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Martin Snead

Showing results (1-10 of 12) with videos related to

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Genes|October 27, 2022
A Novel Transcriptome Approach to the Investigation of the Molecular Pathology of Vitreous and Retinal DetachmentMel Maranian, Martin Snead
Retinal Cases & Brief Reports|October 18, 2016
BILATERAL INTRAOCULAR HEMORRHAGE SECONDARY TO CEREBRAL VENOUS SINUS THROMBOSISFeyi Kunle-Hassan, Minaxi Dattani, Martin Snead, et al.
Acta Ophthalmologica|July 24, 2020
Assessing bulk emulsification at the silicone oil - saline solution interface in a 3D model of the eyeRu Wang, Martin Snead, Philip Alexander, et al.
Journal of Pediatric Ophthalmology and Strabismus|December 31, 2005
Lamellar macular hole as the presenting feature in a child with Coats' diseaseAlexander S Ioannidis, Alki Liasis, James Sheldrick, et al.
JAMA Ophthalmology|May 27, 2016
Clinicopathologic Correlation of Lens Epithelial Metaplasia and Late Intraocular Lens Dislocation After Repair of Retinal DetachmentLing Zhi Heng, Ranjit Sandhu, D R J Snead, et al.
Therapeutic Advances in Rare Disease|May 14, 2023
Therapeutic and diagnostic advances in Stickler syndromeMartin Snead, Howard Martin, Peter Bale, et al.
BMC Medical Genetics|April 30, 2013
Deletions within COL11A1 in Type 2 stickler syndrome detected by multiplex ligation-dependent probe amplification (MLPA)Raymon Vijzelaar, Sarah Waller, Abdellatif Errami, et al.
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|September 9, 2020
Auditory dysfunction in type 2 Stickler SyndromePhilip Alexander, Philip Gomersall, Jack Stancel-Lewis, et al.
American Journal of Medical Genetics. Part A|February 24, 2007
Vitreous phenotype: a key diagnostic sign in Stickler syndrome types 1 and 2 complicated by double heterozygosityAlan Ang, Tsiang Ung, Narman Puvanachandra, et al.
Archives of Disease in Childhood|March 7, 2023
Legg-Calve-Perthes' disease: an opportunity to prevent blindness?Aijing Wang, Thomas Nixon, Howard Martin, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Genes|October 27, 2022
A Novel Transcriptome Approach to the Investigation of the Molecular Pathology of Vitreous and Retinal DetachmentMel Maranian, Martin Snead
Retinal Cases & Brief Reports|October 18, 2016
BILATERAL INTRAOCULAR HEMORRHAGE SECONDARY TO CEREBRAL VENOUS SINUS THROMBOSISFeyi Kunle-Hassan, Minaxi Dattani, Martin Snead, et al.
Acta Ophthalmologica|July 24, 2020
Assessing bulk emulsification at the silicone oil - saline solution interface in a 3D model of the eyeRu Wang, Martin Snead, Philip Alexander, et al.
Journal of Pediatric Ophthalmology and Strabismus|December 31, 2005
Lamellar macular hole as the presenting feature in a child with Coats' diseaseAlexander S Ioannidis, Alki Liasis, James Sheldrick, et al.
JAMA Ophthalmology|May 27, 2016
Clinicopathologic Correlation of Lens Epithelial Metaplasia and Late Intraocular Lens Dislocation After Repair of Retinal DetachmentLing Zhi Heng, Ranjit Sandhu, D R J Snead, et al.
Therapeutic Advances in Rare Disease|May 14, 2023
Therapeutic and diagnostic advances in Stickler syndromeMartin Snead, Howard Martin, Peter Bale, et al.
BMC Medical Genetics|April 30, 2013
Deletions within COL11A1 in Type 2 stickler syndrome detected by multiplex ligation-dependent probe amplification (MLPA)Raymon Vijzelaar, Sarah Waller, Abdellatif Errami, et al.
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|September 9, 2020
Auditory dysfunction in type 2 Stickler SyndromePhilip Alexander, Philip Gomersall, Jack Stancel-Lewis, et al.
American Journal of Medical Genetics. Part A|February 24, 2007
Vitreous phenotype: a key diagnostic sign in Stickler syndrome types 1 and 2 complicated by double heterozygosityAlan Ang, Tsiang Ung, Narman Puvanachandra, et al.
Archives of Disease in Childhood|March 7, 2023
Legg-Calve-Perthes' disease: an opportunity to prevent blindness?Aijing Wang, Thomas Nixon, Howard Martin, et al.
Pageof 2