Role of the sclera in the development and pathological complications of myopia
NA McBrien, A Gentle - Progress in retinal and eye research, 2003 - Elsevier
Myopia is one of the most prevalent ocular conditions and is the result of a mismatch
between the power of the eye and axial length of the eye. As a result images of distant …
between the power of the eye and axial length of the eye. As a result images of distant …
Marfan syndrome
RE Pyeritz - Emery and Rimoin's Principles and Practice of Medical …, 2025 - Elsevier
Heritable disorders of connective tissue can be due to Mendelian defects in the components
of the extracellular matrix, the enzymes that perform posttranslational processing, or in the …
of the extracellular matrix, the enzymes that perform posttranslational processing, or in the …
The molecular genetics of Marfan syndrome and related microfibrillopathies
PN Robinson, M Godfrey - Journal of medical genetics, 2000 - jmg.bmj.com
Mutations in the gene for fibrillin-1 (FBN1) have been shown to cause Marfan syndrome, an
autosomal dominant disorder of connective tissue characterised by pleiotropic …
autosomal dominant disorder of connective tissue characterised by pleiotropic …
[HTML][HTML] ADAMTS proteins as modulators of microfibril formation and function
D Hubmacher, SS Apte - Matrix Biology, 2015 - Elsevier
The ADAMTS (ad isintegrin-like and metalloproteinase domain with thrombospondin-type 1
motifs) protein superfamily includes 19 secreted metalloproteases and 7 secreted ADAMTS …
motifs) protein superfamily includes 19 secreted metalloproteases and 7 secreted ADAMTS …
Current concepts of ocular manifestations in Marfan syndrome
AY Nemet, EI Assia, DJ Apple, IS Barequet - Survey of ophthalmology, 2006 - Elsevier
Marfan syndrome is a widespread disorder of connective tissue. It is characterized by
systemic and ocular features due to mutations in the fibrillin gene. Awareness and prompt …
systemic and ocular features due to mutations in the fibrillin gene. Awareness and prompt …
Marfan syndrome
DM Milewicz, AC Braverman, J De Backer… - Nature reviews Disease …, 2021 - nature.com
Marfan syndrome (MFS) is an autosomal dominant, age-related but highly penetrant
condition with substantial intrafamilial and interfamilial variability. MFS is caused by …
condition with substantial intrafamilial and interfamilial variability. MFS is caused by …
Anterior pituitary, sex hormones, and keratoconus: Beyond traditional targets
D Karamichos, P Escandon, B Vasini… - Progress in Retinal and …, 2022 - Elsevier
Abstract" The Diseases of the Horny-coat of The Eye", known today as keratoconus, is a
progressive, multifactorial, non-inflammatory ectatic corneal disorder that is characterized by …
progressive, multifactorial, non-inflammatory ectatic corneal disorder that is characterized by …
Distribution of myocilin and extracellular matrix components in the juxtacanalicular tissue of human eyes
J Ueda, K Wentz-Hunter… - … ophthalmology & visual …, 2002 - iovs.arvojournals.org
purpose. To examine ultrastructurally the composition of extracellular matrix (ECM)
materials, the distribution of myocilin, and the colocalization of myocilin with ECM …
materials, the distribution of myocilin, and the colocalization of myocilin with ECM …
The genetics of central corneal thickness
DP Dimasi, KP Burdon, JE Craig - British Journal of Ophthalmology, 2010 - bjo.bmj.com
Evidence in the recent literature has highlighted the importance of central corneal thickness
(CCT) in relation to several ocular and non-ocular conditions. Most notably, thinner CCT has …
(CCT) in relation to several ocular and non-ocular conditions. Most notably, thinner CCT has …