نتایج جستجو برای: chorioretinal atrophy

تعداد نتایج: 37027  

Journal: :The British journal of ophthalmology 2005
P J Francis D W Schultz A M Gregory M B Schain R Barra J Majewski J Ott T Acott R G Weleber M L Klein

BACKGROUND The pattern dystrophies (PD) represent a clinically heterogeneous family of inherited macular diseases frequently caused by mutations in the peripherin/RDS gene. Most previous studies have detailed the clinical findings in single families, making it difficult to derive data from which progression and visual outcome can be generalised. METHODS Families were ascertained and clinicall...

2014
Hajji Chaimae Rajae Daoudi

We report a case of 43 years old women who present myopic CNV (A) causing an acute vision loss. That has not been treated at time causing a chorioretinal atrophy as the angiography (B) and her Optical Coherence Tomography (OCT) (C) shows. High myopia is a major cause of legal blindness in many countries, especially in young people. Itis defined as a refraction of at least -6.00 diopters and/or ...

Journal: :Retinal cases & brief reports 2017
Elliott H Sohn Kathleen R Chirco James C Folk Robert F Mullins

PURPOSE Birdshot chorioretinopathy (BCR) is a bilateral, chronic uveitis primarily involving the posterior segment that often results in progressive vision loss. Histopathology on eyes with BCR has been limited, but we had the rare opportunity to study the eyes of a donor with BCR. We sought to compare immunolabeling in the eyes of this donor who was treated with immunosuppression for over 30 y...

2005
P J Francis T Acott R G Weleber M L Klein

Background: The pattern dystrophies (PD) represent a clinically heterogeneous family of inherited macular diseases frequently caused by mutations in the peripherin/RDS gene. Most previous studies have detailed the clinical findings in single families, making it difficult to derive data from which progression and visual outcome can be generalised. Methods: Families were ascertained and clinicall...

Journal: :Archives of ophthalmology 1999
A H Neufeld

BACKGROUND Microglia, the macrophages and immune surveillance cells of the central nervous system, are quiescent normally but become activated in injured neural tissue. We have determined the distribution and potential participation of microglia in glaucomatous optic nerve degeneration. METHODS Microglia were localized by immunohistochemistry on paraffin sections of age-matched normal and gla...

Journal: :journal of current ophthalmology 0
هرمز شمس hormoz chams علیرضا لاشیئی alireza lashay احمد جوادیان ahmad javadian رضا کارخانه reza karkhaneh فرهاد شهرام farhad shahram فریدون دواچی fereidoun davatchi

purpose : to investigate the risk factors and causes for blindness in behcet’s disease (bd). methods : in this preliminary retrospective case series we have investigated 27 bd patients (54 eyes), legally blind (vision 0.1 or less) at least in one eye at the last visit (2006), and compared them with 54 eyes of 27 non-blind patients (control group), matched individually and consequently in terms ...

Journal: :Journal of Biological Engineering 2009
Giovanna Ferrentino Mariacarmela Bruno Giovanna Ferrari Massimo Poletto Murat O Balaban

Apple juice prepared from 'Annurca' apple puree was treated with a HPCD batch system. The pH, degrees Brix, color parameters and microbial load of the treated apple juice were compared with those of thermally processed juice. Thermal processes were carried out at 35, 50, 65, 85 degrees C and treatment times ranging between 10 and 140 minutes. Microbial inactivation kinetics indicated that 5-log...

2016

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Journal: :International journal of food microbiology 2012
J Casas M T Valverde F Marín-Iniesta L Calvo

Alicyclobacillus acidoterrestris (A. acidoterrestris) is a bacillus-type spore former that causes significant alterations in fruit products. It is highly resistant to typical pasteurization regimes; thus, this work explored the use of high-pressure CO₂ (HPCD) for its deactivation in apple cream. The assays were conducted in a high-pressure apparatus where the cream was placed in an agitated ves...

Journal: :The British journal of ophthalmology 1970
D J Hopkins E C Horan

The Hallermann-Streiff syndrome is a complex association of developmental anomalies principally involving structures of ectodermal origin. The constant expressions of the syndrome are dyscephaly with mandibulo-facial malformation, bilateral congenital cataracts, and dental anomalies, while hypotrichosis, cutaneous atrophy, microphthalmos, and proportionate dwarfism are frequently present (Table...

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