{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,8,1]],"date-time":"2024-08-01T14:37:42Z","timestamp":1722523062897},"reference-count":27,"publisher":"Springer Science and Business Media LLC","issue":"2","license":[{"start":{"date-parts":[[2005,2,1]],"date-time":"2005-02-01T00:00:00Z","timestamp":1107216000000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Ophthalmologe"],"published-print":{"date-parts":[[2005,2]]},"DOI":"10.1007\/s00347-004-1158-2","type":"journal-article","created":{"date-parts":[[2005,1,18]],"date-time":"2005-01-18T07:05:03Z","timestamp":1106031903000},"page":"111-115","source":"Crossref","is-referenced-by-count":7,"title":["Morbus Best"],"prefix":"10.1007","volume":"102","author":[{"given":"B.","family":"Lorenz","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M. N.","family":"Preising","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"CR1","first-page":"199","volume":"13","author":"Best","year":"1905","unstructured":"Best F (1905) \u00dcber eine heredit\u00e4re Maculaaffektion. Z Augenheilkunde 13:199?212","journal-title":"Z Augenheilkunde"},{"key":"CR2","first-page":"830","volume":"12","author":"Birndorf","year":"1973","unstructured":"Birndorf LA, Dawson WW (1973) A normal electrooculogram in a patient with a typical vitelliform macular lesion. Invest Ophthalmol 12:830?833","journal-title":"Invest Ophthalmol"},{"key":"CR3","unstructured":"Cavender JC, Everett AI, Soon TL (1993) Hereditary macular dystrophies. In: Tasman W, Jaeger EA (eds) Duane?s Clinical Ophthalmology, vol 3. Lippincott, Philadelphia"},{"key":"CR4","doi-asserted-by":"crossref","first-page":"94","DOI":"10.1159\/000306800","volume":"166","author":"Denden","year":"1973","unstructured":"Denden A, Littann KE (1973) Fluoreszenzangiographie bei den multiplen vitelliformen Retinazysten des hinteren Augenpols. Ophthalmologica 166:94?104","journal-title":"Ophthalmologica"},{"key":"CR5","doi-asserted-by":"crossref","first-page":"1115","DOI":"10.1001\/archopht.1982.01030040093017","volume":"100","author":"Frangieh","year":"1982","unstructured":"Frangieh GT, Green WR, Fine SL (1982) A histopathologic study of Best?s macular dystrophy. Arch Ophthalmol 100:1115?1121","journal-title":"Arch Ophthalmol"},{"key":"CR6","unstructured":"Gass JDM (1997) Heredodystrophic disorders affecting the pigment epithelium and retina. In: Gass JDM (ed) Steroscopic Atlas of Macular Disease?Diagnosis and Treatment, vol 1, 4th edn. Mosby, St. Louis, pp 303?436"},{"key":"CR7","doi-asserted-by":"crossref","first-page":"371","DOI":"10.1016\/0002-9394(50)90335-7","volume":"33","author":"Klien","year":"1950","unstructured":"Klien BA (1950) The heredodegeneration of the macula lutea. Am J Ophthalmol 33:371?379","journal-title":"Am J Ophthalmol"},{"key":"CR8","doi-asserted-by":"crossref","unstructured":"Krieglstein GK, Jonescu-Cuypers CP, Severin M (1999) Atlas der Augenheilkunde. Springer, Berlin Heidelberg New York Tokio","DOI":"10.1007\/978-3-642-59863-0"},{"key":"CR9","doi-asserted-by":"crossref","first-page":"347","DOI":"10.1007\/BF00158923","volume":"60","author":"Marmor","year":"1985","unstructured":"Marmor MF, Donovan WJ, Gaba DM (1985) Effects of hypoxia and hyperoxia on the human standing potential. Doc Ophthalmol 60:347?352","journal-title":"Doc Ophthalmol"},{"key":"CR10","doi-asserted-by":"crossref","first-page":"12758","DOI":"10.1073\/pnas.220402097","volume":"97","author":"Marmorstein","year":"2000","unstructured":"Marmorstein AD, Marmorstein LY, Rayborn M, Wang X, Hollyfield JG, Petrukhin K (2000) Bestrophin, the product of the Best vitelliform macular dystrophy gene (VMD2), localizes to the basolateral plasma membrane of the retinal pigment epithelium. Proc Natl Acad Sci U S A 97:12758?12763","journal-title":"Proc Natl Acad Sci U S A"},{"key":"CR11","doi-asserted-by":"crossref","first-page":"1517","DOI":"10.1093\/hmg\/7.9.1517","volume":"7","author":"Marquardt","year":"1998","unstructured":"Marquardt A, St\u00f6hr H, Passmore LA, Kramer F, Rivera A, Weber BH (1998) Mutations in a novel gene, VMD2, encoding a protein of unknown properties cause juvenile-onset vitelliform macular dystrophy (Best?s disease). Hum Mol Genet 7:1517?1525","journal-title":"Hum Mol Genet"},{"key":"CR12","doi-asserted-by":"crossref","first-page":"224","DOI":"10.1001\/archopht.1955.00930010226009","volume":"53","author":"McFarland","year":"1955","unstructured":"McFarland CB (1955) Heredodegeneration of the macula lutea; a study of the clinical and pathologic aspects. Arch Opthalmol 53:224?228","journal-title":"Arch Opthalmol"},{"key":"CR13","doi-asserted-by":"crossref","first-page":"256","DOI":"10.1136\/bjo.62.4.256","volume":"62","author":"Miller","year":"1978","unstructured":"Miller S (1978) Fluorescence in Best?s vitelliform dystrophy, lipofuscin, and fundus flavimaculatus. Br J Ophthalmol 62:256?260","journal-title":"Br J Ophthalmol"},{"key":"CR14","doi-asserted-by":"crossref","first-page":"688","DOI":"10.1016\/S0161-6420(81)34965-3","volume":"88","author":"Mohler","year":"1981","unstructured":"Mohler CW, Fine SL (1981) Long-term evaluation of patients with Best?s vitelliform dystrophy. Ophthalmology 88:688?692","journal-title":"Ophthalmology"},{"key":"CR15","doi-asserted-by":"crossref","first-page":"1261","DOI":"10.1001\/archopht.1988.01060140421045","volume":"106","author":"O?Gorman","year":"1988","unstructured":"O?Gorman S, Flaherty WA, Fishman GA, Berson EL (1988) Histopathologic findings in Best?s vitelliform macular dystrophy. Arch Ophthalmol 106:1261?1268","journal-title":"Arch Ophthalmol"},{"key":"CR16","doi-asserted-by":"crossref","first-page":"241","DOI":"10.1038\/915","volume":"19","author":"Petrukhin","year":"1998","unstructured":"Petrukhin K, Koisti MJ, Bakall B et al. (1998) Identification of the gene responsible for Best macular dystrophy. Nat Genet 19:241?247","journal-title":"Nat Genet"},{"key":"CR17","doi-asserted-by":"crossref","first-page":"203","DOI":"10.1016\/S0014-4835(02)00280-4","volume":"76","author":"Pianta","year":"2003","unstructured":"Pianta MJ, Aleman TS, Cideciyan AV et al. (2003) In vivo micropathology of Best macular dystrophy with optical coherence tomography. Exp Eye Res 76:203?211","journal-title":"Exp Eye Res"},{"key":"CR18","doi-asserted-by":"crossref","first-page":"49563","DOI":"10.1074\/jbc.M308414200","volume":"278","author":"Qu","year":"2003","unstructured":"Qu Z, Wei RW, Mann W, Hartzell HC (2003) Two bestrophins cloned from Xenopus laevis oocytes express Ca(2+)-activated Cl(-) currents. J Biol Chem 278:49563?49572","journal-title":"J Biol Chem"},{"key":"CR19","doi-asserted-by":"crossref","first-page":"327","DOI":"10.1085\/jgp.200409031","volume":"123","author":"Qu","year":"2004","unstructured":"Qu Z, Fischmeister R, Hartzell C (2004) Mouse bestrophin-2 is a bona fide Cl(-) channel: identification of a residue important in anion binding and conduction. J Gen Physiol 123:327?340","journal-title":"J Gen Physiol"},{"key":"CR20","doi-asserted-by":"crossref","first-page":"91","DOI":"10.1007\/s00417-003-0828-0","volume":"242","author":"Schlingemann","year":"2004","unstructured":"Schlingemann RO (2004) Role of growth factors and the wound healing response in age-related macular degeneration. Graefes Arch Clin Exp Ophthalmol 242:91?101","journal-title":"Graefes Arch Clin Exp Ophthalmol"},{"key":"CR21","unstructured":"St\u00f6hr H, Marquardt A, Cooper P, Nowak NJ, Shows TB, Gerhard DS, Weber BHF (1996) Gene map of the Best?s disease candidate region in 11q12-q13.1. (Abstract) Am J Hum Genet 59 [Suppl.]:A313"},{"key":"CR22","doi-asserted-by":"crossref","first-page":"281","DOI":"10.1038\/sj.ejhg.5200796","volume":"10","author":"St\u00f6hr","year":"2002","unstructured":"St\u00f6hr H, Marquardt A, Nanda I, Schmid M, Weber BH (2002) Three novel human VMD2-like genes are members of the evolutionary highly conserved RFP-TM family. Eur J Hum Genet 10:281?284","journal-title":"Eur J Hum Genet"},{"key":"CR23","doi-asserted-by":"crossref","first-page":"4008","DOI":"10.1073\/pnas.052692999","volume":"99","author":"Sun","year":"2002","unstructured":"Sun H, Tsunenari T, Yau KW, Nathans J (2002) The vitelliform macular dystrophy protein defines a new family of chloride channels. Proc Natl Acad Sci U S A 99:4008?4013","journal-title":"Proc Natl Acad Sci U S A"},{"key":"CR24","doi-asserted-by":"crossref","first-page":"41114","DOI":"10.1074\/jbc.M306150200","volume":"278","author":"Tsunenari","year":"2003","unstructured":"Tsunenari T, Sun H, Williams J, Cahill H, Smallwood P, Yau KW, Nathans J (2003) Structure-function analysis of the bestrophin family of anion channels. J Biol Chem 278:41114?41125","journal-title":"J Biol Chem"},{"key":"CR25","doi-asserted-by":"crossref","first-page":"609","DOI":"10.1001\/archopht.1997.01100150611006","volume":"115","author":"Von R\u00fcckmann","year":"1997","unstructured":"Von R\u00fcckmann A, Fitzke FW, Bird AC (1997) In vivo fundus autofluorescence in macular dystrophies. Arch Ophthalmol 115:609?615","journal-title":"Arch Ophthalmol"},{"key":"CR26","first-page":"Evaluation","volume":"dystrophy","author":"Wabbels","year":"2004","unstructured":"Wabbels BK, Demmler A, Preising MN, Lorenz B (2004) Fundus autofluorescence in patients with genetically determined Best vitelliform macular dystrophy: Evaluation of genotype-phenotype correlation and longitudinal course. Assoc Res Vis Ophthalmol, Bethesda, MD, USA","journal-title":"Fundus autofluorescence in patients with genetically determined Best vitelliform macular"},{"key":"CR27","doi-asserted-by":"crossref","first-page":"1108","DOI":"10.1001\/archopht.1982.01030040086016","volume":"100","author":"Weingeist","year":"1982","unstructured":"Weingeist TA, Kobrin JL, Watzke RC (1982) Histopathology of Best?s macular dystrophy. Arch Ophthalmol 100:1108?1114","journal-title":"Arch Ophthalmol"}],"container-title":["Der Ophthalmologe"],"original-title":[],"language":"de","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s00347-004-1158-2.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/s00347-004-1158-2\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s00347-004-1158-2","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2019,5,28]],"date-time":"2019-05-28T13:46:34Z","timestamp":1559051194000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/s00347-004-1158-2"}},"subtitle":["Ein \ufffdberblick zur Pathologie und deren Ursachen"],"short-title":[],"issued":{"date-parts":[[2005,2]]},"references-count":27,"journal-issue":{"issue":"2","published-print":{"date-parts":[[2005,2]]}},"alternative-id":["1158"],"URL":"https:\/\/doi.org\/10.1007\/s00347-004-1158-2","relation":{},"ISSN":["0941-293X","1433-0423"],"issn-type":[{"value":"0941-293X","type":"print"},{"value":"1433-0423","type":"electronic"}],"subject":[],"published":{"date-parts":[[2005,2]]}}}