The mutation rate in PIG-A is normal in patients with paroxysmal nocturnal hemoglobinuria (PNH)

per Araten, David J., Luzzatto, Lucio
Publicat 2006

No evidence of hypermutability in red cells from patients with paroxysmal nocturnal hemoglobinuria using the XK gene

per Araten, David J., Zamechek, Leah, Halverson, Gregory
Publicat 2014

Clonal populations of hematopoietic cells with paroxysmal nocturnal hemoglobinuria genotype and phenotype are present in normal individuals

per Araten, David J., Nafa, Khedoudja, Pakdeesuwan, Kriangsak, Luzzatto, Lucio
Publicat 1999

Spontaneously arising red cells with a McLeod-like phenotype in normal donors

per Araten, David J., Sanders, Katie J., Pu, Jeffrey, Lee, Soohee
Publicat 2009

Multiple Myeloma Involving Skin and Pulmonary Parenchyma after Autologous Stem Cell Transplantation

per Green David L, Wieczorek Rosemary, Yuan Yuan, Cook Perry, Ballard Harold, Araten David J
Publicat 2009-11-01

Multiple Myeloma Involving Skin and Pulmonary Parenchyma after Autologous Stem Cell Transplantation

per Yuan, Yuan, Wieczorek, Rosemary, Green, David L, Cook, Perry, Ballard, Harold, Araten, David J
Publicat 2009

Analysis of TET2 mutations in paroxysmal nocturnal hemoglobinuria (PNH)

per Lobry, Camille, Bains, Ashish, Zamechek, Leah B., Ibrahim, Sherif, Aifantis, Iannis, Araten, David J.
Publicat a Exp Hematol Oncol (2019)

Leukemic Blasts with the Paroxysmal Nocturnal Hemoglobinuria Phenotype in Children with Acute Lymphoblastic Leukemia

per Araten, David J., Sanders, Katie J., Anscher, Dan, Zamechek, Leah, Hunger, Stephen P., Ibrahim, Sherif
Publicat 2012

Mild Clinical Course of COVID-19 in 3 Patients Receiving Therapeutic Monoclonal Antibodies Targeting C5 Complement for Hematologic Disorders

per Araten, David J., Belmont, H. Michael, Schaefer-Cutillo, Julia, Iyengar, Arjun, Mattoo, Aprajita, Reddy, Ramachandra
Publicat a Am J Case Rep (2020)

A patient with POEMS syndrome responding to modified CyBorD chemotherapy as a bridge to autologous stem cell transplantation

per Milam, Emily C., Martires, Kathryn J., Lo Sicco, Kristen I., Araten, David J., Franks, Andrew G.
Publicat a JAAD Case Rep (2019)

The rate of spontaneous mutations in human myeloid cells

per Araten, David J., Krejci, Ondrej, DiTata, Kimberly, Wunderlich, Mark, Sanders, Katie J., Zamechek, Leah, Mulloy, James C.
Publicat a Mutat Res (2013)

A quantitative analysis of genomic instability in lymphoid and plasma cell neoplasms based on the PIG-A gene

per Araten, David J., Martinez-Climent, Jose A., Perle, Mary Ann, Holm, Eliana, Zamechek, Leah, DiTata, Kimberly, Sanders, Katie J.
Publicat 2010

Baseline clinical characteristics and disease burden in patients with paroxysmal nocturnal hemoglobinuria (PNH): updated analysis from the International PNH Registry

per Schrezenmeier, Hubert, Röth, Alexander, Araten, David J., Kanakura, Yuzuru, Larratt, Loree, Shammo, Jamile M., Wilson, Amanda, Shayan, Gilda, Maciejewski, Jaroslaw P.
Publicat a Ann Hematol (2020)

Selective splenic artery embolization for the treatment of thrombocytopenia and hypersplenism in paroxysmal nocturnal hemoglobinuria

per Araten, David J, Iori, Anna Paola, Brown, Karen, Torelli, Giovanni Fernando, Barberi, Walter, Natalino, Fiammetta, De Propris, Maria Stefania, Girmenia, Corrado, Salvatori, Filippo Maria, Zelig, Orly, Foà, Robin, Luzzatto, Lucio
Publicat 2014

Thrombolytic therapy is effective in paroxysmal nocturnal hemoglobinuria: a series of nine patients and a review of the literature

per Araten, David J., Notaro, Rosario, Thaler, Howard T, Kernan, Nancy, Boulad, Farid, Castro-Malaspina, Hugo, Small, Trudy, Scaradavou, Andromachi, Magnan, Heather, Prockop, Susan, Chaffee, Sara, Gonsky, Jason, Thertulien, Raymond, Tarquini, Roberto, Luzzatto, Lucio
Publicat 2012

MSH6 haploinsufficiency at relapse contributes to the development of thiopurine resistance in pediatric B-lymphoblastic leukemia

per Evensen, Nikki A., Madhusoodhan, P. Pallavi, Meyer, Julia, Saliba, Jason, Chowdhury, Ashfiyah, Araten, David J., Nersting, Jacob, Bhatla, Teena, Vincent, Tiffaney L., Teachey, David, Hunger, Stephen P., Yang, Jun, Schmiegelow, Kjeld, Carroll, William L.
Publicat a Haematologica (2018)