Rod and cone a-waves in three cases of Bietti crystalline chorioretinal dystrophyUSUI, Tomoaki; TANIMOTO, Naoyuki; TAKAGI, Mineo et al.American journal of ophthalmology. 2001, Vol 132, Num 3, pp 395-402, issn 0002-9394Article

Sacsin-related autosomal recessive ataxia without prominent retinal myelinated fibers in JapanHARA, Kenju; ONODERA, Osamu; ENDO, Minoru et al.Movement disorders. 2004, Vol 20, Num 3, pp 380-382, issn 0885-3185, 3 p.Article

R91W mutation in Rpe65 leads to milder early-onset retinal dystrophy due to the generation of low levels of 11-cis-retinalSAMARDZIJA, Marijana; VON LINTIG, Johannes; TANIMOTO, Naoyuki et al.Human molecular genetics (Print). 2008, Vol 17, Num 2, pp 281-292, issn 0964-6906, 12 p.Article

Night blindness with depolarizing pattern of ON/OFF response in electroretinogram : A case reportUSUI, Tomoaki; TANIMOTO, Naoyuki; UEKI, Satoshi et al.Documenta ophthalmologica. 2005, Vol 111, Num 1, pp 15-21, issn 0012-4486, 7 p.Article

Study of Gene-Targeted Mouse Models of Splicing Factor Gene Prpf31 Implicated in Human Autosomal Dominant Retinitis Pigmentosa (RP)BUJAKOWSKA, Kinga; MAUBARET, Cecilia; PAQUET-DURAND, François et al.Investigative ophthalmology & visual science. 2009, Vol 50, Num 12, pp 5927-5933, issn 0146-0404, 7 p.Article

RPE65 is essential for the function of cone photoreceptors in NRL-deficient miceWENZEL, Andreas; VON LINTIG, Johannes; OBERHAUSER, Vitus et al.Investigative ophthalmology & visual science. 2007, Vol 48, Num 2, pp 534-542, issn 0146-0404, 9 p.Article

In vivo confocal imaging of the retina in animal models using scanning laser ophthalmoscopySEELIGER, Mathias W; BECK, Susanne C; ZRENNER, Eberhart et al.Vision research (Oxford). 2005, Vol 45, Num 28, pp 3512-3519, issn 0042-6989, 8 p.Article

Mice lacking Period 1 and Period 2 circadian clock genes exhibit blue cone photoreceptor defectsAIT-HMYED, Ouafa; FELDER-SCHMITTBUHL, Marie-Paule; GARCIA-GARRIDO, Marina et al.European journal of neuroscience (Print). 2013, Vol 37, Num 7-8, pp 1048-1060, issn 0953-816X, 13 p.Article

Gene therapy restores vision and delays degeneration in the CNGB1^―/― mouse model of retinitis pigmentosaKOCH, Susanne; SOTHILINGAM, Vithiyanjali; MÜHLFRIEDEL, Regine et al.Human molecular genetics (Print). 2012, Vol 21, Num 20, pp 4486-4496, issn 0964-6906, 11 p.Article

Long-term fundus changes due to fundus albipunctatus associated with mutations in the RDH5 geneSEKIYA, Keigo; NAKAZAWA, Mitsuru; OHGURO, Hiroshi et al.Archives of ophthalmology (1960). 2003, Vol 121, Num 7, pp 1057-1059, issn 0003-9950, 3 p.Article

PIII and derived PII analysis in a patient with retinal dysfunction with supernormal scotopic ERGTANIMOTO, Naoyuki; USUI, Tomoaki; ICHIBE, Mikio et al.Documenta ophthalmologica. 2005, Vol 110, Num 2-3, pp 219-226, issn 0012-4486, 8 p.Article

Negative scotopic ERG and photopic ERG ON response impairment in a patient with normal dark adaptationTANIMOTO, Naoyuki; USUI, Tomoaki; ICHIBE, Mikio et al.Documenta ophthalmologica. 2006, Vol 113, Num 3, pp 171-177, issn 0012-4486, 7 p.Article

Central and peripheral visual interactions in disparity-induced vergence eye movements: I. Spatial interactionTANIMOTO, Naoyuki; TAKAGI, Mineo; BANDO, Takehiko et al.Investigative ophthalmology & visual science. 2004, Vol 45, Num 4, pp 1132-1138, issn 0146-0404, 7 p.Article

ERG rod a-wave in Oguchi diseaseUSUI, Tomoaki; TANIMOTO, Naoyuki; UEKI, Satoshi et al.Vision research (Oxford). 2004, Vol 44, Num 5, pp 535-540, issn 0042-6989, 6 p.Article

Electroretinographic findings in Three family members with X-linked juvenile retinoschisis associated with a novel Pro192Thr mutation of the XLRS1 geneTANIMOTO, Naoyuki; USUI, Tomoaki; TAKAGI, Mineo et al.Japanese journal of ophthalmology. 2002, Vol 46, Num 5, pp 568-576, issn 0021-5155Article

Advance Access published on December 10, 2010 A key role for cyclic nucleotide gated (CNG) channels in cGMP-related retinitis pigmentosaPAQUET-DURAND, François; BECK, Susanne; BECIROVIC, Elvir et al.Human molecular genetics (Print). 2011, Vol 20, Num 5, pp 941-947, issn 0964-6906, 7 p.Article

In conditions of limited chromophore supply rods entrap 11-cis-retinal leading to loss of cone function and cell deathSAMARDZIJA, Marijana; TANIMOTO, Naoyuki; WENZEL, Andreas et al.Human molecular genetics (Print). 2009, Vol 18, Num 7, pp 1266-1275, issn 0964-6906, 10 p.Article

Mpp4 recruits Psd95 and Veli3 towards the photoreceptor synapseAARTSEN, Wendy M; KANTARDZHIEVA, Albena; SEELIGER, Mathias W et al.Human molecular genetics (Print). 2006, Vol 15, Num 8, pp 1291-1302, issn 0964-6906, 12 p.Article