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Gordon K. Klintworth, MD PhD

Affiliations: 
Pathology Duke University, Durham, NC 
Area:
Ophthalmic Pathology (angiogenesis, eye pathology, cornea dystrophies)
Website:
http://pathology.mc.duke.edu/neuropath/np_faculty_klint2.htm
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"Gordon Klintworth"
Mean distance: 106866
 

Children

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Alan Proia grad student (Neuropathology Tree)
Charleen T. Chu post-doc 1997-1998
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Publications

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Klintworth GK. (2011) The parameters to establish a new corneal dystrophy. American Journal of Ophthalmology. 152: 155-6
Weiss JS, Møller HU, Lisch W, et al. (2011) [The IC3D classification of the corneal dystrophies]. Klinische Monatsblã¤Tter Fã¼R Augenheilkunde. 228: S1-39
Riazuddin SA, Zaghloul NA, Al-Saif A, et al. (2010) Missense mutations in TCF8 cause late-onset Fuchs corneal dystrophy and interact with FCD4 on chromosome 9p. American Journal of Human Genetics. 86: 45-53
Karring H, Runager K, Valnickova Z, et al. (2010) Differential expression and processing of transforming growth factor beta induced protein (TGFBIp) in the normal human cornea during postnatal development and aging. Experimental Eye Research. 90: 57-62
Jonasson F, Sander B, Eysteinsson T, et al. (2007) Sveinsson chorioretinal atrophy: the mildest changes are located in the photoreceptor outer segment/retinal pigment epithelium junction. Acta Ophthalmologica Scandinavica. 85: 862-7
Jonasson F, Hardarson S, Olafsson BM, et al. (2007) Sveinsson chorioretinal atrophy/helicoid peripapillary chorioretinal degeneration: first histopathology report. Ophthalmology. 114: 1541-6
Afshari NA, Pittard AB, Siddiqui A, et al. (2006) Clinical study of Fuchs corneal endothelial dystrophy leading to penetrating keratoplasty: a 30-year experience. Archives of Ophthalmology (Chicago, Ill. : 1960). 124: 777-80
Tanhehco TY, Eifrig DE, Schwab IR, et al. (2006) Two cases of Reis-Bücklers corneal dystrophy (granular corneal dystrophy type III) caused by spontaneous mutations in the TGFBI gene. Archives of Ophthalmology (Chicago, Ill. : 1960). 124: 589-93
Kang PC, Klintworth GK, Kim T, et al. (2005) Trends in the indications for penetrating keratoplasty, 1980-2001. Cornea. 24: 801-3
Aldave AJ, Gutmark JG, Yellore VS, et al. (2004) Lattice corneal dystrophy associated with the Ala546Asp and Pro551Gln missense changes in the TGFBI gene. American Journal of Ophthalmology. 138: 772-81
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