Distrofia endoteliale di Fuchs (Italian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Distrofia endoteliale di Fuchs" in Italian language version.

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20nih.gov

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13doi.org

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4oadoi.org

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1medscape.com

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799^th place

1worldcat.org

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1ias.ac.in

6,086^th place

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1arvojournals.org

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1cochranelibrary.com

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1allaboutvision.com

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allaboutvision.com

(EN) Scleral Lenses Have Many Uses, Including in the Movies!, su All About Vision. URL consultato il 2 settembre 2020.

arvojournals.org

iovs.arvojournals.org

(EN) Danielle N. Meadows, Allen O. Eghrari e S. Amer Riazuddin, Progression of Fuchs Corneal Dystrophy in a Family Linked to the FCD1 Locus, in Investigative Ophthalmology & Visual Science, vol. 50, n. 12, 1º dicembre 2009, pp. 5662–5666, DOI:10.1167/iovs.09-3568. URL consultato il 2 settembre 2020.

cochranelibrary.com

Descemet's membrane endothelial keratoplasty versus Descemet's stripping automated endothelial keratoplasty for corneal endothelial failure, su cochranelibrary.com.

doi.org

dx.doi.org

Gordon K. Klintworth, Corneal dystrophies, in Orphanet Journal of Rare Diseases, vol. 4, 23 febbraio 2009, p. 7, DOI:10.1186/1750-1172-4-7. URL consultato il 24 maggio 2018.
Megan D Louttit, Laura J Kopplin e Robert P Igo, A Multi-Center Study to Map Genes for Fuchs’ Endothelial Corneal Dystrophy: Baseline Characteristics and Heritability, in Cornea, vol. 31, n. 1, 2012-1, pp. 26–35, DOI:10.1097/ICO.0b013e31821c9b8f. URL consultato il 24 maggio 2018.
John D. Gottsch, Olof H. Sundin e Sammy H. Liu, Inheritance of a novel COL8A2 mutation defines a distinct early-onset subtype of fuchs corneal dystrophy, in Investigative Ophthalmology & Visual Science, vol. 46, n. 6, 2005-06, pp. 1934–1939, DOI:10.1167/iovs.04-0937. URL consultato il 2 settembre 2020.
Vilas GL, Loganathan SK, Quon A, Sundaresan P, Vithana EN, Casey J, Oligomerization of SLC4A11 protein and the severity of FECD and CHED2 corneal dystrophies caused by SLC4A11 mutations, in Hum. Mutat., vol. 33, n. 2, febbraio 2012, pp. 419–28, DOI:10.1002/humu.21655, PMID 22072594.
Kelliher C, Chakravarti S, Vij N, et al., A cellular model for the investigation of Fuchs' endothelial corneal dystrophy, in Exp. Eye Res., vol. 93, n. 6, dicembre 2011, pp. 880–8, DOI:10.1016/j.exer.2011.10.001, PMID 22020132.
Kuot A, Hewitt AW, Griggs K, et al., Association of TCF4 and CLU polymorphisms with Fuchs' endothelial dystrophy and implication of CLU and TGFBI proteins in the disease process, in Eur. J. Hum. Genet., vol. 20, n. 6, giugno 2012, pp. 632–8, DOI:10.1038/ejhg.2011.248, PMID 22234156.
Allen O. Eghrari, Elyse J. McGlumphy e Benjamin W. Iliff, Prevalence and severity of fuchs corneal dystrophy in Tangier Island, in American Journal of Ophthalmology, vol. 153, n. 6, 2012-06, pp. 1067–1072, DOI:10.1016/j.ajo.2011.11.033. URL consultato il 2 settembre 2020.
(EN) Danielle N. Meadows, Allen O. Eghrari e S. Amer Riazuddin, Progression of Fuchs Corneal Dystrophy in a Family Linked to the FCD1 Locus, in Investigative Ophthalmology & Visual Science, vol. 50, n. 12, 1º dicembre 2009, pp. 5662–5666, DOI:10.1167/iovs.09-3568. URL consultato il 2 settembre 2020.
Elyse J. McGlumphy, William S. Yeo e S. Amer Riazuddin, Age-Severity Relationships in Families Linked to FCD2 with Retroillumination Photography, in Investigative Ophthalmology & Visual Science, vol. 51, n. 12, 2010-12, pp. 6298–6302, DOI:10.1167/iovs.10-5187. URL consultato il 2 settembre 2020.
Nanavaty MA, Shortt AJ, Endothelial keratoplasty versus penetrating keratoplasty for Fuchs endothelial dystrophy, in Cochrane Database Syst Rev, n. 7, 2011, pp. CD008420, DOI:10.1002/14651858.CD008420.pub2, PMID 21735430.
Naoki Okumura, Yuji Sakamoto e Keita Fujii, Rho kinase inhibitor enables cell-based therapy for corneal endothelial dysfunction, in Scientific Reports, vol. 6, 18 maggio 2016, DOI:10.1038/srep26113. URL consultato il 2 settembre 2020.
Allen O. Eghrari e John D. Gottsch, Fuchs' corneal dystrophy, in Expert Review of Ophthalmology, vol. 5, n. 2, 2010-04, pp. 147–159, DOI:10.1586/eop.10.8. URL consultato il 2 settembre 2020.

doi.org

Gordon K. Klintworth, Corneal dystrophies, in Orphanet Journal of Rare Diseases, vol. 4, 23 febbraio 2009, p. 7, DOI:10.1186/1750-1172-4-7. URL consultato il 24 maggio 2018.

ias.ac.in

Chitra Kannabiran, Genetics of corneal endothelial dystrophies, in Journal of Genetics, vol. 88, n. 4, 2009-12, pp. 487–494. URL consultato il 24 maggio 2018.

medscape.com

emedicine.medscape.com

Fuchs Endothelial Dystrophy: Background, Pathophysiology, Epidemiology, 4 maggio 2018. URL consultato il 24 maggio 2018.

nih.gov

ncbi.nlm.nih.gov

Elhalis H, Azizi B, Jurkunas UV, Fuchs endothelial corneal dystrophy, in Ocul Surf, vol. 8, n. 4, ottobre 2010, pp. 173–84, PMC 3061348, PMID 20964980.
Megan D Louttit, Laura J Kopplin e Robert P Igo, A Multi-Center Study to Map Genes for Fuchs’ Endothelial Corneal Dystrophy: Baseline Characteristics and Heritability, in Cornea, vol. 31, n. 1, 2012-1, pp. 26–35, DOI:10.1097/ICO.0b013e31821c9b8f. URL consultato il 24 maggio 2018.
Vilas GL, Loganathan SK, Quon A, Sundaresan P, Vithana EN, Casey J, Oligomerization of SLC4A11 protein and the severity of FECD and CHED2 corneal dystrophies caused by SLC4A11 mutations, in Hum. Mutat., vol. 33, n. 2, febbraio 2012, pp. 419–28, DOI:10.1002/humu.21655, PMID 22072594.
Kelliher C, Chakravarti S, Vij N, et al., A cellular model for the investigation of Fuchs' endothelial corneal dystrophy, in Exp. Eye Res., vol. 93, n. 6, dicembre 2011, pp. 880–8, DOI:10.1016/j.exer.2011.10.001, PMID 22020132.
(EN) Corneal dystrophy, Fuchs endothelial, 2 - Conditions - GTR - NCBI, su ncbi.nlm.nih.gov. URL consultato il 24 maggio 2018.
(EN) Corneal dystrophy, Fuchs endothelial, 3 - Conditions - GTR - NCBI, su ncbi.nlm.nih.gov. URL consultato il 24 maggio 2018.
(EN) Corneal dystrophy, Fuchs endothelial, 4 - Conditions - GTR - NCBI, su ncbi.nlm.nih.gov. URL consultato il 24 maggio 2018.
(EN) Corneal dystrophy, Fuchs endothelial, 5 - Conditions - GTR - NCBI, su ncbi.nlm.nih.gov. URL consultato il 24 maggio 2018.
(EN) Corneal dystrophy, Fuchs endothelial, 6 - Conditions - GTR - NCBI, su ncbi.nlm.nih.gov. URL consultato il 24 maggio 2018.
(EN) Corneal dystrophy, Fuchs endothelial, 7 - Conditions - GTR - NCBI, su ncbi.nlm.nih.gov. URL consultato il 24 maggio 2018.
(EN) Corneal dystrophy, Fuchs endothelial, 8 - Conditions - GTR - NCBI, su ncbi.nlm.nih.gov. URL consultato il 24 maggio 2018.
Kuot A, Hewitt AW, Griggs K, et al., Association of TCF4 and CLU polymorphisms with Fuchs' endothelial dystrophy and implication of CLU and TGFBI proteins in the disease process, in Eur. J. Hum. Genet., vol. 20, n. 6, giugno 2012, pp. 632–8, DOI:10.1038/ejhg.2011.248, PMID 22234156.
Elyse J. McGlumphy, William S. Yeo e S. Amer Riazuddin, Age-Severity Relationships in Families Linked to FCD2 with Retroillumination Photography, in Investigative Ophthalmology & Visual Science, vol. 51, n. 12, 2010-12, pp. 6298–6302, DOI:10.1167/iovs.10-5187. URL consultato il 2 settembre 2020.
(EN) Fuchs endothelial corneal dystrophy - Conditions - GTR - NCBI, su ncbi.nlm.nih.gov. URL consultato il 24 maggio 2018.
Nanavaty MA, Shortt AJ, Endothelial keratoplasty versus penetrating keratoplasty for Fuchs endothelial dystrophy, in Cochrane Database Syst Rev, n. 7, 2011, pp. CD008420, DOI:10.1002/14651858.CD008420.pub2, PMID 21735430.
Naoki Okumura, Yuji Sakamoto e Keita Fujii, Rho kinase inhibitor enables cell-based therapy for corneal endothelial dysfunction, in Scientific Reports, vol. 6, 18 maggio 2016, DOI:10.1038/srep26113. URL consultato il 2 settembre 2020.

pubmed.ncbi.nlm.nih.gov

John D. Gottsch, Olof H. Sundin e Sammy H. Liu, Inheritance of a novel COL8A2 mutation defines a distinct early-onset subtype of fuchs corneal dystrophy, in Investigative Ophthalmology & Visual Science, vol. 46, n. 6, 2005-06, pp. 1934–1939, DOI:10.1167/iovs.04-0937. URL consultato il 2 settembre 2020.
Allen O. Eghrari, Elyse J. McGlumphy e Benjamin W. Iliff, Prevalence and severity of fuchs corneal dystrophy in Tangier Island, in American Journal of Ophthalmology, vol. 153, n. 6, 2012-06, pp. 1067–1072, DOI:10.1016/j.ajo.2011.11.033. URL consultato il 2 settembre 2020.
Allen O. Eghrari e John D. Gottsch, Fuchs' corneal dystrophy, in Expert Review of Ophthalmology, vol. 5, n. 2, 2010-04, pp. 147–159, DOI:10.1586/eop.10.8. URL consultato il 2 settembre 2020.

rarediseases.info.nih.gov

(EN) Fuchs endothelial corneal dystrophy | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program, su rarediseases.info.nih.gov. URL consultato il 24 maggio 2018.

oadoi.org

Vilas GL, Loganathan SK, Quon A, Sundaresan P, Vithana EN, Casey J, Oligomerization of SLC4A11 protein and the severity of FECD and CHED2 corneal dystrophies caused by SLC4A11 mutations, in Hum. Mutat., vol. 33, n. 2, febbraio 2012, pp. 419–28, DOI:10.1002/humu.21655, PMID 22072594.
Kelliher C, Chakravarti S, Vij N, et al., A cellular model for the investigation of Fuchs' endothelial corneal dystrophy, in Exp. Eye Res., vol. 93, n. 6, dicembre 2011, pp. 880–8, DOI:10.1016/j.exer.2011.10.001, PMID 22020132.
Kuot A, Hewitt AW, Griggs K, et al., Association of TCF4 and CLU polymorphisms with Fuchs' endothelial dystrophy and implication of CLU and TGFBI proteins in the disease process, in Eur. J. Hum. Genet., vol. 20, n. 6, giugno 2012, pp. 632–8, DOI:10.1038/ejhg.2011.248, PMID 22234156.
Nanavaty MA, Shortt AJ, Endothelial keratoplasty versus penetrating keratoplasty for Fuchs endothelial dystrophy, in Cochrane Database Syst Rev, n. 7, 2011, pp. CD008420, DOI:10.1002/14651858.CD008420.pub2, PMID 21735430.

worldcat.org

Kunimoto, Derek Y., Kanitkar, Kunal D. e Makar, Mary., The Wills eye manual : office and emergency room diagnosis and treatment of eye disease., 4th ed., Lippincott Williams & Wilkins, 2004, ISBN 0-7817-4207-2, OCLC 53477145. URL consultato il 2 settembre 2020.