Safety and Efficacy of Mitapivat in Pyruvate Kinase Deficiency von Grace, Rachael F, Rose, Christian, Layton, D. Mark, Galactéros, Frédéric, Barcellini, Wilma, Morton, D. Holmes, van Beers, Eduard J, Yaish, Hassan, Ravindranath, Yaddanapudi, Kuo, Kevin H.M, Sheth, Sujit, Kwiatkowski, Janet L, Barbier, Ann J, Bodie, Susan, Silver, Bruce, Hua, Lei, Kung, Charles, Hawkins, Peter, Jouvin, Marie-Hélène, Bowden, Chris, Glader, Bertil

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Clinical spectrum of pyruvate kinase deficiency: data from the Pyruvate Kinase Deficiency Natural History Study von Grace, Rachael F., Bianchi, Paola, van Beers, Eduard J., Eber, Stefan W., Glader, Bertil, Yaish, Hassan M., Despotovic, Jenny M., Rothman, Jennifer A., Sharma, Mukta, McNaull, Melissa M., Fermo, Elisa, Lezon-Geyda, Kimberly, Morton, D. Holmes, Neufeld, Ellis J., Chonat, Satheesh, Kollmar, Nina, Knoll, Christine M., Kuo, Kevin, Kwiatkowski, Janet L., Pospíšilová, Dagmar, Pastore, Yves D., Thompson, Alexis A., Newburger, Peter E., Ravindranath, Yaddanapudi, Wang, Winfred C., Wlodarski, Marcin W., Wang, Heng, Holzhauer, Susanne, Breakey, Vicky R., Kunz, Joachim, Sheth, Sujit, Rose, Melissa J., Bradeen, Heather A., Neu, Nolan, Guo, Dongjing, Al-Sayegh, Hasan, London, Wendy B., Gallagher, Patrick G., Zanella, Alberto, Barcellini, Wilma

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Voxelotor (GBT440) in pediatric sickle cell disease: A review von Jamalapur, Sri Lakshmi, Glaros, Alexander K., Ravindranath, Yaddanapudi

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Aberrant myelomonocytic CD56 expression in Down syndrome is frequent and not associated with leukemogenesis von Gadgeel, Manisha, AlQanber, Batool, Buck, Steven, Taub, Jeffrey W., Ravindranath, Yaddanapudi, Savaşan, Süreyya

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Genotype‐phenotype correlation and molecular heterogeneity in pyruvate kinase deficiency von Bianchi, Paola, Fermo, Elisa, Lezon‐Geyda, Kimberly, Beers, Eduard J., Morton, Holmes D., Barcellini, Wilma, Glader, Bertil, Chonat, Satheesh, Ravindranath, Yaddanapudi, Newburger, Peter E., Kollmar, Nina, Despotovic, Jenny M., Verhovsek, Madeleine, Sharma, Mukta, Kwiatkowski, Janet L., Kuo, Kevin H. M., Wlodarski, Marcin W., Yaish, Hassan M., Holzhauer, Susanne, Wang, Heng, Kunz, Joachim, Addonizio, Kathryn, Al‐Sayegh, Hasan, London, Wendy B., Andres, Oliver, Wijk, Richard, Gallagher, Patrick G., Grace, Rachael F. F.

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Natural history of transient myeloproliferative disorder clinically diagnosed in Down syndrome neonates: a report from the Children's Oncology Group Study A2971 von Gamis, Alan S., Alonzo, Todd A., Gerbing, Robert B., Hilden, Joanne M., Sorrell, April D., Sharma, Mukta, Loew, Thomas W., Arceci, Robert J., Barnard, Dorothy, Doyle, John, Massey, Gita, Perentesis, John, Ravindranath, Yaddanapudi, Taub, Jeffrey, Smith, Franklin O.

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Prevalence and management of iron overload in pyruvate kinase deficiency: report from the Pyruvate Kinase Deficiency Natural History Study von van Beers, Eduard J, van Straaten, Stephanie, Morton, D Holmes, Barcellini, Wilma, Eber, Stefan W, Glader, Bertil, Yaish, Hassan M, Chonat, Satheesh, Kwiatkowski, Janet L, Rothman, Jennifer A, Sharma, Mukta, Neufeld, Ellis J, Sheth, Sujit, Despotovic, Jenny M, Kollmar, Nina, Pospíšilová, Dagmar, Knoll, Christine M, Kuo, Kevin, Pastore, Yves D, Thompson, Alexis A, Newburger, Peter E, Ravindranath, Yaddanapudi, Wang, Winfred C, Wlodarski, Marcin W, Wang, Heng, Holzhauer, Susanne, Breakey, Vicky R, Verhovsek, Madeleine, Kunz, Joachim, McNaull, Melissa A, Rose, Melissa J, Bradeen, Heather A, Addonizio, Kathryn, Li, Anran, Al-Sayegh, Hasan, London, Wendy B, Grace, Rachael F

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Compound heterozygosity in PKLR gene for a previously unrecognized intronic polymorphism and a rare missense mutation as a novel cause of severe pyruvate kinase deficiency von Bagla, Shruti, Bhambhani, Kanta, Gadgeel, Manisha, Buck, Steven, Jin, Jian-Ping, Ravindranath, Yaddanapudi

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Treatment of Nonmetastatic Unilateral Retinoblastoma in Children von Pérez, Verónica, Sampor, Claudia, Rey, Guadalupe, Parareda-Salles, Andreu, Kopp, Katherine, Dabezies, Agustín P, Dufort, Gustavo, Zelter, Marta, López, Juan P, Urbieta, Marcelo, Alcalde-Ruiz, Elisa, Catala-Mora, Jaume, Suñol, Mariona, Ossandon, Diego, Fandiño, Adriana C, Croxatto, J. Oscar, de Dávila, María T. G, Reaman, Gregory, Ravindranath, Yaddanapudi, Chantada, Guillermo L

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The effects of disruption of genes for peroxiredoxin-2, glutathione peroxidase-1, and catalase on erythrocyte oxidative metabolism von Johnson, Robert M., Ho, Ye-Shih, Yu, Dae-Yeul, Kuypers, Frans A., Ravindranath, Yaddanapudi, Goyette, Gerard W.

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Clinical Diagnosis of Red Cell Membrane Disorders: Comparison of Osmotic Gradient Ektacytometry and Eosin Maleimide (EMA) Fluorescence Test for Red Cell Band 3 (AE1, SLC4A1) Conten... von Zaidi, Ahmar Urooj, Buck, Steven, Gadgeel, Manisha, Herrera-Martinez, Miguel, Mohan, Araathi, Johnson, Kenya, Bagla, Shruti, Johnson, Robert M., Ravindranath, Yaddanapudi

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Impact of Disease Risk on Efficacy of Matched Related Bone Marrow Transplantation for Pediatric Acute Myeloid Leukemia: The Children's Oncology Group von HORAN, John T, ALONZO, Todd A, LYMAN, Gary H, GERBING, Robert B, LANGE, Beverly J, RAVINDRANATH, Yaddanapudi, BECTON, David, SMITH, Franklin O, WOODS, William G

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Biology of childhood acute lymphoblastic leukemia (ALL) in low/middle-income countries-A case for using age at diagnosis for defining low-risk ALL von Ravindranath, Yaddanapudi

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Cardiomyopathy in Children With Down Syndrome Treated for Acute Myeloid Leukemia: A Report From the Children's Oncology Group Study POG 9421 von O'BRIEN, Maureen M, TAUB, Jeffrey W, CHANG, Myron N, MASSEY, Gita V, STINE, Kimo C, RAIMONDI, Susana C, BECTON, David, RAVINDRANATH, Yaddanapudi, DAHL, Gary V

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Duffy-Null Phenotype-Associated Neutropenia is the Most Common Etiology for Leukopenia/Neutropenia Referrals to a Tertiary Children's Hospital von Gay, Kelsey, Dulay, Kristopher, Ravindranath, Yaddanapudi, Savaşan, Süreyya

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Defining Hereditary Pyropoikilocytosis (HPP) in the Molecular Diagnostic Era von Jamalapur, Sri Lakshmi (Sindura), Gadgeel, Manisha, Ozgonenel, Bulent, Ravindranath, Yaddanapudi

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Molecular Characterization of 140 Patients in the Pyruvate Kinase Deficiency (PKD) Natural History Study (NHS): Report of 20 New Variants von Bianchi, Paola, Fermo, Elisa, Lezon-Geyda, Kimberly, Gallagher, Patrick G., Morton, D Holmes, Barcellini, Wilma, Glader, Bertil, Eber, Stefan W., Despotovic, Jenny M., Knoll, Christine M., Yaish, Hassan M., Newburger, Peter E., Rothman, Jennifer, Thompson, Alexis A., Ravindranath, Yaddanapudi, Nottage, Kerri A, Wang, Heng, van Beers, Eduard J., Kunz, Joachim, Wlodarski, Marcin W, Sharma, Mukta, Rose, Melissa J., Pastore, Yves D., Giardina, Patricia J., Rhodes, Melissa, Kuo, Kevin, Guo, Dongjing, London, Wendy B., Grace, Rachael F.

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Congenital dyserythropoietic anemia type IV with KLF1 E325K mutation: A new case with dysmorphic male genitalia von Massey, Gita V., Chesney, Alden, Gadgeel, Manisha, Ravindranath, Yaddanapudi

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CD14/16 monocyte profiling in juvenile myelomonocytic leukemia von Gadgeel, Manisha, Bagla, Shruti, Buck, Steven, Shamoun, Mark, Ravindranath, Yaddanapudi

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Myelodysplastic syndrome in children: Changing definitions from FAB 1976 to WHO 2008 classification systems von Ravindranath, Yaddanapudi

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