R
Richard McMasters
Researcher at Cincinnati Children's Hospital Medical Center
Publications - 13
Citations - 290
Richard McMasters is an academic researcher from Cincinnati Children's Hospital Medical Center. The author has contributed to research in topics: Leukemia & Fanconi anemia. The author has an hindex of 6, co-authored 13 publications receiving 246 citations.
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Journal ArticleDOI
Lineage Switch in MLL-Rearranged Infant Leukemia Following CD19-Directed Therapy.
TL;DR: An infant with ALL with t(4;11)(q21;q23) refractory to cytotoxic chemotherapy who was treated with blinatumomab is reported, and bone marrow evaluation demonstrated a leukemic lineage switch to CD19‐negative monoblastic AML.
Journal ArticleDOI
Low dose decitabine in very high risk relapsed or refractory acute myeloid leukaemia in children and young adults
Christine L Phillips,Stella M. Davies,Richard McMasters,Michael J. Absalon,Maureen M. O'Brien,Jun Mo,Randall Broun,Jeffrey A. Moscow,Teresa A. Smolarek,Ramiro Garzon,William Blum,Sebastian Schwind,Guido Marcucci,John P. Perentesis +13 more
TL;DR: Low‐dose decitabine has encouraging activity and tolerability in adults with acute myeloid leukaemia (AML), but paediatric experience is lacking, and eight patients with refractory/relapsed AML are reported on.
Journal ArticleDOI
The clinical phenotype of children with Fanconi anemia caused by biallelic FANCD1/BRCA2 mutations
Kasiani C. Myers,Stella M. Davies,Richard E. Harris,Sheri L. Spunt,Teresa A. Smolarek,Sarah L. Zimmerman,Richard McMasters,Lars M. Wagner,Robin Mueller,Arleen D. Auerbach,Parinda A. Mehta +10 more
TL;DR: Clinical and molecular features of three patients with FA associated with FANCD1/BRCA2 mutations are reported, including two novel mutations, and treatment of malignancy and associated side effects in this particularly vulnerable group are discussed.
Journal ArticleDOI
CTLA-4 haploinsufficiency in a patient with an autoimmune lymphoproliferative disorder
Zeynep Yesim Kucuk,Louis-Marie Charbonnier,Richard McMasters,Talal A. Chatila,Jack J. Bleesing +4 more
Journal ArticleDOI
11-Month-Old Infant With Periodic Fevers, Recurrent Liver Dysfunction, and Perforin Gene Polymorphism.
Grant S. Schulert,Kevin E. Bove,Richard McMasters,Kathleen M. Campbell,Nancy D. Leslie,Alexei A. Grom +5 more
TL;DR: In this article, a former 32-week premature female infant, born by elective cesarean section due to concern for hydrops, was found to have ascites and ultimately conjugated hyperbilirubinemia, but was without other congenital abnormalities.