Search Results - "Baker, Eva"

Alcohol use among Congolese Babembe male refugees in Tarrant County: A qualitative study by Diese, Elvis Longanga, Raines-Milenkov, Amy, Felini, Martha, Akpan, Idara, Hussain, Arbaz, Baker, Eva

“…Background Refugees are at high risk of alcohol abuse due to experiences in their country of origin, transit camps, and in host countries. Congolese have been…”
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Long-Term Follow-Up of CD19-CAR T-Cell Therapy in Children and Young Adults With B-ALL by Shah, Nirali N, Lee, Daniel W, Yates, Bonnie, Yuan, Constance M, Shalabi, Haneen, Martin, Staci, Wolters, Pamela L, Steinberg, Seth M, Baker, Eva H, Delbrook, Cindy P, Stetler-Stevenson, Maryalice, Fry, Terry J, Stroncek, David F, Mackall, Crystal L

“…CD19 chimeric antigen receptor (CD19-CAR) T cells induce high response rates in children and young adults (CAYAs) with B-cell acute lymphoblastic leukemia…”
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Measures, Metrics, and Indicators for Evaluating Technology-Based Interventions by Baker, Eva L., O'Neil, Harold F.

“…The goal of this article is to reconsider the types of dependent variables used in formal evaluation of technology-based learning programs. This article…”
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Prospective phenotyping of NGLY1-CDDG, the first congenital disorder of deglycosylation by Lam, Christina, Ferreira, Carlos, Krasnewich, Donna, Toro, Camilo, Latham, Lea, Zein, Wadih M., Lehky, Tanya, Brewer, Carmen, Baker, Eva H., Thurm, Audrey, Farmer, Cristan A., Rosenzweig, Sergio D., Lyons, Jonathan J., Schreiber, John M., Gropman, Andrea, Lingala, Shilpa, Ghany, Marc G., Solomon, Beth, Macnamara, Ellen, Davids, Mariska, Stratakis, Constantine A., Kimonis, Virginia, Gahl, William A., Wolfe, Lynne

“…The cytosolic enzyme N-glycanase 1, encoded by NGLY1, catalyzes cleavage of the β-aspartyl glycosylamine bond of N-linked glycoproteins, releasing intact…”
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Autosomal recessive Noonan syndrome associated with biallelic LZTR1 variants by Johnston, Jennifer J, van der Smagt, Jasper J, Rosenfeld, Jill A, Pagnamenta, Alistair T, Alswaid, Abdulrahman, Baker, Eva H, Blair, Edward, Borck, Guntram, Brinkmann, Julia, Craigen, William, Dung, Vu Chi, Emrick, Lisa, Everman, David B, van Gassen, Koen L, Gulsuner, Suleyman, Harr, Margaret H, Jain, Mahim, Kuechler, Alma, Leppig, Kathleen A, McDonald-McGinn, Donna M, Can, Ngoc Thi Bich, Peleg, Amir, Roeder, Elizabeth R, Rogers, R Curtis, Sagi-Dain, Lena, Sapp, Julie C, Schäffer, Alejandro A, Schanze, Denny, Stewart, Helen, Taylor, Jenny C, Verbeek, Nienke E, Walkiewicz, Magdalena A, Zackai, Elaine H, Zweier, Christiane, Zenker, Martin, Lee, Brendan, Biesecker, Leslie G

“…Purpose To characterize the molecular genetics of autosomal recessive Noonan syndrome. Methods Families underwent phenotyping for features of Noonan syndrome…”
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Health information-seeking behavior among Congolese refugees by Longanga Diese, Elvis, Baker, Eva, Akpan, Idara, Acharya, Rushil, Raines-Milenkov, Amy, Felini, Martha, Hussain, Arbaz

“…Background The purpose of this cross-sectional study was to determine the extent to which Congolese refugees seek health information, to identify and assess…”
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Long-term follow-up after lymphodepleting autologous haematopoietic cell transplantation for treatment-resistant systemic lupus erythematosus by Goklemez, Sencer, Hasni, Sarfaraz, Hakim, Frances T, Muraro, Paolo A, Pirsl, Filip, Rose, Jeremy, Memon, Sarfraz, Fowler, Daniel F, Steinberg, Seth M, Baker, Eva H, Panch, Sandya R, Gress, Ronald, Illei, Gabor G, Lipsky, Peter E, Pavletic, Steven Z

“…Abstract Objective Autologous haematopoietic cell transplantation (AHSCT) improves immunologic dysfunction in patients with SLE. However, the curative…”
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Research to Controversy in 10 Decades by Baker, Eva L.

“…This article investigates the persistent and change elements of educational testing and assessment from 1920 to the present day. I show by examining the…”
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Health information-seeking behavior among Congolese refugees by Elvis Longanga Diese, Eva Baker, Idara Akpan, Rushil Acharya, Amy Raines-Milenkov, Martha Felini, Arbaz Hussain

“…Background The purpose of this cross-sectional study was to determine the extent to which Congolese refugees seek health information, to identify and assess…”
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The Chimera of Validity by Baker, Eva L

“…Background/Context: Education policy over the past 40 years has focused on the importance of accountability in school improvement. Although much of the…”
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Classification of learning outcomes: evidence from the computer games literature by O'Neil, Harold F., Wainess, Richard, Baker, Eva L.

“…Following up on an earlier issue of The Curriculum Journal (Vol. 16, No. 1), this article focuses on learning outcomes in the context of video games. Learning…”
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Oral cysteamine bitartrate and N-acetylcysteine for patients with infantile neuronal ceroid lipofuscinosis: a pilot study by Levin, Sondra W, MD, Baker, Eva H, PhD, Zein, Wadih M, MD, Zhang, Zhongjian, MD, Quezado, Zenaide M N, MD, Miao, Ning, MD, Gropman, Andrea, MD, Griffin, Kurt J, MD, Bianconi, Simona, MD, Chandra, Goutam, PhD, Khan, Omar I, MD, Caruso, Rafael C, MD, Liu, Aiyi, PhD, Mukherjee, Anil B, Dr

“…Summary Background Infantile neuronal ceroid lipofuscinosis is a devastating neurodegenerative lysosomal storage disease caused by mutations in the gene ( CLN1…”
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Uptake of cancer screenings among a multiethnic refugee population in North Texas, 2014-2018 by Raines Milenkov, Amy, Felini, Martha, Baker, Eva, Acharya, Rushil, Longanga Diese, Elvis, Onsa, Sara, Fernando, Shane, Chor, Holy

“…Refugees are less likely than US born populations to receive cancer screenings. Building Bridges is a community health worker prevention program designed to…”
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Neurofilament light chain levels correlate with clinical measures in CLN3 disease by Dang Do, An N., Sinaii, Ninet, Masvekar, Ruturaj R., Baker, Eva H., Thurm, Audrey E., Soldatos, Ariane G., Bianconi, Simona E., Bielekova, Bibiana, Porter, Forbes D.

“…CLN3 disease is a neurodegenerative disorder with onset in childhood. It affects multiple functions at different developmental stages. Incomplete understanding…”
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GM1 gangliosidosis type II: Results of a 10-year prospective study by D’Souza, Precilla, Farmer, Cristan, Johnston, Jean M., Han, Sangwoo T., Adams, David, Hartman, Adam L., Zein, Wadih, Huryn, Laryssa A., Solomon, Beth, King, Kelly, Jordan, Christopher P., Myles, Jennifer, Nicoli, Elena-Raluca, Rothermel, Caroline E., Mojica Algarin, Yoliann, Huang, Reyna, Quimby, Rachel, Zainab, Mosufa, Bowden, Sarah, Crowell, Anna, Buckley, Ashura, Brewer, Carmen, Regier, Debra S., Brooks, Brian P., Acosta, Maria T., Baker, Eva H., Vézina, Gilbert, Thurm, Audrey, Tifft, Cynthia J.

“…GM1 gangliosidosis (GM1) a lysosomal disorder caused by pathogenic variants in GLB1, is characterized by relentless neurodegeneration. There are no approved…”
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Brain proton MR spectroscopy measurements in CLN3 disease by Dang Do, An N., Baker, Eva H., Farmer, Cristan A., Soldatos, Ariane G., Thurm, Audrey E., Porter, Forbes D.

“…CLN3 is an autosomal recessive lysosomal disorder with intracellular accumulation of ceroid-lipofuscins. CLN3 classically has onset around 4–6 years of age…”
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From the Assessment OF Education to the Assessment for Education: Policy and Futures by Baker, Eva L

“…Context Educational reform in the United States has had a growing dependence on accountability achieved through large-scale assessment. Despite discussion and…”
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Late diagnosis and atypical brain imaging of Aicardi–Goutières syndrome: are we failing to diagnose Aicardi–Goutières syndrome‐2? by Svingen, Leah, Goheen, Mitchell, Godfrey, Rena, Wahl, Colleen, Baker, Eva H, Gahl, William A, Malicdan, May Christine V, Toro, Camilo

“…Aicardi–Goutières syndrome (AGS) is a rare disorder with in utero or postnatal onset of encephalopathy and progressive neurological deterioration. The seven…”
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Genomic analysis, immunomodulation and deep phenotyping of patients with nodding syndrome by Soldatos, Ariane, Nutman, Thomas B, Johnson, Tory, Dowell, Scott F, Sejvar, James J, Wilson, Michael R, DeRisi, Joseph L, Inati, Sara K, Groden, Catherine, Evans, Colleen, O’Connell, Elise M, Toliva, Bernard Opar, Aceng, Jane R, Aryek-Kwe, Josephine, Toro, Camilo, Stratakis, Constantine A, Buckler, A Gretchen, Cantilena, Cathy, Palmore, Tara N, Thurm, Audrey, Baker, Eva H, Chang, Richard, Fauni, Harper, Adams, David, Macnamara, Ellen F, Lau, C Christopher, Malicdan, May Christine V, Pusey-Swerdzewski, Barbara, Downing, Robert, Bunga, Sudhir, Thomas, Jerry D, Gahl, William A, Nath, Avindra

“…Abstract The aetiology of nodding syndrome remains unclear, and comprehensive genotyping and phenotyping data from patients remain sparse. Our objectives were…”
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Glb1 knockout mouse model shares natural history with type II GM1 gangliosidosis patients by Nicoli, Elena-Raluca, Huebecker, Mylene, Han, Sangwoo T., Garcia, Karolyn, Munasinghe, Jeeva, Lizak, Martin, Latour, Yvonne, Yoon, Robin, Glase, Brianna, Tyrlik, Michal, Peiravi, Morteza, Springer, Danielle, Baker, Eva H., Priestman, David, Sidhu, Rohini, Kell, Pamela, Jiang, Xuntian, Kolstad, Josephine, Kuhn, Anna Luisa, Shazeeb, Mohammed Salman, Acosta, Maria T., Proia, Richard L., Platt, Frances M., Tifft, Cynthia J.

“…GM1 gangliosidosis is a rare lysosomal storage disorder affecting multiple organ systems, primarily the central nervous system, and is caused by functional…”
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