00855nam--2200325---450-99000349839020331620110216140748.0000349839USA01000349839(ALEPH)000349839USA0100034983920110216d1939----km-y0itay50------baitaITa---||||001yyTrattamento delle frattureBohler Lorenzo7 ed.Romas.n.1939XXXIII, 813 p.ill.25 cmFrattureBNCF617.15BOHLER,Lorenzo609452ITsalbcISBD990003498390203316FDC 130663 Med.FDCBKMEDCIANATIEMP9020110216USA011407Trattamento delle fratture1111431UNISA02100nam0 22004333i 450 VAN024953820230531093236.320N978303042950820220902d2020 |0itac50 baengCH|||| |||||Nonlinear Conjugate Gradient Methods for Unconstrained OptimizationNeculai AndreiChamSpringer2020xxviii, 498 p.ill.24 cm001VAN00671972001 Springer optimization and its applications210 Berlin [etc.]Springer2006-158VAN0249539Nonlinear Conjugate Gradient Methods for Unconstrained Optimization241354290C90Applications of mathematical programming [MSC 2020]VANC019710MF90C30Nonlinear programming [MSC 2020]VANC023183MF49M37Numerical methods based on nonlinear programming [MSC 2020]VANC023193MF65K05Numerical mathematical programming methods [MSC 2020]VANC028868MF90C06Large-scale problems in mathematical programming [MSC 2020]VANC028934MFBFGS methodKW:KConjugate Gradient MethodKW:KConjugate gradient algorithmKW:KDai and LaoKW:KQuasi-Newton methodKW:KSteepest Descent MethodKW:KCHChamVANL001889AndreiNeculaiVANV204095767620Springer <editore>VANV108073650ITSOL20240614RICAhttp://doi.org/10.1007/978-3-030-42950-8E-book – Accesso al full-text attraverso riconoscimento IP di Ateneo, proxy e/o ShibbolethBIBLIOTECA DEL DIPARTIMENTO DI MATEMATICA E FISICAIT-CE0120VAN08NVAN0249538BIBLIOTECA DEL DIPARTIMENTO DI MATEMATICA E FISICA08CONS e-book 4762 08eMF4762 20220902 Nonlinear Conjugate Gradient Methods for Unconstrained Optimization2413542UNICAMPANIA05489nam 22005895 450 991030344010332120200703135124.03-319-95046-010.1007/978-3-319-95046-4(CKB)4100000007279040(MiAaPQ)EBC5625467(DE-He213)978-3-319-95046-4(PPN)232960526(EXLCZ)99410000000727904020181221d2018 u| 0engurcnu||||||||txtrdacontentcrdamediacrrdacarrierAtlas of Inherited Retinal Diseases /edited by Stephen H. Tsang, Tarun Sharma1st ed. 2018.Cham :Springer International Publishing :Imprint: Springer,2018.1 online resource (262 pages)Advances in Experimental Medicine and Biology,0065-2598 ;10853-319-95045-2 Section I: Basic Knowledge. Retinal Histology and Anatomical Landmarks -- Fluorescein Angiography -- Optical Coherence Tomography -- Fundus Autofluorescence -- Electroretinography -- Electrooculography -- Glossary of Relevant Genetic and Molecular/Cell Biology -- Section II: X-linked Forms -- X-Linked Retinitis Pigmentosa -- X-Linked Choroideremia -- X-Linked Juvenile Retinoschisis -- X-Linked Ocular Albinism -- Progressive Cone Dystrophy and Cone-Rod Dystrophy -- Congenital Stationary Night Blindness -- Blue Cone Monochromatism -- Section III: Autosomal Dominant Forms -- Autosomal Dominant Retinitis Pigmentosa -- Best Vitelliform Macular Dystrophy -- Pattern Dystrophy -- Doyne Honeycomb Retinal Dystrophy (Malattia Leventinese, Autosomal Dominant Drusen) -- Occult Macular Dystrophy -- Sorsby Pseudoinflammatory Fundus Dystrophy -- North Carolina Macular Dystrophy -- Pigmented Paravenous Chorioretinal Atrophy (PPCRA) -- Late-Onset Retinal Degeneration -- Section IV: Autosomal Recessive Form -- Rod Monochromatism (Achromatopsia) -- Retinitis Pigmentosa (Non-syndromic) -- Leber Congenital Amaurosis -- Stargardt Disease -- Enhanced S-Cone Syndrome (Goldmann-Favre Syndrome) -- Best Vitelliform Macular Dystrophy -- Section V: Systemic Disorders -- Mitochondrial Disorder: Kearns-Sayre Syndrome -- Mitochondrial Disorder: Maternally Inherited Diabetes and Deafness -- Ciliopathy: Usher Syndrome -- Ciliopathy: Bardet-Biedl Syndrome -- Ciliopathy: Senior-Løken Syndrome -- Ciliopathy: Alström Syndrome -- Ciliopathy: Sjögren-Larsson Syndrome -- Inborn Errors of Metabolism: Gyrate Atrophy -- Inborn Errors of Metabolism: Pseudoxanthoma Elasticum -- Inborn Errors of Metabolism: Refsum Disease -- Inborn Errors of Metabolism: Bietti Crystalline Dystrophy -- Extracellular Matrix: Alport Syndrome -- Section VI: Phakomatoses -- Von Hippel-Lindau Disease -- Tuberous Sclerosis -- Neurofibromatosis -- Section VII: Phenocopies -- Rubella Retinopathy -- Syphilis -- Autoimmune Retinopathy -- Drug-Induced Retinal Toxicity -- Acute Zonal Occult Outer Retinopathy (AZOOR) and Related Diseases -- Diffuse Unilateral Subacute Neuroretinitis (DUSN) -- Section VIII: Managing IRDs in Clinics -- A Practical Approach to Retinal Dystrophies -- Genetic Testing for Inherited Retinal Dystrophy: Basic Understanding.This Atlas of Inherited Retinal Disorders provides a thorough overview of various inherited retinal dystrophies with emphasis on phenotype characteristics and how they are related to the most frequently encountered genes. It will also meet the hitherto unmet need of PhD students who would benefit from seeing the phenotypes of the genes they work on and study. Further, because it would help geneticists use and familiarize themselves with the candidate gene approach to test patients' genomes, enabling them to test more efficiently and cost-efficiently (as the cost of genetic testing is quite high and spiralling higher). This invaluable atlas is organized into eight sections starting with the basic knowledge on retinal imaging as an introduction to the subject matter, then diseases are listed according to their inheritance pattern while disorders with extraocular manifestations are grouped by their defining features. This structure will be intuitive to clinicians and students studying IRDs.Advances in Experimental Medicine and Biology,0065-2598 ;1085Gene therapyAnimal geneticsOphthalmologyMedical geneticsGene Therapyhttps://scigraph.springernature.com/ontologies/product-market-codes/B12020Animal Genetics and Genomicshttps://scigraph.springernature.com/ontologies/product-market-codes/L32030Ophthalmologyhttps://scigraph.springernature.com/ontologies/product-market-codes/H44004Gene Functionhttps://scigraph.springernature.com/ontologies/product-market-codes/B12030Gene therapy.Animal genetics.Ophthalmology.Medical genetics.Gene Therapy.Animal Genetics and Genomics.Ophthalmology.Gene Function.616.042Tsang Stephen Hedthttp://id.loc.gov/vocabulary/relators/edtSharma Tarunedthttp://id.loc.gov/vocabulary/relators/edtBOOK9910303440103321Atlas of Inherited Retinal Diseases2513346UNINA