Results 101 to 110 of about 25,332 (224)

54. On the Simulation of Amaurosis [PDF]

open access: yesThe American Journal of the Medical Sciences
n ...
openaire   +1 more source

The Neuro-Ophthalmology of Cerebrovascular Disease [PDF]

open access: yes, 1974
The neuro-ophthalmology of cerebrovascular disease is a vast plain of neuro-ophthalmic vistas, encompassing virtually all areas of disturbances of the eye-brain mechanism.
Harbison, John W.
core   +1 more source

Amaurosis fugax – delay between symptoms and surgery by specialty

open access: yesClinical Ophthalmology, 2016
Pia Kvickström,1 Bertil Lindblom,2,3 Göran Bergström,4,5 Madeleine Zetterberg2,3 1Department of Ophthalmology, Skaraborg Hospital, Skövde, 2Department of Clinical Neuroscience/Ophthalmology, Institute of Neuroscience and Physiology ...
Kvickström P   +3 more
doaj  

Combined Left Central Retinal Artery Occlusion and Bilateral Anterior Ischemic Optic Neuritis: A Rare Presentation of Giant Cell Arteritis

open access: yesCase Reports in Rheumatology, 2019
Giant cell arteritis, a large vessel vasculitis is characterized by headache, visual impairment, constitutional symptoms, and increased inflammatory markers. Visual involvement in giant cell arteritis ranges from amaurosis fugax to permanent visual loss,
Anne D. D. Joseph   +3 more
doaj   +1 more source

A Novel Locus for Leber Congenital Amaurosis (LCA4) with Anterior Keratoconus Mapping to Chromosome 17p13 [PDF]

open access: yes, 2000
5 páginas, 3 figuras, 2 tablas.-- et al.[Purpose]: A two-generation consanguineous Pakistani family with autosomal recessive Leber congenital amaurosis (LCA, MIM 204,000) and keratoconus was identified. All affected individuals have bilateral keratoconus
Bhattacharya, Shom Shanker   +1 more
core  

Identification and Correction of Mechanisms Underlying Inherited Blindness in Human iPSC-Derived Optic Cups [PDF]

open access: yes, 2016
Leber congenital amaurosis (LCA) is an inherited retinal dystrophy that causes childhood blindness. Photoreceptors are especially sensitive to an intronic mutation in the cilia-related gene CEP290, which causes missplicing and premature termination, but ...
Carr, A-JF   +15 more
core  

Arteritis de Takayasu y fiebre de origen desconocido Takayasu's arteritis and unknown origin fever

open access: yesRevista Cubana de Medicina, 2010
La arteritis de Takayasu es una arteritis inflamatoria crónica que afecta a grandes vasos, predomina en la aorta y sus ramas principales. Es una causa poco frecuente de fiebre de origen desconocido (FOD).
Victor Roca Campañá   +4 more
doaj  

Nasoendoscopic treatment of the sphenoid sinus mucoceles

open access: yesInternational Archives of Otorhinolaryngology, 2009
Introduction: Mucoceles is a slow growth benign lesion, composed of mucous or purulent material, may be multiple and cause osseous erosion. The sphenoid sinus mucoceles are uncommon and correspond to 1% of the cases; they are more frequent in the frontal
Silva, Fabrício Boechat do Carmo   +3 more
doaj  

CRB1 gene variant in leber congenital amaurosis: molecular and clinical investigations

open access: yesEgyptian Journal of Medical Human Genetics
Introduction In Iran, due to widespread consanguineous marriages, the emergence of genetic variants is a likely issue. This study aimed to describe an Iranian female patient with a novel variant in the Crumbs homologue 1 (CRB1) associated with Leber ...
Almuthana K. Hameed   +7 more
doaj   +1 more source

Amaurosis bilateral cortical en preeclampsia severa

open access: yesRevista Chilena de Obstetricia y Ginecología, 2004
Se presenta un caso clínico con diagnóstico final de preeclampsia severa que debuta con una complicación excepcional, la amaurosis bilateral cortical. Se discute esta presentación poco frecuente, realizándose una revisión actualizadaWe report a clinical ...
Arlette Adauy E.   +4 more
doaj  

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