Distrofia di Meesmann (Italian Wikipedia)

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

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(EN) Gordon K. Klintworth, Advances in the molecular genetics of corneal dystrophies, in American Journal of Ophthalmology, vol. 128, n. 6, 1999-12, pp. 747–754, DOI:10.1016/S0002-9394(99)00358-X. URL consultato il 22 maggio 2018.

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 22 maggio 2018.
(EN) Gordon K. Klintworth, Advances in the molecular genetics of corneal dystrophies, in American Journal of Ophthalmology, vol. 128, n. 6, 1999-12, pp. 747–754, DOI:10.1016/S0002-9394(99)00358-X. URL consultato il 22 maggio 2018.
Edwin H. A. Allen, David G. Courtney e Sarah D. Atkinson, Keratin 12 missense mutation induces the unfolded protein response and apoptosis in Meesmann epithelial corneal dystrophy, in Human Molecular Genetics, vol. 25, n. 6, 15 marzo 2016, pp. 1176–1191, DOI:10.1093/hmg/ddw001. URL consultato il 22 maggio 2018.
Haihui Liao, Alan D. Irvine e Caroline J. MacEwen, Development of Allele-Specific Therapeutic siRNA in Meesmann Epithelial Corneal Dystrophy, in PLoS ONE, vol. 6, n. 12, 12 dicembre 2011, DOI:10.1371/journal.pone.0028582. URL consultato il 23 maggio 2018.

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 22 maggio 2018.

nih.gov

ncbi.nlm.nih.gov

F. W. Stocker e L. B. Holt, A rare form of hereditary epithelial dystrophy of the cornea: a genetic, clinical, and pathologic study, in Transactions of the American Ophthalmological Society, vol. 52, 1954-1955, pp. 133–144. URL consultato il 23 maggio 2018.
Judy L. Chen, Benjamin R. Lin e Katherine M. Gee, Identification of presumed pathogenic KRT3 and KRT12 gene mutations associated with Meesmann corneal dystrophy, in Molecular Vision, vol. 21, 31 dicembre 2015, pp. 1378–1386. URL consultato il 22 maggio 2018.
Jacek P. Szaflik, Monika Ołdak e Radosław B. Maksym, Genetics of Meesmann corneal dystrophy: a novel mutation in the keratin 3 gene in an asymptomatic family suggests genotype-phenotype correlation, in Molecular Vision, vol. 14, 15 settembre 2008, pp. 1713–1718. URL consultato il 22 maggio 2018.
Edwin H. A. Allen, David G. Courtney e Sarah D. Atkinson, Keratin 12 missense mutation induces the unfolded protein response and apoptosis in Meesmann epithelial corneal dystrophy, in Human Molecular Genetics, vol. 25, n. 6, 15 marzo 2016, pp. 1176–1191, DOI:10.1093/hmg/ddw001. URL consultato il 22 maggio 2018.
Mohammad-Ali Javadi, Mozhgan Rezaei-Kanavi e Atefeh Javadi, Meesmann Corneal Dystrophy; a Clinico-Pathologic, Ultrastructural and Confocal Scan Report, in Journal of Ophthalmic & Vision Research, vol. 5, n. 2, 2010-4, pp. 122–126. URL consultato il 22 maggio 2018.
(EN) Meesman corneal dystrophy - Conditions - GTR - NCBI, su ncbi.nlm.nih.gov. URL consultato il 23 maggio 2018.
P. D. Roca, Meesmann's hereditary epithelial dystrophy (differential diagnosis), in Eye, Ear, Nose & Throat Monthly, vol. 48, n. 7, 1969-7, pp. 424–425. URL consultato il 23 maggio 2018.
Haihui Liao, Alan D. Irvine e Caroline J. MacEwen, Development of Allele-Specific Therapeutic siRNA in Meesmann Epithelial Corneal Dystrophy, in PLoS ONE, vol. 6, n. 12, 12 dicembre 2011, DOI:10.1371/journal.pone.0028582. URL consultato il 23 maggio 2018.

rarediseases.info.nih.gov

(EN) Meesmann corneal dystrophy - Genetic and Rare Diseases Information Center (GARD) – an NCATS Program, su rarediseases.info.nih.gov. URL consultato il 23 maggio 2018.