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Journal articles on the topic 'Wilson'

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Published: 4 June 2021
Last updated: 1 August 2024

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1

Harada, Masaru. "Wilson disease." Kanzo 56, no. 12 (2015): 639–44. http://dx.doi.org/10.2957/kanzo.56.639.

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2

LONGINO, JOHN T. "Additions to the taxonomy of New World Pheidole (Hymenoptera: Formicidae)." Zootaxa 2181, no. 1 (August 6, 2009): 1–90. http://dx.doi.org/10.11646/zootaxa.2181.1.1.

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The hyperdiverse ant genus Pheidole has its center of diversity in the New World, where over 600 species occur. In spite of recent revisonary work (Wilson 2003) new species continue to be discovered and understanding of geographic variation of named species continues to improve. In this report new species and taxonomic changes are proposed for the Central American fauna. The following new species are described: P. bigote, P. branstetteri, P. carinote, P. debilis, P. eowilsoni, P. epiphyta, P. fossimandibula, P. gymnoceras, P. janzeni, P. karolmorae, P. karolsetosa, P. lagunculinoda, P. leoncortesi, P. mesomontana, P. pararugiceps, P. phanigaster, P. picobarva, P. purpurea, P. rhinomontana, P. sebofila, P. sparsisculpta, P. synanthropica, and P. tenuicephala. The following new synonymy is proposed, with the senior synonym listed first and the junior synonym(s) in parentheses: P. angusticeps Wilson (= P. gradifera Wilson); P. arachnion Wilson (= P. iracunda Wilson); P. bilimeki Mayr (=P. rectiluma Wilson); P. boliviana Wilson (= P. mincana Wilson, P. scitula Wilson); P. boltoni Wilson (= P. humida Wilson); P. deceptrix Forel (=P. chiapasana Wilson, P. variceps Wilson); P. erratilis Wilson (= P. petersoni Wilson); P. exarata Emery (= P. grantae Forel); P. harrisonfordi Wilson (= P. prolixa Wilson, P. ruida Wilson, P. tenebra Wilson); P. laselva Wilson (=P. ebenina Wilson); P. mooreorum Wilson (= P. fariasana Wilson); P. nebulosa Wilson (= P. scabriventris Wilson); P. nitidicollis Emery (= P. sagana Wheeler); P. perpusilla Emery (= P. breviscapa Forel); P. pubiventris Mayr (= P. variegata Emery, P. indistincta Forel); P. radoszkowskii Mayr (= P. medialis Wilson); P. sculptior Forel (= P. tayrona Wilson); P. susannae Forel (= P. obscurior Forel and its synonym P. partita Mayr); P. texticeps Wilson (= P. perdiligens Wilson); P. vorax (Fabricius) (= P. cephalica F. Smith and its synonyms P. opaca Mayr, P. incrustata Forel, P. sarrita Forel, P. apterostigmoides Weber); P. walkeri Mann (= P. arietans Wilson, P. glyphoderma Wilson, P. triumbonata Wilson). Pheidole innupta Menozzi is removed from synonymy under P. alfaroi and revalidated.
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3

Odake, Satoru, and Ryu Sasaki. "Multi-indexed Wilson and Askey–Wilson polynomials." Journal of Physics A: Mathematical and Theoretical 46, no. 4 (January 15, 2013): 045204. http://dx.doi.org/10.1088/1751-8113/46/4/045204.

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4

Kaushik, S. K., and Suman Panwar. "An Interplay between Gabor and Wilson Frames." Journal of Function Spaces and Applications 2013 (2013): 1–6. http://dx.doi.org/10.1155/2013/610917.

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Wilson frames{ψjk:w0,w-1∈L2(ℝ)}j∈ℤ,k∈ℕ0as a generalization of Wilson bases have been defined and studied. We give necessary condition for a Wilson system to be a Wilson frame. Also, sufficient conditions for a Wilson system to be a Wilson Bessel sequence are obtained. Under the assumption that the window functionsw0andw-1for odd and even indices ofjare the same, we obtain sufficient conditions for a Wilson system to be a Wilson frame (Wilson Bessel sequence). Finally, under the same conditions, a characterization of Wilson frame in terms of Zak transform is given.
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5

Wilson, Brent. "Transfer of type specimens of Caribbean Foraminifera and Ostracoda to the European Micropalaeontological Reference Centre." Micropaleontology 67, no. 1 (2021): 105. http://dx.doi.org/10.47894/mpal.67.1.07.

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While working on Trinidad and Tobago and the western tropical Atlantic Ocean, the author published four papers (Wilson 2006a, 2006b, 2006c;Wilson et al. 2011) that included descriptions of ten new species of foraminifera and ostracoda from the Neogene of the SE Caribbean Sea. These holotypes and associated paratypes have now been transferred to the European Micropalaeontological Reference Centre, AGH, University of Science and Technology, Krakow, Poland, for safekeeping. Among the foraminifera, these are: Amphistegina martybuzasi Wilson, Ramkissoon and McLean 2011; Bolivina jiattongi Wilson 2006; Textularia carrbrowni Wilson 2006; Textularia framptoni Wilson 2006; and Textularia sawhi Wilson 2006. Regarding ostracodes, they are: Bythoceratina coimbrai Wilson 2006; Cytheropteron bremani Wilson 2006; Polycope swietinia Wilson 2006; Polycope trinitatensis Wilson 2066; and Pterygocythereis fithiani Wilson 2006. The specimen slides have been curated in Cabinet 7, Drawer 27.
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6

Faltin, Kamil, Marta Kostrzewa, Małgorzata Stańczyk, and Marcin Tkaczyk. "Mowat–Wilson syndrome – case study." Pediatria i Medycyna Rodzinna 12, no. 2 (June 30, 2016): 201–8. http://dx.doi.org/10.15557/pimr.2016.0020.

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7

LONGINO, JOHN T. "Pheidole (Hymenoptera, Formicidae) of Middle American Wet Forest." Zootaxa 4599, no. 1 (May 6, 2019): 1. http://dx.doi.org/10.11646/zootaxa.4599.1.1.

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The ant genus Pheidole is a highly diverse lineage of ants that are dominant elements of tropical and subtropical ecosystems throughout the world. Biodiversity inventory projects in Middle American wet forests (southern Mexico to Costa Rica, lowland rainforest to high montane forest) allow an improved taxonomy of the genus in this region. An identification guide to 234 species in the region is provided, using a "bird guide" approach. Species are arranged in order of minor worker head width and scape length, and each species has a fixed layout that includes habitat and microhabitat information, standard views (minor lateral, minor face, major face), and a distribution map. The following new synonyms are proposed: biconstricta Mayr 1870 (= inermis Mayr 1870), carapuna Mann 1916 (= tristicula Wilson 2003), fimbriata Roger 1863 (= soesilae Makhan 2007), insipida Forel 1899 (= fariasana Wilson 2003, mooreorum Wilson 2003), longiscapa Forel 1901 (= cocciphaga Borgmeier 1934), plebecula Forel 1899 (= perdiligens Wilson 2003, texticeps Wilson 2003), nitidicollis Emery 1896 (= chalcoides Wilson 2003), nubicola Wilson 2003 (= cielana Wilson 2003, petrensis Wilson 2003), simonsi Wilson 2003 (= arctos Wilson 2003, gangamon Wilson 2003, thrasys Wilson 2003), striaticeps Mayr 1870 (= chloe Forel 1908), transversostriata Mayr 1887 (= scalaris Wilson 2003), vafra Santschi 1923 (= laticornis Wilson 2003). The following 57 new species are described: ajaxigibba, andersoni, angustinigra, atitlana, balatro, belonorte, besalon, bicornisculpta, brownampla, cahui, caliginosa, carinitida, corniclypeus, costaricensis, cusuco, depressinoda, eosimilis, familiaparra, fincanaranjo, hansoni, hectornitida, hitoy, huarache, imbrilis, indagarama, kasparii, kelainos, lagunculiminor, lamancha, laselvoides, lineafrons, luteagossamer, machaquila, marmor, moskitia, muralla, musacolor, musinermis, natalie, nephele, obturaculum, passivaeferox, perissothrix, platyscapa, probolonotum, rima, rogeripolita, savegre, sensipelada, sepultura, tapanti, tikal, tinamu, tsontekonwei, tuculutan, xiloa, zannia.
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8

Birringer, Johannes. "Wilson/Wagner." Performing Arts Journal 15, no. 1 (January 1993): 62. http://dx.doi.org/10.2307/3245798.

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9

Bowles, Nigel. "Harold Wilson." International Affairs 69, no. 3 (July 1993): 586–87. http://dx.doi.org/10.2307/2622370.

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10

Heale, Elizabeth, Peter E. Medine, Charles W. Crupi, and Michael O'Connell. "Thomas Wilson." Yearbook of English Studies 19 (1989): 309. http://dx.doi.org/10.2307/3508066.

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11

Ozuah, Philip O. "Wilson Disease." Pediatrics in Review 17, no. 12 (December 1996): 448. http://dx.doi.org/10.1542/pir.17-12-448.

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12

Fargnoli, Joseph R., and David Castronovo. "Edmund Wilson." Journal of the Midwest Modern Language Association 19, no. 1 (1986): 77. http://dx.doi.org/10.2307/1315015.

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13

Naylor, John F., and Austen Morgan. "Harold Wilson." American Historical Review 99, no. 1 (February 1994): 238. http://dx.doi.org/10.2307/2166239.

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14

Crunden, Robert M., and August Heckscher. "Woodrow Wilson." American Historical Review 98, no. 1 (February 1993): 267. http://dx.doi.org/10.2307/2166567.

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15

Clements, Kendrick A., and August Heckscher. "Woodrow Wilson." Journal of American History 79, no. 3 (December 1992): 1215. http://dx.doi.org/10.2307/2080909.

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16

Simina, Cozma, Cozma Simina, Paraschiv Andreea, and Vacaras Vitalie. "Wilson disease." Romanian Journal of Neurology 17, no. 2 (June 30, 2018): 113–18. http://dx.doi.org/10.37897/rjn.2018.2.10.

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17

Watson, George. "Angus Wilson." Hudson Review 53, no. 3 (2000): 452. http://dx.doi.org/10.2307/3853033.

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18

AYESHA, HINA, AAMIR ALI CHOUDHRY, and MUHAMMED ASGHAR BUTT. "WILSON DISEASE." Professional Medical Journal 12, no. 04 (December 31, 2005): 446–50. http://dx.doi.org/10.29309/tpmj/2005.12.04.5098.

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Objectives: 1). To study the genotypic differences, if any, betweenPakistani children suffering from Wilson’s disease from those in the west and to correlate phenotype with genotype. 2).To find out the most frequent mutations present in our patients and screen out asymptomatic siblings of the index cases.Setting: Department of Pediatrics, Allied Hospital, Punjab Medical College, Faisalabad. Duration: May 1997 to June2005. Materials and methods: 41 patients ranging from 5-18 years were diagnosed based on clinical and laboratorydata. 13 patients and 6 asymptomatic siblings along with their parents were subjected to mutation analysis. at Universityof Vienna, Austria. Results: None of the patients had His1069Gln, the commonest European mutation. R969Q andI1102T detected in our patients have previously been described. Four novel mutations were found. Asymptomaticsiblings screened were either heterozygote or normal. R969Q appears to be associated with sub-acute liver diseasewith hepatosplenomegaly. I1102T was seen in children with chronic liver disease and L1071W, C1079Y and E583R-fs(insA) with early onset of neurological disease. Conclusion: Our Patients are phenotypicaly as well as genotypicalydifferent. Different genotype could be responsible for the phenotype. Further studies are needed with a larger samplesize so that molecular genetic tests be devised for early diagnosis and family screening.
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19

Ozuah, Philip O. "Wilson Disease." Pediatrics In Review 17, no. 12 (December 1, 1996): 448. http://dx.doi.org/10.1542/pir.17.12.448.

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Wilson disease (hepatolenticular degeneration) is an autosomal recessive, inherited disorder of copper metabolism resulting in excessive accumulation of copper in the liver, brain, and other organs of the body. The manifestations of the disease are related directly to this accumulation of copper. Copper homeostasis normally is a product of the balance between intestinal absorption of dietary copper and hepatic biliary excretion of excess copper. In Wilson disease, incorporation of hepatic copper into ceruloplasmin is defective and excretion of copper in the bile is reduced. A low level of ceruloplasmin, which until a few years ago was erroneously considered to be the basis for the disease, is a consequence of the underlying metabolic defect.
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20

Gordon, Lewis R. "Wilson Harris." CLR James Journal 7, no. 1 (1999): 135–41. http://dx.doi.org/10.5840/clrjames1999/2000719.

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21

Mead, Walter Russell, and H. W. Brands. "Woodrow Wilson." Foreign Affairs 82, no. 3 (2003): 153. http://dx.doi.org/10.2307/20033605.

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22

White, Howard D. "Patrick Wilson." KNOWLEDGE ORGANIZATION 46, no. 4 (2019): 279–307. http://dx.doi.org/10.5771/0943-7444-2019-4-279.

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During 1965-2001, Patrick Wilson brought the acuity of a professional philosopher to library and information science (LIS) and became a major theorist in many aspects of knowledge organization (KO). This article, an extensive critical introduction to his thought, reflects the view that much of his work is of permanent value. He can be read for well-informed critiques of the instruments by which writings are organized for retrieval-the bibliographical side of KO. He can also be read for shrewd accounts of personal knowledge and behavior with respect to societal information systems-the social-epistemological side of KO. Indeed, in his work the two sides converge. One of his themes is the preferability of human consultants over bibliographies and catalogs for answering questions. He thus writes at length about the social organization of possible consultants and their degrees of cognitive authority in communicating what they know. Another theme is the desirability of indexing writings not only by subject but also by their possible utility in helping individuals. For that, however, he saw little hope. A third theme is ideal information systems. Broadly, he can be read for his clarifications of concepts on both sides of KO, such as bibliographical control, relevance, subject indeterminacy, information needs, information overload, librarians’ roles, and LIS as a field.
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23

El-Youssef, Mounif. "Wilson Disease." Mayo Clinic Proceedings 78, no. 9 (September 2003): 1126–36. http://dx.doi.org/10.4065/78.9.1126.

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24

Dopson, Laurence. "Wilson, Kathleen." Nursing Standard 25, no. 9 (November 3, 2010): 33. http://dx.doi.org/10.7748/ns2010.11.25.9.33.p6129.

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25

Grecco, Stephen, Peter Wolfe, and Frank Day. "August Wilson." World Literature Today 74, no. 2 (2000): 378. http://dx.doi.org/10.2307/40155659.

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26

Hollands, Charlotte. "Richard Wilson." Anthropology News 59, no. 4 (July 2018): e244-e244. http://dx.doi.org/10.1111/an.951.

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27

Clements, Kendrick A., and John A. Thompson. "Woodrow Wilson." Journal of Southern History 70, no. 1 (February 1, 2004): 187. http://dx.doi.org/10.2307/27648375.

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28

Hanağası, Figen, and Haşmet A. Hanağası. "Wilson Hastalığı." Türk Nöroloji Dergisi 19, no. 4 (2013): 122–27. http://dx.doi.org/10.4274/tnd.60566.

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29

Kermode-Scott, B. "Wilson Greatbatch." BMJ 343, oct26 3 (October 26, 2011): d6765. http://dx.doi.org/10.1136/bmj.d6765.

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30

Tanner, Stuart. "Wilson Disease." Journal of Pediatric Gastroenterology and Nutrition 54, no. 1 (January 2012): 6–7. http://dx.doi.org/10.1097/mpg.0b013e3182301328.

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31

Taly, Arun B., S. Meenakshi-Sundaram, Sanjib Sinha, H. S. Swamy, and G. R. Arunodaya. "Wilson Disease." Medicine 86, no. 2 (March 2007): 112–21. http://dx.doi.org/10.1097/md.0b013e318045a00e.

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32

Guthrie, V., and A. Wilson. "Eileen Wilson." BMJ 346, feb06 1 (February 6, 2013): f410. http://dx.doi.org/10.1136/bmj.f410.

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33

Wilson, S. W. J. "Harold Wilson." BMJ 347, jul17 1 (July 17, 2013): f4226. http://dx.doi.org/10.1136/bmj.f4226.

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34

Pernell, Ruby B. "Gertrude Wilson." Journal of Teaching in Social Work 6, no. 2 (January 26, 1993): 131–35. http://dx.doi.org/10.1300/j067v06n02_11.

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35

Huster, D., and C. Spranger. "Morbus Wilson." Kinder- und Jugendmedizin 09, no. 04 (2009): 211–14. http://dx.doi.org/10.1055/s-0038-1629065.

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ZusammenfassungDer Morbus Wilson ist eine autosomal-rezessiv vererbte Kupferstoffwechselstörung, die zu einer pathologischen Speicherung von Kupfer in der Leber, im Zentralnervensystem, in der Kornea und anderen Organen führt. Das betroffene Gen ATP7B kodiert für ein hepatisches Kupfertransportprotein mit zentraler Rolle im Kupferstoffwechsel des Menschen. Die klinischen Manifestationen sind Folgen der Kupfertoxizität. Bei Kindern tritt vor allem eine Leberschädigung unterschiedlichen Ausmaßes auf. Die Art der Lebererkrankung reicht von einer asymptomatischen Verlaufsform mit isolierter Transaminasenerhöhung bis hin zu einem fulminanten Leberversagen. Bei Kindern mit einer Hepatopathie unklarer Genese sollte daher ein M. Wilson differenzialdiagnostisch ab einem Alter von 3 Jahren immer in Erwägung gezogen werden. Eine vorwiegend neurologische Verlaufsform mit Tremor, Sprachstörungen und psychischen Veränderungen kann bei Jugendlichen vorgefunden werden. Die frühe Diagnosestellung und rasche Therapieeinleitung mit Chelatoren oder Zinksalzen sind für Verlauf und Prognose von entscheidender Bedeutung. Die Lebertrans-plantation ist bei akutem Leberversagen oder fortgeschrittener Leberzirrhose indiziert.
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36

Voss, H. "Morbus Wilson." Nervenheilkunde 35, no. 04 (2016): 232–41. http://dx.doi.org/10.1055/s-0037-1616377.

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ZusammenfassungMorbus Wilson ist eine autosomal-rezessive Erkrankung, bei der es durch Mutationen des ATP7B-Gens zu einer Störung des Kupferstoffwechsels kommt. Eine verminderte biliäre Kupferausscheidung und massive Kupferablagerungen insbesondere in Leber und Gehirn sind die Folge. Klinisch manifestiert sich der M. Wilson klassischerweise als (akute) hepatische Form im Kindes- und Jugendalter oder im jungen Erwachsenenalter mit extrapyramidalmotorischen oder psychiatrischen Symptomen. Unklare Bewegungsstörungen, insbesondere in Kombination mit (sub)klinischer Leberfunktionsstörung sollten aber auch in höherem Alter an den M. Wilson denken lassen. Unbehandelt kommt es zu schwerer Behinderung und Tod. Rechtzeitig erkannt, kann die Symptomprogredienz zumeist gestoppt und eine Rückbildung der Symptome erreicht werden. Der Einsatz von Chelatbildnern führt zu einer renalen Kupferausscheidung, mit Zinksalzen wird die Resorption von Kupfer im Darm gehemmt. Eine Lebertransplantation ist bei schweren hepatischen Verläufen sinnvoll und wird auch bei anders nicht zu kontrollierenden neurologischen Verlaufsformen diskutiert.
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37

Liederbach, John, and Lawrence F. Travis. "Wilson Redux." Police Quarterly 11, no. 4 (February 29, 2008): 447–67. http://dx.doi.org/10.1177/1098611108314567.

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38

Wilson, Derek. "Derek Wilson." Historically Speaking 9, no. 4 (2008): 19. http://dx.doi.org/10.1353/hsp.2008.0064.

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39

Wilson, John. "John Wilson." Historically Speaking 9, no. 4 (2008): 20. http://dx.doi.org/10.1353/hsp.2008.0069.

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40

Pfeiffer, Ronald F. "Wilson Disease." CONTINUUM: Lifelong Learning in Neurology 22, no. 4 (August 2016): 1246–61. http://dx.doi.org/10.1212/con.0000000000000350.

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41

Mittleman, L. B., and David Castronovo. "Edmund Wilson." World Literature Today 60, no. 2 (1986): 318. http://dx.doi.org/10.2307/40141794.

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42

Carist, Raymond E. "Wilson Popenoe." American Journal of Economics and Sociology 52, no. 1 (January 1993): 78. http://dx.doi.org/10.1111/j.1536-7150.1993.tb02743.x.

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43

Wilson, D. "Frederick Wilson." BMJ 344, feb14 3 (February 14, 2012): e393-e393. http://dx.doi.org/10.1136/bmj.e393.

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Holubar, K. "ERASMUS WILSON." Aktuelle Dermatologie 36, no. 01/02 (February 2010): 1–3. http://dx.doi.org/10.1055/s-0029-1243935.

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45

Goold, Douglas. "Michael Wilson." International Journal: Canada's Journal of Global Policy Analysis 61, no. 2 (June 2006): 468–78. http://dx.doi.org/10.1177/002070200606100214.

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46

Streitfeld, Lisa Paul. "Martha Wilson." Artus 2011 - 2012: The Collector's Edition 32, no. 1 (August 2, 2013): 188–89. http://dx.doi.org/10.1386/artus.32.1.188_4.

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47

Iorio, Raffaele, and Giusy Ranucci. "Wilson Disease." Journal of Pediatric Gastroenterology and Nutrition 60, no. 4 (April 2015): 423–24. http://dx.doi.org/10.1097/mpg.0000000000000725.

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48

Graham, Philip. "Peter Wilson." Child Psychology and Psychiatry Review 4, no. 4 (November 1999): 183–84. http://dx.doi.org/10.1017/s1360641799002075.

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For a relatively new organisation (it was founded only 10 years ago), Young Minds has already made a major impact on the CAMHS field. Its magazine contains lively articles by writers such as Susie Orbach and Adam Phillips and is widely read. It runs a well-used information service for parents concerned about the mental health of their children, and a consultancy service for professionals. High profile personalities such as Spike Milligan, John Bird, John Fortune and Nick Hornby have given their services to its fund-raising events. Who can take the major credit for the success of Young Minds? Stand up, Peter Wilson, the subject of this profile. He was initially Chair of the organisation and has been Director since April 1992.
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49

Kirby, Neil. "Leah Wilson." Australasian Journal on Ageing 22, no. 1 (March 2003): 41–43. http://dx.doi.org/10.1111/j.1741-6612.2003.tb00462.x.

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50

Richardson, Matt. "Ajita Wilson." TSQ: Transgender Studies Quarterly 7, no. 2 (May 1, 2020): 192–207. http://dx.doi.org/10.1215/23289252-8143350.

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Abstract This article puts forward a consideration of Black womanhood by looking at the softcore films starring African American trans model and actress, Ajita Wilson. Wilson starred in many European softcore and hardcore films from the 1970s until her death in 1987. The author is particularly interested in Wilson's 1976 film The Nude Princess and the 1977 film Black Afrodite (Mavri Afroditi) for their use of soul aesthetics. Conceptualized in dialogue with Tanisha Ford's discussion of “soul style,” soul aesthetics are a combination of gestures as well as visual and auditory references in dress, music, literature, and language that were generated by Black people during a period of African and Caribbean anticolonialism and liberatory Black civil rights movements. Because they were born from radical movement politics, these references have transnationally come to symbolize the possibility for Black collective and self-transformation. The author offers an analysis of these films as an example of softcore pornography affirming Black womanhood and focuses on what this process of self-making has to offer Black trans and queer feminist thought.
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