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Dorothea Besch

Showing results (1-10 of 44) with videos related to

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Acta Ophthalmologica Scandinavica|July 21, 2005
Glare sensitivity and professional drivers' safety: a case of rod-cone dystrophy with negative electroretinogramHerbert Jägle, Dorothea Besch
Documenta Ophthalmologica. Advances in Ophthalmology|April 5, 2003
Prevention and therapy in hereditary retinal degenerationsDorothea Besch, Eberhart Zrenner
Klinische Monatsblatter Fur Augenheilkunde|October 12, 2017
[Acute Diplopia: Differential Diagnosis and Treatment Options]Carina Kelbsch, Dorothea Besch, Helmut Wilhelm
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|May 17, 2012
Management of strabismus with hemianopic visual field defectsMelanie van Waveren, Herbert Jägle, Dorothea Besch
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|November 7, 2018
Refractive adaptation and efficacy of occlusion therapy in untreated amblyopic patients aged 12 to 40 yearsBrigitte Simonsz-Tóth, Maurits V Joosse, Dorothea Besch
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|April 5, 2002
A mutational hot spot in the mitochondrial ND6 gene in patients with Leber's hereditary optic neuropathyJanina Luberichs, Beate Leo-Kottler, Dorothea Besch, et al.
Ophthalmic Genetics|September 27, 2002
Confirmation of the 14568 mutation in the mitochondrial ND6 gene as causative in Leber's hereditary optic neuropathySascha Fauser, Beate Leo-Kottler, Dorothea Besch, et al.
Biochemical and Biophysical Research Communications|August 2, 2002
Sequence analysis of the complete mitochondrial genome in patients with Leber's hereditary optic neuropathy lacking the three most common pathogenic DNA mutationsSascha Fauser, Janina Luberichs, Dorothea Besch, et al.
The British Journal of Ophthalmology|November 18, 2021
PandAcuity in paediatrics: a novel clinical measure of visual function based on the panda illusionCarina Kelbsch, Bettina Spieth, Eberhart Zrenner, et al.
Neuropediatrics|January 1, 2013
Visual loss without headache in children with pseudotumor cerebri and growth hormone treatmentDorothea Besch, Christine Makowski, Marc-Matthias Steinborn, et al.
Pageof 5

Showing results (1-10 of 44) with videos related to

Sort By:
Pageof 5
Acta Ophthalmologica Scandinavica|July 21, 2005
Glare sensitivity and professional drivers' safety: a case of rod-cone dystrophy with negative electroretinogramHerbert Jägle, Dorothea Besch
Documenta Ophthalmologica. Advances in Ophthalmology|April 5, 2003
Prevention and therapy in hereditary retinal degenerationsDorothea Besch, Eberhart Zrenner
Klinische Monatsblatter Fur Augenheilkunde|October 12, 2017
[Acute Diplopia: Differential Diagnosis and Treatment Options]Carina Kelbsch, Dorothea Besch, Helmut Wilhelm
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|May 17, 2012
Management of strabismus with hemianopic visual field defectsMelanie van Waveren, Herbert Jägle, Dorothea Besch
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|November 7, 2018
Refractive adaptation and efficacy of occlusion therapy in untreated amblyopic patients aged 12 to 40 yearsBrigitte Simonsz-Tóth, Maurits V Joosse, Dorothea Besch
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|April 5, 2002
A mutational hot spot in the mitochondrial ND6 gene in patients with Leber's hereditary optic neuropathyJanina Luberichs, Beate Leo-Kottler, Dorothea Besch, et al.
Ophthalmic Genetics|September 27, 2002
Confirmation of the 14568 mutation in the mitochondrial ND6 gene as causative in Leber's hereditary optic neuropathySascha Fauser, Beate Leo-Kottler, Dorothea Besch, et al.
Biochemical and Biophysical Research Communications|August 2, 2002
Sequence analysis of the complete mitochondrial genome in patients with Leber's hereditary optic neuropathy lacking the three most common pathogenic DNA mutationsSascha Fauser, Janina Luberichs, Dorothea Besch, et al.
The British Journal of Ophthalmology|November 18, 2021
PandAcuity in paediatrics: a novel clinical measure of visual function based on the panda illusionCarina Kelbsch, Bettina Spieth, Eberhart Zrenner, et al.
Neuropediatrics|January 1, 2013
Visual loss without headache in children with pseudotumor cerebri and growth hormone treatmentDorothea Besch, Christine Makowski, Marc-Matthias Steinborn, et al.
Pageof 5