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Review

Monitoring and Management of the Patient with Stargardt Disease

ORCID Icon, , ORCID Icon, & ORCID Icon
Pages 151-165 | Published online: 28 Nov 2019

Keep up to date with the latest research on this topic with citation updates for this article.

Read on this site (3)

Jiaxin Bian, Hongyu Chen, Junhui Sun, Yuqing Cao, Jianhong An, Qing Pan & Ming Qi. (2021) Gene Therapy for Rdh12-Associated Retinal Diseases Helps to Delay Retinal Degeneration and Vision Loss. Drug Design, Development and Therapy 15, pages 3581-3591.
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Vincenzo Starace, Marco Battista, Maria Brambati, Matteo Pederzolli, Chiara Viganò, Alessandro Arrigo, Maria Vittoria Cicinelli, Francesco Bandello & Maurizio Battaglia Parodi. (2021) Genotypic and phenotypic factors influencing the rate of progression in ABCA-4-related Stargardt disease. Expert Review of Ophthalmology 16:2, pages 67-79.
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Articles from other publishers (8)

Chung-Ting Wang, Yin-Hsi Chang, Gavin S. W. Tan, Shu Yen Lee, R. V. Paul Chan, Wei-Chi Wu & Andrew S. H. Tsai. (2023) Optical Coherence Tomography and Optical Coherence Tomography Angiography in Pediatric Retinal Diseases. Diagnostics 13:8, pages 1461.
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Audrey Voisin, Amaury Pénaguin, Afsaneh Gaillard & Nicolas Leveziel. (2023) Stem cell therapy in retinal diseases. Neural Regeneration Research 18:7, pages 1478.
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Xuan Xiao, Lin Ye, Changzheng Chen, Hongmei Zheng & Jiajia Yuan. (2022) Clinical Observation and Genotype-Phenotype Analysis of ABCA4- Related Hereditary Retinal Degeneration before Gene Therapy. Current Gene Therapy 22:4, pages 342-351.
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S. Peñarrocha-Oltra, Á. Rallo-López & E. Escrivá-Pastor. (2021) Stargardt disease: A clinical case report of two sisters with different clinical development. Archivos de la Sociedad Española de Oftalmología (English Edition) 96:12, pages 673-676.
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S. Peñarrocha-Oltra, Á. Rallo-López & E. Escrivá-Pastor. (2021) Enfermedad de Stargardt: a propósito de dos hermanas con distintas evoluciones clínicas. Archivos de la Sociedad Española de Oftalmología 96:12, pages 673-676.
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Virginie M.M. Buhler, Lieselotte Berger, André Schaller, Martin S. Zinkernagel, Sebastian Wolf & Pascal Escher. (2021) Absence of Genotype/Phenotype Correlations Requires Molecular Diagnostic to Ascertain Stargardt and Stargardt-Like Swiss Patients. Genes 12:6, pages 812.
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Maurizio Battaglia Parodi, Pierluigi Iacono & Stefano Da Pozzo. (2020) Anti-VEGF and Retinal Dystrophies. Current Drug Targets 21:12, pages 1201-1207.
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Maria Vittoria Cicinelli, Alessandro Marchese, Alessandro Bordato, Maria Pia Manitto, Francesco Bandello & Maurizio Battaglia Parodi. (2020) Reviewing the Role of Ultra-Widefield Imaging in Inherited Retinal Dystrophies. Ophthalmology and Therapy 9:2, pages 249-263.
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