Comprehensive Structured Transition Program With Dedicated Transition Navigator Reduced Lost to Follow-Up and Improved Medication Adherence in Adolescents and Young Adults With Sickle Cell Disease and Thalassemia
Allemang, Brooke, MSW, Allan, Kate, MSW, Johnson, Colleen, BScN, MN, CNP, Cheong, Melina, BScN, MN, CNP, Cheung, Patrina, BS, Odame, Isaac, MD, Ward, Richard, MD, Williams, Suzan, MD, Kuo, Kevin, MD
Published in Journal of adolescent health (01.02.2017)
Published in Journal of adolescent health (01.02.2017)
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Hb S/β+-thalassemia due to Hb sickle and a novel deletion of DNase I hypersensitive sites HS3 and HS4 of the β locus control region
Amid, Ali, Cheong, Melina, Eng, Barry, Hanna, Meredith, Hohenadel, Betty-Ann, Nakamura, Lisa M, Walker, Lynda, Odame, Isaac, Kirby-Allen, Melanie, Waye, John S
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Published in Haematologica (Roma) (01.05.2015)
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Pediatric Sickle Cell Disease: A Potential Role for the Complement System
Diatlov, Daniel, Bohorquez, Arlette, Jackson, Melanie, Cheong, Melina, Kahr, Walter H.A., Kuo, Kevin H.M., Kirby-Allen, Melanie, Licht, Christoph
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Published in Blood (15.11.2022)
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Impact of a transition program with navigator on loss to follow‐up, medication adherence, and appointment attendance in hemoglobinopathies
Allemang, Brooke, Allan, Kate, Johnson, Colleen, Cheong, Melina, Cheung, Patrina, Odame, Isaac, Ward, Richard, Williams, Suzan, Mukerji, Geetha, Kuo, Kevin H.M.
Published in Pediatric blood & cancer (01.08.2019)
Published in Pediatric blood & cancer (01.08.2019)
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Comprehensive Structured Transition Program with Dedicated Transition Navigator Reduced Lost to Follow-up and Improved Medication Adherence in Sickle Cell Disease and Thalassemia Adolescents and Young Adults
Allemang, Brooke, Allan, Kate, Johnson, Colleen, Cheong, Melina, Cheung, Patrina, Odame, Isaac, Ward, Richard, Williams, Suzan, Kuo, Kevin H.M.
Published in Blood (02.12.2016)
Published in Blood (02.12.2016)
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Compound Heterozygosity for Hb S and a Novel Deletion of Dnase I Hypersensitivity Sites HS3 and HS4 of β-Globin Locus Control Region Results in Hb S/β+-Thalassemia Phenotype
Amid, Ali, Eng, Barry, Hohenadel, Betty-Ann, Hanna, Meredith, Nakamura, Lisa N., Walker, Lynda, Cheong, Melina, Kirby-Allen, Melanie, Waye, John S.
Published in Blood (06.12.2014)
Published in Blood (06.12.2014)
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Capsule shredding device
Palmer, Marcia, Cheong, Melina, Roy, Renu, Hartman, Michael, Mack, Lynn, Looi, Thomas
Year of Publication 01.11.2022
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Year of Publication 01.11.2022
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CAPSULE SHREDDING DEVICE
HARTMAN, Michael, MACK, Lynn, PALMER, Marcia, CHEONG, Melina, ROY, Renu, LOOI, Thomas
Year of Publication 28.05.2020
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Year of Publication 28.05.2020
Patent
CAPSULE SHREDDING DEVICE
HARTMAN, Michael, MACK, Lynn, PALMER, Marcia, CHEONG, Melina, ROY, Renu, LOOI, Thomas
Year of Publication 06.12.2018
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Year of Publication 06.12.2018
Patent
CAPSULE SHREDDING DEVICE
PALMER, MARCIA, LOOI, THOMAS, HARTMAN, MICHAEL, ROY, RENU, CHEONG, MELINA, MACK, LYNN
Year of Publication 06.12.2018
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Year of Publication 06.12.2018
Patent
Hb S/β+-thalassemia due to Hb sickle and a novel deletion of DNase I hypersensitive sites HS3 and HS4 of the β locus control region
Amid, Ali, Cheong, Melina, Eng, Barry, Hanna, Meredith, Hohenadel, Betty-Ann, Nakamura, Lisa M, Walker, Lynda, Odame, Isaac, Kirby-Allen, Melanie, Waye, John S
Published in Haematologica (01.05.2015)
Published in Haematologica (01.05.2015)
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