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Klinische Monatsblatter Fur Augenheilkunde
|
September 18, 2025
[An (Un)Classical Venous Event]
Emanuel Valentin Reitemeyer, Maximilian Hammer, Annette Schmidt-Bacher, et al.
Plos One
|
May 13, 2016
Adding Papillomacular Bundle Measurements to Standard Optical Coherence Tomography Does Not Increase Sensitivity to Detect Prior Optic Neuritis in Patients with Multiple Sclerosis
Mona Laible, Sven Jarius, Friedericke Mackensen, et al.
Journal of the Neurological Sciences
|
March 15, 2011
An unusual case of optic neuritis
Daniela Doegel, Wolf Mueller, Martina Deckert, et al.
The Journal of Rheumatology
|
November 19, 2013
Experiences with rituximab for the treatment of autoimmune diseases with ocular involvement
Laura Pelegrin, Eva Jakob, Annette Schmidt-Bacher, et al.
European Journal of Human Genetics : EJHG
|
March 26, 2015
SIPA1L3 identified by linkage analysis and whole-exome sequencing as a novel gene for autosomal recessive congenital cataract
Christina Evers, Nagarajan Paramasivam, Katrin Hinderhofer, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 5) with videos related to
Sort By:
Page
of 1
Klinische Monatsblatter Fur Augenheilkunde
|
September 18, 2025
[An (Un)Classical Venous Event]
Emanuel Valentin Reitemeyer, Maximilian Hammer, Annette Schmidt-Bacher, et al.
Plos One
|
May 13, 2016
Adding Papillomacular Bundle Measurements to Standard Optical Coherence Tomography Does Not Increase Sensitivity to Detect Prior Optic Neuritis in Patients with Multiple Sclerosis
Mona Laible, Sven Jarius, Friedericke Mackensen, et al.
Journal of the Neurological Sciences
|
March 15, 2011
An unusual case of optic neuritis
Daniela Doegel, Wolf Mueller, Martina Deckert, et al.
The Journal of Rheumatology
|
November 19, 2013
Experiences with rituximab for the treatment of autoimmune diseases with ocular involvement
Laura Pelegrin, Eva Jakob, Annette Schmidt-Bacher, et al.
European Journal of Human Genetics : EJHG
|
March 26, 2015
SIPA1L3 identified by linkage analysis and whole-exome sequencing as a novel gene for autosomal recessive congenital cataract
Christina Evers, Nagarajan Paramasivam, Katrin Hinderhofer, et al.
Page
of 1