Year |
Citation |
Score |
2021 |
Shapiro E, Ziegler R. Pediatric Neuropsychology and Pediatric Neurology: Kenneth Swaiman's Legacy. Pediatric Neurology. 122: 122-124. PMID 34294470 DOI: 10.1016/j.pediatrneurol.2021.05.003 |
0.527 |
|
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, ... ... Shapiro E, 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 |
0.301 |
|
2020 |
Seo JH, Okuyama T, Shapiro E, Fukuhara Y, Kosuga M. Natural history of cognitive development in neuronopathic mucopolysaccharidosis type II (Hunter syndrome): Contribution of genotype to cognitive developmental course. Molecular Genetics and Metabolism Reports. 24: 100630. PMID 32775211 DOI: 10.1016/J.Ymgmr.2020.100630 |
0.312 |
|
2018 |
Whitley CB, Cleary M, Eugen Mengel K, Harmatz P, Shapiro E, Nestrasil I, Haslett P, Whiteman D, Alexanderian D. Observational Prospective Natural History of Patients with Sanfilippo Syndrome Type B. The Journal of Pediatrics. PMID 29661560 DOI: 10.1016/J.Jpeds.2018.01.044 |
0.303 |
|
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 |
0.619 |
|
2017 |
van der Lee JH, Morton J, Adams HR, Clarke L, Ebbink BJ, Escolar ML, Giugliani R, Harmatz P, Hogan M, Jones S, Kearney S, Muenzer J, Rust S, Semrud-Clikeman M, Wijburg FA, ... ... Shapiro E, et al. Cognitive endpoints for therapy development for neuronopathic mucopolysaccharidoses: Results of a consensus procedure. Molecular Genetics and Metabolism. PMID 28501294 DOI: 10.1016/J.Ymgme.2017.05.004 |
0.308 |
|
2017 |
Nestrasil I, Shapiro E, Svatkova A, Dickson P, Chen A, Wakumoto A, Ahmed A, Stehel E, McNeil S, Gravance C, Maher E. Intrathecal enzyme replacement therapy reverses cognitive decline in mucopolysaccharidosis type I. American Journal of Medical Genetics. Part A. 173: 780-783. PMID 28211988 DOI: 10.1002/Ajmg.A.38073 |
0.343 |
|
2015 |
Nestrasil I, Shapiro E, Kovac V, Wakumoto A, Ahmed A, Delaney K, Yund B, Rudser K, Barbier A, Haslett P, Whitley C. OP47 – 2274: Brain MRI patterns of disease progression in Sanfilippo syndrome type A (MPS IIIA) European Journal of Paediatric Neurology. 19. DOI: 10.1016/S1090-3798(15)30048-9 |
0.331 |
|
2015 |
Abdelwahab M, Shapiro E, Nestrasil I. Abnormal behavioral features in Egyptian children with type III Gaucher disease Molecular Genetics and Metabolism. 114. DOI: 10.1016/J.Ymgme.2014.12.003 |
0.3 |
|
2014 |
Kovac V, Yund BD, Ahmed A, Rudser K, Shapiro E, Nestrasil I. The development of brain and neurocognitive function in typically developing children ages 4-7 years Molecular Genetics and Metabolism. 111. DOI: 10.1016/J.Ymgme.2013.12.139 |
0.302 |
|
2014 |
Aldenhoven M, Orchard P, Kurtzberg J, Wynn R, O'Meara A, Veys P, Fischer A, Valayannopoulos V, Neven B, Rovelli A, Prasad VK, Tolar J, Shapiro E, Jones S, Parini R, et al. Predictors of Long-Term Clinical Outcome in Hurler Syndrome Patients after Successful Hematopoietic Cell Transplantation: An International Study Biology of Blood and Marrow Transplantation. 20. DOI: 10.1016/J.Bbmt.2013.12.095 |
0.325 |
|
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 |
0.57 |
|
2013 |
Yund B, Kovac V, Nestrasil I, Delaney K, Rudser K, Nguyen-Driver M, Steiner R, Shapiro E. Neuropsychological function and brain abnormalities in Children with attenuated Mucopolysaccharidosis type II Molecular Genetics and Metabolism. 108. DOI: 10.1016/J.Ymgme.2012.11.276 |
0.325 |
|
2012 |
Ziegler R, King K, Whitley C, Shapiro E. Brain Function in Children with Fabry Disease Molecular Genetics and Metabolism. 105: S68. DOI: 10.1016/J.Ymgme.2011.11.185 |
0.601 |
|
2011 |
Eisengart J, Rudser K, Ahmed A, Nestrasil I, King K, Ziegler R, Shapiro E. Differences in attention and executive functioning between MPS types IH, IA, and II: analysis of test performance and quantitative MRI Molecular Genetics and Metabolism. 102: S17. DOI: 10.1016/J.Ymgme.2010.11.058 |
0.571 |
|
2009 |
Ziegler R, Bjoraker K, Shapiro E. 156. The role of neuropsychological testing in clinical research on lysosomal diseases Molecular Genetics and Metabolism. 96: S46-S47. DOI: 10.1016/J.Ymgme.2008.11.157 |
0.564 |
|
2008 |
Ziegler RS, Shapiro E. Neurogenetic Developmental Disorders: Variation and Manifestation in Childhood Child Neuropsychology. 14: 562-564. DOI: 10.1080/09297040701770827 |
0.551 |
|
2008 |
Ziegler R, Bjoraker K, Shapiro E, Adams H. 116. Neurobehavioral core Molecular Genetics and Metabolism. 93: 44. DOI: 10.1016/J.Ymgme.2007.10.128 |
0.53 |
|
2007 |
Tolar J, Orchard PJ, Bjoraker KJ, Ziegler RS, Shapiro EG, Charnas L. N-acetyl-L-cysteine improves outcome of advanced cerebral adrenoleukodystrophy. Bone Marrow Transplantation. 39: 211-5. PMID 17290278 DOI: 10.1038/sj.bmt.1705571 |
0.567 |
|
2004 |
Peters C, Charnas LR, Tan Y, Ziegler RS, Shapiro EG, DeFor T, Grewal SS, Orchard PJ, Abel SL, Goldman AI, Ramsay NK, Dusenbery KE, Loes DJ, Lockman LA, Kato S, et al. Cerebral X-linked adrenoleukodystrophy: the international hematopoietic cell transplantation experience from 1982 to 1999. Blood. 104: 881-8. PMID 15073029 DOI: 10.1182/blood-2003-10-3402 |
0.575 |
|
2002 |
Grewal SS, Krivit W, Defor TE, Shapiro EG, Orchard PJ, Abel SL, Lockman LA, Ziegler RS, Dusenbery KE, Peters C. Outcome of second hematopoietic cell transplantation in Hurler syndrome. Bone Marrow Transplantation. 29: 491-6. PMID 11960268 DOI: 10.1038/Sj.Bmt.1703395 |
0.598 |
|
2001 |
Corbett B, Khan K, Czapansky-Beilman D, Brady N, Dropik P, Goldman DZ, Delaney K, Sharp H, Mueller I, Shapiro E, Ziegler R. A double-blind, placebo-controlled crossover study investigating the effect of porcine secretin in children with autism. Clinical Pediatrics. 40: 327-31. PMID 11824175 DOI: 10.1177/000992280104000604 |
0.547 |
|
2000 |
Shapiro E, Krivit W, Lockman L, Jambaqué I, Peters C, Cowan M, Harris R, Blanche S, Bordigoni P, Loes D, Ziegler R, Crittenden M, Ris D, Berg B, Cox C, et al. Long-term effect of bone-marrow transplantation for childhood-onset cerebral X-linked adrenoleukodystrophy. Lancet. 356: 713-8. PMID 11085690 DOI: 10.1016/S0140-6736(00)02629-5 |
0.551 |
|
1999 |
Krivit W, Aubourg P, Shapiro E, Peters C. Bone marrow transplantation for globoid cell leukodystrophy, adrenoleukodystrophy, metachromatic leukodystrophy, and Hurler syndrome. Current Opinion in Hematology. 6: 377-82. PMID 10546790 DOI: 10.1097/00062752-199911000-00004 |
0.308 |
|
1990 |
Krivit W, Shapiro E, Kennedy W, Lipton M, Lockman L, Smith S, Summers CG, Wenger DA, Tsai MY, Ramsay NKC, Kersey JH, Yao JK, Kaye E. Treatment of late infantile metachromatic leukodystrophy by bone marrow transplantation. The New England Journal of Medicine. 322: 28-32. PMID 1967188 DOI: 10.1056/Nejm199001043220106 |
0.304 |
|
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