Zobrazeno 1 - 10
of 23
pro vyhledávání: '"L Vandy Black"'
Autor:
Diana J Wilkie, Guettchina Telisnor, Keesha Powell-Roach, Andrea P Rangel, Amelia L Greenlee, Miriam O Ezenwa, Agatha M Gallo, L Vandy Black, Alexandre Gomes de Siqueira, Brenda W Dyal, Sriram Kalyanaraman, Yingwei Yao
Publikováno v:
PLoS ONE, Vol 18, Iss 12, p e0294907 (2023)
Our long-term goal is to foster genetically informed reproductive health knowledge and behaviors among young adults with sickle cell disease (SCD) or sickle cell trait (SCT) with a web-based, tailored, multimedia intervention called CHOICES. CHOICES
Externí odkaz:
https://doaj.org/article/b470d2c9ce794d4b82c7d06fd4b6172f
Publikováno v:
Journal of Pediatric Hematology/Oncology. 45:e433-e440
Autor:
Dominik Ochocinski, Mansi Dalal, L. Vandy Black, Silvana Carr, Judy Lew, Kevin Sullivan, Niranjan Kissoon
Publikováno v:
Frontiers in Pediatrics, Vol 8 (2020)
Sickle cell disease (SCD) results in chronic hemolytic anemia, recurrent vascular occlusion, insidious vital organ deterioration, early mortality, and diminished quality of life. Life-threatening acute physiologic crises may occur on a background of
Externí odkaz:
https://doaj.org/article/0804655b889b4105b479d95ccb89497d
Publikováno v:
Journal of Pediatric Hematology/Oncology. 43:e777-e779
Tacrolimus-induced immune thrombocytopenia (ITP) is a rare entity that can occur years after initiation of tacrolimus therapy following solid organ transplantation, and platelet recovery can be substantially delayed following discontinuation of tacro
Publikováno v:
Pediatric bloodcancerREFERENCES. 67(11)
BACKGROUND In children with sickle cell disease (SCD), comorbid asthma is associated with increased disease severity and morbidity, but it remains underdiagnosed and optimal management paradigms are not well defined. The purpose of this study was to
Autor:
Ahmed A. Daak, Lee Hilliard, L. Vandy Black, Fredrick Sancilio, Matthew M. Heeney, Beng Fuh, Carlton Dampier, Alex George, Melissa A. McNaull, Adrian L. Rabinowicz, Lynne Neumayr, Ofelia A. Alvarez, Michael U. Callaghan, Julie Kanter
Publikováno v:
Blood Advances. 2:1969-1979
Blood cell membranes in sickle cell disease (SCD) have low docosahexaenoic acid (DHA). DHA treatment reduces sickle cell crisis (SCC) rate and ameliorates the inflammation, oxidative stress, and hypercoagulable state of SCD. SC411 is a novel DHA ethy
Publikováno v:
Journal of Pediatric Hematology/Oncology. 41:158-160
Chronic transfusion therapy with the goal of maintaining a hemoglobin (Hb) S
Autor:
Hanieh Razzaghi, L. Vandy Black, Jordan Smallwood, David M. Hartley, Jennifer McCafferty-Fernandez, Rahul A Darwar, Kathryn M. Shaw, Lloyd N. Werk, Keith Marsolo, Amy Kelly, Kathleen E Walsh, Jonathan A. Finkelstein, Mary Goodick, Charles P. Bailey, Michael A. Shapiro, Levon Utidjian, Al Ozonoff, Elizabeth Shenkman, Shannon Alford, Susannah Jonas
Publikováno v:
Pediatric Quality & Safety
Introduction Health systems spend $1.5 billion annually reporting data on quality, but efficacy and utility for benchmarking are limited due, in part, to limitations of data sources. Our objective was to implement and evaluate measures of pediatric q
Autor:
Sharada A. Sarnaik, Ofelia A. Alvarez, William Owen, Murtadha Al-Khabori, Ashok Raj, Thomas Moulton, Bruce A. Barton, Charles T. Quinn, Suzie A. Noronha, Beng Fuh, Connie M. Piccone, Mark T. Gladwin, Philip Maes, Jennifer Keates-Baleeiro, Ed Parsley, Emad Salman, Nirmish Shah, Cameron K. Tebbi, Lewis L. Hsu, Abdulkareem Al-Momen, Kamar Godder, Yasser Wali, Jason M. Fixler, Claudia R. Morris, Yurdanur Kilinç, Christophe F. Chantrain, Suvankar Majumdar, Natalie L. Kamberos, Elena Cela de Julián, L. Vandy Black, Meenakshi Goyal-Khemka, Rebecca T. Gorney, Julie Kanter, Courtney D. Thornburg, Alex George, Zeynep Karakas, Betty S. Pace, Clarisse Lopes De Castro Lobo, Debra E. Cohen, Tammuella Singleton, Alexis A. Thompson, Clifford M. Takemoto, Joseph L. Lasky, Miguel R. Abboud, India Sisler, Rachelle Nuss, Shari S. Kronsberg, Claire S. Padgett, Adlette Inati, James F. Casella, Marty Emanuele, Richard A. Drachtman, Gregory J. Kato, Anne Schaefer, Anne M. Marsh
Publikováno v:
JAMA : the journal of the American Medical Association
Key PointsQuestionCan poloxamer 188, an agent that is reported to reduce blood viscosity and cell-cell interactions, effectively reduce the duration of vaso-occlusive episodes (painful crises) in hospitalized patients with sickle cell disease? Findin
Publikováno v:
The Journal of Pain. 10:1065-1072
Anecdotal evidence suggests that chronic bladder pain improves while breastfeeding. The present study sought to identify potential mechanisms for such a phenomenon by investigating the effects of the lactogenic hormones prolactin (PL) and oxytocin (O