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M Andrassi

Showing results (1-10 of 8) with videos related to

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Klinische Monatsblatter Fur Augenheilkunde|January 1, 1996
[Incomplete congenital stationary night blindness (CSNB). An important differential diagnosis of congenital nystagmus]B Lorenz, M Andrassi, K D Miliczek
Documenta Ophthalmologica. Advances in Ophthalmology|April 15, 2000
A comparison of two multifocal ERG systemsM Bock, M Andrassi, L Belitsky, et al.
Klinische Monatsblatter Fur Augenheilkunde|September 16, 2016
[Handheld Optical Coherence Tomography in Paediatric Ophthalmology: Experience of the Department of Ophthalmology in Giessen]W Bowl, M Andrassi-Darida, K Holve, et al.
Clinical Genetics|August 18, 1999
Assessment of RS1 in X-linked juvenile retinoschisis and sporadic senile retinoschisisA Gehrig, K White, B Lorenz, et al.
The British Journal of Ophthalmology|December 3, 2015
Correlation of central visual function and ROP risk factors in prematures with and without acute ROP at the age of 6-13 years: the Giessen long-term ROP studyW Bowl, B Lorenz, K Stieger, et al.
Klinische Monatsblatter Fur Augenheilkunde|October 26, 2012
[Autosomal recessive bestrophinopathy (ARB): a clinical and molecular description of two patients at childhood]M N Preising, C Pasquay, C Friedburg, et al.
Investigative Ophthalmology & Visual Science|August 11, 2000
Early-onset severe rod-cone dystrophy in young children with RPE65 mutationsB Lorenz, P Gyürüs, M Preising, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
Mutations in the VMD2 gene are associated with juvenile-onset vitelliform macular dystrophy (Best disease) and adult vitelliform macular dystrophy but not age-related macular degenerationF Krämer, K White, D Pauleikhoff, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Klinische Monatsblatter Fur Augenheilkunde|January 1, 1996
[Incomplete congenital stationary night blindness (CSNB). An important differential diagnosis of congenital nystagmus]B Lorenz, M Andrassi, K D Miliczek
Documenta Ophthalmologica. Advances in Ophthalmology|April 15, 2000
A comparison of two multifocal ERG systemsM Bock, M Andrassi, L Belitsky, et al.
Klinische Monatsblatter Fur Augenheilkunde|September 16, 2016
[Handheld Optical Coherence Tomography in Paediatric Ophthalmology: Experience of the Department of Ophthalmology in Giessen]W Bowl, M Andrassi-Darida, K Holve, et al.
Clinical Genetics|August 18, 1999
Assessment of RS1 in X-linked juvenile retinoschisis and sporadic senile retinoschisisA Gehrig, K White, B Lorenz, et al.
The British Journal of Ophthalmology|December 3, 2015
Correlation of central visual function and ROP risk factors in prematures with and without acute ROP at the age of 6-13 years: the Giessen long-term ROP studyW Bowl, B Lorenz, K Stieger, et al.
Klinische Monatsblatter Fur Augenheilkunde|October 26, 2012
[Autosomal recessive bestrophinopathy (ARB): a clinical and molecular description of two patients at childhood]M N Preising, C Pasquay, C Friedburg, et al.
Investigative Ophthalmology & Visual Science|August 11, 2000
Early-onset severe rod-cone dystrophy in young children with RPE65 mutationsB Lorenz, P Gyürüs, M Preising, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
Mutations in the VMD2 gene are associated with juvenile-onset vitelliform macular dystrophy (Best disease) and adult vitelliform macular dystrophy but not age-related macular degenerationF Krämer, K White, D Pauleikhoff, et al.
Pageof 1