Annie M. Mcninch
Cambridge, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 24 publications
Vitreous phenotyping distinguishes Wagner syndrome from ocular-only Stickler syndrome: a case series.
Journal: Eye (London, England)
Published: April 03, 2026
A simple questionnaire to prevent blindness-a cross-sectional study screening for Stickler syndrome in children.
Journal: Rheumatology (Oxford, England)
Published: January 22, 2026
Peripapillary Hyperreflective Ovoid Mass-Like Structures in Stickler Syndrome.
Journal: Ophthalmology. Retina
Published: April 11, 2024
Retinal detachment in Type IX collagen recessive Stickler syndrome.
Journal: Eye (London, England)
Published: January 24, 2024
Use of vitreous phenotype as a key clinical marker to identify Ocular-only Stickler syndrome in a family with Marfan syndrome.
Journal: European journal of ophthalmology
Published: April 09, 2023
Cambridge Prophylactic Protocol, Retinal Detachment, and Stickler Syndrome.
Journal: The New England journal of medicine
Published: April 05, 2023
Legg-Calve-Perthes' disease: an opportunity to prevent blindness?
Journal: Archives of disease in childhood
Published: November 18, 2022
Stickler syndrome - lessons from a national cohort.
Journal: Eye (London, England)
Published: March 16, 2021
Therapeutic and diagnostic advances in Stickler syndrome.
Journal: Therapeutic advances in rare disease
Published: October 07, 2020
Auditory dysfunction in type 2 Stickler Syndrome.
Journal: European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery
Published: June 05, 2020
Inherited and de novo biallelic pathogenic variants in COL11A1 result in type 2 Stickler syndrome with severe hearing loss.
Journal: Molecular genetics & genomic medicine
Published: March 10, 2020
Last Updated: 09/26/2026