Search Results - "Degar, A"

Recurrent BRAF mutations in Langerhans cell histiocytosis by Badalian-Very, Gayane, Vergilio, Jo-Anne, Degar, Barbara A., MacConaill, Laura E., Brandner, Barbara, Calicchio, Monica L., Kuo, Frank C., Ligon, Azra H., Stevenson, Kristen E., Kehoe, Sarah M., Garraway, Levi A., Hahn, William C., Meyerson, Matthew, Fleming, Mark D., Rollins, Barrett J.

“…Langerhans cell histiocytosis (LCH) has a broad spectrum of clinical behaviors; some cases are self-limited, whereas others involve multiple organs and cause…”
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Recent advances in the understanding of Langerhans cell histiocytosis by Badalian-Very, Gayane, Vergilio, Jo-Anne, Degar, Barbara A., Rodriguez-Galindo, Carlos, Rollins, Barrett J.

“…Summary Langerhans cell histiocytosis (LCH) is a proliferative disease of cells that share phenotypic characteristics with the primary antigen presenting cells…”
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Calm in the midst of cytokine storm: a collaborative approach to the diagnosis and treatment of hemophagocytic lymphohistiocytosis and macrophage activation syndrome by Halyabar, Olha, Chang, Margaret H, Schoettler, Michelle L, Schwartz, Marc A, Baris, Ezgi H, Benson, Leslie A, Biggs, Catherine M, Gorman, Mark, Lehmann, Leslie, Lo, Mindy S, Nigrovic, Peter A, Platt, Craig D, Priebe, Gregory P, Rowe, Jared, Sundel, Robert P, Surana, Neeraj K, Weinacht, Katja G, Mann, Alison, Yuen, Jenny Chan, Meleedy-Rey, Patricia, Starmer, Amy, Banerjee, Taruna, Dedeoglu, Fatma, Degar, Barbara A, Hazen, Melissa M, Henderson, Lauren A

“…Hemophagocytic lymphohistiocytosis (HLH) and macrophage activation syndrome (MAS) were historically thought to be distinct entities, often managed in…”
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Langerhans cell histiocytosis: malignancy or inflammatory disorder doing a great job of imitating one? by Degar, Barbara A, Rollins, Barrett J

“…Langerhans cell histiocytosis (LCH) is the unifying designation for a rare proliferative disorder that occurs predominantly in childhood and involves the main…”
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Retrograde signaling by a mtDNA-encoded non-coding RNA preserves mitochondrial bioenergetics by Blumental-Perry, A., Jobava, R., Bederman, I., Degar, A. J., Kenche, H., Guan, B. J., Pandit, K., Perry, N. A., Molyneaux, N. D., Wu, J., Prendergas, E., Ye, Z.-W., Zhang, J., Nelson, C. E., Ahangari, F., Krokowski, D., Guttentag, S. H., Linden, P. A., Townsend, D. M., Miron, A., Kang, M.-J., Kaminski, N., Perry, Y., Hatzoglou, M.

“…Alveolar epithelial type II (AETII) cells are important for lung epithelium maintenance and function. We demonstrate that AETII cells from mouse lungs exposed…”
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HLH treatment: smarter, not harder by Henderson, Lauren A., Degar, Barbara A.

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Dr. Degar et al reply by Degar, Barbara A, Halyabar, Olha, Hazen, Melissa M, Henderson, Lauren A

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Pharmacogenomic Score Effectively Personalizes Treatment of Acute Myeloid Leukemia by Marrero, Richard J, Wu, Huiyun, Cao, Xueyuan, Parcha, Phani Krishna, Elsayed, Abdelrahman H, Inaba, Hiroto, Kuo, Dennis John, Degar, Barbara A, Heym, Kenneth, Taub, Jeffrey W, Lacayo, Norman, Pui, Ching-Hon, Ribeiro, Raul C, Rubnitz, Jeffrey E, Pounds, Stanley B, Lamba, Jatinder K

“…Cytarabine (also known as ara-C) has been the backbone of acute myeloid leukemia (AML) chemotherapy for over five decades. Recent pharmacogenomics-based 10-SNP…”
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The added value of skeletal surveys in the initial evaluation of children diagnosed with Langerhans cell histiocytosis in the era of staging 18 F-FDG PET/CT: A retrospective study by Rameh, Vanessa, Voss, Stephan, Bedoya, M Alejandra, Beaulieu, Danielle, Zhang, Da, Degar, Barbara A, Tsai, Andy

“…Currently, there is no consensus protocol on the initial staging evaluation for Langerhans cell histiocytosis (LCH). Our institutional protocol consists of a…”
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The added value of skeletal surveys in the initial evaluation of children diagnosed with Langerhans cell histiocytosis in the era of staging 18F‐FDG PET/CT: A retrospective study by Rameh, Vanessa, Voss, Stephan, Bedoya, M. Alejandra, Beaulieu, Danielle, Zhang, Da, Degar, Barbara A., Tsai, Andy

“…Objective Currently, there is no consensus protocol on the initial staging evaluation for Langerhans cell histiocytosis (LCH). Our institutional protocol…”
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Treatment of Epstein Barr virus‐induced haemophagocytic lymphohistiocytosis with rituximab‐containing chemo‐immunotherapeutic regimens by Chellapandian, DeepakBabu, Das, Rupali, Zelley, Kristin, Wiener, Susan J., Zhao, Huaqing, Teachey, David T., Nichols, Kim E., Hale, Gregory, Minkov, Milen, Karlhuber, Susanne, Weinstein, Joanna L., Weitzman, Sheila, Moshous, Despina, Fischer, Alain, Jeng, Michael, Henry, Michael, Haupt, Riccardo, Svahn, Joanna, Zapotocka, Ester, Wolfson, Julie, Yacobovich, Joanne, Van Laar, Jan A.M., Talano, Julie, Astigarraga, Itziar, Beutel, Karin, Berglöf, Elisabet, Henter, Jan‐Inge, Imashuku, Shinsaku, Ho, Marco Hok‐kung, Fraser, Chris, Greene Welch, Jennifer, Kitchen, Brenda, Jasty, Rama, Degar, Barbara A., Gunnes, Maria Winther, McMahon, Corrina, Garrington, Timothy, Filipovich, Alexandra H., Jordan, Michael B., Bleesing, Jacob J., Marsh, Rebecca A.

“…Summary Haemophagocytic lymphohistiocytosis (HLH) is a life threatening complication of Epstein–Barr virus (EBV) infection. The anti‐CD20 antibody rituximab…”
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BRAF V600E-Positive Multisite Langerhans Cell Histiocytosis in a Preterm Neonate by Bates, Sara V, Lakshmanan, Ashwini, Green, Adam L, Terry, Jefferson, Badalian-Very, Gayane, Rollins, Barrett J, Fleck, Patricia, Aslam, Muhammad, Degar, Barbara A

“…Hemorrhagic pustules with a "blueberry muffin" appearance accompanied by respiratory failure in a neonate present a challenging differential diagnosis that…”
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Histopathologic Correlates of Familial Hemophagocytic Lymphohistiocytosis Isolated to the Central Nervous System by Solomon, Isaac H, Li, Hojun, Benson, Leslie A, Henderson, Lauren A, Degar, Barbara A, Gorman, Mark P, Duncan, Christine N, Lidov, Hart G, Alexandrescu, Sanda

“…Abstract Familial hemophagocytic lymphohistiocytosis (HLH) is an immune hyperactivation syndrome caused by mutations in genes associated with cytotoxic T-cell…”
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Pediatric leukemia cutis: A case series by Andriescu, Elena Corina, Coughlin, Carrie C., Cheng, Carol E., Prajapati, Vimal H., Huang, Jennifer T., Schmidt, Birgitta A., Degar, Barbara A., Aplenc, Richard, Pillai, Vinodh, Yan, Albert C., Liang, Marilyn G.

“…Background Pediatric leukemia cutis (LC) is often difficult to diagnose due to similarity in appearance to other dermatologic diseases. Several case reports…”
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Pediatric CNS-isolated hemophagocytic lymphohistiocytosis by Benson, Leslie A, Li, Hojun, Henderson, Lauren A, Solomon, Isaac H, Soldatos, Ariane, Murphy, Jennifer, Bielekova, Bibiana, Kennedy, Alyssa L, Rivkin, Michael J, Davies, Kimberly J, Hsu, Amy P, Holland, Steven M, Gahl, William A, Sundel, Robert P, Lehmann, Leslie E, Lee, Michelle A, Alexandrescu, Sanda, Degar, Barbara A, Duncan, Christine N, Gorman, Mark P

“…OBJECTIVETo highlight a novel, treatable syndrome, we report 4 patients with CNS-isolated inflammation associated with familial hemophagocytic…”
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Imaging Features of Juvenile Xanthogranuloma of the Pediatric Head and Neck by Ginat, D T, Vargas, S O, Silvera, V M, Volk, M S, Degar, B A, Robson, C D

“…Juvenile xanthogranuloma is a non-Langerhans cell histiocytosis primarily affecting children. The purpose of this study was to characterize the imaging…”
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Familial Erythrocytosis Associated With a Short Deletion in the Erythropoietin Receptor Gene by Arcasoy, Murat O., Degar, Barbara A., Harris, Kevin W., Forget, Bernard G.

“…Familial erythrocytosis (familial polycythemia) inherited as an autosomal dominant trait has recently been reported to be associated with mutations in the gene…”
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Pharmacogenomics, Race, and Treatment Outcome in Pediatric Acute Myeloid Leukemia by Lamba, Jatinder K, Marrero, Richard, Wu, Huiyun, Cao, Xueyuan, Parcha, Phani Krisha, Karol, Seth E, Inaba, Hiroto, Kuo, Dennis John, Degar, Barbara A, Heym, Kenneth, Taub, Jeffrey W, Lacayo, Norman J, Pui, Ching-Hon, Ribeiro, Raul C, Pounds, Stanley B, Rubnitz, Jeffrey E

“…Disparities in outcomes exist between Black and White patients with acute myeloid leukemia (AML), with Black patients experiencing poorer prognosis compared…”
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Rapid next-generation sequencing aids in diagnosis of transient abnormal myelopoiesis in a phenotypically normal newborn by Aziz-Bose, Rahela, Wachter, Franziska, Chiarle, Roberto, Lindeman, Neal I., Kim, Annette S., Degar, Barbara A., Davies, Kimberly, Pikman, Yana

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Hemophagocytosis exacerbated by G‐CSF/GM‐CSF treatment in a patient with myelodysplasia by Wang, Sa, Degar, Barbara A., Zieske, Arthur, Shafi, Nelofar Q., Rose, Michal G.

“…We describe a 75‐year‐old man with neutropenia in whom bone marrow aspirate and biopsy demonstrated hemophagocytosis associated with myelodysplasia (MDS)…”
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