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Barbara Käsmann-Kellner

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Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|January 14, 2021
[MDVI patients - Multiply disabled visually impaired : On the situation of the child, parents and ophthalmologist with MDVI children]Barbara Käsmann-Kellner, Berthold Seitz
Die Ophthalmologie|August 28, 2023
[Achromatopsia : Clinical aspects, diagnostics, genes, brain and quality of life]Barbara Käsmann-Kellner, Michael B Hoffmann
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|April 8, 2022
[Optical rehabilitation and pediatric ophthalmological care following keratoplasty for childhood corneal opacities]Barbara Käsmann-Kellner, Kayed Moslemani, Berthold Seitz
Klinische Monatsblatter Fur Augenheilkunde|February 9, 2019
[Clinical and Genetic Characteristics of Ocular Developmental Disorders: MAC-Spectrum, Anterior Segment Dysgenesis]Barbara Käsmann-Kellner, Kayed Moslemani, Berthold Seitz
Journal of Personalized Medicine|July 29, 2023
Morphological and Functional Aspects and Quality of Life in Patients with AchromatopsiaCaroline Chan, Berthold Seitz, Barbara Käsmann-Kellner
Klinische Monatsblatter Fur Augenheilkunde|November 25, 2003
[Prevalence of optic atrophy and associated ocular and systemic diseases in a department of paediatric ophthalmology]Christian Denne, Barbara Käsmann-Kellner, Klaus W Ruprecht
Retinal Cases & Brief Reports|September 21, 2016
MYCOPLASMA PNEUMONIA-ASSOCIATED CHOROIDAL NEOVASCULARIZATION-BEVACIZUMAB INTRAVITREAL INJECTION AND LASER TREATMENTMiltiadis Fiorentzis, Barbara Käsmann-Kellner, Sascha Meyer, et al.
Contact Lens & Anterior Eye : the Journal of the British Contact Lens Association|March 4, 2015
Can retinoscopy keep up in keratoconus diagnosis?Susanne Goebels, Barbara Käsmann-Kellner, Timo Eppig, et al.
Human Mutation|January 15, 2004
Mutations in the MATP gene in five German patients affected by oculocutaneous albinism type 4Uta Rundshagen, Christine Zühlke, Sven Opitz, et al.
Human Mutation|May 18, 2004
Detection of 53 novel DNA variations within the tyrosinase gene and accumulation of mutations in 17 patients with albinismSven Opitz, Barbara Käsmann-Kellner, Markus Kaufmann, et al.
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Showing results (1-10 of 48) with videos related to

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Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|January 14, 2021
[MDVI patients - Multiply disabled visually impaired : On the situation of the child, parents and ophthalmologist with MDVI children]Barbara Käsmann-Kellner, Berthold Seitz
Die Ophthalmologie|August 28, 2023
[Achromatopsia : Clinical aspects, diagnostics, genes, brain and quality of life]Barbara Käsmann-Kellner, Michael B Hoffmann
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|April 8, 2022
[Optical rehabilitation and pediatric ophthalmological care following keratoplasty for childhood corneal opacities]Barbara Käsmann-Kellner, Kayed Moslemani, Berthold Seitz
Klinische Monatsblatter Fur Augenheilkunde|February 9, 2019
[Clinical and Genetic Characteristics of Ocular Developmental Disorders: MAC-Spectrum, Anterior Segment Dysgenesis]Barbara Käsmann-Kellner, Kayed Moslemani, Berthold Seitz
Journal of Personalized Medicine|July 29, 2023
Morphological and Functional Aspects and Quality of Life in Patients with AchromatopsiaCaroline Chan, Berthold Seitz, Barbara Käsmann-Kellner
Klinische Monatsblatter Fur Augenheilkunde|November 25, 2003
[Prevalence of optic atrophy and associated ocular and systemic diseases in a department of paediatric ophthalmology]Christian Denne, Barbara Käsmann-Kellner, Klaus W Ruprecht
Retinal Cases & Brief Reports|September 21, 2016
MYCOPLASMA PNEUMONIA-ASSOCIATED CHOROIDAL NEOVASCULARIZATION-BEVACIZUMAB INTRAVITREAL INJECTION AND LASER TREATMENTMiltiadis Fiorentzis, Barbara Käsmann-Kellner, Sascha Meyer, et al.
Contact Lens & Anterior Eye : the Journal of the British Contact Lens Association|March 4, 2015
Can retinoscopy keep up in keratoconus diagnosis?Susanne Goebels, Barbara Käsmann-Kellner, Timo Eppig, et al.
Human Mutation|January 15, 2004
Mutations in the MATP gene in five German patients affected by oculocutaneous albinism type 4Uta Rundshagen, Christine Zühlke, Sven Opitz, et al.
Human Mutation|May 18, 2004
Detection of 53 novel DNA variations within the tyrosinase gene and accumulation of mutations in 17 patients with albinismSven Opitz, Barbara Käsmann-Kellner, Markus Kaufmann, et al.
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