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[null,"1.","Record Nr.",null,"UNINA9910815201303321"]
[null,null,"Titolo",null,"Radiochemical synthesis . Volume I Radiopharmaceuticals for positron emission tomography / / edited by Peter J.H. Scott, Brian G. Hockley"]
[null,null,"Pubbl/distr/stampa",null,"Hoboken, N.J., : Wiley, 2012"]
[null,null,"ISBN",null,"9786613400932"]
[{"$nulls":4},"9781283400930"]
[{"$nulls":4},"1283400936"]
[{"$nulls":4},"9781118140338"]
[{"$nulls":4},"1118140338"]
[{"$nulls":4},"9781118140345"]
[{"$nulls":4},"1118140346"]
[{"$nulls":4},"9781118140314"]
[{"$nulls":4},"1118140311"]
[null,null,"Edizione",null,"[1st ed.]"]
[null,null,"Descrizione fisica",null,"1 online resource (371 p.)"]
[null,null,"Collana",null,"Wiley Series on Radiochemical Syntheses ; ; v.1"]
[null,null,"Disciplina",null,"616.07575"]
[null,null,"Soggetti",null,"Radiopharmaceuticals - Synthesis"]
[{"$nulls":4},"Tomography, Emission"]
[null,null,"Lingua di pubblicazione",null,"Inglese"]
[null,null,"Formato",null,"Materiale a stampa"]
[null,null,null,"Livello bibliografico","Monografia"]
[null,null,null,"Note generali","Description based upon print version of record."]
[null,null,null,"Nota di bibliografia","Includes bibliographical references and index."]
[null,null,"Nota di contenuto",null,"Radiochemical Syntheses; CONTENTS; Contributors; Foreword; Preface; Abbreviations; PART I FLUORINE-18 LABELED RADIOPHARMACEUTICALS; 1. Synthesis of [18F]-Fluorodeoxyglucose ([18F]FDG); 2. Synthesis of Sodium [18F]Fluoride (Na[18F]F); 3. Radiosynthesis of 3'-Deoxy-3''-[18F]Fluorothymidine ([18F]FLT); 4. Synthesis of [18F]Fluoroazomycin Arabinoside ([18F]FAZA); 5. Synthesis of [18F]Fluoromisonidazole (1-(2-Hydroxy-3-[18F]Fluoropropyl)-2-Nitroimidazole, [18F]FMISO); 6. Synthesis of [18F]FPPRGD2; 7. Synthesis of [18F]Fluorocholine ([18F]FCH)"]
[{"$nulls":4},"8. Clinical Manufacturing of [18F]-16-a-Fluoroestradiol ([18F]FES)9. Synthesis of N-Succinimidyl 4-[18F]Fluorobenzoate ([18F]SFB); 10. Synthesis of 4-(2'-Methoxyphenyl)-1-[2'-(N-2'Pyridinyl)-p-[18F]Fluorobenzamido]Ethylpiperazine [18F]MPPF; 11. Synthesis of [18F]-Fallypride; 12. Synthesis of [18F]Fluoroethyltyrosine (18F-FET); 13. Synthesis of [18F]Flumazenil ([18F]FZ); 14. Synthesis of 6-[18F]Fluorodopamine (6-[18F]FDA); 15. Synthesis of 2-([18F]Fluoro)-3-[(2S)"]
[{"$nulls":4},"-2-Azetidinylmethoxy]Pyridine ([18F]2FA); 16. Synthesis of [18F]-Substance-P Antagonist-Receptor Quantifier ([18F]SPA-RQ)"]
[{"$nulls":4},"PART II CARBON-11 LABELED RADIOPHARMACEUTICALS17. Synthesis of [11C]Choline Chloride ([11C]CHL); 18. Synthesis of 2-(4-N-[11C]Methylaminophenyl)-6-Hydroxybenzothiazole ([11C]6-OH-BTA-1;  [11C]PIB); 19. Synthesis of [11C]-meta-Hydroxyephedrine ([11C]MHED); 20. Synthesis of l-[methyl-11C]Methionine ([11C]MET); 21. Synthesis of (+)-a-[11C]Dihydrotetrabenazine ([11C]DTBZ); 22. Synthesis of [11C]Flumazenil([11C]FMZ); 23. Synthesis of [11C]Hexadecanoic Acid ([11C]Palmitic Acid); 24. Synthesis of O-methyl-11C]Metomidate ([11C]-MTO); 25. Synthesis of [11C]Carfentanil ([11C]CFN)"]
[{"$nulls":4},"26. Synthesis of [carbonyl-11C]Way-10063527. Synthesis of [11C]Raclopride; 28. Synthesis of 3-Amino-4-[2-(N-Methyl-N-[11C]Methyl-Amino-Methyl)Phenylsulfanyl]-Benzonitrile ([11C]Dasb); 29. Synthesis of [11C]Acetate; 30. Synthesis of N-(2-[11C]Methoxybenzyl)-N-(4-Phenoxypyridin-3-yl)Acetamide ([11C]PBR28); PART III OTHER RADIOPHARMACEUTICALS; 31. Synthesis of [13N]Ammonia ([13N]NH3); 32. Synthesis of [68Ga]Gallium Dota-(Tyr3)-Octreotide Acetate ([68Ga]-Dotatoc); Appendix 1 Supplier Information; Index"]
[null,null,null,"Sommario/riassunto","The ultimate reference guide to the synthesis of radiopharmaceuticals The Radiochemical Syntheses series provides scientists and professionals with a comprehensive reference to proven synthetic methods for radiochemical reactions, along with step-by-step guidance on how to replicate these syntheses in the laboratory. Volume 1 in the series focuses on the synthesis and purification of radiopharmaceuticals in clinical use today. It brings together in one complete, self-contained volume a collection of monographs containing a wealth of practical information from across the liter"]
[null,"2.","Record Nr.",null,"UNISA996675482503316"]
[null,null,"Autore",null,"ENNODIUS, Magnus Felix"]
[null,null,"Titolo",null,"Epitalamio per Massimo : vir spectabilis / Magno Felice Ennodio ; a cura di Marino Neri"]
[null,null,"Pubbl/distr/stampa",null,"Milano, : La vita felice, 2020"]
[null,null,"Titolo uniforme",null,"Epithalamium dictum Maximo"]
[null,null,"ISBN",null,"978-88-93464-03-1"]
[null,null,"Descrizione fisica",null,"185 p. ; 17 cm"]
[null,null,"Collana",null,"Saturnalia ; 52"]
[null,null,"Disciplina",null,"871.02"]
[null,null,"Collocazione",null,"V.3. Coll. 29/ 52"]
[null,null,"Lingua di pubblicazione",null,"Italiano"]
[{"$nulls":4},"Latino"]
[null,null,"Formato",null,"Materiale a stampa"]
[null,null,null,"Livello bibliografico","Monografia"]
[null,null,null,"Note generali","Testo originale a fronte"]
[null,null,null,"Sommario/riassunto","L’epitalamio è un canto nuziale, un sottogenere lirico greco imitato più tardi dai Romani, destinato a celebrare in versi un matrimonio, presso la camera degli sposi. Nelle poesie, benché una volta protesti contro le falsità degli antichi e invochi lo Spirito Santo, Ennodio non sdegna di rappresentare Apollo, Venere, le Muse: nell’epitalamio per Massimo, Amore si lamenta con Venere dell’ascetismo introdotto dal cristianesimo. Il poeta più imitato è Virgilio; i sette mediocri inni religiosi arieggiano quelli di sant’Ambrogio. Un epitalamio in chiave di conversione, quella di Massimo, dalla precedente vita ascetica a quella coniugale. (Fonte: editore)"]
[null,"3.","Record Nr.",null,"UNISA996672457003316"]
[null,null,"Autore",null,"Frost Jetta <1968->"]
[null,null,"Titolo",null,"Mehrebenen-Steuerung von Universitäten : von der professionellen Bürokratie zu kollaborativen Wissensnetzwerken / Jetta Frost, Fabian Hattke, Markus Reihlen und Ferdinand Wenzlaff"]
[null,null,"Pubbl/distr/stampa",null,"Köln, : Kölner Wissenschaftsverlag, 2015"]
[null,null,"ISBN",null,"9783942720731"]
[null,null,"Descrizione fisica",null,"1 Online-Ressource"]
[null,null,"Classificazione",null,"PJ 2660"]
[{"$nulls":4},"PZ 4700"]
[{"$nulls":4},"340"]
[{"$nulls":4},"360"]
[null,null,"Disciplina",null,"342.430858"]
[null,null,"Soggetti",null,"Hochschulforschung"]
[{"$nulls":4},"Hochschulpartnerschaft"]
[{"$nulls":4},"Hochschulplanung"]
[{"$nulls":4},"Hochschulpolitik"]
[{"$nulls":4},"Innovationsmanagement"]
[{"$nulls":4},"Organisationsentwicklung"]
[{"$nulls":4},"Datenschutz"]
[{"$nulls":4},"Datenverarbeitung"]
[{"$nulls":4},"Elektronische Gesundheitskarte"]
[{"$nulls":4},"Gesundheitswesen"]
[{"$nulls":4},"Informationelles Selbstbestimmungsrecht"]
[{"$nulls":4},"Personenbezogene Daten"]
[{"$nulls":4},"Deutschland"]
[null,null,"Lingua di pubblicazione",null,"Tedesco"]
[null,null,"Formato",null,"Materiale a stampa"]
[null,null,null,"Livello bibliografico","Monografia"]