Multimodal imaging of Hypotrichosis with juvenile macular dystrophy: a case report
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1471-2415
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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Multimodal imaging of Hypotrichosis with juvenile macular dystrophy: a case report ; volume:21 ; number:1 ; day:23 ; month:7 ; year:2021 ; pages:1-6 ; date:12.2021
BMC ophthalmology ; 21, Heft 1 (23.7.2021), 1-6, 12.2021
- Creator
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Scalzo, Giovanna Carnovale
Carnevali, Adriano
Piccoli, Gabriele
Ceravolo, Domenico
Bruzzichessi, Donatella
Iuliano, Rodolfo
Tallerico, Rossana
Gatti, Valentina
Giannaccare, Giuseppe
Scorcia, Vincenzo
- Contributor
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SpringerLink (Online service)
- DOI
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10.1186/s12886-021-02037-8
- URN
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urn:nbn:de:101:1-2021102321513565146746
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:27 AM CEST
Data provider
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Scalzo, Giovanna Carnovale
- Carnevali, Adriano
- Piccoli, Gabriele
- Ceravolo, Domenico
- Bruzzichessi, Donatella
- Iuliano, Rodolfo
- Tallerico, Rossana
- Gatti, Valentina
- Giannaccare, Giuseppe
- Scorcia, Vincenzo
- SpringerLink (Online service)
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Correction: Multimodal imaging of Hypotrichosis with juvenile macular dystrophy: a case report
Multimodal imaging features and genetic findings in Bietti crystalline dystrophy
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Non-syndromic OTX2-associated pattern dystrophy: a 10-year multimodal imaging study
New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
Varied clinical presentations of RP1L1 variants in Chinese patients: a study of occult macular dystrophy and vitelliform macular dystrophy
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The possible pathogenesis of macular caldera in patients with North Carolina macular dystrophy
Best vitelliform macular dystrophy in a large Brazilian family
Macular dystrophy in Kabuki syndrome due to de novo KMT2D variants: refining the phenotype with multimodal imaging and follow-up over 10 years: insight into pathophysiology
Comments on “The possible pathogenesis of macular caldera in patients with North Carolina macular dystrophy”