Results 91 to 100 of about 18,407 (215)

Amaurosis secondary to sphenoid mucocele

International Archives of Otorhinolaryngology, 2011
Introduction: The mucocele of the sphenoide sinus its a benign rare lesion. Those lesions are probably diagnosed late because they are asymptomatic or cause non-specific symptoms. The clinical characteristics depend on its location and can include fronto-
Melo, Antonio Antunes, Caldas Neto, Sílvio da Silva, Gouveia, Mariana Carvalho Leal, Santos, Patrícia Ferreira   +3 more
doaj  

Sneeze-Induced Amaurosis (.pdf)

, 2016
We present the first case of a patient with recurrent amaurosis fugax (AF) induced by sneezing.
Kondapalli Swathi; Michael L. Rosenberg; Mohammad Moussavi
core  

Acute disseminated encephalomyelitis presenting with bilateral transient amaurosis

, 2005
A 4-year-old male presented with acute disseminated encephalomyelitis with seizures and transient amaurosis after initial symptoms of a flulike febrile infection I week earlier.
Aydin, ADEM, Cakmakci, HANDAN, Atasever, S   +2 more
core   +1 more source

54. On the Simulation of Amaurosis [PDF]

The American Journal of the Medical Sciences
n ...
openaire   +1 more source

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

Revista 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, Luis Senra Armas, Héctor Rodríguez Silva, Hierro García-Junseda Daniel Ernesto, Bárbara Cepero Rosales   +4 more
doaj  

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

Case 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, Jebananthy Anandaselvam Pradeepan, Thirunavukarasu Kumanan, Muthusamy Malaravan   +3 more
doaj   +1 more source

A Novel Recessive RPGRIP1 Mutation Causing Leber Congenital Amaurosis

, 2016
Background: Leber congenital amaurosis is an early-onset childhood severe retinal dystrophy, of significant genetic heterogeneity. RPGRIP1 is ubiquitously expressed, but mutations in RPGRIP1 lead to a retina-restricted phenotype, such as Leber congenital
Abouzeid, Hana, Othman, I S, Othman, I. S., Abouzeid, H., Schorderet, D. F., Schorderet, D F   +5 more
core   +1 more source

Amaurosis fugax in a Danish community: a prospective study.

, 1988
A prospective study of amaurosis fugax was carried out in a Danish community (population 481,000); case ascertainment was based on the collaboration of practicing ophthalmologists and general practitioners.
J Marquardsen, T Vesterlund, B Mikkelsen, C U Andersen, J H Nehen, K K Pedersen   +5 more
core   +1 more source

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

Egyptian 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, Ahmed M. Amshawee, Sahar Kareem Al-Mozani, Mostafa Neissi, Javad Mohammadi-Asl, Kamele Jorfi, Doaa Haqi Ismael, Elaheh Nekouei   +7 more
doaj   +1 more source

Quinine Amaurosis [PDF]

British Journal of Ophthalmology, 1955
openaire   +2 more sources