Diagnosis and treatment of bilateral Coats disease in a 5-year-old girl - Journal of American Association for Pediatric Ophthalmology and Strabismus {JAAPOS}
How to Diagnose and Manage Coats' Disease
Coats plus syndrome (cerebroretinal microangiopathy with calcifications and cysts‐1): A case report - Morgado - 2021 - Pediatric Dermatology - Wiley Online Library
Coats Disease and Coats Plus Syndrome - ScienceDirect
Novel compound heterozygous STN1 variants are associated with Coats Plus syndrome - Acharya - 2021 - Molecular Genetics & Genomic Medicine - Wiley Online Library
Coats Disease | Ento Key
Coats-plus syndrome: when imaging leads to genetic diagnosis | BMJ Case Reports
Coats plus syndrome
FAQs - Jack McGovern Coats' Disease Foundation
Coats Plus : la version systémique de la maladie de Coats | Semantic Scholar
Researchers identify a new genetic cause of C | EurekAlert!
Coats Plus Syndrome and Mutation of the TERT Gene: A Case Report
Coats Plus Syndrome.,JAMA Neurology - X-MOL
Coats plus syndrome (cerebroretinal microangiopathy with calcifications and cysts‐1): A case report - Morgado - 2021 - Pediatric Dermatology - Wiley Online Library
Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus | Nature Genetics
Teaching NeuroImages: Adult-onset leukoencephalopathy with intracranial calcifications and cysts (Labrune syndrome) | Neurology
Coats disease causes, symptoms, diagnosis, treatment & prognosis
Cerebro-retinal microangiopathy with calcifications and cysts due to recessive mutations in the CTC1 gene - ScienceDirect
Coats plus syndrome: MedlinePlus Genetics
Coats Plus : la version systémique de la maladie de Coats | Semantic Scholar
Coats' disease - Wikipedia
Coats Plus Syndrome and Mutation of the TERT Gene: A Case Report
Coats Plus Syndrome Archives - NORD (National Organization for Rare Disorders)
Cerebroretinal microangiopathy with calcifications and cysts - Wikipedia
