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Felix Tonagel

Showing results (31-40 of 38) with videos related to

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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 21, 2009
Loss of the cholesterol-binding protein prominin-1/CD133 causes disk dysmorphogenesis and photoreceptor degenerationSerena Zacchigna, Hideyasu Oh, Michaela Wilsch-Bräuninger, et al.
Human Molecular Genetics|March 8, 2006
Mpp4 recruits Psd95 and Veli3 towards the photoreceptor synapseWendy M Aartsen, Albena Kantardzhieva, Jan Klooster, et al.
Advances in Experimental Medicine and Biology|January 26, 2007
Disease mechanisms and gene therapy in a mouse model for X-linked retinoschisisLaurie L Molday, Seok-Hong Min, Mathias W Seeliger, et al.
Brain : a Journal of Neurology|June 28, 2014
Pure and syndromic optic atrophy explained by deep intronic OPA1 mutations and an intralocus modifierTobias Bonifert, Kathrin N Karle, Felix Tonagel, et al.
Vision Research|September 29, 2005
In vivo confocal imaging of the retina in animal models using scanning laser ophthalmoscopyMathias W Seeliger, Susanne C Beck, Naira Pereyra-Muñoz, et al.
Journal of Medical Genetics|September 21, 2023
Diagnostic genome sequencing improves diagnostic yield: a prospective single-centre study in 1000 patients with inherited eye diseasesNicole Weisschuh, Pascale Mazzola, Theresia Zuleger, et al.
BMJ Open|March 3, 2016
Treatment of optic neuritis with erythropoietin (TONE): a randomised, double-blind, placebo-controlled trial-study protocolRicarda Diem, Fanni Molnar, Flemming Beisse, et al.
Brain Communications|May 31, 2021
Dominant <i>ACO2</i> mutations are a frequent cause of isolated optic atrophyMajida Charif, Naïg Gueguen, Marc Ferré, et al.
Pageof 4

Showing results (31-40 of 38) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 38 results.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 21, 2009
Loss of the cholesterol-binding protein prominin-1/CD133 causes disk dysmorphogenesis and photoreceptor degenerationSerena Zacchigna, Hideyasu Oh, Michaela Wilsch-Bräuninger, et al.
Human Molecular Genetics|March 8, 2006
Mpp4 recruits Psd95 and Veli3 towards the photoreceptor synapseWendy M Aartsen, Albena Kantardzhieva, Jan Klooster, et al.
Advances in Experimental Medicine and Biology|January 26, 2007
Disease mechanisms and gene therapy in a mouse model for X-linked retinoschisisLaurie L Molday, Seok-Hong Min, Mathias W Seeliger, et al.
Brain : a Journal of Neurology|June 28, 2014
Pure and syndromic optic atrophy explained by deep intronic OPA1 mutations and an intralocus modifierTobias Bonifert, Kathrin N Karle, Felix Tonagel, et al.
Vision Research|September 29, 2005
In vivo confocal imaging of the retina in animal models using scanning laser ophthalmoscopyMathias W Seeliger, Susanne C Beck, Naira Pereyra-Muñoz, et al.
Journal of Medical Genetics|September 21, 2023
Diagnostic genome sequencing improves diagnostic yield: a prospective single-centre study in 1000 patients with inherited eye diseasesNicole Weisschuh, Pascale Mazzola, Theresia Zuleger, et al.
BMJ Open|March 3, 2016
Treatment of optic neuritis with erythropoietin (TONE): a randomised, double-blind, placebo-controlled trial-study protocolRicarda Diem, Fanni Molnar, Flemming Beisse, et al.
Brain Communications|May 31, 2021
Dominant <i>ACO2</i> mutations are a frequent cause of isolated optic atrophyMajida Charif, Naïg Gueguen, Marc Ferré, et al.
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