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International Journal of Molecular Sciences
|
July 12, 2025
Novel Genetic Variants and Clinical Profiles in Peters Anomaly Spectrum Disorders
Flora Delas, Samuel Koller, Jordi Maggi, et al.
BMC Medical Genetics
|
March 2, 2017
Characterization of two novel intronic OPA1 mutations resulting in aberrant pre-mRNA splicing
Ramona Bolognini, Christina Gerth-Kahlert, Mathias Abegg, et al.
Investigative Ophthalmology & Visual Science
|
November 4, 2024
Retinal Function in Advanced Multiple Sclerosis
James V M Hanson, Sara Single, Rahel B Eberle, et al.
Genes
|
January 8, 2025
Retinal Dystrophy Associated with Homozygous Variants in <i>NRL</i>
Jordi Maggi, James V M Hanson, Lisa Kurmann, et al.
American Journal of Medical Genetics. Part A
|
June 2, 2021
Confirmation of Ogden syndrome as an X-linked recessive fatal disorder due to a recurrent NAA10 variant and review of the literature
Laura Gogoll, Katharina Steindl, Pascal Joset, et al.
Investigative Ophthalmology & Visual Science
|
January 27, 2018
Outer Retinal Dysfunction in the Absence of Structural Abnormalities in Multiple Sclerosis
James V M Hanson, Michael Hediger, Praveena Manogaran, et al.
Investigative Ophthalmology & Visual Science
|
January 27, 2018
Outer Retinal Dysfunction in the Absence of Structural Abnormalities in Multiple Sclerosis
James V M Hanson, Michael Hediger, Praveena Manogaran, et al.
Journal of Ophthalmology
|
April 24, 2018
Outcome of Pediatric Cataract Surgeries in a Tertiary Center in Switzerland
Sarah Claudia Ambroz, Marc Töteberg-Harms, James V M Hanson, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society
|
April 19, 2021
The "Eyelet Sign" as an MRI Clue for Inflammatory Brown Syndrome
Fabienne C Fierz, Klara Landau, Raimund Kottke, et al.
Eye (London, England)
|
May 23, 2024
Flicker electroretinogram in preterm infants
Aylin F Taner, James V M Hanson, Caroline Weber, et al.
Page
of 9
Search research articles
Search
Showing results (41-50 of 85) with videos related to
Sort By:
Page
of 9
International Journal of Molecular Sciences
|
July 12, 2025
Novel Genetic Variants and Clinical Profiles in Peters Anomaly Spectrum Disorders
Flora Delas, Samuel Koller, Jordi Maggi, et al.
BMC Medical Genetics
|
March 2, 2017
Characterization of two novel intronic OPA1 mutations resulting in aberrant pre-mRNA splicing
Ramona Bolognini, Christina Gerth-Kahlert, Mathias Abegg, et al.
Investigative Ophthalmology & Visual Science
|
November 4, 2024
Retinal Function in Advanced Multiple Sclerosis
James V M Hanson, Sara Single, Rahel B Eberle, et al.
Genes
|
January 8, 2025
Retinal Dystrophy Associated with Homozygous Variants in <i>NRL</i>
Jordi Maggi, James V M Hanson, Lisa Kurmann, et al.
American Journal of Medical Genetics. Part A
|
June 2, 2021
Confirmation of Ogden syndrome as an X-linked recessive fatal disorder due to a recurrent NAA10 variant and review of the literature
Laura Gogoll, Katharina Steindl, Pascal Joset, et al.
Investigative Ophthalmology & Visual Science
|
January 27, 2018
Outer Retinal Dysfunction in the Absence of Structural Abnormalities in Multiple Sclerosis
James V M Hanson, Michael Hediger, Praveena Manogaran, et al.
Investigative Ophthalmology & Visual Science
|
January 27, 2018
Outer Retinal Dysfunction in the Absence of Structural Abnormalities in Multiple Sclerosis
James V M Hanson, Michael Hediger, Praveena Manogaran, et al.
Journal of Ophthalmology
|
April 24, 2018
Outcome of Pediatric Cataract Surgeries in a Tertiary Center in Switzerland
Sarah Claudia Ambroz, Marc Töteberg-Harms, James V M Hanson, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society
|
April 19, 2021
The "Eyelet Sign" as an MRI Clue for Inflammatory Brown Syndrome
Fabienne C Fierz, Klara Landau, Raimund Kottke, et al.
Eye (London, England)
|
May 23, 2024
Flicker electroretinogram in preterm infants
Aylin F Taner, James V M Hanson, Caroline Weber, et al.
Page
of 9