{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,9,27]],"date-time":"2025-09-27T17:01:43Z","timestamp":1758992503401},"reference-count":19,"publisher":"Springer Science and Business Media LLC","issue":"1","license":[{"start":{"date-parts":[[2009,1,10]],"date-time":"2009-01-10T00:00:00Z","timestamp":1231545600000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Doc Ophthalmol"],"published-print":{"date-parts":[[2009,8]]},"DOI":"10.1007\/s10633-008-9161-6","type":"journal-article","created":{"date-parts":[[2009,1,9]],"date-time":"2009-01-09T15:16:41Z","timestamp":1231514201000},"page":"1-7","source":"Crossref","is-referenced-by-count":7,"title":["Visually impaired children: \u201ccoming to better terms\u201d"],"prefix":"10.1007","volume":"119","author":[{"given":"Frans C. C.","family":"Riemslag","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","published-online":{"date-parts":[[2009,1,10]]},"reference":[{"key":"9161_CR1","unstructured":"Talsma H, Blom Th and Riemslag, FCC (2002) Working with ICIDH-2 in Practice. Vision 2002 Goteborg (Abstract)"},{"issue":"6","key":"9161_CR2","doi-asserted-by":"crossref","first-page":"799","DOI":"10.1111\/j.1600-0420.2006.00717.x","volume":"84","author":"MM Genderen Van","year":"2006","unstructured":"Van Genderen MM, Riemslag FCC, Jorritsma F, Hoeben F, Meire F, Stilma J (2006) The key role of electrophysiology in the diagnosis of visually impaired children. Acta Ophthalmol Scand 84(6):799. doi: 10.1111\/j.1600-0420.2006.00717.x","journal-title":"Acta Ophthalmol Scand"},{"issue":"2","key":"9161_CR3","doi-asserted-by":"crossref","first-page":"75","DOI":"10.1016\/0039-6257(85)90077-3","volume":"30","author":"PE Kinnear","year":"1985","unstructured":"Kinnear PE, Jay B, Witkop CJ Jr (1985) Albinism. Surv Ophthalmol 30(2):75\u2013101. doi: 10.1016\/0039-6257(85)90077-3","journal-title":"Surv Ophthalmol"},{"key":"9161_CR4","first-page":"57","volume":"29","author":"E Nettleship","year":"1909","unstructured":"Nettleship E (1909) On some hereditary diseases of the eye. Trans Opthalmol Soc UK 29:57\u2013198","journal-title":"Trans Opthalmol Soc UK"},{"issue":"6","key":"9161_CR5","first-page":"430","volume":"13","author":"D Creel","year":"1974","unstructured":"Creel D, Witkop CJ Jr, King RA (1974) Asymmetric visually evoked potentials in human albinos: evidence for visual system anomalies. Investig Opthalmol Vis Sci 13(6):430\u2013440","journal-title":"Investig Opthalmol Vis Sci"},{"key":"9161_CR6","doi-asserted-by":"crossref","first-page":"595","DOI":"10.1016\/0013-4694(81)91433-4","volume":"52","author":"D Creel","year":"1981","unstructured":"Creel D, Spekreijse H, Reits D (1981) Evoked potentials in albinos: efficacy of pattern stimuli in detecting misrouted optic fibres. Electorenc Clin Neurophysiol 52:595\u2013603. doi: 10.1016\/0013-4694(81)91433-4","journal-title":"Electorenc Clin Neurophysiol"},{"key":"9161_CR7","doi-asserted-by":"crossref","first-page":"285","DOI":"10.1007\/BF00238157","volume":"53","author":"P Apkarian","year":"1984","unstructured":"Apkarian P, Reits D, Spekerijse H (1984) Component specificity in albino asymmetry: maturation of the visual pathway anomaly. Exp Brain Res 53:285\u2013294. doi: 10.1007\/BF00238157","journal-title":"Exp Brain Res"},{"issue":"9","key":"9161_CR8","first-page":"2653","volume":"32","author":"P Apkarian","year":"1991","unstructured":"Apkarian P, Shallo-Hoffmann J (1991) VEP projections in congenital nystogmus; VEP asymmetry in albinism: a comparison study. Investig Opthalmol Vis Sci 32(9):2653\u20132661","journal-title":"Investig Opthalmol Vis Sci"},{"key":"9161_CR9","doi-asserted-by":"crossref","first-page":"1098","DOI":"10.1136\/bjo.2006.091702","volume":"90","author":"MM Genderen Van","year":"2006","unstructured":"Van Genderen MM, Riemslag FCC, Schuil J, Hoeben FP, Stilma JS, Meire FM (2006) Chiasmal misrouting and foveal hypoplasia without Albinism. Br J Ophthalmol 90:1098\u20131102. doi: 10.1136\/bjo.2006.091702","journal-title":"Br J Ophthalmol"},{"key":"9161_CR10","doi-asserted-by":"crossref","first-page":"1825","DOI":"10.1111\/j.1460-9568.2005.04364.x","volume":"22","author":"MM Neveu","year":"2005","unstructured":"Neveu MM, Holder GE, Sloper JJ, Jeffery G (2005) Optic chiasm formation is independent of foveal development. Eur J Neurosci 22:1825\u20131829. doi: 10.1111\/j.1460-9568.2005.04364.x","journal-title":"Eur J Neurosci"},{"key":"9161_CR11","doi-asserted-by":"crossref","first-page":"432","DOI":"10.1016\/j.ejmg.2007.08.003","volume":"50","author":"M Poot","year":"2007","unstructured":"Poot M, Eleveld MJ, van \u2019t Slot R, van Genderen MM, Verrijn Stuart AA, Hochstenbach R, Beemer FA (2007) Proportional growth failure and oculocutaneous albinism in a girl with 6.87\u00a0Mb deletion of region 15q26.2 -> qter. Eur J Med Genet 50:432\u2013440. doi: 10.1016\/j.ejmg.2007.08.003","journal-title":"Eur J Med Genet"},{"key":"9161_CR12","doi-asserted-by":"crossref","first-page":"547","DOI":"10.1016\/S0002-9394(00)00737-6","volume":"130","author":"TP Dryja","year":"2000","unstructured":"Dryja TP (2000) Molecular genetics of oguchi disease, fundus albipunctatus, and other forms of stationary night blindness: LVII Edward Jackson memorial lecture. Am J Ophthalmol 130:547\u2013563. doi: 10.1016\/S0002-9394(00)00737-6","journal-title":"Am J Ophthalmol"},{"key":"9161_CR13","doi-asserted-by":"crossref","first-page":"657","DOI":"10.1086\/508067","volume":"79","author":"C Zeitz","year":"2006","unstructured":"Zeitz C, Kloeckener-Gruissem B, Forster U, Kohl S, Magyar I, Wissinger B, Matyas G, Borruat F, Schorderet DF, Zrenner E, Munier FL, Berger W (2006) Mutations in CABP4, the gene encoding the Ca2+-binding protein 4. Cause autosomal recessive night blindness. Am J Hum Genet 79:657\u2013667","journal-title":"Am J Hum Genet"},{"issue":"12","key":"9161_CR14","doi-asserted-by":"crossref","first-page":"4884","DOI":"10.1073\/pnas.0501233102","volume":"102","author":"TP Dryja","year":"2005","unstructured":"Dryja TP, McGee TL, Berson EL, Fishman GA, Sandberg MA, Alexander KR, Derlacki DJ, Rajagopalan AS (2005) Night blindness and abnormal cone electroretinogram ON responses in patients with mutations in the GRM6 gene encoding mGluR6. Proc Natl Acad Sci USA 102(12):4884\u20134889. doi: 10.1073\/pnas.0501233102","journal-title":"Proc Natl Acad Sci USA"},{"key":"9161_CR15","doi-asserted-by":"crossref","first-page":"1013","DOI":"10.1001\/archopht.1986.01050190071042","volume":"104","author":"Y Miyake","year":"1986","unstructured":"Miyake Y, Yagasaki K, Horiguchi M, Kawase Y, Kanda T (1986) Congenital stationary nightblindness with a negative electroretinogram: a new classification. Arch Ophthalmol 104:1013\u20131020","journal-title":"Arch Ophthalmol"},{"issue":"2","key":"9161_CR16","doi-asserted-by":"crossref","first-page":"71","DOI":"10.1076\/opge.23.2.71.2214","volume":"23","author":"RG Weleber","year":"2002","unstructured":"Weleber RG (2002) Infantile and childhood retinal blindness: a molecular perspective. Ophthalmic Genet 23(2):71\u201397. doi: 10.1076\/opge.23.2.71.2214","journal-title":"Ophthalmic Genet"},{"key":"9161_CR17","volume-title":"Vision research: a practical guide to laboratory methods","author":"W Makous","year":"1997","unstructured":"Makous W (1997) Optics and photometry. In: Carpenter RHS, Robson JG (eds) Vision research: a practical guide to laboratory methods. Oxford University Press, Oxford"},{"key":"9161_CR18","first-page":"78","volume-title":"Studies in health technology and informatics, volume 11. Low vision research and developments in rehabilitation","author":"FW Cornelissen","year":"1994","unstructured":"Cornelissen FW, Kooijman AC, Bootsma A, van der Wildt GJ (1994) Light and objects; perceiving \u201cthe real thing\u201d. In: Kooijman AC, Looijestijn PL, Welling JA, van der Wildt GJ (eds) Studies in health technology and informatics, volume 11. Low vision research and developments in rehabilitation. IOS Press, Amsterdam, pp 78\u201384"},{"key":"9161_CR19","doi-asserted-by":"crossref","unstructured":"Littink KW, van Genderen MM, Collin RW, Roosing S, de Brouwer AP, Riemslag FC, Venselaar H, Thiadens AA, Hoyng CB, Rohrschneider K, den Hollander AI, Cremers FP, van den Born LI (2008) A novel homozygous nonsense mutation in CABP4 causes congenital cone-rod synaptic disorder. Investig Opthalmol Vis Sci. doi: 10.1167\/iovs.08-2553","DOI":"10.1167\/iovs.08-2553"}],"container-title":["Documenta Ophthalmologica"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s10633-008-9161-6.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/s10633-008-9161-6\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s10633-008-9161-6","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2019,5,30]],"date-time":"2019-05-30T20:00:29Z","timestamp":1559246429000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/s10633-008-9161-6"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2009,1,10]]},"references-count":19,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2009,8]]}},"alternative-id":["9161"],"URL":"https:\/\/doi.org\/10.1007\/s10633-008-9161-6","relation":{},"ISSN":["0012-4486","1573-2622"],"issn-type":[{"value":"0012-4486","type":"print"},{"value":"1573-2622","type":"electronic"}],"subject":[],"published":{"date-parts":[[2009,1,10]]}}}