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14篇 您的检索式:作者名="Stavern"
    题名 作者 年代 出处 被引量
1Atypical idiopathic intracranial hypertension:normal BMI and older patients显示文摘Bruce B B Kedar S Van Stavern G P 0,,22:1
2Adalimumab-associated optic neuritis 显示文摘CHUNG JH VAN STAVERN GP FROHMAN LP 2006J Neurolog Sci2006,244,12:1
3Are pa- tients receiving maximal medical therapy following carotid endarterectomy? 显示文摘Betancourt M Van Stavern RB Share D 2004Neurology2004,63,11:1
4Natural History,Prognosis,and Outcomes显示文摘Renee B Van Stavern MD 2005Semin Cerebrovasc Dis Stroke2005,5,:1
5Hyperintense optic nerve heads on diffusion-weighted imaging:a potential imaging sign of papilledema显示文摘Viers R Parsons M Van Stavern G 0,,:1
6Clinical,genetic,and biochenmical characterization of a Leber's bereditary optic neuropathy family containing both the 11778 and 14484 primary mutations?显示文摘Brown MD Allen JC Van Stavern GP 2001Am J Med Genet2001,104,4:1
7Sticky platelet syndrome and anterior ischaemic optic neuropathy显示文摘 Van Stavern GP 2007Clin Experiment Ophthalmol2007,35,8:1
8Idiopathic intracranial hypertension in men显示文摘Bruce BB Kedar S Van Stavern GP 0,,04:1
9Leber hereditary optic neuropathy : current perspectives显示文摘Meyerson C Van Stavern G Mcclelland C 2015Clin Ophthalmol2015,9,:1
10Idiopathicintracranial hypertension in men显示文摘Bruce BB Kedar S Van Stavern GP 2009Neurology2009,72,:1
11Psychometric properties of theBrief Pain Inventory among patients with osteoarthritis undergo-ing total hip replacement surgery 显示文摘Kapstad H Rokne B Stavern K 2010Health Qual Life Outcomes2010,8,:1
12Clinical, genetic, and biochenmical characterization of a Leber's hereditary optic neuropathy family containing both the 11778 and 14484 primary mutations显示文摘Brown MD Allen JC van Stavern GP 2001Am J Med Genet2001,104,:1
13Downbeat nystagmus from heat stroke显示文摘Van Stavern GP Biousse V Newman N J 0,,:1
14Application of optical coherence tomography in hereditary,toxic and metabolic optic neuropathies显示文摘Hereditary,metabolic and toxic optic neuropathies cause bilateral,central vision loss and therefore can result in severe impairment in visual function.Accurate,early diagnosis is critical,as nutritional and toxic optic neuropathies may be reversible if identified early,and diagnosis of hereditary optic neuropathies can prevent unnecessary invasive workup,provide prognostic information,and allow for effective genetic counseling.Optical coherence tomography(OCT)is a valuable tool that aids in the diagnosis and prognostication of optic neuropathies as it allows for quantification of changes in the retinal ganglion cells(RGCs)and retinal nerve fiber layer(RNFL)over time.We review the characteristic clinical presentations of hereditary,metabolic and toxic optic neuropathies,with an emphasis on OCT findings.Jennifer Enright Gregory Van Stavern 2020Annals of Eye Science2020,,2:0
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