Literature DB >> 5087603

Retinal involvement in hereditary hemorrhagic telangiectasia.

D G Davis, J L Smith.   

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Year:  1971        PMID: 5087603     DOI: 10.1001/archopht.1971.00990050620018

Source DB:  PubMed          Journal:  Arch Ophthalmol        ISSN: 0003-9950


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  6 in total

1.  Coats' disease and congenital vascular retinopathy.

Authors:  F P Campbell
Journal:  Trans Am Ophthalmol Soc       Date:  1976

2.  A patient with polycythemia.

Authors:  J E Olerud; H T Robertson; K F Hossack; W B Nelp; G F Odland; W D Bowman; C A Finch
Journal:  West J Med       Date:  1981-11

3.  Spontaneous thrombosis of an orbital arteriovenous malformation revealing hereditary haemorrhagic telangiectasia (Rendu-Osler-Weber disease). A case report.

Authors:  Charles Van Went; A Ozanne; G Saliou; G Dethorey; I De Monchy; T Krings; D Ducreux; M Labetoulle
Journal:  Interv Neuroradiol       Date:  2011-12-16       Impact factor: 1.610

4.  Organ specific optical imaging of mitochondrial redox state in a rodent model of hereditary hemorrhagic telangiectasia-1.

Authors:  Zahra Ghanian; Sepideh Maleki; SunYoung Park; Christine M Sorenson; Nader Sheibani; Mahsa Ranji
Journal:  J Biophotonics       Date:  2013-06-06       Impact factor: 3.207

5.  Prevalence of ocular manifestations in hereditary hemorrhagic telangiectasia.

Authors:  Urban W Geisthoff; Konrad Hille; Klaus W Ruprecht; Thomas Verse; Peter K Plinkert
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2007-08       Impact factor: 3.535

6.  Renal arteriovenous malformation demonstrated angiographically in hereditary haemorrhagic telangiectasia (Rendu-Osler-Weber disease).

Authors:  D A Cooke
Journal:  J R Soc Med       Date:  1986-12       Impact factor: 18.000

  6 in total

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