01654nam0 2200385 i 450 VAN010154720211109021859.522N978331904417020150428d2014 |0itac50 baengCH|||| |||||Lectures on formal and rigid geometrySiegfried BoschChamSpringer2014VIII, 254 p.24 cm001VAN01022502001 Lecture notes in mathematics210 Berlin [etc.]Springer2105VAN0234065Lectures on formal and rigid geometry139228714G22Rigid analytic geometry [MSC 2020]VANC024467MF14D15Formal methods and deformations in algebraic geometry [MSC 2020]VANC025088MFFormal blowing-upKW:KFormal schemeKW:KRigid analytic spaceKW:KTate algebraKW:KTate's Acyclicity TheoremKW:KCHChamVANL001889BoschSiegfriedVANV04196441946Springer <editore>VANV108073650ITSOL20240614RICAhttp://doi.org/10.1007/978-3-319-04417-0E-book – Accesso al full-text attraverso riconoscimento IP di Ateneo, proxy e/o ShibbolethBIBLIOTECA DEL DIPARTIMENTO DI MATEMATICA E FISICAIT-CE0120VAN08NVAN0101547BIBLIOTECA DEL DIPARTIMENTO DI MATEMATICA E FISICA08CONS e-book 08LNM2105 20150428 Lectures on formal and rigid geometry1392287UNICAMPANIA03120nam 22004695 450 991037395950332120200706231655.0981-15-0414-810.1007/978-981-15-0414-3(CKB)4100000010121906(DE-He213)978-981-15-0414-3(MiAaPQ)EBC6033746(PPN)242843417(EXLCZ)99410000001012190620200129d2020 u| 0engurnn|008mamaatxtrdacontentcrdamediacrrdacarrierHereditary Chorioretinal Disorders /edited by Gemmy Cheung1st ed. 2020.Singapore :Springer Singapore :Imprint: Springer,2020.1 online resource (VII, 147 p. 126 illus., 110 illus. in color.) Retina Atlas,2662-5741981-15-0413-X Retinits 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.This 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. .Retina Atlas,2662-5741OphthalmologyOphthalmologyhttps://scigraph.springernature.com/ontologies/product-market-codes/H44004Ophthalmology.Ophthalmology.617.73Cheung Gemmyedthttp://id.loc.gov/vocabulary/relators/edtMiAaPQMiAaPQMiAaPQBOOK9910373959503321Hereditary Chorioretinal Disorders2257573UNINA