Results 61 to 70 of about 3,916 (200)
Meretojan taudista uutta tietoa kansallisen potilasrekisterin avulla [PDF]
Tiedot Meretojan taudin eli suomalaisen perinnöllisen gelsoliiniamyloidoosin taudinkulusta ovat tähän saakka perustuneet suhteellisen pieniin potilassarjoihin.
Atula, Sari +3 more
core
Exploring the histopathological signature of repeat‐mediated Fuchs endothelial corneal dystrophy
Abstract Purpose To determine the histological differences between Fuchs endothelial corneal dystrophy (FECD) cases with and without the most common genetic risk factor, expansion of a CTG repeat (CTG18.1) within the TCF4 gene. Methods Formalin‐fixed paraffin‐embedded corneal tissues were compared retrospectively, and CTG18.1 status was determined from
Anne‐Marie S. Kladny +5 more
wiley +1 more source
Corneal Dystrophies and Degenerations [PDF]
The cornea is a complex structure with complex functions aiming to protect the internal ocular tissues and transmit and refract the coming light rays. Corneal dystrophies are a group of relatively infrequent genetic corneal disorders in which an abnormal
Alkatan, Hind +2 more
core +2 more sources
Advances in the genetics of refractive errors: Contributions from the CREAM consortium
Abstract The Consortium for Refractive Error and Myopia (CREAM) was established in 2011, bringing together an international team of researchers studying more than 30 cohorts. Since its establishment, CREAM has played a pivotal role in research investigating the genetics of myopia and other refractive errors, serving as a key driver of progress in the ...
Sze Wai Rosa Li +11 more
wiley +1 more source
ABSTRACT Objective To compare unsedated noncontact specular microscopy imaging techniques for the canine corneal endothelium and identify the most effective technique. Animals Studied Nineteen eyes of 10 systemically healthy, staff‐owned dogs with clinically normal corneas were studied.
Hyunwoo Suk +4 more
wiley +1 more source
Infantile nystagmus: an optometrist's perspective [PDF]
Infantile nystagmus (IN), previously known as congenital nystagmus, is an involuntary to-and-fro movement of the eyes that persists throughout life.
Binti Ahmad Zahidi, Asma +3 more
core +1 more source
This review charts the evolution of corneal hydrogels from passive replacements to active and intelligent systems, evaluating natural and synthetic materials while addressing design challenges such as transparency and strength. Advanced applications such as scarless wound healing, three‐dimensional bioprinting, and smart wearables are highlighted to ...
Xinwei Wang +9 more
wiley +1 more source
Epidemiological and Histopathological Assessment of Corneal Dystrophies Leading to Corneal Transplantation [PDF]
Purpose: To carry out an epidemiological assessment of corneal dystrophies leading to corneal transplantation and to determine different subtype frequencies.
Asadi-Amoli, Fahimeh +5 more
core +2 more sources
Aplasia Cutis Congenita in Bart's Syndrome: A Case Report and Literature Review
ABSTRACT Aplasia cutis congenita (ACC) is a partial or complete absence of skin layers which can be a part of a syndromic disease. Bart's syndrome is a combination of clinical manifestations including ACC, epidermolysis bullosa, blistering in the oral mucosa, nail dystrophy, or congenital absence of nails. Additional anomalies, such as pyloric atresia,
Parvaneh Sadeghimoghadam +4 more
wiley +1 more source
Childhood blindness in the context of VISION 2020: the right to sight
The major causes of blindness in children vary widely from region to region, being largely determined by socioeconomic development, and the availability of primary health care and eye care services.
Gilbert Clare, Foster Allen
doaj

