01796nam 2200421 n 450 99638564470331620221108085615.0(CKB)1000000000610978(EEBO)2240901290(UnM)99846224(EXLCZ)99100000000061097819911021d1556 uy |engurbn||||a|bb|The bayte [and] snare of fortune[electronic resource] Wherin may be seen that money is not the only cause of mischefe and vnfortunat endes: but a necessary mean to mayntayne a vertuous quiet lyfe. Treated in a dialoge betwene man and moneyImprinted at London By Iohn Wayland, at the signe of the Sunne ouer against the Conduite in Fletestrete[1556?][20] p"Tr[anslated]. [by Roger Bieston] probably from the French version by C. Platin, Le debat de lhomme et de l'argent, of an Italian original"--STC. Bieston's name appears in acrostic on the last page.In verse.At foot of title: Cum priuilegio per septennium.Publication date conjectured by STC.Signatures: A⁶ B⁴.In this edition the headline on A2r has: bayte.Reproduction of original in the Harvard University Library.eebo-0018Dialogues, EnglishEarly works to 1800WealthMoral and ethical aspectsPoetryEarly works to 1800Dialogues, EnglishWealthMoral and ethical aspectsBieston Roger1007282Cu-RivESCu-RivESCStRLINWaOLNBOOK996385644703316The bayte snare of fortune2320258UNISA01275nam 2200385Ka 450 991069095780332120010511135423.0(CKB)5470000002342765(OCoLC)45410616ocm45410616(OCoLC)995470000002342765(EXLCZ)99547000000234276520001121d1999 ua 0engtxtrdacontentcrdamediacrrdacarrierImplementing distance learning in urban schools[electronic resource] /Majdalany, Gibran [and] Guiney, SusanNew York, NY :ERIC Clearinghouse on Urban Education,[1999]ERIC/CUE digest ;no. 150Distributed to depository libraries in microfiche, shipping list no.: 2001-0191-M.Title from title screen.Distance educationUrban schoolsDistance education.Urban schools.Majdalany Gibran1384972Guiney Susan1384973ERIC Clearinghouse on Urban Education.GPOGPOBOOK9910690957803321Implementing distance learning in urban schools3431919UNINA05759nam 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