检索结果 - Kenney, Amy
- Showing 1 - 17 results of 17
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Clinical, Immunophenotypic, and Genetic Characterization of Small Lymphocyte–Like Plasma Cell Myeloma: A Potential Mimic of Mature B-Cell Lymphoma 由 Heerema-McKenney, Amy, Waldron, James, Hughes, Steven, Zhan, Fenghuang, Sawyer, Jeffery, Barlogie, Bart, Shaughnessy, John D.
出版 2010Text -
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Gemtuzumab ozogamicin in infants with AML: results from the Children’s Oncology Group trials AAML03P1 and AAML0531 由 Guest, Erin M., Aplenc, Richard, Sung, Lillian, Raimondi, Susana C., Hirsch, Betsy A., Alonzo, Todd A., Gerbing, Robert B., Wang, Yi-Cheng Jim, Kahwash, Samir B., Heerema-McKenney, Amy, Meshinchi, Soheil, Gamis, Alan S.
出版 2017Text -
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Disease Characteristics and Prognostic Implications of Cell Surface FLT3 Receptor (CD135) Expression in Pediatric Acute Myeloid Leukemia: A Report from the Children’s Oncology Grou... 由 Tarlock, Katherine, Alonzo, Todd A., Loken, Michael R., Gerbing, Robert B., Ries, Rhonda E., Aplenc, Richard, Sung, Lillian, Raimondi, Susana C., Hirsch, Betsy A., Kahwash, Samir B., McKenney, Amy, Kolb, E Anders, Gamis, Alan S., Meshinchi, Soheil
出版 2017Text -
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Gemtuzumab Ozogamicin in Children and Adolescents With De Novo Acute Myeloid Leukemia Improves Event-Free Survival by Reducing Relapse Risk: Results From the Randomized Phase III C... 由 Gamis, Alan S., Alonzo, Todd A., Meshinchi, Soheil, Sung, Lillian, Gerbing, Robert B., Raimondi, Susana C., Hirsch, Betsy A., Kahwash, Samir B., Heerema-McKenney, Amy, Winter, Laura, Glick, Kathleen, Davies, Stella M., Byron, Patti, Smith, Franklin O., Aplenc, Richard
出版 2014Text -
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Expanding the clinical and phenotypic heterogeneity associated with biallelic variants in ACO2 由 Blackburn, Patrick R., Schultz, Matthew J., Lahner, Carrie A., Li, Dong, Bhoj, Elizabeth, Fisher, Laura J., Renaud, Deborah L., Kenney, Amy, Ibrahim, Niema, Hashem, Mais, Zain Seidahmed, Mohammed, Hasadsri, Linda, Schrier Vergano, Samantha A., Alkuraya, Fowzan S., Lanpher, Brendan C.
出版 2020Text -
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Acute erythroid leukemia is enriched in NUP98 fusions: a report from the Children’s Oncology Group 由 Chisholm, Karen M., Heerema-McKenney, Amy E., Choi, John K., Smith, Jenny, Ries, Rhonda E., Hirsch, Betsy A., Raimondi, Susana C., Alonzo, Todd A., Wang, Yi-Cheng, Aplenc, Richard, Sung, Lillian, Gamis, Alan S., Meshinchi, Soheil, Kahwash, Samir B.
出版 2020Text -
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Bi-allelic POLR3A Loss-of-Function Variants Cause Autosomal-Recessive Wiedemann-Rautenstrauch Syndrome 由 Wambach, Jennifer A., Wegner, Daniel J., Patni, Nivedita, Kircher, Martin, Willing, Marcia C., Baldridge, Dustin, Xing, Chao, Agarwal, Anil K., Vergano, Samantha A. Schrier, Patel, Chirag, Grange, Dorothy K., Kenney, Amy, Najaf, Tasnim, Nickerson, Deborah A., Bamshad, Michael J., Cole, F. Sessions, Garg, Abhimanyu
出版 2018Text -
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High-dose AraC is essential for the treatment of ML-DS independent of postinduction MRD: results of the COG AAML1531 trial 由 Hitzler, Johann, Alonzo, Todd, Gerbing, Robert, Beckman, Amy, Hirsch, Betsy, Raimondi, Susana, Chisholm, Karen, Viola, Shelton, Brodersen, Lisa, Loken, Michael, Tong, Spencer, Druley, Todd, O’Brien, Maureen, Hijiya, Nobuko, Heerema-McKenney, Amy, Wang, Yi-Chang, Schore, Reuven, Taub, Jeffrey, Gamis, Alan, Kolb, E. Anders, Berman, Jason N.
出版 2021Text -
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The CHD4-Related Syndrome: A Comprehensive Investigation of the Clinical Spectrum, Genotype-Phenotype Correlations and Molecular Basis 由 Weiss, Karin, Lazar, Hayley P., Kurolap, Alina, Martinez, Ariel, Paperna, Tamar, Cohen, Lior, Smeland, Marie F., Wallen, Sandra, Heide, Solveig, Keren, Boris, Terhal, Pauline, Irving, Melita, Takaku, Motoki, Roberts, John D., Petrovich, Robert M., Vergano, Samantha A. Schrier, Kenney, Amy, Hove, Hanne, DeChene, Elizabeth, Quinonez, Shane C., Colin, Estelle, Ziegler, Alban, Rumple, Melissa, Jain, Mahim, Monteil, Danielle, Roeder, Elizabeth R., Nugent, Kimberly, van Haeringen, Arie, Gambello, Michael, Santani, Avni, Medne, Līvija, Krock, Bryan, Skraban, Cara M., Zackai, Elaine H., Dubbs, Holly A., Smol, Thomas, Ghoumid, Jamal, Parker, Michael J., Wright, Michael, Turnpenny, Peter, Clayton-Smith, Jill, Metcalfe, Kay, Kurumizaka, Hitoshi, Gelb, Bruce D., Feldman, Hagit Baris, Campeau, Philippe M., Muenke, Maximilian, Wade, Paul A., Lachlan, Katherine
出版 2020Text -
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CTCF variants in 39 individuals with a variable neurodevelopmental disorder broaden the mutational and clinical spectrum 由 Konrad, Enrico D. H., Nardini, Niels, Caliebe, Almuth, Nagel, Inga, Young, Dana, Horvath, Gabriella, Santoro, Stephanie L., Shuss, Christine, Ziegler, Alban, Bonneau, Dominique, Kempers, Marlies, Pfundt, Rolph, Legius, Eric, Bouman, Arjan, Stuurman, Kyra E., Õunap, Katrin, Pajusalu, Sander, Wojcik, Monica H., Vasileiou, Georgia, Le Guyader, Gwenaël, Schnelle, Hege M., Berland, Siren, Zonneveld-Huijssoon, Evelien, Kersten, Simone, Gupta, Aditi, Blackburn, Patrick R., Ellingson, Marissa S., Ferber, Matthew J., Dhamija, Radhika, Klee, Eric W., McEntagart, Meriel, Lichtenbelt, Klaske D., Kenney, Amy, Vergano, Samantha A., Abou Jamra, Rami, Platzer, Konrad, Ella Pierpont, Mary, Khattar, Divya, Hopkin, Robert J., Martin, Richard J., Jongmans, Marjolijn C. J., Chang, Vivian Y., Martinez-Agosto, Julian A., Kuismin, Outi, Kurki, Mitja I., Pietiläinen, Olli, Palotie, Aarno, Maarup, Timothy J., Johnson, Diana S., Venborg Pedersen, Katja, Laulund, Lone W., Lynch, Sally A., Blyth, Moira, Prescott, Katrina, Canham, Natalie, Ibitoye, Rita, Brilstra, Eva H., Shinawi, Marwan, Fassi, Emily, Sticht, Heinrich, Gregor, Anne, Van Esch, Hilde, Zweier, Christiane
出版 2019Text