Klintworth, Gordon K.
Gordon K. Klintworth
Klintworth, Gordon Kenneth (1932-2014).
VIAF ID: 39472553 (Personal)
Permalink: http://viaf.org/viaf/39472553
Preferred Forms
- 100 0 _ ‡a Gordon K. Klintworth
- 200 _ | ‡a Klintworth ‡b Gordon K.
- 100 1 0 ‡a Klintworth, Gordon K.
-
- 100 1 _ ‡a Klintworth, Gordon K.
-
- 100 1 _ ‡a Klintworth, Gordon K.
- 100 1 _ ‡a Klintworth, Gordon K.
-
-
-
4xx's: Alternate Name Forms (1)
Works
Title | Sources |
---|---|
Allelic and locus heterogeneity in autosomal recessive gelatinous drop-like corneal dystrophy | |
Applications of energy dispersive microprobe analysis in ophthalmic pathology | |
Clinical study of Fuchs corneal endothelial dystrophy leading to penetrating keratoplasty: a 30-year experience | |
Corneal angiogenesis : a comprehensive critical review | |
A dataset of human cornea proteins identified by Peptide mass fingerprinting and tandem mass spectrometry. | |
Duke University honors Gordon Klintworth. | |
The eye | |
Genetic screen of African Americans with Fuchs endothelial corneal dystrophy | |
The human cornea proteome: bioinformatic analyses indicate import of plasma proteins into the cornea | |
Human phenotypically distinct TGFBI corneal dystrophies are linked to the stability of the fourth FAS1 domain of TGFBIp | |
Insight into the Protein Composition of Immunoglobulin Light Chain Deposits of Eyelid, Orbital and Conjunctival Amyloidosis. | |
The insoluble TGFBIp fraction of the cornea is covalently linked via a disulfide bond to type XII collagen | |
Missense mutations in TCF8 cause late-onset Fuchs corneal dystrophy and interact with FCD4 on chromosome 9p. | |
Mitochondrial polymorphism A10398G and Haplogroup I are associated with Fuchs' endothelial corneal dystrophy | |
The molecular genetics of the corneal dystrophies--current status | |
Mycoses of the central nervous system | |
Novel mutations of the carbohydrate sulfotransferase-6 (CHST6) gene causing macular corneal dystrophy in India | |
Pathobiology of ocular disease : a dynamic approach | |
Phenotype associated with the H626P mutation and other changes in the TGFBI gene in Czech families | |
Primary intraocular T-cell-rich large B-cell lymphoma. | |
Proteomic analysis of the soluble fraction from human corneal fibroblasts with reference to ocular transparency | |
Replication of TCF4 through association and linkage studies in late-onset Fuchs endothelial corneal dystrophy | |
Research into the pathogenesis and non surgical treatment of keratoconus and corneal dystrophies | |
Sveinsson chorioretinal atrophy: the mildest changes are located in the photoreceptor outer segment/retinal pigment epithelium junction | |
Transforming growth factor beta induced protein accumulation in granular corneal dystrophy type III | |
Trends in the indications for penetrating keratoplasty, 1980-2001. | |
Trilateral retinoblastoma: clinical and radiologic progression | |
Two cases of Reis-Bücklers corneal dystrophy (granular corneal dystrophy type III) caused by spontaneous mutations in the TGFBI gene. | |
Two mutations in the TGFBI (BIGH3) gene associated with lattice corneal dystrophy in an extensively studied family. |