Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Erin, Dainer"'
Autor:
Amit Kaushal, Erin Taub, Erin Dainer, Tracey Spinnato, Kimberly Noel, Mark Lerman, Patricia Ng, Alice Fernan, Rachel Wong
Publikováno v:
J Grad Med Educ
Background Despite increasing use of telehealth, there are limited published curricula training primary care providers in utilizing telehealth to deliver complex interdisciplinary care. Objective To describe and evaluate a telehealth curriculum with
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:
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