectasia causing epistaxis. Johns Hopkins Medical Bulletin 20: 63–67.Google Scholar
Harrison, D. F. N. (1956) Babington's disease, hereditary haemorrhagic telangiectasia. Guy's Hospital Reports 104: 246–266.Google Scholar
Harrison, D. F. N. (1964) Familial haemorrhagic telangiectasia: 20 cases treated with systemic oestrogen. Quarterly Journal of Medicine New Series 129: 25–38.Google Scholar
Harrison, D. F. N. (1982) Use of oestrogen in treatment of familial haemorrhagic telangiectasia. Laryngoscope 92: 314–320.CrossRefGoogle Scholar
Harrison, D. F. N., Lund, V. J. (1993) Tumours of the Upper Jaw. 1st Edition, Churchill Livingstone, Edinburgh.Google Scholar
Illum, P., Bjerring, P. (1988) Hereditary haemorrhagic telangiectasia treated by laser surgery. Rhinology 26: 19–24.Google ScholarPubMed
Kluger, P. B., Shapsay, S. M., Hybels, R. L., Bohigian, R. K. (1987) Neodymium-Yag laser intranasal photocoagulation in hereditary haemorrhagic telangiectasis: an update report. Laryngoscope 97: 1397–1401.CrossRefGoogle ScholarPubMed
Levine, H. L. (1989) Endoscopy and KTP532 laser. Annals of Otology, Rhinology and Laryngology 98: 46–51.CrossRefGoogle ScholarPubMed
Lund, V. J., Howard, D. J. (1996) Closure of the nasal cavities in the treatment of refractory hereditary haemorrhagic telangiectasia. Journal of Laryngology and Otology 111: 30–33.CrossRefGoogle Scholar
Piccirillo, J. F., Edwards, D., Haiduk, A., Yonan, B. S., Thawley, J. F. (1995) Psychometric and clinimetric validity of the 31-Item rhinosinusitis outcome measure (RSOM-31). American Journal of Rhinology 9: 297–306.CrossRefGoogle Scholar
Van-Cutsem, E., Rutgeerts, P., Geboes, K., Van Gompel, F., Vantrappen, G. (1988) Oestrogen-progesterone treatment of Osier-Weber-Rendu disease. Journal of Clinical Gastroenterology 10: 676–679.CrossRefGoogle ScholarPubMed