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Artigos de revistas sobre o tema "Turner Co"

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Autor: Grafiati

Publicado: 26 de julho de 2024

Última modificação: 29 de julho de 2024

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1

AN Yan, 安岩, 孙强 SUN Qiang, 刘英 LIU Ying e 李淳 LI Chun. "Design of astigmatism-free crossed Czerny-Turner spectrometer". Chinese Journal of Optics and Applied Optics 5, n.º 5 (2012): 470–75. http://dx.doi.org/10.3788/co.20120505.0470.

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2

Guimarães, Marília M., Carla T. G. Guerra, Solange T. F. Alves, Maria C. S. A. Cunha, Luiz A. Marins, Luiz F. M. Barreto, Evelyn Teich et al. "Intercorrências clínicas na Síndrome de Turner". Arquivos Brasileiros de Endocrinologia & Metabologia 45, n.º 4 (agosto de 2001): 331–38. http://dx.doi.org/10.1590/s0004-27302001000400004.

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Neste trabalho descrevemos as malformações e co-morbidades observadas em pacientes com síndrome de Turner (ST). Foi realizado um estudo retrospectivo, avaliando os prontuários de 60 pacientes cujo diagnóstico de ST foi confirmado através do cariótipo, desde a fase pré-natal até a idade de 49 anos. As pacientes encontram-se com idades entre 1 e 50 anos e foram evoluídas num período de 4 meses a 29 anos. Trinta e uma apresentavam o cariótipo 45XO, 24 eram mosaico e 5 apresentavam o padrão 46Xi, (i,Xq). Todas tinham baixa estatura e algum tipo de estigma. Cinco (8,3%) não apresentavam outras malformações congênitas e eram saudáveis; 55 (91,6%) apresentavam doenças associadas, sendo que em 23 (38,3%) foram detectadas doenças endócrinas, em 16 (26,6%) otorrinolaringológicas, 15 (25%) cardiológicas, 14 (23,3%) nefrológicas e 6 (10%) gastrointestinais. Entre as doenças endócrinas mais comuns, observamos hipotireoidismo (36,6%), seguido de osteoporose (18,3%) e hiperlipemia (11,6%). As doenças otorrinolaringológicas mais comuns foram as infecções (otite média e amigdalite); das doenças cardiológicas, as valvulopatias (principalmente aorta bicúspide), das nefrológicas as duplicações do sistema coletor e rotações renais e das gastrointestinais foram observados dois casos de divertículo de Meckel. Encontramos maior prevalência de malformações cardíacas nas pacientes com cariótipo 45XO, embora sem significância estatística quando considerados os demais cariótipos. Concluímos que, devido à alta ocorrência de doenças nesta síndrome, estas devem ser acompanhadas periodicamente em diferentes especialidades.

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3

Mikheev, R. K., O. R. Grigoryan, M. S. Pankratova, E. N. Andreeva, E. V. Sheremetyeva, Yu S. Absatarova e N. G. Mokrysheva. "Telomere pathology in ontogenesis in patients with Turner syndrome". Problems of Endocrinology 68, n.º 2 (17 de fevereiro de 2022): 128–32. http://dx.doi.org/10.14341/probl12869.

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According to present medical databases there many trials to provide in vivo researches in vivo to confirm/refute shortening process of telomeres among patients with Turner syndrome. Despite the successful clinical experience of providing such patients with Turner syndrome, a lot of omics (proteomic and metabolomic) aspects still stay unclear. Main disadvantages of most researches are small volume and minimized mathematical correlation with chronic disease (coronary heart disease, essential hypertension, cardiovascular malformations). Finally, organization of international prospective multi-centered researches in vivo including patients with mosaic cariotype and co-operation between physicians and biologists are optimal solutions for this present problem.

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4

Turner, Leah. "market view: AVERAGE COST". Nursery World 2024, n.º 4 (2 de abril de 2024): 52. http://dx.doi.org/10.12968/nuwa.2024.4.52.

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5

Turner, Leah. "Market View: By the Book". Nursery World 2024, n.º 3 (2 de março de 2024): 44. http://dx.doi.org/10.12968/nuwa.2024.3.44.

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6

Turner, J. L. "6.3. Physical conditions of the gas in the center of the nearby spiral galaxy IC 342". Symposium - International Astronomical Union 184 (1998): 267–68. http://dx.doi.org/10.1017/s0074180900084862.

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One of our nearest neighbors is a large spiral galaxy with abundant molecular gas in its nucleus. IC 342, a face-on Scd galaxy at a distance of 1.8 Mpc, is close enough to give us a view of individual molecular clouds with millimeter interferometry. The CO distribution in the nucleus of IC 342 consists of two very open spiral arms (Lo et al. 1984; Ishizuki et al. 1990) that continue to within 50 pc of the dynamical center (Turner & Hurt 1992). The total extent of the nuclear “mini-spiral” is ~ 500 pc. Corresponding arms are observed in Hα (J.S. Young, private comm.). However, the Hα arms are systematically offset by 50-100 pc from the CO arms (Turner & Hurt 1992). The offset of the Hα arms to the outer, leading edge of the CO arms is consistent with a picture of density wave-induced star formation in the arms (Turner & Hurt 1992). Energy dissipation and angular momentum transfer in spiral arms is believed to drive a slow drift of gas inward; if this is the case, the molecular “mini-spiral” in IC 342 is short-lived, and will probably no longer exist in another 108 years.

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7

Turner, Leah. "Market view: SELL AND TELL". Nursery World 2024, n.º 2 (2 de fevereiro de 2024): 44. http://dx.doi.org/10.12968/nuwa.2024.2.44.

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8

Turner, Leah. "Market view: WHAT IS ‘NAV’?" Nursery World 2024, n.º 1 (2 de janeiro de 2024): 44. http://dx.doi.org/10.12968/nuwa.2024.1.44.

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9

Mortensen, Kristian Havmand, Britta Eilersen Hjerrild, Niels Holmark Andersen, Keld Ejvind Sørensen, Arne Hørlyck, Erik Morre Pedersen, Erik Lundorf, Jens Sandahl Christiansen e Claus Højbjerg Gravholt. "Abnormalities of the major intrathoracic arteries in Turner syndrome as revealed by magnetic resonance imaging". Cardiology in the Young 20, n.º 2 (22 de março de 2010): 191–200. http://dx.doi.org/10.1017/s1047951110000041.

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AbstractBackgroundEctatic aortopathy and arterial abnormalities cause excess morbidity and mortality in Turner syndrome, where a state of vasculopathy seemingly extends into the major head and neck branch arteries.ObjectiveWe investigated the prevalence of abnormalities of the major intrathoracic arteries, their interaction with arterial dimensions, and their association with karyotype.DesignMagnetic resonance imaging scans determined the arterial abnormalities as well as head and neck branch artery and aortic dimensions in 99 adult women with Turner syndrome compared with 33 healthy female controls. Echocardiography determined aortic valve morphology.ResultsIn Turner syndrome, the relative risk of any congenital abnormality was 7.7 (p = 0.003) and 6.7 of ascending aortic dilation (p = 0.02). A bovine aortic arch was seen in both Turner syndrome and controls. Other abnormalities were only encountered in Turner syndrome: elongated transverse aortic arch (47%), bicuspid aortic valve (27%), aortic coarctation (13%), aberrant right subclavian artery (8%), and aortic arch hypoplasia (2%). The innominate and left common carotid arteries were enlarged in Turner syndrome (p < 0.001). Significant associations were first, bicuspid aortic valve with aortic coarctation, elongated transverse aortic arch, and ascending aortic dilation; second, aortic coarctation with elongated aortic arch and descending aortic dilation; third, 45,X with aortic coarctation, elongated transverse aortic arch and ascending aortic dilation; and fourth, branch artery dilation with bicuspid aortic valve, aortic coarctation, elongated transverse aortic arch and 45,X.ConclusionAn increased risk of arterial abnormalities, aortic dilation, and enlargement of the branch arteries was found in Turner syndrome without distinct patterns of co-segregation.

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10

Prior, Trevor I., Pierre S. Chue e Philip Tibbo. "Investigation of Turner syndrome in schizophrenia". American Journal of Medical Genetics 96, n.º 3 (2000): 373–78. http://dx.doi.org/10.1002/1096-8628(20000612)96:3<373::aid-ajmg26>3.0.co;2-z.

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11

Shahid, Mohammad Moin. "MRKH syndrome and Turner syndrome co-existing in a patient with primary amenorrhoea". Sri Lanka Journal of Diabetes Endocrinology and Metabolism 10, n.º 1 (1 de junho de 2020): 30. http://dx.doi.org/10.4038/sjdem.v10i1.7419.

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12

Schorry, Elizabeth K., Anne M. Lovell, Athena Milatovich e Howard M. Saal. "Ullrich-Turner syndrome and neurofibromatosis-1". American Journal of Medical Genetics 66, n.º 4 (30 de dezembro de 1996): 423–25. http://dx.doi.org/10.1002/(sici)1096-8628(19961230)66:4<423::aid-ajmg6>3.0.co;2-l.

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13

Ross, Judith, Andrew Zinn e Elizabeth McCauley. "Neurodevelopmental and psychosocial aspects of Turner syndrome". Mental Retardation and Developmental Disabilities Research Reviews 6, n.º 2 (2000): 135–41. http://dx.doi.org/10.1002/1098-2779(2000)6:2<135::aid-mrdd8>3.0.co;2-k.

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14

Vincent, A. J., H. H. Nguyen, S. Ranasinha e B. Vollenhoven. "Increased detection of co-morbidities with evaluation at a dedicated adult Turner syndrome clinic". Climacteric 20, n.º 5 (28 de julho de 2017): 442–47. http://dx.doi.org/10.1080/13697137.2017.1350841.

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15

Alvesalo, Lassi, John T. Mayhall e Juha Varrela. "Torus mandibularis in 45,X females (Turner syndrome)". American Journal of Physical Anthropology 101, n.º 2 (outubro de 1996): 145–49. http://dx.doi.org/10.1002/(sici)1096-8644(199610)101:2<145::aid-ajpa2>3.0.co;2-1.

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16

AMIEL, A., D. KIDRON, I. KEDAR, E. GABER, O. REISH e M. D. FEJGIN. "ARE ALL PHENOTYPICALLY-NORMAL TURNER SYNDROME FETUSES MOSAICS?" Prenatal Diagnosis 16, n.º 9 (setembro de 1996): 791–95. http://dx.doi.org/10.1002/(sici)1097-0223(199609)16:9<791::aid-pd944>3.0.co;2-3.

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17

Kjær, Inger, e Birgit Fischer Hansen. "Cervical ribs in fetuses with Ullrich-Turner syndrome". American Journal of Medical Genetics 71, n.º 2 (8 de agosto de 1997): 219–21. http://dx.doi.org/10.1002/(sici)1096-8628(19970808)71:2<219::aid-ajmg19>3.0.co;2-h.

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18

Garavelli, L., A. Donadio, G. Banchini, G. Fornaciari, A. C. Plancher, F. Franchi e G. Gardini. "Liver abnormalities and portal hypertension in Ullrich-Turner syndrome". American Journal of Medical Genetics 80, n.º 2 (2 de novembro de 1998): 180–82. http://dx.doi.org/10.1002/(sici)1096-8628(19981102)80:2<180::aid-ajmg18>3.0.co;2-u.

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19

Uematsu, Ayumi, Tohru Yorifuji, Junko Muroi, Chutaro Yamanaka e Toru Momoi. "Relatively longer hand in patients with Ullrich-Turner syndrome". American Journal of Medical Genetics 82, n.º 3 (29 de janeiro de 1999): 254–56. http://dx.doi.org/10.1002/(sici)1096-8628(19990129)82:3<254::aid-ajmg11>3.0.co;2-j.

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20

GRIFFITHS, M. J., P. R. MILLER e H. M. STIBBE. "A FALSE-POSITIVE DIAGNOSIS OF TURNER SYNDROME BY AMNIOCENTESIS". Prenatal Diagnosis 16, n.º 5 (maio de 1996): 463–66. http://dx.doi.org/10.1002/(sici)1097-0223(199605)16:5<463::aid-pd876>3.0.co;2-n.

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21

Ross, Judith L., Harvey Kushner e Andrew R. Zinn. "Discriminant analysis of the Ullrich-Turner syndrome neurocognitive profile". American Journal of Medical Genetics 72, n.º 3 (31 de outubro de 1997): 275–80. http://dx.doi.org/10.1002/(sici)1096-8628(19971031)72:3<275::aid-ajmg4>3.0.co;2-q.

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22

Wolstencroft, Jeanne, William Mandy e David Skuse. "Mental health and neurodevelopment in children and adolescents with Turner syndrome". Women's Health 18 (janeiro de 2022): 174550572211336. http://dx.doi.org/10.1177/17455057221133635.

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Objectives: Turner syndrome (TS) is a rare sex chromosome aneuploidy, with an incidence of four in 10,000 new-born girls. TS is often associated with impaired social communication skills, but the extent to which these are attributable to Autism Spectrum Disorders (ASD) is uncertain. We made standardized assessments of the mental health and associated neurodevelopmental disorders in children and adolescents with TS and report on the prevalence of concurrent conditions. Methods: Our sample comprised 127 girls with TS, 5–19 years of age. We obtained reports of their mental health from a combination of diagnostic interview (the Development and Wellbeing Assessment (DAWBA)), from the Strengths and Difficulties Questionnaire (SDQ) and from the Social Responsiveness Scale (SRS-2). Sources of information included parents, teachers and self-reports. The prevalence of mental health disorders in this sample was compared with age/sex matched national English data from typical controls. Results: Most individuals with TS (83%) had experienced significant social communication difficulties and nearly one in four (23%) met diagnostic criteria for ASD on the DAWBA. One-third (34%) had at least one mental health or neurodevelopmental condition, and those girls with an ASD were at a greater risk of a co-occurring emotional disorder and/or attention deficit hyperactivity disorder (ADHD). Conclusion: Children and adolescents with TS are substantially more likely to meet criteria for ASD than their typically developing peers. Our finding has clinical implications for appropriate behavioural management from preschool through to adolescence.

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23

Kuhns, Roger J., e Hart W. Baitis. "Preliminary study of the Turner Albright Zn-Cu-Ag-Au-Co massive sulfide deposit, Josephine County, Oregon". Economic Geology 82, n.º 5 (1 de agosto de 1987): 1362–76. http://dx.doi.org/10.2113/gsecongeo.82.5.1362.

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24

Romans, Sarah M., Gerry Stefanatos, David P. Roeltgen, Harvey Kushner e Judith L. Ross. "Transition to young adulthood in Ullrich-Turner syndrome: Neurodevelopmental changes". American Journal of Medical Genetics 79, n.º 2 (1 de setembro de 1998): 140–47. http://dx.doi.org/10.1002/(sici)1096-8628(19980901)79:2<140::aid-ajmg10>3.0.co;2-j.

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25

Morava, Eva, Robert Hermann, M�rta Czak�, Gyula Solt�sz e Gy�rgy Kosztol�nyi. "Isodicentric Y chromosome in an Ullrich-Turner patient without virilization". American Journal of Medical Genetics 91, n.º 2 (13 de março de 2000): 99–101. http://dx.doi.org/10.1002/(sici)1096-8628(20000313)91:2<99::aid-ajmg3>3.0.co;2-c.

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26

Kaiser, Christiane, e Klaus Abt. "Recognizing Ullrich-Turner syndrome by discriminant analysis of craniofacial structure". American Journal of Medical Genetics 62, n.º 2 (15 de março de 1996): 113–19. http://dx.doi.org/10.1002/(sici)1096-8628(19960315)62:2<113::aid-ajmg3>3.0.co;2-x.

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27

JOHNSON, RICHARD I. "MOLLUSCAN TAXA AND BIBLIOGRAPHIES OF WILLIAM JAMES CLENCH AND RUTH DIXON TURNER". Bulletin of the Museum of Comparative Zoology 158, n.º 1 (2 de setembro de 2003): 1–46. http://dx.doi.org/10.3099/0027-4100(2003)158[1:mtabow]2.0.co;2.

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28

Sinkar, Prachi, e Sandhya Iyer. "Double Chromosomal Anomalies in Turner Syndrome: Rare Co-existence of Robertsonian Translocation with Monosomy X and Isochromosome XQ". Asian Journal of Biological and Life sciences 9, n.º 3 (27 de janeiro de 2021): 421–23. http://dx.doi.org/10.5530/ajbls.2020.9.64.

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29

Abd, Samaa El, Michael A. Patton, Jeremy Turk, Hilary Hoey e Patricia Howlin. "Social, communicational, and behavioral deficits associated with ring X Turner syndrome". American Journal of Medical Genetics 88, n.º 5 (15 de outubro de 1999): 510–16. http://dx.doi.org/10.1002/(sici)1096-8628(19991015)88:5<510::aid-ajmg14>3.0.co;2-z.

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30

Magee, Alex C., Norman C. Nevin, Mike J. Armstrong, David McGibbon e Jean Nevin. "Ullrich-Turner syndrome: Seven pregnancies in an apparent 45,X woman". American Journal of Medical Genetics 75, n.º 1 (6 de janeiro de 1998): 1–3. http://dx.doi.org/10.1002/(sici)1096-8628(19980106)75:1<1::aid-ajmg1>3.0.co;2-z.

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31

Mauersberger, R., A. Schulz, J. W. M. Baars e H. Steppe. "An 8″ resolution CO (J=3−2) map of IC342". Symposium - International Astronomical Union 147 (1991): 460–61. http://dx.doi.org/10.1017/s0074180900240035.

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IC342 (Distance 4 Mpc) is one of the most suitable sources for extragalactic molecular line studies. Toward its nucleus, a great number of molecular species have been found (see Henkel and Mauersberger, 1990); it is also one of the few galaxies investigated in molecular multi-level studies (Mauersberger and Henkel, 1989). In particular, CO shows strong emission: A 7″ resolution interferometric map of the central parts of this galaxy in the 12CO(1—0) transition by Lo et al. (1984) reveals that the circumnuclear molecular gas is distributed in a bar (size 15″ × 70″) (330 × 1500 pc) extending from the nucleus towards the spiral arms. An interferometric map of the 1—0 line of CO by Ishizuki et al. (1990) shows that the inner part of the bar forms a molecular ring of diameter 110 pc. This inner ring also emits 2 and 6 cm continuum radiation (Turner and Ho, 1983). The kinetic temperature of the denser molecular gas is > 50 K (Martin and Ho, 1986). The H2 density of the gas component seen in CO (Eckart et al., 1990) and CS (Mauersberger and Henkel, 1989) is ∼ 104 cm−3.

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32

Mauersberger, R., A. Schulz, J. W. M. Baars e H. Steppe. "An 8″ resolution CO (J=3−2) map of IC342". Symposium - International Astronomical Union 147 (1991): 460–61. http://dx.doi.org/10.1017/s0074180900199413.

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IC342 (Distance 4 Mpc) is one of the most suitable sources for extragalactic molecular line studies. Toward its nucleus, a great number of molecular species have been found (see Henkel and Mauersberger, 1990); it is also one of the few galaxies investigated in molecular multi-level studies (Mauersberger and Henkel, 1989). In particular, CO shows strong emission: A 7″ resolution interferometric map of the central parts of this galaxy in the 12CO(1—0) transition by Lo et al. (1984) reveals that the circumnuclear molecular gas is distributed in a bar (size 15″ × 70″) (330 × 1500 pc) extending from the nucleus towards the spiral arms. An interferometric map of the 1—0 line of CO by Ishizuki et al. (1990) shows that the inner part of the bar forms a molecular ring of diameter 110 pc. This inner ring also emits 2 and 6 cm continuum radiation (Turner and Ho, 1983). The kinetic temperature of the denser molecular gas is > 50 K (Martin and Ho, 1986). The H2 density of the gas component seen in CO (Eckart et al., 1990) and CS (Mauersberger and Henkel, 1989) is ∼ 104 cm−3.

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33

Carter, Ellen C. "The Munsell Color System: A language for color, by Joy Turner Luke". Color Research & Application 23, n.º 2 (abril de 1998): 119–20. http://dx.doi.org/10.1002/(sici)1520-6378(199804)23:2<119::aid-col11>3.0.co;2-a.

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Godoy Assump��o, Juliana, Christine Hackel, Antonia Paula Marques-de-Faria e Maricilda Palandi de Mello. "Molecular mapping of an idic(Yp) chromosome in an Ullrich-Turner patient". American Journal of Medical Genetics 91, n.º 2 (13 de março de 2000): 95–98. http://dx.doi.org/10.1002/(sici)1096-8628(20000313)91:2<95::aid-ajmg2>3.0.co;2-j.

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LAUNDON, CAROLINE H., KEVIN SPENCER, JAMES N. MACRI, ROBERT W. ANDERSON e PHILIP D. BUCHANAN. "FREE BETA hCG SCREENING OF HYDROPIC AND NON-HYDROPIC TURNER SYNDROME PREGNANCIES". Prenatal Diagnosis 16, n.º 9 (setembro de 1996): 853–56. http://dx.doi.org/10.1002/(sici)1097-0223(199609)16:9<853::aid-pd945>3.0.co;2-9.

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Gedeon, Agi, John Mulley e Gillian Turner. "Letter to the editor: Gene localisation for Wilson-Turner syndrome (WTS:MIM 309585)". American Journal of Medical Genetics 64, n.º 1 (12 de julho de 1996): 80–81. http://dx.doi.org/10.1002/(sici)1096-8628(19960712)64:1<80::aid-ajmg13>3.0.co;2-o.

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L�pez, Marisol, Patricia Canto, M�nica Aguinaga, Leda Torres, Alicia Cervantes, Guillermo Alfaro, Juan Pablo M�ndez e Susana Kofman-Alfaro. "Frequency of Y chromosomal material in Mexican patients with Ullrich-Turner syndrome". American Journal of Medical Genetics 76, n.º 2 (5 de março de 1998): 120–24. http://dx.doi.org/10.1002/(sici)1096-8628(19980305)76:2<120::aid-ajmg3>3.0.co;2-x.

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Sutton, Carrie. "Interview". Alphaville: Journal of Film and Screen Media, n.º 19 (23 de julho de 2020): 203–10. http://dx.doi.org/10.33178/alpha.19.18.

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Carrie Sutton is a freelance directors’ representative working with independent creatives as well as music video directors signed to Biscuit Filmworks, Blindeye Films, Good Co., Kode Media, Rankin and The Graft. In her role as Music Video Commissioner, she has commissioned videos for Blur, Tina Turner, Pet Shop Boys, Snow Patrol and Robbie Williams amongst many others, with artists picking up 3 Brit Awards for Best Video, an MTV Award and a D&AD Yellow Pencil Nomination. In 2018, she was awarded the ‘Outstanding Achievement’ award at the UK Music Video Awards in recognition of her career as a Creative Commissioner, Directors’ Rep., Executive Producer and Producer

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39

Yu, Peter K. "Moral Rights 2.0". 2013 Fall Intellectual Property Symposium Articles 1, n.º 4 (março de 2014): 873–900. http://dx.doi.org/10.37419/lr.v1.i4.3.

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When the protection of moral rights is brought up in the United States, commentators have always emphasized the differences between continental Europe and the United States.2 Cases that have been widely used as textbook illustrations include Soc. Le Chant de Monde v. Soc. Fox Europe3 and Turner Entertainment Co. v. Huston.4 While the Anglo-American copyright regime and the French author’s right (droit d’auteur) regime were quite similar in the eighteenth century, 5 the protection of moral rights did not attain formal international recognition until 1928.6 The gap between the U.S. and French systems has also grown considerably since the enactment of the 1909 U.S. Copyright Act.

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40

Wilkin, Helen, Jeremy Tuohy e Wilhelmina Theewis. "Prenatal diagnosis of fragile X and Turner mosaicism in a 12-week fetus". Prenatal Diagnosis 20, n.º 10 (2000): 854–55. http://dx.doi.org/10.1002/1097-0223(200010)20:10<854::aid-pd928>3.0.co;2-1.

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41

STARN, ORIN. "American Indians and the American Imaginary: Cultural Representation across the Centuries. Pauline Turner Strong. Boulder, CO: Paradigm, 2011. 277 pp." American Ethnologist 40, n.º 4 (novembro de 2013): 802–3. http://dx.doi.org/10.1111/amet.12054_19.

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Hikade, Katie R., George J. Bitar, Milton T. Edgerton e Raymond F. Morgan. "Modified Z-Plasty Repair of Webbed Neck Deformity Seen in Turner and Klippel-Feil Syndrome". Cleft Palate-Craniofacial Journal 39, n.º 3 (maio de 2002): 261–66. http://dx.doi.org/10.1597/1545-1569(2002)039<0261:mzprow>2.0.co;2.

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Mier, Constance M., Michael J. Turner, Ali A. Ehsani e Robert J. Spina. "Cardiovascular adaptations to 10 days of cycle exercise". Journal of Applied Physiology 83, n.º 6 (1 de dezembro de 1997): 1900–1906. http://dx.doi.org/10.1152/jappl.1997.83.6.1900.

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Mier, Constance M., Michael J. Turner, Ali A. Ehsani, and Robert J. Spina. Cardiovascular adaptations to 10 days of cycle exercise. J. Appl. Physiol. 83(6): 1900–1906, 1997.—We hypothesized that 10 days of training would enhance cardiac output (CO) and stroke volume (SV) during peak exercise and increase the inotropic response to β-adrenergic stimulation. Ten subjects [age 26 ± 2 (SE) yr] trained on a cycle ergometer for 10 days. At peak exercise, training increased O2 uptake, CO, and SV ( P < 0.001). Left ventricular (LV) size and function at rest were assessed with two-dimensional echocardiography before (baseline) and after atropine injection (1.0 mg) and during four graded doses of dobutamine. LV end-diastolic diameter increased with training ( P< 0.02), whereas LV wall thickness was unchanged. LV contractile performance was assessed by relating fractional shortening (FS) to the estimated end-systolic wall stress (ςES). Training increased the slope of the FS-ςES relationship ( P < 0.05), indicating enhanced systolic function. The increase in slope correlated with increases in CO ( r = −0.71, P < 0.05) and SV ( r = −0.70, P < 0.05). The increase in blood volume also correlated with increases in CO ( r = 0.80, P < 0.01) and SV ( r= 0.85, P < 0.004). These data show that 10 days of training enhance the inotropic response to β-adrenergic stimulation, associated with increases in CO and SV during peak exercise.

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Fejgin, M. D., Y. Arbel-DeRowe, N. Shul e A. Amiel. "Letter to the Editor. A false-positive diagnosis of Turner syndrome by amniocentesis". Prenatal Diagnosis 17, n.º 1 (janeiro de 1997): 88–89. http://dx.doi.org/10.1002/(sici)1097-0223(199701)17:1<88::aid-pd17>3.0.co;2-h.

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Beradze, Sopia, e Nino Kochiashvili. "Possible connection between P Cygni and neighboring open clusters". Proceedings of the International Astronomical Union 14, S351 (maio de 2019): 181–84. http://dx.doi.org/10.1017/s1743921319006999.

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AbstractAccording to earlier investigations by Turner and co-authors, P Cygni could be a member of a hypothetical, sparsely populated open cluster. The star lies near the east boundary of this hypothetical cluster. There is another known open cluster, IC 4996, in the vicinity of P Cygni. The same authors believe that the above mentioned two clusters are connected to each other and they could represent a double cluster. As P Cygni is a hypergiant and consequently has very strong and variable stellar wind, so a cluster membership can enable us to determine the age, distance, and reddening of the star relatively precisely. We used new data of different catalogues, for example, PPMXL and Gaia and tried to resolve the problem.

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Gyuró, Monika. "HUMOR AND METAPHORS IN MEDICAL LANGUAGE". Discourse and Interaction 10, n.º 2 (15 de dezembro de 2017): 47–60. http://dx.doi.org/10.5817/di2017-2-47.

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The study makes an attempt to analyze cognitive models of metaphor and humor developedby Fauconnier and Turner (1994) and Attardo and Raskin (1991). Although metaphorand humor are different categories, their cognitive models demonstrate similarities whichmay create a joint category, metaphorical humor. The study focuses on the co-existenceof metaphorical and humorous characteristics in a single expression taken from medicalslang. Similarities between the metaphor and humor can be found in the analogies andimplications between the contrasting conceptual domains. The difference between themetaphor and humor lies only in the weights of between- and within-domain relationships(Hillson & Martin 1994). The aim of the paper is to show that the existence of humor andmetaphor in a single phrase may reveal common cognitive processes in the creation ofmetaphorical humor.

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Gupta, Bhavna, Munisha Agarwal, Rohan Sharma e Vandana Saith. "Anesthesia management in a case of Turner syndrome with anti-NMDA limbic encephalitis and multiple co-morbidities for repair of fracture femur". Korean Journal of Anesthesiology 71, n.º 4 (1 de agosto de 2018): 330–31. http://dx.doi.org/10.4097/kja.d.18.00073.

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Hasegawa, Yuh, James Rogers, Graham Scriven e Grant Townsend. "Carabelli Trait in Australian Twins: Reliability and Validity of Different Scoring Systems". Dental Anthropology Journal 23, n.º 1 (2 de setembro de 2018): 7–15. http://dx.doi.org/10.26575/daj.v23i1.65.

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We assessed the intra- and inter-observer reliability of two methods of scoring or categorizing Carabelli trait in both primary and permanent dentitions (Hanihara, 1961; Dahlberg, 1963). By using dental casts obtained from twins, we also compared the expression of Carabelli trait within and between monozygotic (MZ) co-twins to clarify the ontogenetic processes leading to different forms of trait expression. While intra-observer concordance rates were generally good (70 - 90%), inter-observer concordance rates were poor (35 - 60%). This indicates that considerable caution is needed when comparing data for Carabelli trait derived from different samples by different researchers. By comparing categories or scores for Carabelli trait in both dentitions of MZ co-twins, we found inter-relationships between groove and cuspal forms of the feature. Although the Arizona State University system developed by Turner is commonly used nowadays to score the Carabelli trait, we would encourage researchers interested in clarifying genetic influences and ontogenetic processes in both dentitions to refer to the often over-looked plaque of Hanihara and also Dahlberg’s plaque P12B. This should improve the reliability and validity of data obtained by helping to clarify the inter-relationships between the different phenotypic expressions of Carabelli trait.

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Højbjerg Gravholt, Claus, e Rune Weis Naeraa. "Reference values for body proportions and body composition in adult women with Ullrich-Turner syndrome". American Journal of Medical Genetics 72, n.º 4 (12 de novembro de 1997): 403–8. http://dx.doi.org/10.1002/(sici)1096-8628(19971112)72:4<403::aid-ajmg6>3.0.co;2-r.

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Bernard, Catherine. "Out of Bounds: Confronting War Crimes and the Breakdown of Justice with Contemporary Art". Synthesis: an Anglophone Journal of Comparative Literary Studies, n.º 13 (19 de julho de 2021): 52. http://dx.doi.org/10.12681/syn.27561.

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Recent art has turned to judiciary and extra-judiciary practices, specifically in the context of international conflicts, in order to assert art’s political accountability and relevance to our capacity to historicise the present. The war in Iraq inspired works that directly address issues of representation and remediation, such as Marc Quinn’s Mirage (2008), in which the aesthetic experience opens onto an ambiguous experience of the breakdown of justice. Other works have chosen to turn carceral space itself into the site of a collective remembering that harnesses affect to a critical reflection on the administration of justice, on assent and dissent. This article will turn to key works by Marc Quinn and Trevor Paglen that confront extra-judiciary malpractices, but also to recent collective art projects involving an interdisciplinary take on the experience of imprisonment, such as Inside. Artists and Writers in Reading Prison (2016), in which artists of all backgrounds responded to Oscar Wilde’s De Profundis on the very premises of Wilde’s incarceration, as well as the work of 2019 Turner Prize co-recipient: Jordanian sound artist Lawrence Abu Hamdan whose recent works rely on testimonies from Syrian detainees and probe the political pragmatics of aural art. All these works have turned to the document—literary, visual, aural—to reflect on the process of experiential mediation. How does the experience of imprisonment, or extra-judiciary malpractices, come to the spectator? How are they read, heard, interpreted, remediated? The article ponders the remediation and displacement of aesthetic experience itself and the “response-ability”—following Donna Haraway’s coinage—of such a repoliticised embodied experience. It will assess the way by which such interdisciplinary works rethink the poetics of the documentary for an embodied intellection of justice—and injustice—in the present.

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