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F. Weber (1907)
MULTIPLE HEREDITARY DEVELOPMENTAL ANGIOMATA (TELANGIECTASES) OF THE SKIN AND MUCOUS MEMBRANES ASSOCIATED WITH RECURRING HÆMORRHAGES.The Lancet, 170
Osler W (1901)
On a family form of recurring epistaxis, associated with multiple telangiectases of the skin and mucous membranesJohns Hopkins Med J, 12
V. Jahnke (1970)
Ultrastructure of hereditary telangiectasia.Archives of otolaryngology, 91 3
PeterT. Rowley, John Kurnick, Richard Cheville (1970)
Hereditary haemorrhagic telangiectasia: aggravation by oral contraceptives?Lancet, 1 7644
R. Stecker, C. Lake (1965)
Hereditary hemorrhagic telangiectasia; review of 102 cases and presentation of an innovation to septodermoplasty.Archives of otolaryngology, 82 5
Russell Williams (1957)
Utilization of rhinoplastic technique hemi‐lateral rhinotomy. For the removal of intranasal tumorsThe Laryngoscope, 67
Babington BG (1865)
Hereditary epistaxisLancet, 2
D. Harrison (1964)
FAMILIAL HAEMORRHAGIC TELANGIECTASIA. 20 CASES TREATED WITH SYSTEMIC OESTROGEN.The Quarterly journal of medicine, 33
Rendu M (1896)
Epistaxis repétées chez un sujet porteur de petits angiomes cutanés et muqueuxBull Soc Med Hop Paris, 13
Hanes FM (1909)
Multiple hereditary telangiectases causing hemorrhage (hereditary hemorrhagic telangiectasia)Johns Hopkins Med J, 20
Saunders Wh (1960)
Septal dermoplasty for control of nosebleeds caused by hereditary hemorrhagic telangiectasia or septal perforations.Transactions - American Academy of Ophthalmology and Otolaryngology, 64
Abstract Of the numerous treatment modalities for hemorrhagic hereditary telangiectasia, skin grafting the nasal cavity affords the best prognosis. In patients with absent nasal septa or large perforations, the hemilateral rhinotomy approach offers excellent exposure and convenient graft placement without increased morbidity. References 1. Sutton, cited in Harrison DFN: Familial haemorrhagic telangiectasia: Twenty cases treated with systemic oestrogen . Quart J. Med 33: 25-38, 1964. 2. Babington BG: Hereditary epistaxis . Lancet 2:362-363, 1865. 3. Osler W: On a family form of recurring epistaxis, associated with multiple telangiectases of the skin and mucous membranes . Johns Hopkins Med J 12:333-337, 1901. 4. Weber FP: Multiple hereditary developmental angiomata (telangiectases) of the skin and mucous membranes associated with recurring haemorrhages . Lancet 2:160-162, 1907. 5. Rendu M: Epistaxis repétées chez un sujet porteur de petits angiomes cutanés et muqueux . Bull Soc Med Hop Paris 13:731-733, 1896. 6. Hanes FM: Multiple hereditary telangiectases causing hemorrhage (hereditary hemorrhagic telangiectasia) . Johns Hopkins Med J 20:63-73, 1909. 7. Jahnke V: Ultrastructure of hereditary telangiectasia . Arch Otolaryng 91:262-265, 1970.Crossref 8. Harrison DFN: Familial haemorrhagic telangiectasia: Twenty cases treated with systemic oestrogen . Quart J Med 33:25-38, 1964. 9. Rowley PT, Kurnick J, Cheville R: Hereditary haemorrhagic telangiectasia: Aggravation by oral contraceptives? Lancet 1:474-475, 1970.Crossref 10. Saunders WH: Septal dermoplasty for control of nosebleeds caused by hereditary hemorrhagic telangiectasia or septal perforations . Trans Amer Acad Ophthal Otolaryng 64:500-506, 1960. 11. Williams RI: Utilization of rhinoplastic technique hemi-lateral rhinotomy: For the removal of intranasal tumors . Laryngoscope 67:796-814, 1957.Crossref 12. Stecker RH, Lake CF: Hereditary hemorrhagic telangiectasia: Review of 102 cases and presentation of an innovation to septodermoplasty . Arch Otolaryng 82:522-526, 1965.Crossref
Archives of Otolaryngology – American Medical Association
Published: Oct 1, 1972
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