| P50 | author | Kristina Narfström | Q4968951 |
| P2093 | author name string | Joan R Coates | |
| | Martin L Katz | |
| | Rebecca E H Whiting | |
| | Jacqueline W Pearce | |
| | Leilani J Castaner | |
| | Gang Yao | |
| P2860 | cites work | A mutation in the cathepsin D gene (CTSD) in American Bulldogs with neuronal ceroid lipofuscinosis | Q46874383 |
| | Sex-specific lateralization of contraction anisocoria in transient pupillary light reflex | Q47312350 |
| | The neuronal ceroid-lipofuscinoses: a historical introduction | Q48384621 |
| | Intrathecal tripeptidyl-peptidase 1 reduces lysosomal storage in a canine model of late infantile neuronal ceroid lipofuscinosis | Q49017608 |
| | Ultraviolet light-induced and green light-induced transient pupillary light reflex in mice. | Q50707637 |
| | A truncating mutation in ATP13A2 is responsible for adult-onset neuronal ceroid lipofuscinosis in Tibetan terriers. | Q54608818 |
| | Automated standardized pupillometry with optical method for purposes of clinical practice and research | Q74261318 |
| | Effect of gene therapy on visual function in Leber's congenital amaurosis | Q28277981 |
| | Distinct contributions of rod, cone, and melanopsin photoreceptors to encoding irradiance. | Q33872959 |
| | A mutation in canine PPT1 causes early onset neuronal ceroid lipofuscinosis in a Dachshund | Q34092211 |
| | Diminished pupillary light reflex at high irradiances in melanopsin-knockout mice. | Q34169762 |
| | Use of model organisms for the study of neuronal ceroid lipofuscinosis | Q34323680 |
| | A missense mutation in canine CLN6 in an Australian shepherd with neuronal ceroid lipofuscinosis | Q34460688 |
| | The neuronal ceroid-lipofuscinoses: from past to present | Q34557117 |
| | Neuronal ceroid lipofuscinoses therapeutic strategies: past, present and future | Q34574898 |
| | Neuronal ceroid lipofuscinosis in 3 Australian shepherd littermates | Q34589771 |
| | Treatment of lysosomal storage disorders: focus on the neuronal ceroid-lipofuscinoses. | Q34594922 |
| | Toward a clinical protocol for assessing rod, cone, and melanopsin contributions to the human pupil response | Q35221107 |
| | Cone-based vision in the aging mouse | Q36103372 |
| | Pupillometric analysis for assessment of gene therapy in Leber Congenital Amaurosis patients | Q36478463 |
| | Functional biology of the neuronal ceroid lipofuscinoses (NCL) proteins. | Q36535298 |
| | Three-year follow-up after unilateral subretinal delivery of adeno-associated virus in patients with Leber congenital Amaurosis type 2 | Q36906324 |
| | Quantitative assessment of the canine pupillary light reflex | Q37095330 |
| | Gene therapy for late infantile neuronal ceroid lipofuscinosis: neurosurgical considerations. | Q39851951 |
| | The eclectroretinogram: its components and their origins | Q40012949 |
| | A frame shift mutation in canine TPP1 (the ortholog of human CLN2) in a juvenile Dachshund with neuronal ceroid lipofuscinosis | Q40333380 |
| | In vivo gene therapy in young and adult RPE65-/- dogs produces long-term visual improvement. | Q40594379 |
| | Guidelines for clinical electroretinography in the dog. | Q40618068 |
| | Gene therapy restores vision in a canine model of childhood blindness | Q43590733 |
| | Autonomic components of the human pupillary light reflex | Q44157613 |
| | Functional and structural recovery of the retina after gene therapy in the RPE65 null mutation dog. | Q44376450 |
| | Standard for clinical electroretinography (2004 update). | Q45084219 |
| | A mutation in the CLN8 gene in English Setter dogs with neuronal ceroid-lipofuscinosis | Q45209232 |
| | Retinal pathology in a canine model of late infantile neuronal ceroid lipofuscinosis | Q46698740 |
| P921 | main subject | Infantile neuronal ceroid lipofuscinosis | Q4357262 |
| P304 | page(s) | 402-410 | |
| P577 | publication date | 2013-10-14 | |
| P1433 | published in | Experimental Eye Research | Q15754753 |
| P1476 | title | Pupillary light reflex deficits in a canine model of late infantile neuronal ceroid lipofuscinosis | |
| P478 | volume | 116 | |