4.0 Article

Multimodal imaging analysis of macular dystrophy in patient with maternally inherited diabetes and deafness (MIDD) with m.3243A>G mutation

Related references

Note: Only part of the references are listed.
Review Ophthalmology

Mitochondrial disorders and the eye

Eli Kisilevsley et al.

SURVEY OF OPHTHALMOLOGY (2020)

Article Multidisciplinary Sciences

Quantitative Variation in m.3243A > G Mutation Produce Discrete Changes in Energy Metabolism

Ryan P. McMillan et al.

SCIENTIFIC REPORTS (2019)

Article Medicine, Research & Experimental

mtDNA heteroplasmy level and copy number indicate disease burden in m.3243A>G mitochondrial disease

John P. Grady et al.

EMBO MOLECULAR MEDICINE (2018)

Article Genetics & Heredity

Ophthalmological findings in 74 patients with mitochondrial disease

Cheng-Cheng Zhu et al.

OPHTHALMIC GENETICS (2017)

Article Ophthalmology

ISCEV Standard for full-field clinical electroretinography (2015 update)

Daphne L. McCulloch et al.

DOCUMENTA OPHTHALMOLOGICA (2015)

Article Ophthalmology

ANATOMICAL CORRELATES TO THE BANDS SEEN IN THE OUTER RETINA BY OPTICAL COHERENCE TOMOGRAPHY Literature Review and Model

Richard F. Spaide et al.

RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES (2011)

Review Pathology

Mitochondrial Energetics and Therapeutics

Douglas C. Wallace et al.

ANNUAL REVIEW OF PATHOLOGY-MECHANISMS OF DISEASE (2010)

Article Endocrinology & Metabolism

The Clinical Variability of Maternally Inherited Diabetes and Deafness Is Associated with the Degree of Heteroplasmy in Blood Leukocytes

M. Laloi-Michelin et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2009)

Article Genetics & Heredity

Mitochondrial DNA mutations in human disease

S Dimauro et al.

AMERICAN JOURNAL OF MEDICAL GENETICS (2001)