02473nam0-2200361 --450 991049455300332120211013121252.06563 lia, lal- 8.am (3) 1828 (R)feiIT-NA010520210916d1828----km-y0itay5050----bagrclatDEa-----------------bb0-------Leonis Diaconi Caloënsis Historiae libri decem et Liber de velitatione bellica Nicephori Augusti e recensione Caroli Benedicti Hasii ... Addita eiusdem versione atque annotationibus ab ipso recognitis. Accedunt Theodosii Acroases De Creta capta e recensione Fr. Iacobsii et Luitprandi legatio cum aliis libellis qui Nicephori Phocae et Ioannis Tzimiscis historiam illustrantEditio emendatior et copiosior, consilio B.G. Niebuhrii C.F. instituta, opera eiusdem Niebuhrii, Imm. Bekkeri, L. Schopeni, G. et L. Dindorfiorum aliorumque philologorum parataBonnaeimpensis Ed. Weberi1828XXXVIII, 624 p.4°Corpus scriptorum historiae byzantinae11Segn.: [a]⁸ b⁸ c⁴ 1-39⁸Historiae libri decem et Liber de velitatione bellica Nicephori Augusti e recensione Caroli Benedicti Hasii ... Addita eiusdem versione atque annotationibus ab ipso recognitis. Accedunt Theodosii Acroases De Creta capta e recensione Fr. Iacobsii et Luitprandi legatio cum aliis libellis qui Nicephori Phocae et Ioannis Tzimiscis historiam illustrantGermania.BonnLeo : Diaconus443184Liutprandus Cremonensis<ca. 920-972>Jacobs,Friedrich<1764-1847>Hase,Charles Benoit<1780-1864>Weber,Eduard650ITUNINAREICATUNIMARCVisualizza la versione elettronica in SBNWebhttps://books.google.it/books?id=TMEjN4758gAC&printsec=frontcover&hl=it&source=gbs_ge_summary_r&cad=0#v=onepage&q&f=false20210916AQ9910494553003321SG 880/B 1283938FLFBCFLFBCLeonis Diaconi Caloënsis Historiae libri decem et Liber de velitatione bellica Nicephori Augusti e recensione Caroli Benedicti Hasii ... Addita eiusdem versione atque annotationibus ab ipso recognitis. Accedunt Theodosii Acroases De Creta capta e recensione Fr. Iacobsii et Luitprandi legatio cum aliis libellis qui Nicephori Phocae et Ioannis Tzimiscis historiam illustrant1867545UNINA03780nam 2200697 450 991046338720332120210518000506.01-4008-5229-310.1515/9781400852291(CKB)2670000000572996(EBL)1753615(OCoLC)894169840(SSID)ssj0001367886(PQKBManifestationID)12538400(PQKBTitleCode)TC0001367886(PQKBWorkID)11447945(PQKB)10895664(MiAaPQ)EBC1753615(MdBmJHUP)muse43443(DE-B1597)454023(OCoLC)1013947436(OCoLC)979905406(DE-B1597)9781400852291(Au-PeEL)EBL1753615(CaPaEBR)ebr10960903(CaONFJC)MIL654484(EXLCZ)99267000000057299620141107h20152015 uy 0engurun#---|u||utxtccrThe emerging Republican majority /Kevin P. PhillipsUpdated edition with a New PrefacePrinceton, New Jersey ;Oxford, England :Princeton University Press,2015.©20151 online resource (599 p.)James Madison Library in American PoliticsDescription based upon print version of record.0-691-16324-3 1-322-23204-0 Includes bibliographical references and index.Front matter --Contents --General Editor's Introduction --Preface to the Princeton University Press Edition --Preface to the 1970 paperback edition --I. Introduction --II. The Northeast --III. The South --IV. The Heartland --V. The Pacific States --VI. The Future of American Politics --IndexOne of the most important and controversial books in modern American politics, The Emerging Republican Majority (1969) explained how Richard Nixon won the White House in 1968-and why the Republicans would go on to dominate presidential politics for the next quarter century. Rightly or wrongly, the book has widely been seen as a blueprint for how Republicans, using the so-called Southern Strategy, could build a durable winning coalition in presidential elections. Certainly, Nixon's election marked the end of a "New Deal Democratic hegemony" and the beginning of a conservative realignment encompassing historically Democratic voters from the South and the Florida-to-California "Sun Belt," in the book's enduring coinage. In accounting for that shift, Kevin Phillips showed how two decades and more of social and political changes had created enormous opportunities for a resurgent conservative Republican Party. For this new edition, Phillips has written a preface describing his view of the book, its reception, and how its analysis was borne out in subsequent elections. A work whose legacy and influence are still fiercely debated, The Emerging Republican Majority is essential reading for anyone interested in American politics or history.James Madison library in American politics.POLITICAL SCIENCE / Political Ideologies / Conservatism & LiberalismbisacshUnited StatesPolitics and governmentElectronic books.POLITICAL SCIENCE / Political Ideologies / Conservatism & Liberalism.324.2734Phillips Kevin1940-304078Phillips Kevin P304078Wilentz Sean506895MiAaPQMiAaPQMiAaPQBOOK9910463387203321The emerging Republican majority2456633UNINA05759nam 2201441z- 450 991055757800332120220111(CKB)5400000000043869(oapen)https://directory.doabooks.org/handle/20.500.12854/76272(oapen)doab76272(EXLCZ)99540000000004386920202201d2021 |y 0engurmn|---annantxtrdacontentcrdamediacrrdacarrierHereditary Hemorrhagic TelangiectasiaRecent Advances and Future ChallengesBasel, SwitzerlandMDPI - Multidisciplinary Digital Publishing Institute20211 online resource (228 p.)3-0365-0590-3 3-0365-0591-1 Hereditary hemorrhagic telangiectasia (HHT) is an inherited disease that affects the blood vessels, and is characterized by direct connections between arteries and veins with no intervening capillaries. These abnormal vessels may appear in the skin as tiny red dilated blood vessels in the mouth, lips, fingers and toes. The presence of these vascular lesions in the mucosa can lead to spontaneous and recurrent nose bleeding, typically beginning in mid-childhood, and this is the most common clinical manifestation of HHT, occurring in over 90% of patients. Gastrointestinal bleeding, derived from mucocutaneous vascular lesions, affects approximately 25% of patients, almost always presenting after the age of 50. Chronic nasal and gastrointestinal bleeding can cause iron-deficiency anemia, and current therapeutic strategies are trying to minimize iron and blood transfusions. HHT patients also present large vascular lesions, known as arteriovenous malformations, that occur in internal organs like lungs, liver, and brain, and may result in life-threatening complications often related to the shunting of blood. This book not only highlights the current knowledge regarding diagnosis and treatment of HHT, but also the newest insights in the molecular basis of HHT, the understanding of which is essential for the development of new medicines or therapeutic strategies.Hereditary Hemorrhagic Telangiectasia Research and information: generalbicsscactivin receptor-like kinase 1 (ALK1)activin-receptor-like kinase 1ACVRL1ALK1angiogenesisantiangiogenic propertiesanticoagulantsantiplateletsantithrombotic therapyarteriovenous malformationarteriovenous malformation (AVM)arteriovenous malformations (AVMs)AVMbazedoxifenebevacizumabbiomarkerbiomarkersbleedingbone morphogenetic protein (BMP)catheter based embolization therapycell adhesioncerebral ischemic lesionscontrast enhanced magnetic resonance angiographyendoglinEndoglinendothelial cellsENGepistaxisepistaxis severity scoreetamsylateFK506gastrointestinal bleedinggenetic diseasegenotype-phenotype correlationguidelineshereditary hemorrhagichereditary hemorrhagic telangiectasiaHereditary hemorrhagic telangiectasiaHereditary Hemorrhagic Telangiectasiahereditary hemorrhagic telangiectasia (HHT)hereditary hemorrhagic telangiectasia (HHT), second-hithereditary hemorrhagic telangiectasia/HHT/osler's diseaseHHTinflammationlife expectancyliverlong non-coding RNAsmechanical damagemicroRNAmicroRNAsMRIN-acetylcysteinenasal endoscopynasal ointmentnon-coding RNAsnosebleedsOsler-Weber-Rendupediatricsplasmapropranololpropranolol gelpulmonary arteriovenous malformationpulmonary arteriovenous malformationsraloxifenerare diseaserare diseasessafetyscreeningshear stressSmad pathwaySmad4SMAD4somatic mutationsun-induced traumasurvivaltacrolimustelangiectasestelangiectasiatelangiectasistranexamic acidtranscatheter embolotherapytransforming growth factor beta (TGF-β)transforming growth factor-beta (TGF-β)ultrasoundvascular endothelial growth factor (VEGF)vascular injuryvascular malformationsResearch and information: generalMager Hans-Jurgenedt1299262Bernabeu CarmeloedtPost MarcoedtMager Hans-JurgenothBernabeu CarmeloothPost MarcoothBOOK9910557578003321Hereditary Hemorrhagic Telangiectasia3025091UNINA