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Philip Alexander

Showing results (71-80 of 114) with videos related to

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American Journal of Medical Genetics. Part A|May 16, 2019
Homozygous Type IX collagen variants (COL9A1, COL9A2, and COL9A3) causing recessive Stickler syndrome-Expanding the phenotypeThomas R W Nixon, Philip Alexander, Allan Richards, et al.
Methods in Molecular Biology (Clifton, N.J.)|September 7, 2023
Construction of Human Immune and Naive scFv Phage Display LibrariesMaximilian Ruschig, Philip Alexander Heine, Viola Fühner, et al.
Frontiers in Microbiology|December 22, 2018
Development of Neutralizing and Non-neutralizing Antibodies Targeting Known and Novel Epitopes of TcdB of <i>Clostridioides difficile</i>Viola Fühner, Philip Alexander Heine, Saskia Helmsing, et al.
European Journal of Ophthalmology|April 9, 2023
Use of vitreous phenotype as a key clinical marker to identify Ocular-only Stickler syndrome in a family with Marfan syndromeHammad Malik, Zack Soh, Thomas R W Nixon, et al.
Eye (London, England)|October 15, 2024
Retinal detachment in Type IX collagen recessive Stickler syndromeDaniel Maghsoudi, Thomas Rw Nixon, Howard Martin, et al.
Journal of Diabetes Science and Technology|February 3, 2016
The Evolution of Teleophthalmology Programs in the United Kingdom: Beyond Diabetic Retinopathy ScreeningDawn A Sim, Danny Mitry, Philip Alexander, 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.
European Journal of Human Genetics : EJHG|December 21, 2018
Bone morphogenetic protein 4 (BMP4) loss-of-function variant associated with autosomal dominant Stickler syndrome and renal dysplasiaThomas R W Nixon, Allan Richards, Laura K Towns, et al.
Journal of Neurology|June 29, 2026
Quantification of amyotrophic lateral sclerosis (ALS) disease accumulation with T1-weighted high-resolution magnetic resonance imaging: validation in an independent cohortPhilip Alexander Gremmler, Janina von der Gablentz, Julia Meyer, et al.
The New England Journal of Medicine|April 5, 2023
Cambridge Prophylactic Protocol, Retinal Detachment, and Stickler SyndromePhilip Alexander, Gregory S Fincham, Senjah Brown, et al.
Pageof 12

Showing results (71-80 of 114) with videos related to

Sort By:
Pageof 12
American Journal of Medical Genetics. Part A|May 16, 2019
Homozygous Type IX collagen variants (COL9A1, COL9A2, and COL9A3) causing recessive Stickler syndrome-Expanding the phenotypeThomas R W Nixon, Philip Alexander, Allan Richards, et al.
Methods in Molecular Biology (Clifton, N.J.)|September 7, 2023
Construction of Human Immune and Naive scFv Phage Display LibrariesMaximilian Ruschig, Philip Alexander Heine, Viola Fühner, et al.
Frontiers in Microbiology|December 22, 2018
Development of Neutralizing and Non-neutralizing Antibodies Targeting Known and Novel Epitopes of TcdB of <i>Clostridioides difficile</i>Viola Fühner, Philip Alexander Heine, Saskia Helmsing, et al.
European Journal of Ophthalmology|April 9, 2023
Use of vitreous phenotype as a key clinical marker to identify Ocular-only Stickler syndrome in a family with Marfan syndromeHammad Malik, Zack Soh, Thomas R W Nixon, et al.
Eye (London, England)|October 15, 2024
Retinal detachment in Type IX collagen recessive Stickler syndromeDaniel Maghsoudi, Thomas Rw Nixon, Howard Martin, et al.
Journal of Diabetes Science and Technology|February 3, 2016
The Evolution of Teleophthalmology Programs in the United Kingdom: Beyond Diabetic Retinopathy ScreeningDawn A Sim, Danny Mitry, Philip Alexander, 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.
European Journal of Human Genetics : EJHG|December 21, 2018
Bone morphogenetic protein 4 (BMP4) loss-of-function variant associated with autosomal dominant Stickler syndrome and renal dysplasiaThomas R W Nixon, Allan Richards, Laura K Towns, et al.
Journal of Neurology|June 29, 2026
Quantification of amyotrophic lateral sclerosis (ALS) disease accumulation with T1-weighted high-resolution magnetic resonance imaging: validation in an independent cohortPhilip Alexander Gremmler, Janina von der Gablentz, Julia Meyer, et al.
The New England Journal of Medicine|April 5, 2023
Cambridge Prophylactic Protocol, Retinal Detachment, and Stickler SyndromePhilip Alexander, Gregory S Fincham, Senjah Brown, et al.
Pageof 12