Resultats de la cerca - Lori Luchtman‐Jones

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  1. 1
    Knowledge insufficient: the management of haemoglobin SC disease

    Knowledge insufficient: the management of haemoglobin SC disease per Lydia H. Pecker, Beverly A. Schaefer, Lori Luchtman‐Jones

    Publicat 2016
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  2. 2
    Frontline treatment of localized osteosarcoma without methotrexate

    Frontline treatment of localized osteosarcoma without methotrexate per Najat C. Daw, Michael D. Neel, Bhaskar N. Rao, Catherine A. Billups, Jianrong Wu, Jesse J. Jenkins, Juan A. Quintana, Lori Luchtman‐Jones, Milena Villarroel, Victor M. Santana

    Publicat 2011
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  3. 3
    Immunologic Effects of Hydroxyurea in Sickle Cell Anemia

    Immunologic Effects of Hydroxyurea in Sickle Cell Anemia per Howard M. Lederman, Margaret A. Connolly, Ram Kalpatthi, Russell E. Ware, Winfred C. Wang, Lori Luchtman‐Jones, Myron A. Waclawiw, Jonathan C. Goldsmith, Andrea J. Swift, James F. Casella

    Publicat 2014
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  4. 4
    Differences in the clinical and genotypic presentation of sickle cell disease around the world

    Differences in the clinical and genotypic presentation of sickle cell disease around the world per Santosh L. Saraf, Robert E. Molokie, Mehdi Nouraie, Craig Sable, Lori Luchtman‐Jones, Gregory J. Ensing, Andrew Campbell, Sohail Rana, Xiao Niu, Roberto F. Machado, Mark T. Gladwin, Victor R. Gordeuk

    Publicat 2013
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  5. 5
    Elevated tricuspid regurgitation velocity and decline in exercise capacity over 22 months of follow up in children and adolescents with sickle cell anemia

    Elevated tricuspid regurgitation velocity and decline in exercise capacity over 22 months of follow up in children and adolescents with sickle cell anemia per Victor R. Gordeuk, Caterina P. Minniti, Mehdi Nouraie, Andrew Campbell, Sohail Rana, Lori Luchtman‐Jones, Craig Sable, Niti Dham, Gregory J. Ensing, Josef T. Prchal, Gregory J. Kato, Mark T. Gladwin, Oswaldo Castro

    Publicat 2010
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  6. 6
    Prospective evaluation of haemoglobin oxygen saturation at rest and after exercise in paediatric sickle cell disease patients

    Prospective evaluation of haemoglobin oxygen saturation at rest and after exercise in paediatric sickle cell disease patients per Andrew Campbell, Caterina P. Minniti, Mehdi Nouraie, Manuel Arteta, Sohail Rana, Onyinye Onyekwere, Craig Sable, Gregory J. Ensing, Niti Dham, Lori Luchtman‐Jones, Gregory J. Kato, Mark T. Gladwin, Oswaldo Castro, Victor R. Gordeuk

    Publicat 2009
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  7. 7
    Abnormal Pulmonary Function and Associated Risk Factors in Children and Adolescents With Sickle Cell Anemia

    Abnormal Pulmonary Function and Associated Risk Factors in Children and Adolescents With Sickle Cell Anemia per Manuel Arteta, Andrew Campbell, Mehdi Nouraie, Sohail Rana, Onyinye Onyekwere, Gregory J. Ensing, Craig Sable, Niti Dham, Deepika S. Darbari, Lori Luchtman‐Jones, Gregory J. Kato, Mark T. Gladwin, Oswaldo Castro, Caterina P. Minniti, Victor R. Gordeuk

    Publicat 2013
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  8. 8
    Markers of Severe Vaso-Occlusive Painful Episode Frequency in Children and Adolescents with Sickle Cell Anemia

    Markers of Severe Vaso-Occlusive Painful Episode Frequency in Children and Adolescents with Sickle Cell Anemia per Deepika S. Darbari, Onyinye Onyekwere, Mehdi Nouraie, Caterina P. Minniti, Lori Luchtman‐Jones, Sohail Rana, Craig Sable, Gregory J. Ensing, Niti Dham, Andrew Campbell, Manuel Arteta, Mark T. Gladwin, Oswaldo Castro, James G. Taylor, Gregory J. Kato, Victor R. Gordeuk

    Publicat 2011
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  9. 9
    Phase II Study of Clofarabine in Pediatric Patients With Refractory or Relapsed Acute Myeloid Leukemia

    Phase II Study of Clofarabine in Pediatric Patients With Refractory or Relapsed Acute Myeloid Leukemia per Sima Jeha, Bassem I. Razzouk, Michael Rytting, Susan R. Rheingold, Edythe A. Albano, Richard Kadota, Lori Luchtman‐Jones, Lisa Bomgaars, Paul S. Gaynon, Stewart Goldman, Kim Ritchey, R.J. Arceci, Arnold J. Altman, Kimo C. Stine, Laurel J. Steinherz, Peter G. Steinherz

    Publicat 2009
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  10. 10
    The pediatric hydroxyurea phase III clinical trial (BABY HUG): Challenges of study design

    The pediatric hydroxyurea phase III clinical trial (BABY HUG): Challenges of study design per Bruce Thompson, Scott T. Miller, Zora R. Rogers, Renée C. Rees, Russell E. Ware, Myron A. Waclawiw, Rathi V. Iyer, James F. Casella, Lori Luchtman‐Jones, Sohail Rana, Courtney D. Thornburg, Ram Kalpatthi, Julio C. Barredo, R. Clark Brown, Sharada A. Sarnaik, Thomas H. Howard, Lori Luck, Winfred C. Wang

    Publicat 2009
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  11. 11
    Genetic determinants of haemolysis in sickle cell anaemia

    Genetic determinants of haemolysis in sickle cell anaemia per Jacqueline N. Milton, Helen Rooks, Emma Drašar, Elizabeth L. McCabe, Clinton T. Baldwin, Efi Melista, Victor R. Gordeuk, Mehdi Nouraie, Gregory J. Kato, Caterina P. Minniti, James G. Taylor, Andrew Campbell, Lori Luchtman‐Jones, Sohail Rana, Oswaldo Castro, Yingze Zhang, Swee Lay Thein, Paola Sebastiani, Mark T. Gladwin, Martin H. Steinberg

    Publicat 2013
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  12. 12
    Phase II Study of Clofarabine in Pediatric Patients With Refractory or Relapsed Acute Lymphoblastic Leukemia

    Phase II Study of Clofarabine in Pediatric Patients With Refractory or Relapsed Acute Lymphoblastic Leukemia per Sima Jeha, Paul S. Gaynon, Bassem I. Razzouk, Janet Franklin, Richard Kadota, Violet Shen, Lori Luchtman‐Jones, Michael Rytting, Lisa Bomgaars, Susan R. Rheingold, Kim Ritchey, Edythe A. Albano, R.J. Arceci, Stewart Goldman, Timothy J. Griffin, Arnold J. Altman, Bruce G. Gordon, Laurel J. Steinherz, Steven Weitman, Peter G. Steinherz

    Publicat 2006
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  13. 13
    Effects of hydroxyurea treatment for patients with hemoglobin <scp>SC</scp> disease

    Effects of hydroxyurea treatment for patients with hemoglobin <scp>SC</scp> disease per Lori Luchtman‐Jones, Sara Pressel, Lee Hilliard, R. Clark Brown, Mary G. Smith, Alexis A. Thompson, Margaret T. Lee, Jennifer Rothman, Zora R. Rogers, William Owen, Hamayun Imran, Courtney D. Thornburg, Janet L. Kwiatkowski, Banu Aygün, Stephen C. Nelson, Carla W. Roberts, Cynthia Gauger, Connie M. Piccone, Theodosia A. Kalfa, Ofelia Álvarez, Kathryn L. Hassell, Barry R. Davis, Russell E. Ware

    Publicat 2015
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  14. 14
    Meta-analysis of 2040 sickle cell anemia patients: BCL11A and HBS1L-MYB are the major modifiers of HbF in African Americans

    Meta-analysis of 2040 sickle cell anemia patients: BCL11A and HBS1L-MYB are the major modifiers of HbF in African Americans per Harold Bae, Clinton T. Baldwin, Paola Sebastiani, Marilyn J. Telen, Allison E. Ashley‐Koch, Melanie E. Garrett, W. Craig Hooper, Christopher J. Bean, Michael R. DeBaun, Dan E. Arking, Pallav Bhatnagar, James F. Casella, Jeffrey R. Keefer, Emily Barron‐Casella, Victor R. Gordeuk, Gregory J. Kato, Caterina P. Minniti, James G. Taylor, Andrew Campbell, Lori Luchtman‐Jones, Carolyn Hoppe, Mark T. Gladwin, Yingze Zhang, Martin H. Steinberg

    Publicat 2012
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  15. 15
    Organ iron accumulation in chronically transfused children with sickle cell anaemia: baseline results from the <scp>TW</scp>i<scp>TCH</scp> trial

    Organ iron accumulation in chronically transfused children with sickle cell anaemia: baseline results from the <scp>TW</scp>i<scp>TCH</scp> trial per John C. Wood, Alan R. Cohen, Sara Pressel, Banu Aygün, Hamayun Imran, Lori Luchtman‐Jones, Alexis A. Thompson, Beng Fuh, William H. Schultz, Barry R. Davis, Russell E. Ware, Alex George, Brigitta U. Mueller, Matthew M. Heeney, Theodosia A. Kalfa, Stephen C. Nelson, R. Clark Brown, Beatrice E. Gee, Janet L. Kwiatkowski, Kim Smith Whitley, Isaac Odame, Jennifer Webb, Elizabeth Yang, Margaret T. Lee, Connie M. Piccone, Sherron M. Jackson, Sharon Singh, Kerri Nottage, Jane S. Hankins, Scott T. Miller, Lee Hilliard, Ofelia Álvarez, Melissa Rhodes, Zora R. Rogers, Sharada A. Sarnaik, William Owen, Cynthia Gauger, Carla W. Roberts, Jennifer Rothman

    Publicat 2015
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  16. 16
    Hydroxycarbamide versus chronic transfusion for maintenance of transcranial doppler flow velocities in children with sickle cell anaemia—TCD With Transfusions Changing to Hydroxyurea (TWiTCH): a multicentre, open-label, phase 3, non-inferiority trial

    Hydroxycarbamide versus chronic transfusion for maintenance of transcranial doppler flow velocities in children with sickle cell anaemia—TCD With Transfusions Changing to Hydroxyur... per Russell E. Ware, Barry R. Davis, William H. Schultz, R. Clark Brown, Banu Aygün, Sharada A. Sarnaik, Isaac Odame, Beng Fuh, Alex George, William Owen, Lori Luchtman‐Jones, Zora R. Rogers, Lee Hilliard, Cynthia Gauger, Connie M. Piccone, Margaret T. Lee, Janet L. Kwiatkowski, Sherron M. Jackson, Scott T. Miller, Carla W. Roberts, Matthew M. Heeney, Theodosia A. Kalfa, Stephen C. Nelson, Hamayun Imran, Kerri Nottage, Ofelia Álvarez, Melissa Rhodes, Alexis A. Thompson, Jennifer Rothman, Kathleen J. Helton, Donna R. Roberts, Jamie L. Coleman, Melanie J. Bonner, Abdullah Kutlar, Niren Patel, John C. Wood, Linda B. Piller, Peng Wei, Judy Luden, Nicole A. Mortier, Susan E. Stuber, Naomi L.C. Luban, Alan R. Cohen, Sara Pressel, Robert J. Adams

    Publicat 2015
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