Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 226,017,875 papers from all fields of science
Search
Sign In
Create Free Account
Schnyder crystalline corneal dystrophy
Known as:
Crystalline corneal dystrophy
, CORNEAL DYSTROPHY, SCHNYDER
, CORNEAL DYSTROPHY, CRYSTALLINE, OF SCHNYDER
Expand
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
1 relation
Broader (1)
Hereditary corneal dystrophy
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Schnyder corneal dystrophy-associated UBIAD1 inhibits ER-associated degradation of HMG CoA reductase in mice
Y. Jo
,
Jason S Hamilton
,
+8 authors
R. DeBose-Boyd
eLife
2019
Corpus ID: 71148837
Autosomal-dominant Schnyder corneal dystrophy (SCD) is characterized by corneal opacification owing to overaccumulation of…
Expand
2019
2019
Schnyder's crystalline corneal dystrophy.
S. Handa
,
A. Thakur
,
D. Rajneesh
,
A. Kulshrestha
,
A. Gupta
QJM : monthly journal of the Association of…
2019
Corpus ID: 171092985
2016
2016
Identification of the First De Novo UBIAD1 Gene Mutation Associated with Schnyder Corneal Dystrophy
B. Lin
,
R. Frausto
,
Rosalind C. Vo
,
Stephan Y Chiu
,
Judy L. Chen
,
A. Aldave
Journal of Ophthalmology
2016
Corpus ID: 1063110
Purpose. To report the identification of the first de novo UBIAD1 missense mutation in an individual with Schnyder corneal…
Expand
2010
2010
Newly Reported p.Asp240Asn Mutation in UBIAD1 Suggests Central Discoid Corneal Dystrophy Is a Variant of Schnyder Corneal Dystrophy
J. Weiss
,
C. Wiaux
,
+4 authors
A. Aldave
Cornea
2010
Corpus ID: 22058321
Purpose: To determine whether central discoid corneal dystrophy (CDCD), previously reported as a novel corneal dystrophy, is…
Expand
2009
2009
A novel UBIAD1 mutation identified in a Chinese family with Schnyder crystalline corneal dystrophy
Yang Jing
,
Chun Liu
,
Junmin Xu
,
Liya Wang
Molecular Vision
2009
Corpus ID: 387537
Purpose To identify the molecular defect causing Schnyder crystalline corneal dystrophy (SCCD) in a Chinese family with bilateral…
Expand
2009
2009
Surgical management and genetic analysis of a Chinese family with the S171P mutation in the UBIAD1 gene, the gene for Schnyder corneal dystrophy
J. Mehta
,
E. Vithana
,
+4 authors
D. Tan
British Journal of Ophthalmology
2009
Corpus ID: 40418979
Background: To describe the underlying molecular genetic basis, surgical management and phenotypic variation of Schnyder corneal…
Expand
2004
2004
Phototherapeutic Keratectomy in Schnyder Crystalline Corneal Dystrophy
M. Köksal
,
S. Kargi
,
G. Gürelik
,
F. Akata
Cornea
2004
Corpus ID: 21484944
Objective: To emphasize the effectiveness of phototherapeutic keratectomy (PTK) in a patient with Schnyder crystalline corneal…
Expand
2004
2004
Fine mapping of the Schnyder’s crystalline corneal dystrophy locus
V. Theendakara
,
G. Tromp
,
+20 authors
J. Weiss
Human Genetics
2004
Corpus ID: 2856915
Schnyder’s crystalline corneal dystrophy (SCCD) is a rare autosomal dominant eye disease with a spectrum of clinical…
Expand
1997
1997
Immunohistochemical expression of cathepsin D in correlation with extracellular matrix component, steroid receptor status and proliferative indices in breast cancer
E. Ioachim
,
S. Kamina
,
M. Kontostolis
,
N. Agnantis
Virchows Archiv
1997
Corpus ID: 34706146
Abstract In 87 breast cancer patients, the immunohistochemical expression of the basement membrane (BM)-degrading enzyme…
Expand
Highly Cited
1989
Highly Cited
1989
Physicochemical properties of MoO3TiO2 prepared by an equilibrium adsorption method
Du Soung Kim
,
Y. Kurusu
,
I. Wachs
,
F. Hardcastle
,
K. Segawa
1989
Corpus ID: 39956896
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE