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Gordon K Klintworth

Showing results (1-10 of 41) with videos related to

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Orphanet Journal of Rare Diseases|February 25, 2009
Corneal dystrophiesGordon K Klintworth
Frontiers in Bioscience : a Journal and Virtual Library|April 18, 2003
The molecular genetics of the corneal dystrophies--current statusGordon K Klintworth
Human Mutation|May 10, 2006
TGFBI gene mutations in corneal dystrophiesChitra Kannabiran, Gordon K Klintworth
Investigative Ophthalmology & Visual Science|April 28, 2004
Two mutations in the TGFBI (BIGH3) gene associated with lattice corneal dystrophy in an extensively studied familyGordon K Klintworth, Wenjun Bao, Natalie A Afshari
Molecular Vision|March 29, 2006
CHST6 mutations in North American subjects with macular corneal dystrophy: a comprehensive molecular genetic reviewGordon K Klintworth, Clayton F Smith, Brandy L Bowling
Ophthalmology|March 7, 2007
Sveinsson chorioretinal atrophy/helicoid peripapillary chorioretinal degeneration: first histopathology reportFridbert Jonasson, Sverrir Hardarson, Bjorn Mar Olafsson, et al.
Biochemistry|April 6, 2013
The insoluble TGFBIp fraction of the cornea is covalently linked via a disulfide bond to type XII collagenKasper Runager, Gordon K Klintworth, Henrik Karring, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|June 14, 2006
Clinical study of Fuchs corneal endothelial dystrophy leading to penetrating keratoplasty: a 30-year experienceNatalie A Afshari, Aaron B Pittard, Adnan Siddiqui, et al.
Acta Ophthalmologica Scandinavica|August 9, 2007
Sveinsson chorioretinal atrophy: the mildest changes are located in the photoreceptor outer segment/retinal pigment epithelium junctionFridbert Jonasson, Birgit Sander, Thor Eysteinsson, et al.
Journal of Proteomics & Bioinformatics|October 27, 2015
Insight into the Protein Composition of Immunoglobulin Light Chain Deposits of Eyelid, Orbital and Conjunctival AmyloidosisNadia Sukusu Nielsen, Ebbe Toftgaard Poulsen, Gordon K Klintworth, et al.
Pageof 5

Showing results (1-10 of 41) with videos related to

Sort By:
Pageof 5
Orphanet Journal of Rare Diseases|February 25, 2009
Corneal dystrophiesGordon K Klintworth
Frontiers in Bioscience : a Journal and Virtual Library|April 18, 2003
The molecular genetics of the corneal dystrophies--current statusGordon K Klintworth
Human Mutation|May 10, 2006
TGFBI gene mutations in corneal dystrophiesChitra Kannabiran, Gordon K Klintworth
Investigative Ophthalmology & Visual Science|April 28, 2004
Two mutations in the TGFBI (BIGH3) gene associated with lattice corneal dystrophy in an extensively studied familyGordon K Klintworth, Wenjun Bao, Natalie A Afshari
Molecular Vision|March 29, 2006
CHST6 mutations in North American subjects with macular corneal dystrophy: a comprehensive molecular genetic reviewGordon K Klintworth, Clayton F Smith, Brandy L Bowling
Ophthalmology|March 7, 2007
Sveinsson chorioretinal atrophy/helicoid peripapillary chorioretinal degeneration: first histopathology reportFridbert Jonasson, Sverrir Hardarson, Bjorn Mar Olafsson, et al.
Biochemistry|April 6, 2013
The insoluble TGFBIp fraction of the cornea is covalently linked via a disulfide bond to type XII collagenKasper Runager, Gordon K Klintworth, Henrik Karring, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|June 14, 2006
Clinical study of Fuchs corneal endothelial dystrophy leading to penetrating keratoplasty: a 30-year experienceNatalie A Afshari, Aaron B Pittard, Adnan Siddiqui, et al.
Acta Ophthalmologica Scandinavica|August 9, 2007
Sveinsson chorioretinal atrophy: the mildest changes are located in the photoreceptor outer segment/retinal pigment epithelium junctionFridbert Jonasson, Birgit Sander, Thor Eysteinsson, et al.
Journal of Proteomics & Bioinformatics|October 27, 2015
Insight into the Protein Composition of Immunoglobulin Light Chain Deposits of Eyelid, Orbital and Conjunctival AmyloidosisNadia Sukusu Nielsen, Ebbe Toftgaard Poulsen, Gordon K Klintworth, et al.
Pageof 5