Okuläre Veränderungen bei Patienten mit Alport-Syndrom – ein Update
Author:
Funder
Deutsche Forschungsgemeinschaft
Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s00347-022-01805-1.pdf
Reference37 articles.
1. Ahmed F, Kamae KK, Jones DJ et al (2013) Temporal macular thinning associated with X‑linked Alport syndrome. JAMA Ophthalmol 131:777–782. https://doi.org/10.1001/jamaophthalmol.2013.1452
2. Alport AC (1927) Hereditary familial congenital haemorrhagic nephritis. Br Med J 1:504–506
3. Ameln J, Reiniger JL, Hess K et al (2022) Supernormal foveal photoreceptor density in Alport syndrome: A case report. Eur J Ophthalmol. https://doi.org/10.1177/11206721221093197
4. Barozzi S, Soi D, Intieri E et al (2020) Vestibular and audiological findings in the Alport syndrome. Am J Med Genet A 182:2345–2358. https://doi.org/10.1002/ajmg.a.61796
5. Bekheirnia MR, Reed B, Gregory MC et al (2010) Genotype–phenotype correlation in X‑linked Alport syndrome. J Am Soc Nephrol 21:876–883. https://doi.org/10.1681/ASN.2009070784
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