Search Results - Kirby-Allen, Melanie Ann

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  1. 1
    Reassessing the Need for Pre-Operative Transfusions in Sickle Cell Disease Patients with a High Baseline Hemoglobin

    Reassessing the Need for Pre-Operative Transfusions in Sickle Cell Disease Patients with a High Baseline Hemoglobin by Tole, Soumitra, Yan, Adam Paul, Wagner, Amanda, Bair, Lissa, Tang, Ken, Kirby-Allen, Melanie Ann, Simpson, Ewurabena, Williams, Suzan

    Published in Blood
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  2. 2
    Serum Ferritin Underestimates Liver Iron Concentration in Patients with Homozygous Alpha-0 Thalassemia

    Serum Ferritin Underestimates Liver Iron Concentration in Patients with Homozygous Alpha-0 Thalassemia by Amid, Ali, Chen, Shiyi, Athale, Uma, Charpentier, Karen, Merelles-Pulcini, Manuela, Odame, Isaac, Kirby-Allen, Melanie Ann

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  3. 3
    Increasing Incidence and Prevalence of Pathologic Hemoglobinopathies Among Children in Ontario, Canada from 1991-2013

    Increasing Incidence and Prevalence of Pathologic Hemoglobinopathies Among Children in Ontario, Canada from 1991-2013 by Simpson, Ewurabena, Klaassen, Robert J, Chakraborty, Pranesh, Potter, Beth, Kirby-Allen, Melanie Ann, Odame, Isaac, Williams, Suzan, Athale, Uma, Jardine, Lawrence, Gibson, Paul J., Silva, Mariana, Merelles-Pulcini, Manuela, Bowerman, Brooke, Petrcich, William, Benchimol, Eric I

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  4. 4
    Genotype/Phenotype Correlations in 103 Children from 87 Families with Hereditary Spherocytosis

    Genotype/Phenotype Correlations in 103 Children from 87 Families with Hereditary Spherocytosis by Pugi, Jakob, Drury, Luke J., Langer, Jacob C., Butchart, Sheila, Fantauzzi, Michelle, Baker, Jillian, Blanchette, Victor S., Kirby-Allen, Melanie Ann, Carcao, Manuel

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  5. 5
    Silent cerebral infarction, income, and grade retention among students with sickle cell anemia

    Silent cerebral infarction, income, and grade retention among students with sickle cell anemia by King, Allison A., Rodeghier, Mark J., Panepinto, Julie Ann, Strouse, John J., Casella, James F., Quinn, Charles T., Dowling, Michael M., Sarnaik, Sharada A., Thompson, Alexis A., Woods, Gerald M., Minniti, Caterina P., Redding‐Lallinger, Rupa C., Kirby‐Allen, Melanie, Kirkham, Fenella J., McKinstry, Robert, Noetzel, Michael J., White, Desiree A., Kwiatkowski, Janet K., Howard, Thomas H., Kalinyak, Karen A., Inusa, Baba, Rhodes, Melissa M., Heiny, Mark E., Fuh, Ben, Fixler, Jason M., Gordon, Mae O., DeBaun, Michael R.

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  6. 6
    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

    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 by 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 (Roma)
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  7. 7
    Associated risk factors for silent cerebral infarcts in sickle cell anemia: low baseline hemoglobin, sex, and relative high systolic blood pressure

    Associated risk factors for silent cerebral infarcts in sickle cell anemia: low baseline hemoglobin, sex, and relative high systolic blood pressure by DeBaun, Michael R., Sarnaik, Sharada A., Rodeghier, Mark J., Minniti, Caterina P., Howard, Thomas H., Iyer, Rathi V., Inusa, Baba, Telfer, Paul T., Kirby-Allen, Melanie, Quinn, Charles T., Bernaudin, Françoise, Airewele, Gladstone, Woods, Gerald M., Panepinto, Julie Ann, Fuh, Beng, Kwiatkowski, Janet K., King, Allison A., Rhodes, Melissa M., Thompson, Alexis A., Heiny, Mark E., Redding-Lallinger, Rupa C., Kirkham, Fenella J., Sabio, Hernan, Gonzalez, Corina E., Saccente, Suzanne L., Kalinyak, Karen A., Strouse, John J., Fixler, Jason M., Gordon, Mae O., Miller, J. Phillip, Noetzel, Michael J., Ichord, Rebecca N., Casella, James F.

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  8. 8
    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

    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 by Amid, Ali, Eng, Barry, Hohenadel, Betty-Ann, Hanna, Meredith, Nakamura, Lisa N., Walker, Lynda, Cheong, Melina, Kirby-Allen, Melanie, Waye, John S.

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  9. 9
    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

    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 by 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
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