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Naveed Nilforushan

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Investigative Ophthalmology & Visual Science|March 27, 2012
Structure-function relationships between spectral-domain OCT and standard achromatic perimetryNaveed Nilforushan, Nariman Nassiri, Sasan Moghimi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 30, 2022
Huntington's disease and neurovascular structure of retinaElahe Amini, Mehdi Moghaddasi, Seyed Amir Hassan Habibi, et al.
Journal of Glaucoma|October 3, 2014
Technique of combined glaucoma tube shunt and keratoprosthesis implantationSimon K Law, Jennifer S Huang, Nariman Nassiri, et al.
Human Molecular Genetics|August 7, 2009
Loss of function mutations in the gene encoding latent transforming growth factor beta binding protein 2, LTBP2, cause primary congenital glaucomaMehrnaz Narooie-Nejad, Seyed Hassan Paylakhi, Seyedmehdi Shojaee, et al.
Human Mutation|April 28, 2012
LTBP2 mutations cause Weill-Marchesani and Weill-Marchesani-like syndrome and affect disruptions in the extracellular matrixRamona Haji-Seyed-Javadi, Sahar Jelodari-Mamaghani, Seyed Hassan Paylakhi, et al.
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Showing results (41-50 of 45) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 45 results.
Investigative Ophthalmology & Visual Science|March 27, 2012
Structure-function relationships between spectral-domain OCT and standard achromatic perimetryNaveed Nilforushan, Nariman Nassiri, Sasan Moghimi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 30, 2022
Huntington's disease and neurovascular structure of retinaElahe Amini, Mehdi Moghaddasi, Seyed Amir Hassan Habibi, et al.
Journal of Glaucoma|October 3, 2014
Technique of combined glaucoma tube shunt and keratoprosthesis implantationSimon K Law, Jennifer S Huang, Nariman Nassiri, et al.
Human Molecular Genetics|August 7, 2009
Loss of function mutations in the gene encoding latent transforming growth factor beta binding protein 2, LTBP2, cause primary congenital glaucomaMehrnaz Narooie-Nejad, Seyed Hassan Paylakhi, Seyedmehdi Shojaee, et al.
Human Mutation|April 28, 2012
LTBP2 mutations cause Weill-Marchesani and Weill-Marchesani-like syndrome and affect disruptions in the extracellular matrixRamona Haji-Seyed-Javadi, Sahar Jelodari-Mamaghani, Seyed Hassan Paylakhi, et al.
Pageof 5