Search Results - "Hinson, Ashley"

Hemophagocytic Lymphohistiocytosis in Langerhans Cell Histiocytosis: A Case Report and Review of the Literature by Hinson, Ashley R.P., Patel, Niraj, Kaplan, Joel

“…A toddler undergoing treatment for refractory Langerhans cell histiocytosis (LCH) developed concurrent hemophagocytic lymphohistiocytosis (HLH). These are…”
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Human rhabdomyosarcoma cell lines for rhabdomyosarcoma research: utility and pitfalls by Hinson, Ashley R P, Jones, Rosanne, Crose, Lisa E S, Belyea, Brian C, Barr, Frederic G, Linardic, Corinne M

“…Rhabdomyosarcoma (RMS) is the most common soft tissue sarcoma of childhood and adolescence. Despite intergroup clinical trials conducted in Europe and North…”
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Emapalumab Treatment in Patients With Rheumatologic Disease–Associated Hemophagocytic Lymphohistiocytosis in the United States: A Retrospective Medical Chart Review Study by Chandrakasan, Shanmuganathan, Allen, Carl E., Bhatla, Deepika, Carter, John, Chien, May, Cooper, Robert, Draper, Lauren, Eckstein, Olive S., Hanna, Rabi, Hays, J. Allyson, Hermiston, Michelle L., Hinson, Ashley P., Hobday, Patricia M., Isakoff, Michael S., Jordan, Michael B., Leiding, Jennifer W., Modica, Renee, Nakano, Taizo A., Oladapo, Abiola, Patel, Sachit A., Pednekar, Priti, Riskalla, Mona, Sarangi, Susmita N., Satwani, Prakash, Tandra, Anand, Walkovich, Kelly J., Yee, John D., Zoref‐Lorenz, Adi, Behrens, Edward M.

“…Rheumatologic disease-associated hemophagocytic lymphohistiocytosis (HLH), a rare, life-threatening, systemic hyperinflammatory syndrome, occurs as a…”
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The Transcriptional Coactivator TAZ Is a Potent Mediator of Alveolar Rhabdomyosarcoma Tumorigenesis by Deel, Michael D, Slemmons, Katherine K, Hinson, Ashley R, Genadry, Katia C, Burgess, Breanne A, Crose, Lisa E S, Kuprasertkul, Nina, Oristian, Kristianne M, Bentley, Rex C, Linardic, Corinne M

“…Alveolar rhabdomyosarcoma (aRMS) is a childhood soft tissue sarcoma driven by the signature (P3F) fusion gene. Five-year survival for aRMS is <50%, with no…”
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Secreted Frizzled-Related Protein 3 (SFRP3) Is Required for Tumorigenesis of PAX3-FOXO1-Positive Alveolar Rhabdomyosarcoma by Kephart, Julie J G, Tiller, Rosanne G J, Crose, Lisa E S, Slemmons, Katherine K, Chen, Po-Han, Hinson, Ashley R, Bentley, Rex C, Chi, Jen-Tsan Ashley, Linardic, Corinne M

“…Rhabdomyosarcoma (RMS) is a soft tissue sarcoma associated with the skeletal muscle lineage. Of the two predominant subtypes, known as embryonal (eRMS) and…”
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Levocarnitine for pegaspargase‐induced hepatotoxicity in older children and young adults with acute lymphoblastic leukemia by Schulte, Rachael, Hinson, Ashley, Huynh, Van, Breese, Erin H., Pierro, Joanna, Rotz, Seth, Mixon, Benjamin A., McNeer, Jennifer L., Burke, Michael J., Orgel, Etan

“…Background Pegaspargase (PEG‐ASP) is an integral component of therapy for acute lymphoblastic leukemia (ALL) but is associated with hepatotoxicity that may…”
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Germ cells are not required to establish the female pathway in mouse fetal gonads by Maatouk, Danielle M, Mork, Lindsey, Hinson, Ashley, Kobayashi, Akio, McMahon, Andrew P, Capel, Blanche

“…The fetal gonad is composed of a mixture of somatic cell lineages and germ cells. The fate of the gonad, male or female, is determined by a population of…”
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Neonatal thrombosis after antenatal treatment of neonatal alloimmune thrombocytopenia with intravenous immunoglobulin by Hinson, Ashley, Saxonhouse, Matthew

“…Neonatal alloimmune thrombocytopenia (NAIT) may lead to serious complications, including perinatal intracranial hemorrhage and death. Mothers with a history of…”
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Where Children Die: Obstacles to Quality End-of-Life Care by Hinson, Ashley P., Rosoff, Philip M.

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Real-world treatment patterns and outcomes in patients with primary hemophagocytic lymphohistiocytosis treated with emapalumab by Chandrakasan, Shanmuganathan, Jordan, Michael B., Baker, Ashley, Behrens, Edward M., Bhatla, Deepika, Chien, May, Eckstein, Olive S., Henry, Michael M., Hermiston, Michelle L., Hinson, Ashley P., Leiding, Jennifer W., Oladapo, Abiola, Patel, Sachit A., Pednekar, Priti, Ray, Anish K., Dávila Saldaña, Blachy, Sarangi, Susmita N., Walkovich, Kelly J., Yee, John D., Zoref-Lorenz, Adi, Allen, Carl E., Weinstein, Joanna, Hinson, Ashley P., Allen, Carl E., Eckstein, Olive S., Gulati, Nitya, Chandrakasan, Shanmuganathan, Haines, Hilary, Nakano, Taizo, Patel, Sachit A., Behrens, Edward M, Intzes, Stefanos, Hays, Allyson, Dávila Saldaña, Blachy, Jordan, Michael B., Zoref-Lorenz, Adi, Hanna, Rabi, Isakoff, Michael, Ray, Anish K., Rothman, Jennifer, Tandra, Anand, Cooper, Robert, Leiding, Jennifer W., Chien, May, Sarangi, Susmita, Gidvani, Diaz, Satwani, Prakesh, Carter, John, Henry, Michael, Gloude, Nicholas, Bhatt, Sima, Bhatla, Deepika, Draper, Lauren, Panigrahi, Arun, Hermiston, Michelle, Modica, Renee, Riskalla, Mona, Baker, Ashley, Ward, Brant

“…•Addition of emapalumab improves laboratory parameters and overall survival in patients with pHLH in real-world clinical practice.•Addition of emapalumab…”
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Spontaneous resolution of Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis by Belyea, Brian, Hinson, Ashley, Moran, Cassandra, Hwang, Eugene, Heath, Jessica, Barfield, Raymond

“…Secondary hemophagocytic lymphohistiocytosis (sHLH) is a reactive, proliferative disorder of the immune system resulting in lymphohistiocytic proliferation,…”
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Asparaginase-Induced Hypertriglyceridemia Presenting as Pseudohyponatremia during Leukemia Treatment by Hinson, Ashley, Linardic, Corinne M., Newbern, Dorothee

“…Asparaginase is a chemotherapeutic agent used to induce disease remission in children with acute lymphoblastic leukemia (ALL). We describe the cases of two…”
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Recombinant von Willebrand factor for perioperative bleeding management in pediatric patient with allergy to plasma‐derived von Willebrand factor by Tran, Thuy B., Arnall, Justin R., Kleiboer, Brendan, Hinson, Ashley

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Severe Thromboses in Neonates by Saxonhouse, Matthew A, Hinson, Ashley

“…Severe thrombosis in the neonate presents a diagnostic challenge to the clinician as the benefits and risks for treatment must be weighed with every medical…”
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Real‐world experience in treating pediatric relapsed/refractory or therapy‐related myeloid malignancies with decitabine, vorinostat, and FLAG therapy based on a phase 1 study run by the TACL consortium by Schafer, Eric S., Chao, Karen, Stevens, Alexandra M., Jo, Eunji, Hilsenbeck, Susan G., Gossai, Nathan P., Doan, Andrew, Colace, Susan I., Guinipero, Terri, Otterson, Daniel, Kaplan, Joel A., Hinson, Ashley, Pommert, Lauren, Wayne, Alan S., Bhojwani, Deepa, Burke, Michael J.

“…Current therapies for relapsed/refractory (R/R) pediatric myeloid neoplasms are inadequately effective. Real‐world data (RWD) can improve care by augmenting…”
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Congenital hemophagocytic lymphohistiocytosis presenting as thrombocytopenia in a newborn by Hinson, Ashley, Owen, William, Prose, Neil, Parikh, Suhag, Thornburg, Courtney

“…Hemophagocytic lymphohistiocytosis (HLH) is a disease caused by dysregulation and hyperactivation of the immune system, and can be familial or acquired. HLH…”
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The transcriptional co-activator TAZ is a potent mediator of alveolar rhabdomyosarcoma tumorigenesis by Deel, Michael D., Slemmons, Katherine K., Hinson, Ashley R., Genadry, Katia C., Burgess, Breanne A., Crose, Lisa E.S., Kuprasertkul, Nina, Oristian, Kristianne M., Bentley, Rex C., Linardic, Corinne M.

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Emapalumab Use in Patients With Rheumatologic Disease-Associated Hemophagocytic Lymphohistiocytosis in the United States: the REAL-HLH Study by Chandrakasan, Shanmuganathan, Allen, Carl E, Bhatla, Deepika, Carter, John, Chien, May, Cooper, Robert, Draper, Lauren, Eckstein, Olive S, Hanna, Rabi, Hays, J Allyson, Hermiston, Michelle L, Hinson, Ashley P, Hobday, Patricia M, Isakoff, Michael S, Jordan, Michael B, Leiding, Jennifer W, Modica, Renee, Nakano, Taizo A, Oladapo, Abiola, Patel, Sachit A, Pednekar, Priti, Riskalla, Mona, Sarangi, Susmita N, Satwani, Prakash, Tandra, Anand, Walkovich, Kelly J, Yee, John D, Zoref-Lorenz, Adi, Behrens, Edward M

“…Rheumatologic disease-associated hemophagocytic lymphohistiocytosis (HLH), a rare, life-threatening, systemic hyperinflammatory syndrome, occurs as a…”
Get full text