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1. |
Record Nr. |
UNINA9910706841003321 |
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Autore |
Adolph Charles E. <1935-> |
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Titolo |
A career in test and evaluation : reflections and observations: from an oral history interview of Charles E. "Pete" Adolph / / conducted by Richard P. Hallion |
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Pubbl/distr/stampa |
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[Washington, D.C.] : , : Air Force History and Museums Program in association with Air University Press, , 1998 |
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Descrizione fisica |
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1 online resource (xi, 221 pages) : illustrations, maps |
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Soggetti |
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Aeronautical engineers - United States |
Airplanes, Military - United States - Flight testing - History |
Aeronautical engineers |
Airplanes, Military - Flight testing |
History |
Interviews. |
United States |
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Lingua di pubblicazione |
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Formato |
Materiale a stampa |
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Livello bibliografico |
Monografia |
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Nota di bibliografia |
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Includes bibliographical references (page 114) and index. |
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2. |
Record Nr. |
UNIORUON00192439 |
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Autore |
BLAKE, William |
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Titolo |
Cielo e inferno / William Blake ; introduzione, traduzione e nota di Pasquale Maffeo ; con cinque disegni e due acqueforti originali di Sandro Stenico |
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Pubbl/distr/stampa |
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Edizione |
[Napoli : Fiorentino Editrice] |
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Descrizione fisica |
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Disciplina |
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Lingua di pubblicazione |
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Formato |
Materiale a stampa |
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Livello bibliografico |
Monografia |
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3. |
Record Nr. |
UNINA9910557578003321 |
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Autore |
Mager Hans-Jurgen |
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Titolo |
Hereditary Hemorrhagic Telangiectasia : Recent Advances and Future Challenges |
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Pubbl/distr/stampa |
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Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021 |
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Descrizione fisica |
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1 online resource (228 p.) |
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Soggetti |
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Research and information: general |
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Lingua di pubblicazione |
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Formato |
Materiale a stampa |
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Livello bibliografico |
Monografia |
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Sommario/riassunto |
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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 |
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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. |
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