Relevant bibliographies by topics / Vizi occulti

Academic literature on the topic 'Vizi occulti'

Author: Grafiati
Published: 9 March 2023
Last updated: 10 March 2023

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Journal articles on the topic "Vizi occulti"

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Ortu, Rosanna. "Alle origini della tutela giuridica del consumatore: fondamenti romanistici della disciplina europea." Zeszyty Naukowe KUL 60, no. 3 (October 27, 2020): 281–97. http://dx.doi.org/10.31743/zn.2017.60.3.281-297.

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Nel presente contributo si sono voluti comparare taluni aspetti della disciplina della tutela del contraente debole nel contratto di compravendita, figura che attualmente coincide con quella del consumatore, concentrando l’attenzione su alcuni istituti presenti nel diritto romano, in cui emergono alcune situazioni di disparità contrattuale. Nella disciplina dell’Editto degli edili curuli, i magistrati repubblicani stabilirono una normativa speciale per la dichiarazione dei vizi occulti nelle vendite di schiavi ed animali, presupponendo una responsabilità oggettiva del venditore che non si fosse attenuto alle disposizioni edilizie. Un intervento importante che andò a definire una settorializzazione della materia, inquadrata all’interno della vendita in generale. Da ciò derivava una sovrapposizione in livelli della disciplina giuridica negoziale: sul piano orizzontale si collocava la regolamentazione della vendita prevista dal ius civile, mentre sul piano verticale si innestava quella speciale, di ius honorarium, prevista dall’Editto degli edili curuli. Tale modalità si riscontra anche in ambito europeo con la Direttiva 1999/44/CE, a proposito della vendita di beni di consumo, che rappresenta la manifestazione più eclatante del ruolo che il legislatore europeo ha nell’ambito della protezione del consumatore in materia contrattuale. Come nel mondo antico, nella Direttiva 1999/44/CE l’intervento normativo è giustificato dall’esigenza di creare uno spazio di tutele maggiori destinate a determinati soggetti, nonché delimitate per contenuto e ambito.
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Pacheco Cano, Carlos I., Marilyn A. Arosemena, Roumen B. Iordanov, Ankitha Lingamaneni, and Ankur Aneja. "Acquired Factor VIII Inhibitor Presenting as Occult GI Bleeding." Case Reports in Hematology 2018 (June 19, 2018): 1–3. http://dx.doi.org/10.1155/2018/1910854.

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An acquired coagulation factor deficiency is characterized by acquired autoantibodies against specific clotting factors in those without diagnosed hemophilia. It is a relatively rare condition with an incidence of approximately one case per million per year. We present a case report of an elderly male who initially presented with an occult GI bleed that was identified with a positive fecal occult blood test result. This is the first case reported to our knowledge of an acquired factor inhibitor deficiency presenting in this manner. We postulate the importance of acquired factor inhibitors in the setting of unexplained anemia given absence of overt clinical symptoms that could contribute to aggravate an established GI bleed, especially in the elderly population.
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Tan, Chieh Suai, Kenneth P. Chan, Charles T. Chuah, Heng Joo Ng, Foong Koon Cheah, Felicia S. Teo, and Philip CT Eng. "Life Threatening and Occult Mediastinal Haemorrhage Secondary to Acquired Factor VIII Deficiency." Annals of the Academy of Medicine, Singapore 38, no. 3 (March 15, 2009): 280–81. http://dx.doi.org/10.47102/annals-acadmedsg.v38n3p280.

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Gibeili, Chloé, Arek Sulukdjian, Audrey Chanlon, and Nathan Moreau. "Unilateral glossodynia as a harbinger of an occult cerebellopontine angle tumour." BMJ Case Reports 15, no. 4 (April 2022): e249408. http://dx.doi.org/10.1136/bcr-2022-249408.

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A woman in her late 80s with severe bronchomalacia was referred to a tertiary orofacial pain clinic for unexplained right unilateral glossodynia of progressive and continuous evolution for the past 8 months, spreading to the ipsilateral labiomental region, associated with ipsilateral hypoacusia. Local and general clinical examinations were unremarkable and routine blood work could not reveal any underlying systemic disease explaining the glossodynia and burning/pricking labiomental pain. Suspecting a painful trigeminal neuropathy secondary to a space-occupying lesion, a cerebral MRI was prescribed, revealing an ipsilateral cerebellopontine angle lesion, compatible with either a schwannoma or meningioma. This lesion invaded the root entry zones of cranial nerves V and VIII explaining the patient’s oral pain and hypoacusia. Following a neurosurgical consultation where surgical treatment was rejected, her pain was successfully managed by topical pregabalin mouthwashes, to prevent any risk of respiratory depression related to her underlying severe bronchomalacia.
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Tibesar, Eric E. "Bleeding Gastric Heterotopic Polyp in the Duodenum of a Teenager with Severe Factor VII Deficiency." Case Reports in Gastroenterology 14, no. 3 (October 8, 2020): 467–71. http://dx.doi.org/10.1159/000508441.

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Heterotopic gastric tissue can be found throughout the intestinal tract, and when it is present in the small intestine, it can present with symptoms that include gastrointestinal bleeding, chronic abdominal pain, diarrhea, and chronic dyspepsia. This finding is incredibly rare in pediatrics, but if present, it can lead to significant morbidity and mortality. This can be especially true if a patient presents with a comorbidity of a bleeding disorder. We here present the case of a teenage male with a history of severe factor VII deficiency who was found to have iron deficiency anemia resulting in multiple blood transfusions from an occult lower gastrointestinal bleed. He was ultimately found to have a bleeding gastric heterotopic polyp in his duodenum that was successfully removed via surgery.
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Mahendradas, Padmamalini, Rohit Shetty, Kavitha Avadhani, Cecil Ross, Anchal Gupta, and Bhujang K. Shetty. "Polycythemia Vera and Increased Hemophilic Factor VIII Causing Acute Zonal Occult Outer Retinopathy: A Case Report." Ocular Immunology and Inflammation 18, no. 4 (July 21, 2010): 319–21. http://dx.doi.org/10.3109/09273941003798767.

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7

Lopetegui Lia, Nerea, Abigael Luke, Syed Daniyal Asad, Shashank Sama, Leo J. Wolansky, and Upendra P. Hegde. "Intracranial bleeding following soccer‐related head trauma in a young student with occult factor VII deficiency." Clinical Case Reports 8, no. 11 (October 3, 2020): 2148–51. http://dx.doi.org/10.1002/ccr3.3094.

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8

Agostini, Vanessa, Chiara Biasoli, Rino Biguzzi, Rita Santarelli, and Pietro Leoni. "Case Report: Coexistence of Factor VIII Inhibitor and Lupus Anticoagulant." Blood 110, no. 11 (November 16, 2007): 3948. http://dx.doi.org/10.1182/blood.v110.11.3948.3948.

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Abstract Acquired haemophilia is a very rare (1,5 per million per year) and serious coagulophaty that is associated with significant morbidity and mortality. This disorder is caused by the development of autoantibodies directed against coagulaton factor, usually for factor (F) VIII. About half of the cases occurred in apparently healthy people and were considered idiopathic, although there were others known associations, including postpartum period, autoimmune disease, cancer and drugs. The simultaneous presence of F VIII inhibitor and lupus anticoagulant (LAC) is extremely rare and the differentiation between these two conditions is crucial because the clinical manifestation range from massive, life-threatening haemorrhage to thrombosis. We report a case of 78 years old men affected by acquired haemophilia presentig with gluteus and right forearm non traumatic haematoma and anemia. The activated partial thromboplastin time (aPTT) was prolonged at 158,5s (normal 20–35s), with a normal prothrombin time (PT) of 9,88s (normal 9–13s). An aPTT inhibitor screening was positive, with demonstration of time-dependent inhibition. F VIII activity was reduced at 0,26% (normal 58,5–131,7%) and F VIII inhibition level was 41,53 Bethesda Units (BU). The patient was also found to have LAC. Screening tests for antinuclear antibodies, viral titres, occult cancer and cardiolipin antibodies were negative, chest Xray was negative and venous ultrasonografy of lower limbs was performed in order to exclude a concomitant deep venous thrombosis. At the admittance in hospital the patient received packed red cells transfusions for the anemia and treatment with prednisone 1mg/kg once daily in order to autoantibody eradication. After a week was associated therapy with cyclophosfamide 500mg per meter squared every 21 days. The acute bleeding stopped without using bypassing agents or recombinant activated F VII. One month after the institution of the immunosoppressive therapy the F VIII level was 0,9% and the inhibitor level was decreased at 9 B.U. After six cycles of cyclophosfamide and prednisone, tapered at 12,5 mg once daily, F VIII level raised at 16,05% but the inhibitor level remined 6,49 B.U., so was decided to change the immunosoppressive treatment and cyclosporin was administrated at the dose of 50 mg once daily. three months later the aPTT was 26s and factor level was 118% and the cyclosporin treatment discontinuated; thirty days after the aPTT was again 58 s and FVIII levels decreased at 78% so the immunosoppressive treatment was reintroduced at the same dosage of 50 mg daily. The patient had a good performance status without side-effects treatment related and without haemorragic complications. cyclosporin was tailed off successfully two months later after obtained a stabilization of F VIII level at 80% and disappearance of the inhibitor. The aPTT value was 52s and LAC persisted present without thromboembolic manifestation and evidence of autoimmune disorder. Conclusion: idiophatic acquired haemophilia A occurs most frequently in older adults and often presents acutely with life-threatening haemorragies; the advanced age of patients sometimes limits the therapeutic options precluding the most aggressive treatments and necessitating dose reductions of drugs. Our patieny outlines the potential role of cyclosporin in the treatment of acquired haemophilia even at the lower doses of 50 mg daily. The concomitant presence of LAC probably mitigates the bleeding episodes caused by acquired F VIII deficiency and viceversa.
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Roe, Sophie. "Monica Black and Eric Kurlander, eds.: Revisiting the “Nazi Occult”: Histories, Realities, Legacies . Rochester, NY: Camden House, 2015; pp. viii + 297." Journal of Religious History 43, no. 4 (December 2019): 560–61. http://dx.doi.org/10.1111/1467-9809.12615.

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Monas, Sidney. "Book ReviewsThe Occult in Russian and Soviet Culture.Edited by Bernice Glatzer Rosenthal. Ithaca, N.Y.: Cornell University Press, 1997. Pp. vii+468." Journal of Modern History 71, no. 2 (June 1999): 517–18. http://dx.doi.org/10.1086/235287.

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Dissertations / Theses on the topic "Vizi occulti"

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XU, WENHUA. "RETICENZA DEL VENDITORE SUI VIZI OCCULTI. LA VIOLAZIONE DELLA BUONA FEDE TRA DIRITTO ROMANO E DIRITTO CINESE." Doctoral thesis, Università degli Studi di Milano, 2020. http://hdl.handle.net/2434/721044.

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Seller's reticence on hidden defects can be approached in different ways. In this thesis, I will deal with this issue by investigating the relation between hidden defects and the principle of good faith in the field of sales. The first part is devoted to Roman Law: it highlights the role that good faith has assumed in the elaboration of the emptio vendito and also in the specific evolution of protection against hidden defects through the actio empti. After dealing with these issues in Roman legal experience, I will proceed to examine current Chinese law in a perspective of diachronic comparison, aiming at verifying to what extent Roman jurisprudential solutions on this topic can inspire Chinese legislators. The second part of the thesis will be devoted to the legal protection against hidden defect in relation to the role of good faith in Chinese law, specifically addressing the issue of seller’s reticence on hidden defects.
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Books on the topic "Vizi occulti"

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Fontana, Alessandro. Il vizio occulto. Ancona: Transeuropa, 1989.

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2

Yates, Frances Amelia. The Rosicrucian enlightenment. London: Routledge, 1999.

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Lytton, Lytton Edward Bulwer. Alice or the Mysteries: Book VII & VIII & IX. IndyPublish.com, 2005.

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Yates, Frances Amelia. The Rosicrucian enlightenment. Barnes & Noble, 1996.

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Book chapters on the topic "Vizi occulti"

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Becker, Richard C., and Frederick A. Spencer. "Fundamentals and Patient Evaluation." In Fibrinolytic and Antithrombotic Therapy. Oxford University Press, 2006. http://dx.doi.org/10.1093/oso/9780195155648.003.0033.

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Thrombophilia is the term used to describe a tendency toward developing thrombosis. This tendency may be inherited, involving polymorphism in gene coding for platelet or clotting factor proteins, or acquired due to alterations in the constituents of blood and/or blood vessels. An inherited thrombophilia is likely if there is a history of repeated episodes of thrombosis or a family history of thromboembolism. One should also consider an inherited thrombophilia when there are no obvious predisposing factors for thrombosis or when clots occur in a patient under the age of 45. Repeated episodes of thromboembolism occurring in patients over the age of 45 raise suspicion for an occult malignancy. A summary of inherited thrombophilias are summarized in Table 24.1. This list continues to grow, as new genetic polymorphisms and combined mutations are being detected. The prevalence of common thrombophilias is shown in Figure 24.1. Factor V Leiden (FVL) mutation and hyperhomocysteinemia are present in nearly 5% of the general population and are often found in patients with venous thrombosis, while deficiencies of antithrombin (AT), protein C, and protein S are relatively uncommon. Elevated levels of factor VIII (FVIII) are uncovered frequently in the general population and in patients with thrombosis. This is not surprising as FVIII is an acute-phase reactant that increases rapidly after surgery or trauma; however, prospective studies have shown that FVIII elevation in some patients cannot be attributed to a stress reaction and probably represents mutations in the genes regulating FVIII synthesis or release (Kyrle et al., 2000). The same may be true for factors IX and XI. The relative risks for thrombosis among patients with inherited thrombophilias have been determined. While AT mutations are the least common, they are associated with a substantial risk of venous thrombosis; similar risk is seen with protein C and S deficiency. In contrast, the lifetime risk of having a thromboembolic event in an individual heterozygous for FVL is comparatively low (Martinelli et al., 1998). Incidence rates markedly increase with age, and are highest among those with AT deficiency, followed by protein C and protein S, and least with FVL.
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Conference papers on the topic "Vizi occulti"

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Almeida, Nathália, José Barros, Letícia Campos, Natália Spitz, Carlos Brandão, Catarina Santana, and Vanessa Paula. "Prevalence of occult Hepatitis B in patients infected with the hepatitis C will be treated with oral direct acting antivirals." In IV International Symposium on Immunobiologicals & VII Seminário Anual Científico e Tecnológico. Instituto de Tecnologia em Imunobiológicos, 2019. http://dx.doi.org/10.35259/isi.sact.2019_32819.

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