Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Leslie Holley"'
Autor:
Danielle Pichette, Leslie Holley, Marguerite E. O’Haire, Amy McCullough, Noémie A. Guérin, Shirley Sierra-Rivera, Ashleigh Ruehrdanz, Cynthia Hellman, Janice Olson, Mary Jo Gilmer, Anjali S Pawar, Deborah E. Linder, Neil J. Grossman, Molly Jenkins
Publikováno v:
Applied Animal Behaviour Science. 200:86-95
Over the past two decades, animal-assisted interventions (AAIs), defined as the purposeful incorporation of specially trained animals in services to improve human health, have become increasingly popular in clinical settings. However, to date, there
Autor:
Ashleigh Ruehrdanz, Janice Olson, Danielle Pichette, Cynthia Hellman, Neil J. Grossman, Molly Jenkins, Leslie Holley, Mary Jo Gilmer, Noémi A. Guérin, Marguerite E. O’Haire, Deborah E. Linder, Shirley Sierra-Rivera, Amy McCullough, Anjali S Pawar
Publikováno v:
Journal of Pediatric Oncology Nursing. 35:159-177
Objective: This multicenter, parallel-group, randomized trial examined the effects of an animal-assisted intervention on the stress, anxiety, and health-related quality of life for children diagnosed with cancer and their parents. Method: Newly diagn
Autor:
Amy, McCullough, Ashleigh, Ruehrdanz, Molly A, Jenkins, Mary Jo, Gilmer, Janice, Olson, Anjali, Pawar, Leslie, Holley, Shirley, Sierra-Rivera, Deborah E, Linder, Danielle, Pichette, Neil J, Grossman, Cynthia, Hellman, Noémi A, Guérin, Marguerite E, O'Haire
Publikováno v:
Journal of pediatric oncology nursing : official journal of the Association of Pediatric Oncology Nurses. 35(3)
This multicenter, parallel-group, randomized trial examined the effects of an animal-assisted intervention on the stress, anxiety, and health-related quality of life for children diagnosed with cancer and their parents.Newly diagnosed patients, aged
Autor:
Leslie Holley, Ferdane Kutlar, Harris Carmichael, Abdullah Kutlar, Rhea-Beth Markowitz, Sean M. McKeown
Publikováno v:
Annals of Hematology. 88:545-548
Hb Lepore is the hybrid hemoglobin (Hb) composed of two alpha-globin chains and two deltabeta hybrid chains and is associated with the clinical findings of thalassemia minor in its heterozygous form. Hb Lepore can be found in many ethnic groups, comm
Autor:
Dedrey Elam, Ruth Luddy, Ferdane Kutlar, Robert E. Wenk, Erin Dainer, Abdullah Kutlar, Leslie Holley
Publikováno v:
Hemoglobin. 32:588-591
Neonatal screening for hemoglobinopathies occasionally results in the detection of novel hemoglobin (Hb) variants. Two heterozygous infants were found with different beta chain mutations, neither of which produced obvious clinical or laboratory abnor
Autor:
Leslie Holley, Richard Shell, Ferdane Kutlar, Debra H. Davis, Randy R. Miller, Abdullah Kutlar, Matt Pastore, Erin Dainer, Joan F. Atkin, Lina Zhuang
Publikováno v:
Hemoglobin. 32:596-600
Neonatal cyanosis can result from a multitude of acquired and inherited causes. Cyanosis resulting from fetal M hemoglobin (Hb) variants is very rare. Only two (G)gamma variants causing methemoglobinemia and cyanosis in the newborn have been reported
Autor:
Frances Wright, Leslie Holley, Ferdane Kutlar, Gaye Tankut, Rupa Redding-Lallinger, Abdullah Kutlar
Publikováno v:
Hemoglobin. 26:129-134
Hb D-Ibadan [beta87(F3)Thr-->Lys] is a common variant in the Nigerian population, which has been reported in association with Hb S [beta6(A3)Glu-->Val] and with beta-thalassemia. Unlike the Hb S/Hb D-Los Angeles [beta121(GH4)Glu-->Gln] combination, c
Autor:
Leigh Wells, Leslie Holley, Erin Dainer, Adekunle Adekile, Betsy Clair, Lisa Daitch, Sule M. Bakanay, David M. Smith, Abdullah Kutlar
Publikováno v:
Blood. 105:545-547
The efficacy of hydroxyurea (HU) and its role in the reduction in mortality in sickle cell patients has been established. Nevertheless, many patients still die of complications of this disease while on HU. Of the 226 patients treated with HU at our c
Autor:
Erin, Dainer, Robert E, Wenk, Ruth, Luddy, Dedrey, Elam, Leslie, Holley, Abdullah, Kutlar, Ferdane, Kutlar
Publikováno v:
Hemoglobin. 32(6)
Neonatal screening for hemoglobinopathies occasionally results in the detection of novel hemoglobin (Hb) variants. Two heterozygous infants were found with different beta chain mutations, neither of which produced obvious clinical or laboratory abnor
Autor:
Dedrey Elam, Leslie Holley, Abdullah Kutlar, A. Addington, Ferdane Kutlar, Adekunle Adekile, Betsy Clair, K. McKie
Publikováno v:
European journal of haematology. 75(2)
PURPOSE Homozygosity for the (AT)7 allele of uridine diphosphate glucuronosyl transferase 1A (UGT1A1) gene polymorphism is associated with increased bilirubin levels in sickle cell anemia (SCA). In the present study, in addition to UGT1A1 promoter ge