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1101“…The results disagree with the narrow sense Trivers & Willard hypothesis, which states that in polygynous mammals that show higher variation in male than in female reproductive success, high-quality mothers are expected to invest more in sons than in daughters.…”
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1102por Tarimo, Edith A.M., Thorson, Anna, Bakari, Muhammad, Mwami, Joachim, Sandström, Eric, Kulane, Asli“…OBJECTIVE: The objective of this study was to analyse the willingness to volunteer (WTV) in a Phase I/II HIV vaccine trial among police officers in Dar es Salaam, Tanzania. …”
Publicado 2009
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1103“…This study examines the prevalence of anxiety disorders in children with Williams syndrome (WS), their sibling closest in age, and their mothers as well as the predictors of anxiety in these groups. …”
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1104
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1105por Uzochukwu, Benjamin SC, Onwujekwe, Obinna E, Uguru, Nkoli P, Ughasoro, Maduka D, Ezeoke, Ogochukwu P“…Urban dwellers were more willing to pay than the rural dwellers. The mean WTP should be considered when designing suitable financial strategies for making RDTs available to communities.…”
Publicado 2010
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1106“…The results indicated that only 32% of Florida healthcare providers were competent and willing to respond to a bioterrorism attack, 82.7% of providers were willing to respond in their local community, and 53.6% within the State. …”
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1107“…OBJECTIVE: To determine the extent of hypoplasia of the component vessels of the circle of Willis (CW) and the anatomical variations in the anterior communicating artery (AcomA) in the subjects who have died of causes unrelated to the brain and compare with previous autopsy studies. …”
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1109por Voetagbe, Gertrude, Yellu, Nathaniel, Mills, Joseph, Mitchell, Ellen, Adu-Amankwah, Amanda, Jehu-Appiah, Koma, Nyante, Felix“…The aim of this study is to assess the capacity and willingness of midwifery tutors to teach contraception, post abortion care and legal termination in Ghana. …”
Publicado 2010
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1110“…BACKGROUND: Prader–Willi syndrome (PWS) is a rare genetic disorder resulting in obesity. …”
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1111por Barnett, Daniel J., Levine, Roger, Thompson, Carol B., Wijetunge, Gamunu U., Oliver, Anthony L., Bentley, Melissa A., Neubert, Patrick D., Pirrallo, Ronald G., Links, Jonathan M., Balicer, Ran D.“…Confidence in workplace safety is a positively influential modifier of their response willingness. These findings can inform insights into interventions for enhancing EMS workers' willingness to respond in the face of a global infectious disease threat.…”
Publicado 2010
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1112“…To determine the sedative and respiratory effects of clonidine when used to evaluate growth hormone (GH) secretion in children with Prader Willi Syndrome (PWS). Methods. The study prospectively evaluated children with PWS who received clonidine (0.15 mg/m(2)) to assess GH responsiveness. …”
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1113por Kim, Su Jin, Paik, Kyung Hoon, Kim, Dong-Ik, Choe, Yon Ho, Kim, Seon Woo, Jin, Dong-Kyu“…PURPOSE: Prader-Willi syndrome (PWS) is a genetic disorder characterized by childhood-onset obesity and endocrine dysfunction that leads to cardiovascular disability. …”
Publicado 2010
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1114por Gao, Michael C., Bellugi, Ursula, Dai, Li, Mills, Debra L., Sobel, Eric M., Lange, Kenneth, Korenberg, Julie R.“…To accelerate understanding in this area, we have taken a new approach by studying the relationship between quantitative gene expression and intelligence in a cohort of 65 patients with Williams Syndrome (WS), a neurodevelopmental disorder caused by a 1.5 Mb deletion on chromosome 7q11.23. …”
Publicado 2010
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1115“…Both sexes of Scandinavian and Scottish Willow grouse (Lagopus lagopus) display marked differences in their winter phenotypes, with Scottish grouse retaining a pigmented plumage year-round and Scandinavian Willow grouse molting to a white morph during winter. …”
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1116“…Prader–Willi syndrome (PWS) is a complex neurodevelopmental disorder caused by an abnormality on the long arm of chromosome 15 (q11–q13) that results in a host of phenotypic characteristics, dominated primarily by hyperphagia and insatiable appetite. …”
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1117“…BACKGROUND: Prader-Willi syndrome (PWS) and Angelman syndrome (AS) are clinically distinct neurodevelopmental genetic disorders that map to 15q11-q13. …”
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1118“…Williams-Beuren syndrome (WBS) is a neurodevelopmental disorder caused by the hemizygous deletion of 28 genes on chromosome 7, including the general transcription factor GTF2IRD1. …”
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1119por Martín-Fernández, Jesús, del Cura-González, Ma Isabel, Gómez-Gascón, Tomás, Oliva-Moreno, Juan, Domínguez-Bidagor, Julia, Beamud-Lagos, Milagros, Pérez-Rivas, Francisco Javier“…This value can differ from the perspectives of Willingness to Pay (WTP) and Willingness to Accept [Compensation] (WTA). …”
Publicado 2010
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1120“…RESULTS: The majority of those surveyed would like to work in Budapest or a large town. Fewer than 7% were willing to work in a town with less than 50 000 inhabitants. …”
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