LEADER 00969nam a2200289 i 4500 001 991000833719707536 005 20020507174200.0 008 971218s1965 it ||| | ita 035 $ab10763636-39ule_inst 035 $aLE01303011$9ExL 040 $aDip.to Matematica$beng 082 0 $a510 084 $aAMS 00A08 084 $aZDM A30 100 1 $aJohnson, Donovan A.$040845 245 10$aDivertimenti matematici /$cdi Donovan A. Johnson e William H. Glenn 260 $aBologna :$bZanichelli,$cc1965 300 $a55 p. ;$c21 cm 490 0 $aMatematica. M ;$v4 650 0$aMathematical recreations 700 1 $aGlenn, William H. 907 $a.b10763636$b23-02-17$c28-06-02 912 $a991000833719707536 945 $aLE013 A30 GLE11 (1965)$g1$i2013000093420$lle013$o-$pE0.00$q-$rl$s- $t0$u3$v0$w3$x0$y.i10859160$z28-06-02 996 $aDivertimenti matematici$9923201 997 $aUNISALENTO 998 $ale013$b01-01-97$cm$da $e-$fita$git $h0$i1 LEADER 00923nam a22002411i 4500 001 991000992799707536 005 20030130171326.0 008 021111s1967 it a||||||||||||||||ita 035 $ab12084682-39ule_inst 035 $aARCHE-017448$9ExL 040 $aDip.to Filologia Ling. e Lett.$bita$cA.t.i. Arché s.c.r.l. Pandora Sicilia s.r.l. 100 1 $aRewald, John$0153203 245 13$aIl Postimpressionismo :$bda van Gogh a Gauguin /$cJohn Rewald 260 $aFirenze :$bSansoni,$c1967 300 $a639 p. :$bill. ;$c19 cm 650 4$aPittura francese$ySec. 19.-20. 650 4$aPostimpressionismo 907 $a.b12084682$b02-04-14$c01-04-03 912 $a991000992799707536 945 $aLE008 FL.M. FR. XVI A 25$g1$i2008000308254$lle008$o-$pE0.00$q-$rl$s- $t0$u0$v0$w0$x0$y.i12384227$z01-04-03 996 $aPostimpressionismo$9140852 997 $aUNISALENTO 998 $ale008$b01-04-03$cm$da $e-$fita$git $h3$i1 LEADER 03120nam 22004695 450 001 9910373959503321 005 20200706231655.0 010 $a981-15-0414-8 024 7 $a10.1007/978-981-15-0414-3 035 $a(CKB)4100000010121906 035 $a(DE-He213)978-981-15-0414-3 035 $a(MiAaPQ)EBC6033746 035 $a(PPN)242843417 035 $a(EXLCZ)994100000010121906 100 $a20200129d2020 u| 0 101 0 $aeng 135 $aurnn|008mamaa 181 $ctxt$2rdacontent 182 $cc$2rdamedia 183 $acr$2rdacarrier 200 10$aHereditary Chorioretinal Disorders /$fedited by Gemmy Cheung 205 $a1st ed. 2020. 210 1$aSingapore :$cSpringer Singapore :$cImprint: Springer,$d2020. 215 $a1 online resource (VII, 147 p. 126 illus., 110 illus. in color.) 225 1 $aRetina Atlas,$x2662-5741 311 $a981-15-0413-X 327 $aRetinits pigmentosa and allied disorders -- Best's disease -- Congenital X-linked retinoschisis -- Progressive cone dystrophy and cone-rod dystrophy -- Pattern dystrophy of the retinal pigment epithelium -- Stargardt's disease and fundus flavimaculatus -- North Carolina macular dystrophy -- Choroideremia -- Malattia Leventinese or Doyne honeycomb retinal dystrophy -- Bietti's crystalline dystrophy -- Albinism. 330 $aThis volume of the retina atlas focuses on hereditary chorioretinal disorders. The topics covered include retinitis pigmentosa, Best disease, congenital X-linked retinoschisis, cone dystrophy, Stargardt?s disease, pattern dystrophy, North Carolina macular dystrophy, choroideremia, Mallattia Leventinese, Bietti?s crystalline dystrophy, and albinism. All clinical features are clearly illustrated with multimodal imaging techniques. The utility of some of the latest imaging tools such as OCT angiography, adaptive optics-scanning laser ophthalmoscopy, and microperimetery is discussed. Readers will gain valuable new insights into pathogenesis at the molecular level, which have been facilitated by recent genetic discoveries. The use of genetic testing and the latest advances in and challenges of gene therapy and cell-based therapy are also covered in detail. Hereditary Chorioretinal Disorders atlas is one of nine volumes in the series Retina Atlas. The series provides validated and comprehensive information on vitreoretinal diseases, covering imaging basics, retinal vascular diseases, macular disorders, ocular inflammatory and infectious disorders, retinal degeneration, the surgical retina, ocular oncology, pediatric retina and trauma. . 410 0$aRetina Atlas,$x2662-5741 606 $aOphthalmology 606 $aOphthalmology$3https://scigraph.springernature.com/ontologies/product-market-codes/H44004 615 0$aOphthalmology. 615 14$aOphthalmology. 676 $a617.73 702 $aCheung$b Gemmy$4edt$4http://id.loc.gov/vocabulary/relators/edt 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910373959503321 996 $aHereditary Chorioretinal Disorders$92257573 997 $aUNINA