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Julie B. Eisengart, Ph.D. - Publications

Affiliations: 
2009 Clinical Psychology Northwestern University, Evanston, IL 
Area:
Mental Health and Public Policy
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27 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 van der Lee JH, Morton J, Adams HR, Clarke L, Eisengart JB, Escolar ML, Giugliani R, Harmatz P, Hogan M, Kearney S, Muenzer J, Muschol N, Rust S, Saville BR, Semrud-Clikeman M, et al. Therapy development for the mucopolysaccharidoses: Updated consensus recommendations for neuropsychological endpoints. Molecular Genetics and Metabolism. PMID 32917509 DOI: 10.1016/J.Ymgme.2020.08.007  0.317
2020 Hampe CS, Eisengart JB, Lund TC, Orchard PJ, Swietlicka M, Wesley J, McIvor RS. Mucopolysaccharidosis Type I: A Review of the Natural History and Molecular Pathology. Cells. 9. PMID 32764324 DOI: 10.3390/Cells9081838  0.328
2020 Pierpont EI, Nascene DR, Shanley R, Kenney-Jung DL, Ziegler RS, Miller WP, Gupta AO, Lund TC, Orchard PJ, Eisengart JB. Neurocognitive benchmarks following transplant for emerging cerebral adrenoleukodystrophy. Neurology. PMID 32616675 DOI: 10.1212/Wnl.0000000000009929  0.352
2019 Chen AH, Harmatz P, Nestrasil I, Eisengart JB, King KE, Rudser K, Kaizer AM, Svatkova A, Wakumoto A, Le SQ, Madden J, Young S, Zhang H, Polgreen LE, Dickson PI. Intrathecal enzyme replacement for cognitive decline in mucopolysaccharidosis type I, a randomized, open-label, controlled pilot study. Molecular Genetics and Metabolism. PMID 31839529 DOI: 10.1016/J.Ymgme.2019.11.007  0.332
2019 Polgreen LE, Lund TC, Braunlin E, Tolar J, Miller BS, Fung E, Whitley CB, Eisengart JB, Northrop E, Rudser K, Miller WP, Orchard PJ. Clinical trial of laronidase in Hurler syndrome after hematopoietic cell transplantation. Pediatric Research. PMID 31434105 DOI: 10.1038/S41390-019-0541-2  0.396
2019 Lund TC, Miller WP, Eisengart JB, Simmons K, Pollard L, Renaud DL, Wenger DA, Patterson MC, Orchard PJ. Biochemical and clinical response after umbilical cord blood transplant in a boy with early childhood-onset beta-mannosidosis. Molecular Genetics & Genomic Medicine. e712. PMID 31115173 DOI: 10.1002/Mgg3.712  0.303
2019 Eisengart JB, Pierpont EI, Kaizer AM, Rudser KD, King KE, Pasquali M, Polgreen LE, Dickson PI, Le SQ, Miller WP, Tolar J, Orchard PJ, Lund TC. Intrathecal enzyme replacement for Hurler syndrome: biomarker association with neurocognitive outcomes. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 31019279 DOI: 10.1038/S41436-019-0522-1  0.319
2019 Lund T, Eisengart J, Pierpont R, Kaizer A, Rudser K, Pasqualli M, Dickson P, Miller W, Polgreen L, Orchard P. Predicting intelligence in MPS IH with biomarkers Molecular Genetics and Metabolism. 126. DOI: 10.1016/J.Ymgme.2018.12.240  0.357
2019 King KE, Shapiro EG, Whitley CB, Muenzer J, Eisengart JB. Feasibility of quantifying behavior in early progressive MPS II Molecular Genetics and Metabolism. 126. DOI: 10.1016/J.Ymgme.2018.12.210  0.311
2019 Gupta A, Lund T, Anderson N, Miettunen K, Eisengart J, Braunlin E, Orchard P. Allogeneic hematopoietic stem cell transplant improves outcomes in fucosidosis Molecular Genetics and Metabolism. 126. DOI: 10.1016/J.Ymgme.2018.12.156  0.314
2018 Shapiro EG, Whitley CB, Eisengart JB. Beneath the floor: re-analysis of neurodevelopmental outcomes in untreated Hurler syndrome. Orphanet Journal of Rare Diseases. 13: 76. PMID 29751845 DOI: 10.1186/S13023-018-0817-3  0.353
2018 Eisengart JB, Rudser KD, Xue Y, Orchard P, Miller W, Lund T, Van der Ploeg A, Mercer J, Jones S, Mengel KE, Gökce S, Guffon N, Giugliani R, de Souza CFM, Shapiro EG, et al. Long-term outcomes of systemic therapies for Hurler syndrome: an international multicenter comparison. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 29517765 DOI: 10.1038/Gim.2018.29  0.389
2018 Polgreen LE, Lund TC, Eisengart J, Miller W, Orchard PJ. Open-label, single arm, pilot study of intravenous laronidase following allogeneic transplantation for Hurler syndrome Molecular Genetics and Metabolism. 123. DOI: 10.1016/J.Ymgme.2017.12.318  0.332
2018 Eisengart JB, Miller W, Kaizer A, Rudser K, King K, Ziegler RS, Pierpont E, Whitley C, Raymond G, Tolar J, Lund T, Shapiro EG, Orchard P. Neurocognitive outcomes of intrathecal enzyme replacement therapy and transplant in Hurler syndrome Molecular Genetics and Metabolism. 123: S41. DOI: 10.1016/J.Ymgme.2017.12.089  0.359
2017 Eisengart JB, Jarnes J, Ahmed A, Nestrasil I, Ziegler R, Delaney K, Shapiro E, Whitley C. Long-term cognitive and somatic outcomes of enzyme replacement therapy in untransplanted Hurler syndrome. Molecular Genetics and Metabolism Reports. 13: 64-68. PMID 28983455 DOI: 10.1016/J.Ymgmr.2017.07.012  0.395
2017 Pierpont EI, Eisengart JB, Shanley R, Nascene D, Raymond GV, Shapiro EG, Ziegler RS, Orchard PJ, Miller WP. Neurocognitive Trajectory of Boys Who Received a Hematopoietic Stem Cell Transplant at an Early Stage of Childhood Cerebral Adrenoleukodystrophy. Jama Neurology. PMID 28418523 DOI: 10.1001/Jamaneurol.2017.0013  0.337
2016 Shapiro EG, Rudser K, Ahmed A, Steiner RD, Delaney KA, Yund B, King K, Kunin-Batson A, Eisengart J, Whitley CB. A longitudinal study of emotional adjustment, quality of life and adaptive function in attenuated MPS II. Molecular Genetics and Metabolism Reports. 7: 32-9. PMID 27114914 DOI: 10.1016/J.Ymgmr.2016.03.005  0.314
2016 McKinney AM, Benson J, Nascene DR, Eisengart J, Salmela MB, Loes DJ, Zhang L, Patel K, Raymond GV, Miller WP. Childhood Cerebral Adrenoleukodystrophy: MR Perfusion Measurements and Their Use in Predicting Clinical Outcome after Hematopoietic Stem Cell Transplantation. Ajnr. American Journal of Neuroradiology. PMID 27079370 DOI: 10.3174/Ajnr.A4773  0.34
2016 Pierpont E, Eisengart J, Ziegler R, Raymond G, Orchard PJ, Lund T, Miller WP. Neurocognitive Trajectory of Patients with Childhood Cerebral Adrenoleukodystrophy Who Received Allogeneic Hematopoietic Cell Transplantation at an Early Stage of Cerebral Disease Blood. 128: 4682-4682. DOI: 10.1182/Blood.V128.22.4682.4682  0.375
2016 Eisengart JB, Shapiro E, Delaney K, Nestrasil I, Ahmed A, Hampton L, Whitley CB. Outcomes of enzyme replacement therapy in a 14-year-old female with Hurler syndrome Molecular Genetics and Metabolism. 117. DOI: 10.1016/J.Ymgme.2015.12.246  0.309
2015 Shapiro EG, Nestrasil I, Rudser K, Delaney K, Kovac V, Ahmed A, Yund B, Orchard PJ, Eisengart J, Niklason GR, Raiman J, Mamak E, Cowan MJ, Bailey-Olson M, Harmatz P, et al. Neurocognition across the spectrum of mucopolysaccharidosis type I: Age, severity, and treatment. Molecular Genetics and Metabolism. PMID 26095521 DOI: 10.1016/J.Ymgme.2015.06.002  0.338
2015 Eisengart JB, Shapiro EG, Rudser KD, Ahmed A, Kovac V, Delaney K, Mercer J, Jones S, Ploeg AVd, Mengel K, Goekce S, Whitley CB. Clinical outcomes of Hurler syndrome treated exclusively with enzyme replacement therapy from a young age Molecular Genetics and Metabolism. 114. DOI: 10.1016/J.Ymgme.2014.12.074  0.329
2013 Eisengart JB, Rudser KD, Tolar J, Orchard PJ, Kivisto T, Ziegler RS, Whitley CB, Shapiro EG. Enzyme replacement is associated with better cognitive outcomes after transplant in Hurler syndrome. The Journal of Pediatrics. 162: 375-80.e1. PMID 22974573 DOI: 10.1016/J.Jpeds.2012.07.052  0.398
2013 McKinney AM, Nascene D, Miller WP, Eisengart J, Loes D, Benson M, Tolar J, Orchard PJ, Ziegler RS, Zhang L, Provenzale J. Childhood cerebral X-linked adrenoleukodystrophy: diffusion tensor imaging measurements for prediction of clinical outcome after hematopoietic stem cell transplantation. Ajnr. American Journal of Neuroradiology. 34: 641-9. PMID 22899791 DOI: 10.3174/Ajnr.A3232  0.322
2011 Miller WP, Rothman SM, Nascene D, Kivisto T, DeFor TE, Ziegler RS, Eisengart J, Leiser K, Raymond G, Lund TC, Tolar J, Orchard PJ. Outcomes after allogeneic hematopoietic cell transplantation for childhood cerebral adrenoleukodystrophy: the largest single-institution cohort report. Blood. 118: 1971-8. PMID 21586746 DOI: 10.1182/Blood-2011-01-329235  0.359
2011 Eisengart J, Delaney K, Rudser K, Potegal M, Shapiro E. Age and cognitive/adaptive function in MPS IIIA (Sanfilippo syndrome) Molecular Genetics and Metabolism. 102. DOI: 10.1016/J.Ymgme.2010.11.056  0.314
2008 Eisengart J, Martinovich Z, Lyons JS. Discharge due to running away from residential treatment: Youth and setting effects Residential Treatment For Children and Youth. 24: 327-343. DOI: 10.1080/08865710802174418  0.432
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