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Günter Rudolph

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

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Klinische Monatsblatter Fur Augenheilkunde|October 18, 2022
Safety Aspects of DIMS Technology Glasses, Fixation as a Marker for Amblyopia, Bielschowsky Head Tilt Test in Superior Oblique Paresis and Successful Late Topical Treatment of Orbital Infantile HemangiomaHerbert Jägle, Günter Rudolph, Göran Darius Hildebrand
Klinische Monatsblatter Fur Augenheilkunde|October 23, 2023
Keratoconus, Dry Eye Syndrome, Overnight Orthokeratology, Achromatopsia and Uveitis in ChildrenGöran Darius Hildebrand, Günter Rudolph, Herbert Jägle
Klinische Monatsblatter Fur Augenheilkunde|September 27, 2021
[Waardenburg's Syndrome Type IIA with Partial Albinism]Dominik Knebel, Günter Rudolph, Tina Herold, et al.
Klinische Monatsblatter Fur Augenheilkunde|October 23, 2019
[Leber's Hereditary Optic Neuropathy]Claudia Priglinger, Thomas Klopstock, Günter Rudolph, et al.
Klinische Monatsblatter Fur Augenheilkunde|March 30, 2021
Gene Therapy for Inherited Retinal Disorders: Update on Clinical TrialsStylianos Michalakis, Maximilian Gerhardt, Günter Rudolph, et al.
Klinische Monatsblatter Fur Augenheilkunde|March 30, 2021
Diagnosis of Inherited Retinal DiseasesJohannes Birtel, Imran H Yusuf, Claudia Priglinger, et al.
Die Ophthalmologie|July 12, 2023
[Corneal disease in childhood-Hereditary, degenerative or infectious?]Barbara S Brunner, Stefan Kassumeh, Günter Rudolph, et al.
Orphanet Journal of Rare Diseases|August 9, 2022
Vitamin B12 in Leber hereditary optic neuropathy mutation carriers: a prospective cohort studyJulia Zibold, Bettina von Livonius, Hana Kolarova, et al.
Molecular Genetics & Genomic Medicine|December 8, 2022
Characterization of a novel non-canonical splice site variant (c.886-5T>A) in NBAS and description of the associated phenotypeClaudia S Priglinger, Günter Rudolph, Irene Schmid, et al.
Human Mutation|September 2, 2011
Large deletions of the KCNV2 gene are common in patients with cone dystrophy with supernormal rod responseBernd Wissinger, Simone Schaich, Britta Baumann, et al.
Pageof 1

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

Sort By:
Pageof 1
Klinische Monatsblatter Fur Augenheilkunde|October 18, 2022
Safety Aspects of DIMS Technology Glasses, Fixation as a Marker for Amblyopia, Bielschowsky Head Tilt Test in Superior Oblique Paresis and Successful Late Topical Treatment of Orbital Infantile HemangiomaHerbert Jägle, Günter Rudolph, Göran Darius Hildebrand
Klinische Monatsblatter Fur Augenheilkunde|October 23, 2023
Keratoconus, Dry Eye Syndrome, Overnight Orthokeratology, Achromatopsia and Uveitis in ChildrenGöran Darius Hildebrand, Günter Rudolph, Herbert Jägle
Klinische Monatsblatter Fur Augenheilkunde|September 27, 2021
[Waardenburg's Syndrome Type IIA with Partial Albinism]Dominik Knebel, Günter Rudolph, Tina Herold, et al.
Klinische Monatsblatter Fur Augenheilkunde|October 23, 2019
[Leber's Hereditary Optic Neuropathy]Claudia Priglinger, Thomas Klopstock, Günter Rudolph, et al.
Klinische Monatsblatter Fur Augenheilkunde|March 30, 2021
Gene Therapy for Inherited Retinal Disorders: Update on Clinical TrialsStylianos Michalakis, Maximilian Gerhardt, Günter Rudolph, et al.
Klinische Monatsblatter Fur Augenheilkunde|March 30, 2021
Diagnosis of Inherited Retinal DiseasesJohannes Birtel, Imran H Yusuf, Claudia Priglinger, et al.
Die Ophthalmologie|July 12, 2023
[Corneal disease in childhood-Hereditary, degenerative or infectious?]Barbara S Brunner, Stefan Kassumeh, Günter Rudolph, et al.
Orphanet Journal of Rare Diseases|August 9, 2022
Vitamin B12 in Leber hereditary optic neuropathy mutation carriers: a prospective cohort studyJulia Zibold, Bettina von Livonius, Hana Kolarova, et al.
Molecular Genetics & Genomic Medicine|December 8, 2022
Characterization of a novel non-canonical splice site variant (c.886-5T>A) in NBAS and description of the associated phenotypeClaudia S Priglinger, Günter Rudolph, Irene Schmid, et al.
Human Mutation|September 2, 2011
Large deletions of the KCNV2 gene are common in patients with cone dystrophy with supernormal rod responseBernd Wissinger, Simone Schaich, Britta Baumann, et al.
Pageof 1