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M Meire

Showing results (31-40 of 40) with videos related to

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International Ophthalmology|August 11, 2000
Retinopathy following measles, mumps, and rubella vaccination in an immuno-incompetent girlJ Schuil, E M van de Putte, C M Zwaan, et al.
Ophthalmology|November 14, 2008
A new locus for congenital cataract, microcornea, microphthalmia, and atypical iris coloboma maps to chromosome 2Hana Abouzeid, Françoise M Meire, Ihab Osman, et al.
Cryobiology|December 6, 2011
Pulpal regeneration and root development after subcutaneous transplantation of cryopreserved immature teeth in ratsL Temmerman, A Vral, M Meire, et al.
The British Journal of Ophthalmology|May 19, 2006
Chiasmal misrouting and foveal hypoplasia without albinismM M van Genderen, F C C Riemslag, J Schuil, et al.
Journal of Medical Genetics|January 16, 2007
Borate transporter SLC4A11 mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophyJulie Desir, Graciela Moya, Orit Reish, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|March 14, 2014
Congenital fixed dilated pupils due to ACTA2- multisystemic smooth muscle dysfunction syndromeFrançoise M J Roulez, Fran Faes, Patricia Delbeke, et al.
Biofilm|January 15, 2021
Laser-induced vapor nanobubbles improve diffusion in biofilms of antimicrobial agents for wound careE Teirlinck, J C Fraire, H Van Acker, et al.
American Journal of Ophthalmology|November 9, 2004
Dominant optic atrophy, sensorineural hearing loss, ptosis, and ophthalmoplegia: a syndrome caused by a missense mutation in OPA1Marielle Payne, Zhenglin Yang, Bradley J Katz, et al.
Molecular Genetics and Metabolism|June 30, 2000
Prevalence of AIPL1 mutations in inherited retinal degenerative diseaseM M Sohocki, I Perrault, B P Leroy, et al.
American Journal of Human Genetics|November 10, 2009
Mutations in TRPM1 are a common cause of complete congenital stationary night blindnessMaria M van Genderen, Mieke M C Bijveld, Yvonne B Claassen, et al.
Pageof 4

Showing results (31-40 of 40) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 40 results.
International Ophthalmology|August 11, 2000
Retinopathy following measles, mumps, and rubella vaccination in an immuno-incompetent girlJ Schuil, E M van de Putte, C M Zwaan, et al.
Ophthalmology|November 14, 2008
A new locus for congenital cataract, microcornea, microphthalmia, and atypical iris coloboma maps to chromosome 2Hana Abouzeid, Françoise M Meire, Ihab Osman, et al.
Cryobiology|December 6, 2011
Pulpal regeneration and root development after subcutaneous transplantation of cryopreserved immature teeth in ratsL Temmerman, A Vral, M Meire, et al.
The British Journal of Ophthalmology|May 19, 2006
Chiasmal misrouting and foveal hypoplasia without albinismM M van Genderen, F C C Riemslag, J Schuil, et al.
Journal of Medical Genetics|January 16, 2007
Borate transporter SLC4A11 mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophyJulie Desir, Graciela Moya, Orit Reish, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|March 14, 2014
Congenital fixed dilated pupils due to ACTA2- multisystemic smooth muscle dysfunction syndromeFrançoise M J Roulez, Fran Faes, Patricia Delbeke, et al.
Biofilm|January 15, 2021
Laser-induced vapor nanobubbles improve diffusion in biofilms of antimicrobial agents for wound careE Teirlinck, J C Fraire, H Van Acker, et al.
American Journal of Ophthalmology|November 9, 2004
Dominant optic atrophy, sensorineural hearing loss, ptosis, and ophthalmoplegia: a syndrome caused by a missense mutation in OPA1Marielle Payne, Zhenglin Yang, Bradley J Katz, et al.
Molecular Genetics and Metabolism|June 30, 2000
Prevalence of AIPL1 mutations in inherited retinal degenerative diseaseM M Sohocki, I Perrault, B P Leroy, et al.
American Journal of Human Genetics|November 10, 2009
Mutations in TRPM1 are a common cause of complete congenital stationary night blindnessMaria M van Genderen, Mieke M C Bijveld, Yvonne B Claassen, et al.
Pageof 4