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  1. 1181
    “…Personal history was not associated with the students’ willingness to treat, but men were less willing to treat. …”
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    Willingness to treat drug dependence and depression: comparisons of future health professionals
  2. 1182
    por Gogate, Bageshri, Gogate, Parikshit
    Publicado 2011
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    Eye donation: Mere awareness and willingness not enough. Only a catalyst can improve corneal harvesting rates
  3. 1183
    “…INTRODUCTION: Williams-Beuren syndrome (WBS; OMIM 194050) is caused by a hemizygous contiguous gene microdeletion at 7q11.23. …”
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    Detection of deletions at 7q11.23 in Williams-Beuren syndrome by polymorphic markers
  4. 1184
    “…Participants were asked what amount they would be willing to pay as taxes to continue accessing the services of the municipality hospital for one year by using open-ended questions in face-to-face interviews. …”
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    Willingness to pay for municipality hospital services in rural Japan: a contingent valuation study
  5. 1185
    “…The results of the study revealed that around 86% of the respondents were willing to buy ITNs. The average maximum willingness-to-pay for three different types of bednets was statistically different. …”
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    Factors Influencing People's Willingness-to-buy Insecticide-treated Bednets in Arbaminch Zuria District, Southern Ethiopia
  6. 1186
    “…CONCLUSIONS: Willingness to risk one's life for a patient is related to knowledge of safety measures, and trust in colleagues and work place preparedness. …”
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    Who is willing to risk his life for a patient with a potentially fatal, communicable disease during the peak of A/H1N1 pandemic in Israel?
  7. 1187
    “…The size of von Willebrand factor (VWF), controlled by ADAMTS13-dependent proteolysis, is associated with its hemostatic activity. …”
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    A Conformation-Sensitive Monoclonal Antibody against the A2 Domain of von Willebrand Factor Reduces Its Proteolysis by ADAMTS13
  8. 1188
    por Butler, Merlin G
    Publicado 2011
    “…Prader-Willi syndrome (PWS) is a complex neurodevelopmental disorder due to errors in genomic imprinting with loss of imprinted genes that are paternally expressed from the chromosome 15q11-q13 region. …”
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    Prader-Willi Syndrome: Obesity due to Genomic Imprinting
  9. 1189
    “…BACKGROUND: Prader-Willi syndrome (PWS) is a complex neurodevelopmental genetic disorder with hypothalamic dysfunction, early morbid obesity with hyperphagia, and specific psychiatric phenotypes including cognitive and behavioural problems, particularly disruptive behaviours and frequent temper outbursts that preclude socialization. …”
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    Oxytocin may be useful to increase trust in others and decrease disruptive behaviours in patients with Prader-Willi syndrome: a randomised placebo-controlled trial in 24 patients
  10. 1190
    por SUTTON, EMMA K.
    Publicado 2011
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    When Misery and Metaphysics Collide: William James on ‘the Problem of Evil’
  11. 1191
    “…von Willebrand factor (VWF) multimers mediate primary adhesion and aggregation of platelets. …”
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    Calcium modulates force sensing by the von Willebrand factor A2 domain
  12. 1192
    “…The prevalence of Prader-Willi syndrome is estimated to be one in 10,000 to 25,000. …”
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    Periodontal disease in a patient with Prader-Willi syndrome: a case report
  13. 1193
    “…Using dual-color confocal microscopy and correlative electron microscopy in human endothelial cells, we visually distinguished two sequential steps of secretagogue-stimulated exocytosis: fusion of individual secretory granules (Weibel–Palade bodies [WPBs]) and subsequent expulsion of von Willebrand factor (VWF) content. Based on our observations, we conclude that for fusion, WPBs are released from cellular sites of actin anchorage. …”
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    Actomyosin II contractility expels von Willebrand factor from Weibel–Palade bodies during exocytosis
  14. 1194
    “…Persons with Williams syndrome (WS) demonstrate pronounced deficits in visuo-spatial processing. …”
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    Electrophysiological study of local/global processing in Williams syndrome
  15. 1195
    “…Prader-Willi syndrome (PWS) is a genetic imprinting disease that causes developmental and behavioral disturbances resulting from loss of expression of genes from the paternal chromosome 15q11-q13 region. …”
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    TPH2 polymorphisms and expression in Prader-Willi syndrome subjects with differing genetic subtypes
  16. 1196
    “…Von Willebrand factor (VWF) is a pro-hemostatic multimeric plasma protein that promotes platelet aggregation and stabilizes coagulation factor VIII (FVIII) in plasma. …”
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    Cleavage of von Willebrand Factor by Granzyme M Destroys Its Factor VIII Binding Capacity
  17. 1197
    “…BACKGROUND: Point mutations resulting in reduced factor VIII (FVIII) binding to von Willebrand factor (VWF) are an important cause of mild/moderate hemophilia A. …”
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    Storage of Factor VIII Variants with Impaired von Willebrand Factor Binding in Weibel-Palade Bodies in Endothelial Cells
  18. 1198
    “…Considering the role of von Willebrand factor (vWf) in hemostasis, and the role of oxidative stress in the development of endothelial dysfunction and atherosclerotic disease, the aim of our study was to investigate the relationship between vWf, parameters of oxidative stress and different types of acute coronary syndromes (ACS). …”
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    von Willebrand Factor and Oxidative Stress Parameters in Acute Coronary Syndromes
  19. 1199
    “…After controlling for demographic characteristics and rural exposure, motivational factors did not influence willingness to practice in rural areas. High family PPES was consistently associated with lower willingness to work in rural areas. …”
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    Willingness to work in rural areas and the role of intrinsic versus extrinsic professional motivations - a survey of medical students in Ghana
  20. 1200
    “…METHODS: 11 adult patients affected by Prader-Willi Syndrome (PWS) and 20 age-matched individuals (Control group: CG) were included in this study. …”
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    Fractal dimension approach in postural control of subjects with Prader-Willi Syndrome
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