Passage et écriture de l'entre-deux dans El Pasajero de Cristóbal Suárez de Figueroa / / Blandine Daguerre

• Record Nr.: UNINA9910687945303321
• Autore: Daguerre Blandine
• Pubbl/distr/stampa: Pessac : , : Presses universitaires de Pau et des Pays de l'Adour, , 2020
• Descrizione fisica: 1 online resource (312 pages)
• Disciplina: 006.32
• Soggetti: Description logics
• Lingua di pubblicazione: Francese
• Formato: Materiale a stampa
• Livello bibliografico: Monografia
• Note generali: Includes bibliographies and indexes.
• Nota di bibliografia: Includes bibliographies and indexes.
• Sommario/riassunto: Spain, first quarter of the 17th century: four men meet during a trip between Madrid and Barcelona where they have to leave for Italy to try their luck. To fight against the hardship of their journey and to avoid boredom, they decide to converse. There follows an exchange of more than 200 pages about their destination, their respective personal journeys, and the society of the time, interspersed with stories of a more playful nature. This is the plot of El Pasajero, advertencias utilísimas a la vida humana, a work cited by many specialists of the Golden Age, who all praise its literary qualities and to which no in-depth literary study has been devoted. How can such a paradox be explained? El Pasajero offers a kaleidoscope of the society of the time, hence the sociological orientation of most of the studies carried out on this text. The bad press of its author, known for his unattractive temperament and for his opposition to Cervantes, may also have contributed to it in a more tangential way. Last but not least, the textual, literary and ideological richness of El Pasajero may have hindered certain analytical ambitions. Figueroa's text is of a deeply hybrid nature, characterized by a perpetual oscillation between Italian inspiration, decameronian accents, transtextual borrowings and Hispanic folklore substratum. He plays on the porosity of the borders between reality and fiction to elaborate a text in which all the elements seem to be in dialogue and between which the reader passes as if on the stones of a ford. In the end, El Pasajero is a true laboratory of ; literary experimentation, where deep-rooted literary traditions and more innovative writing proposals emerge. This perpetual dialogue is decisive in the work: beyond the first obvious dialogue between the characters, the text proposes others in filigree, between literary forms and genres. They function as so many structuring elements within this work, which is conceived as a place of passage where literary experimentation and societal reflections are mixed. El Pasajero can sometimes leave the reader perplexed, it's a fact. Nevertheless, it is one of those texts that fascinate and that have not yet revealed all their secrets. One thing is certain: El Pasajero does not leave the reader indifferent and deserves to be studied in depth. This is what this book proposes to do.

L'Inde dans tous ses états / / Guy Taillefer

• Record Nr.: UNINA9910495720403321
• Autore: Taillefer Guy
• Pubbl/distr/stampa: [Montréal, Québec] : , : Les Presses de l'Université de Montréal, , [2015]; ©2015; Ottawa, Ontario : , : Canadian Electronic Library, , 2015
• ISBN: 2-8218-9500-3; 2-7606-3581-3
• Descrizione fisica: 1 online resource (292 p.)
• Collana: Collection Champ Libre
• Disciplina: 954
• Soggetti: Libros electronicos.; Inde Civilisation 21e siècle; Inde Politique et gouvernement 21e siècle; Inde Conditions économiques 21e siècle; Inde Conditions sociales 21e siècle; India Civilization 21st century; India Politics and government 21st century; India Economic conditions 21st century; India Social conditions 21st century
• Lingua di pubblicazione: Francese
• Formato: Materiale a stampa
• Livello bibliografico: Monografia
• Note generali: Description based upon print version of record.
• Nota di bibliografia: Includes bibliographical references.
• Nota di contenuto: Les champs de bataille de la démocratie -- Traits de personnalité -- La ville comme bouée de sauvetage -- Film catastrophe -- La révolution au long cours -- L'étau des castes et de la religion -- L'anglais est un tremplin, mais la piscine est vide -- Dedans et le dehors.
• Sommario/riassunto: Guy Taillefer est journaliste et éditorialiste à la section internationale du Devoir depuis la fin des années 1990. Il a passé cinq années en Inde où il a pu constater le dynamisme politique et l'énergie délirante de cette démocratie plus grande que nature. Dans ces chroniques au ton personnel et parfois incisif, il rend compte, entre autres choses, de l'avancée de la condition des femmes, de la grande liberté d'expression des Indiens et de la question du développement durable. Il raconte aussi l'état de délabrement du système de santé, l'obésité - cadeau des sauces au ghee autant que des pizzas de Domino et des poulets de Kentucky -, la pollution de l'eau, ou sa rareté, ou encore les centaines de milliers de waste pickers et de junk dealers, humains bas de gamme dans le système de castes toujours en vigueur dans une Inde qui évolue entre tradition et modernité.

Audiovision zwischen Hand und Haut : : Zu einer hapto-taktilen Filmtheorie / / Sonja Kirschall

• Record Nr.: UNINA9910861957303321
• Autore: Kirschall Sonja
• Pubbl/distr/stampa: [s.l.] : , : transcript Verlag, , 2024
• ISBN: 9783732871285; 3732871282
• Descrizione fisica: 1 online resource
• Soggetti: Social Science / Media Studies; Social sciences
• Lingua di pubblicazione: Tedesco
• Formato: Materiale a stampa
• Livello bibliografico: Monografia
• Nota di contenuto: Cover; -- Inhalt -- Danksagung -- 1. Annäherung: Augenhände -- Augenhände -- Haptische Bilder -- Zur Geschichtlichkeit haptischer Filmtheorien -- Zur (Un‑)Geschichtlichkeit des Tastsinns -- Zur Geschichtlichkeit des Tastsinnlichen als ästhetisches Denkmodell -- Zur Methode -- Audiovisuelle Taktilität online: ASMR -- ASMR‐Videos -- ASMR und Film -- Sensorische Maschinen -- 2. Das Tastsinnliche als Projektionsfläche -- 2.1 Den Tastsinn handhabbar machen – Definitionen -- Verwirrende Begriffsvielfalt -- Grenzen verwalten -- Tasthandeln und Fühlen -- Berührung, nicht Vermischung -- 2.2 Den Tastsinn deuten – Sinnesgeschichte und Subjektivierung -- Erleidende Sinne, herrschender Geist -- Die ungreifbare Medialität des Tastsinns -- Sensorische Hierarchien als Subjekthierarchien -- Tastsinn und Racial Othering -- Männliche Umwertungsversuche: Sensualismus und ›erkennendes Tasten‹ -- Weibliche Umwertungsversuche: Differenzfeminismus nach Irigaray -- Zusammenfassung -- Ambivalenz‐ versus Heterogenitätskonzept des Tastsinnlichen -- 2.3 Das Tastsinnliche (audio‑)visuell denken – Konzeptgeschichte
• Sommario/riassunto: Welche Funktion hat der Tastsinn für die Sinnlichkeit von Film? Filmtheoretische Konzeptualisierungen, die diese Frage zu beantworten versuchen, sind seit mehr als zwei Jahrzehnten maßgeblich von Gegenüberstellungen »optischer« und »haptischer« Bilder bestimmt. Sonja Kirschall nimmt eine kritische Revision dieses Denkens vor, indem sie es einerseits mit seiner eigenen etwa hundertjährigen Konzeptgeschichte, andererseits mit den teletaktilen ästhetischen Praktiken der seit 2010 in den sozialen Medien produktiven ASMR-Community konfrontiert. Aus der Kombination von kritischer Theoriearbeit mit ästhetischer und Erfahrungsanalyse entwickelt sie so eine ordnende Zusammenschau möglicher Modi filmischer Tastsinnlichkeit und eine hapto-taktile Art der Filmanalyse.

Blombäck's Essential Guide to Blood Coagulation : A Practical Guide to Diagnosis and Treatment of Hemostatic Disorders

• Record Nr.: UNINA9911027077003321
• Autore: Antovic Jovan P
• Pubbl/distr/stampa: Newark : , : John Wiley & Sons, Incorporated, , 2025; ©2025
• ISBN: 1-394-22315-3; 1-394-22313-7
• Edizione: [3rd ed.]
• Descrizione fisica: 1 online resource (258 pages)
• Altri autori (Persone): MagnussonMaria
• Disciplina: 616.157
• Lingua di pubblicazione: Inglese
• Formato: Materiale a stampa
• Livello bibliografico: Monografia
• Nota di contenuto: Cover -- Title Page -- Copyright Page -- Dedication -- Contents -- Contributors -- Preface -- Abbreviations -- PART 1 General hemostasis -- CHAPTER 1 Overview of normal hemostasis -- CHAPTER 2 Sampling instructions and preanalytical issues in hemostasis -- Points to note prior to blood sampling -- Sampling time and patient preparation -- Referrals for coagulation analyses -- Sampling -- Preparation before sampling -- Sampling technique -- Sample handling -- Centrifugation -- Storage -- Selected References -- CHAPTER 3 Laboratory investigation -- Nomenclature -- Screening analyses -- cB/B-platelet particle concentration/platelet count (PLT) -- p/B/cB-prothrombin time (PT [INR]) -- Spontaneous increase or decrease in PT (INR) -- Point-of-care cB-PT (INR) -- P-activated partial thromboplastin time (APTT) -- Point-of-care cB-APTT -- Point-of-care cB-ACT -- P-fibrin D-dimer (DDI) and S-fibrin(ogen) degradation products (FDP) -- Point-of-care cB/P-fibrin-D-dimer -- P-fibrinogen -- Point-of-care cB-fibrinogen -- B-bleeding time according to Ivy (BT) -- S-soluble fibrin (SF) and fibrin monomers (FM) -- P-antithrombin (AT) -- P-anti-factor Xa analysis (aFXa)/anti-Xa analysis (aXa) -- P-anti-factor IIa analysis (aFIIa)/direct thrombin inhibition assays (DTI) -- P-thrombin time (TT) -- Special analyses -- Coagulation factors -- Protein C anticoagulant system -- Antiphospholipid syndrome -- Thrombotic microangiopathies -- Fibrinolysis -- Markers of coagulation activation (hypercoagulation ; markers) -- Platelet assays -- B-platelet indices (MPV, PDW) -- B-immature platelet fraction (IPF) -- B/PRP-platelet light transmission aggregometry (LTA) -- B-platelet flow cytometry -- PRP-platelet transmission electron microscopy (PTEM) -- B-multiple impedance aggregometry (Multiplate®) -- Point-of-care B-VerifyNowTM.; Point-of-care B-platelet function analyzer (PFA-100/INNOVANCE® PFA-200) -- Genetic testing -- Genetic testing for hemophilia A and B -- Genetic testing for VWD -- Genetic testing for other hereditary bleeding disorders including platelet defects -- Genetic testing for thrombophilia -- Global hemostatic assays -- Endogenous thrombin potential (ETP) -- Overall hemostatic potential (OHP) -- Viscoelastic testing -- Useful assays in research studies -- P-tissue factor (TF) -- P/S-extracellular vesicles (EVs) -- P/S-neutrophil extracellular traps (NETs) -- Fibrin structure -- P-C1-esterase inhibitor -- P-protein C inhibitor -- P-APC-protein C inhibitor (PCI) complex -- P-thrombin activatable fibrinolysis inhibitor (TAFI) -- P-tissue factor pathway inhibitor (TFPI) -- P-thrombomodulin (TM) -- P-plasmin-plasmin inhibitor complex (PAP) -- P-plasminogen activator, tissue type (t-PA) -- P-t-PA/PAI-1 complex -- Other nonhemostatic variables of importance -- S-cytokines -- P-complement -- S-lipoprotein(a) (Lp[a]), P-apolipoprotein -- Selected References -- PART 2 Bleeding disorders -- CHAPTER 4 Clinical and laboratory investigation of increased bleeding tendency -- Introduction -- Clinical investigation -- Bleeding history -- Family history -- Other medical conditions -- Concomitant medications -- Physical examination -- Laboratory investigations -- Laboratory investigations -- Screening assays -- Confirmatory assays -- Genetic testing -- Nondetectable conditions in laboratory tests despite positive bleeding history -- Selected References -- Hereditary bleeding disorders -- CHAPTER 5 Hemophilia -- Introduction -- Bleeding symptoms in hemophilia -- Treatment -- Prophylaxis -- Nonfactor replacement therapy -- Immune tolerance induction -- Antibodies against emicizumab -- Treatment of bleeding events -- Pain relievers.; Clinical follow-up of patients with bleeding disorders -- Selected References -- CHAPTER 6 Von Willebrand disease -- Introduction -- Classification -- Diagnosis -- Management -- On-demand treatment -- Prophylaxis -- Surgery -- Pain treatment -- Follow-up -- Selected References -- CHAPTER 7 Rare bleeding disorders including inherited platelet function defects -- Inherited platelet function defects -- Background -- Diagnosis -- Management -- Very rare coagulation factor deficiencies -- Fibrinogen deficiency -- Factor II (prothrombin) deficiency -- Factor V deficiency -- Combined factor V and factor VIII defect -- Factor VII deficiency -- Factor X deficiency -- Factor XI deficiency (hemophilia C) -- Factor XIII deficiency -- Vitamin K-dependent coagulation factor deficiency (VKDCFD) -- Vascular bleeding disorders -- Hereditary hemorrhagic telangiectasia (HHT, Osler-Weber-Rendu) -- Ehlers-Danlos syndrome (EDS) -- Bleeding disorder of unknown cause (BDUC) -- Background -- Diagnosis -- Management -- Selected References -- CHAPTER 8 Specific issues of hemostasis in children - focus on bleeding -- Developmental hemostasis -- Bleeding in children -- Vitamin K deficiency bleeding -- Coagulation factor deficiencies -- Hemophilia A and B -- Rare hereditary coagulation factor disorders -- Acquired coagulation factor deficiencies -- Platelet function defects and thrombocytopenia -- Platelet function defects -- Thrombocytopenia -- Selected References -- CHAPTER 9 Hereditary bleeding disorders and aging -- Cardiovascular disease (CVD) -- Atrial fibrillation -- Atherosclerotic cardiovascular disease (ASCVD) -- Management of incident coronary artery disease -- Cancer -- Chronic ; kidney disease -- Selected references -- CHAPTER 10 Paradigm change - new treatment for hereditary bleeding disorders -- Coagulation factor concentrates -- Nonfactor replacement therapy.; Factor VIII-mimicking agents -- Rebalancing agents -- Gene therapy -- Selected References -- Acquired bleeding disorders -- CHAPTER 11 Acquired inhibitors of coagulation factors -- Acquired hemophilia -- Background -- Diagnosis -- Management -- Treatment of bleeding -- Eradication of antibodies -- Follow-up -- Relapse -- Acquired von Willebrand disease -- Background -- Diagnosis -- Management -- Selected References -- Critical Bleedings -- CHAPTER 12 Critical bleeding in trauma and surgery -- Background -- Pathophysiology, resuscitation, and surgical management of traumatic bleeding -- Judicious volume replacement aimed at maintaining adequate circulating blood volume -- A blood product transfusion strategy aimed at preventing and treating coagulopathy -- Avoiding acidosis, hypothermia, and hypocalcemia -- Surgical control of the bleeding -- Management of acute bleeding in surgery -- Treatment protocols -- Pediatric considerations -- Selected References -- CHAPTER 13 Gastrointestinal bleeding -- Background -- Diagnosis -- Disease history and symptom assessment -- Physical examination -- Acute management -- Immediate actions -- Early pharmacological treatment -- Diagnostic-therapeutic procedures -- Endoscopy -- Angiography -- Surgery -- Secondary prophylaxis after GI bleeding -- Considerations regarding hemostasis in GI bleeding -- Selected References -- CHAPTER 14 Intracranial bleeding -- Intracerebral hemorrhage -- Background -- Causes and risk factors -- Diagnosis -- Management -- Subarachnoid hemorrhage -- Background -- Causes and risk factors -- Diagnosis -- Management -- Traumatic brain injury -- Background -- Management -- Selected References -- CHAPTER 15 Obstetric massive bleeding -- Background -- Management -- Specific treatments -- Follow-up -- Selected References.; CHAPTER 16 Bleedings associated with anticoagulant and antiplatelet treatment (including reversal of antithrombotic treatment) -- Background -- Antiplatelet drugs -- Anticoagulant therapy -- Combination of anticoagulant and antiplatelet therapies -- Management -- Selected References -- PART 3 Thromboembolic disorders -- Venous thrombosis -- CHAPTER 17 Venous thromboembolism -- Background -- Risk factor review -- Diagnosis -- Clinical signs and symptoms -- Differential diagnoses from clinical assessment -- Assessing probability for incident VTE -- Diagnostic imaging -- Management -- VTE severity assessment -- Clinical symptoms -- Location and size -- Echocardiography -- Biomarkers -- Bleeding risk -- Short-term prognostic stratification -- Treatment -- Follow-up and secondary prevention -- Further investigations to consider -- Hereditary thrombophilia -- Antiphospholipid syndrome (APS) -- Malignancy screening -- Rare underlying causes -- Hyperhomocysteinemia -- Myeloproliferative neoplasms -- Paroxysmal nocturnal hemoglobinuria -- Continued follow-up -- Selected References -- CHAPTER 17.1 Cerebral venous thrombosis -- Background -- Causes and risk factors -- Diagnosis -- Clinical presentation -- Imaging -- Blood tests -- Management -- Selected References -- Anticoagulation -- Endovascular and surgical treatment -- Papillary edema -- Selected References -- CHAPTER 17.2 Splanchnic vein thrombosis -- Background -- Diagnosis -- Imaging -- Laboratory tests -- Pathology -- Endoscopy -- Management -- Treatment of acute/recent portal vein thrombosis without liver cirrhosis (nontumoral) -- Treatment of chronic portal vein thrombosis without liver cirrhosis -- Treatment of portal vein thrombosis in liver cirrhosis ; -- Treatment of Budd-Chiari syndrome -- Selected References -- CHAPTER 18 Specific issues of hemostasis in children - focus on thrombosis.; Background.
• Sommario/riassunto: New edition of a concise, comprehensive, easy-to-read pocket book distilling the most clinically up-to-date information on thrombotic and bleeding disorders In a concise manner, Blombäck's Essential Guide to Blood Coagulation distills the most clinically up-to-date information on thrombotic and bleeding disorders, including the latest treatment.