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  1. 1241
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    The Williams-Beuren Syndrome—A Window into Genetic Variants Leading to the Development of Cardiovascular Disease
  2. 1242
    “…A hallmark feature of Williams-Beuren Syndrome (WBS) is a generalized arteriopathy due to elastin deficiency, presenting as stenoses of medium and large arteries and leading to hypertension and other cardiovascular complications. …”
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    Reduction of NADPH-Oxidase Activity Ameliorates the Cardiovascular Phenotype in a Mouse Model of Williams-Beuren Syndrome
  3. 1243
    “…Compared with other angiosperm trees, the two willows harbor intermediate levels of silent polymorphisms. …”
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    Polymorphism and Divergence in Two Willow Species, Salix viminalis L. and Salix schwerinii E. Wolf
  4. 1244
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    Magel2, a Prader-Willi syndrome candidate gene, modulates the activities of circadian rhythm proteins in cultured cells
  5. 1245
    “…The objective of this study was to assess the impact of melasma on quality of life by using a health status measurement - the Dermatology Life Quality Index (DLQI) - and a preference-based measurement - Willingness to Pay (WTP) and Time Trade-Off (TTO). METHODS: A cross-sectional descriptive study was conducted. …”
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    Measuring melasma patients' quality of life using willingness to pay and time trade-off methods in thai population
  6. 1246
    “…Williams syndrome (WS) is a rare genetic neurodevelopmental disorder characterized by increased non-social anxiety, sensitivity to sounds and hypersociability. …”
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    Regional Brain Differences in Cortical Thickness, Surface Area and Subcortical Volume in Individuals with Williams Syndrome
  7. 1247
    por Breathnach, C S, Moynihan, J B
    Publicado 2011
    “…In the middle of the nineteenth century the cataclysmic Famine opened the floodgates of poverty and urban overcrowding that resulted in an alarming death rate that continued to increase until the early years of the twentieth century. It is to William Wilde (1815-1876) we owe the nuanced investigation of the earliest numerical records of consumption and related disorders in Ireland.…”
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    William Wilde and the Early Records of Consumption in Ireland
  8. 1248
    “…Plusieurs syndromes microdélétionnels peuvent être confirmés aisément, les plus recherchés sont Le syndrome de Williams (microdélétion en 7q11.23) et le syndrome de la délétion 22q11 (microdélétion en 22q11.2). …”
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    Syndromes microdélétionnels (syndrome de Williams et syndrome de la délétion 22q11) au CHU Hassan II de Fès: à propos de 3 observations
  9. 1249
    “…Contents of Cd and Zn in the stems of willows were combination-specific, but were always increased in dual inoculated plants. …”
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    Interactive and Single Effects of Ectomycorrhiza Formation and Bacillus cereus on Metallothionein MT1 Expression and Phytoextraction of Cd and Zn by Willows
  10. 1250
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    Engaging Undergraduates in Science Research: Not Just About Faculty Willingness
  11. 1251
    “…Complications associated with morbid obesity are recognized as the main risk factors for death the lifespan of patients with Prader-Willi syndrome. We experienced desaturation and bronchospasm during arteriovenous fistula surgery in an obese adult with Prader-Willi syndrome.…”
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    Experience of severe desaturation during anesthetic induction period in an obese adult patient with Prader-Willi syndrome -A case report-
  12. 1252
    “…BACKGROUND: Williams-Beuren syndrome (WBS; OMIM 194050) is caused by a hemizygous contiguous gene microdeletion at 7q11.23. …”
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    Copy number variation in Williams-Beuren syndrome: suitable diagnostic strategy for developing countries
  13. 1253
    “…CONCLUSIONS: BICAD with concomitant inadequate collaterals from the circle of Willis may predispose to hypoperfusion which might not respond to the usual conservative treatment prompting for flow reestablishment. …”
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    Therapeutic and Diagnostic Implication of Inadequate Circle of Willis in a Patient with Acute Spontaneous Bilateral Internal Carotid Artery Dissection: Case Report and Review of the Literature
  14. 1254
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    Phenolic content and antioxidant property of the bark extracts of Ziziphus mucronata Willd. subsp. mucronata Willd
  15. 1255
    “…BACKGROUND: Williams-Beuren syndrome (WBS), a rare developmental disorder caused by deletion of contiguous genes at 7q11.23, has been characterized by strengths in socialization (overfriendliness) and communication (excessive talkativeness). …”
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    Autistic Disorder in Patients with Williams-Beuren Syndrome: A Reconsideration of the Williams-Beuren Syndrome Phenotype
  16. 1256
    “…Half of the participants were willing to get circumcised and 79% of men would accept circumcision for their sons. …”
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    Determinants of circumcision and willingness to be circumcised by Rwandan men, 2010
  17. 1257
    “…Percentages of those willing to use models and the average amount (with 95% confidence intervals) they are willing to pay were estimated. …”
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    Willingness to use and pay for options of care for community-dwelling older people in rural Vietnam
  18. 1258
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    Quantification and visualization of flow in small vessels of the Circle of Willis: time-resolved three-dimensional phase contrast MRI at 7T compared with 3T
  19. 1259
    Publicado 2012
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    Exploring the World of Phospholipids and Their Interactions with Proteins: The Work of William Dowhan
  20. 1260
    “…The aim of this study was to characterize the anti-inflammatory mode of action of botanical extracts from rosehip (Rosa canina), willow bark (Salix alba), and nettle leaf (Urtica dioica) in an in vitro model of primary canine articular chondrocytes. …”
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    Botanical Extracts from Rosehip (Rosa canina), Willow Bark (Salix alba), and Nettle Leaf (Urtica dioica) Suppress IL-1β-Induced NF-κB Activation in Canine Articular Chondrocytes
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