Elsa Shapiro

Affiliations: 
University of Minnesota, Twin Cities, Minneapolis, MN 
Area:
Pediatric neuropsychology, degenerative and metabolic disorders
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"Elsa Shapiro"
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Parents

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Robert D. Wirt grad student UMN (PsychTree)

Children

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Suzanne T Mallery grad student UMN (PsychTree)
John Pina grad student 2000 UMN
Richard Ziegler post-doc UMN

Collaborators

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Karen Elizabeth Wills collaborator Mayo Clinc, Rochester
 (Co-wrote Div 40 PIAC brochure on Pediatric Neuropsychology.)
Richard Ziegler collaborator UMN
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Publications

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Shapiro E, Ziegler R. (2021) Pediatric Neuropsychology and Pediatric Neurology: Kenneth Swaiman's Legacy. Pediatric Neurology. 122: 122-124
van der Lee JH, Morton J, Adams HR, et al. (2020) Therapy development for the mucopolysaccharidoses: Updated consensus recommendations for neuropsychological endpoints. Molecular Genetics and Metabolism
Seo JH, Okuyama T, Shapiro E, et al. (2020) 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
Whitley CB, Cleary M, Eugen Mengel K, et al. (2018) Observational Prospective Natural History of Patients with Sanfilippo Syndrome Type B. The Journal of Pediatrics
Eisengart JB, Jarnes J, Ahmed A, et al. (2017) Long-term cognitive and somatic outcomes of enzyme replacement therapy in untransplanted Hurler syndrome. Molecular Genetics and Metabolism Reports. 13: 64-68
van der Lee JH, Morton J, Adams HR, et al. (2017) Cognitive endpoints for therapy development for neuronopathic mucopolysaccharidoses: Results of a consensus procedure. Molecular Genetics and Metabolism
Nestrasil I, Shapiro E, Svatkova A, et al. (2017) Intrathecal enzyme replacement therapy reverses cognitive decline in mucopolysaccharidosis type I. American Journal of Medical Genetics. Part A. 173: 780-783
Nestrasil I, Shapiro E, Kovac V, et al. (2015) OP47 – 2274: Brain MRI patterns of disease progression in Sanfilippo syndrome type A (MPS IIIA) European Journal of Paediatric Neurology. 19
Abdelwahab M, Shapiro E, Nestrasil I. (2015) Abnormal behavioral features in Egyptian children with type III Gaucher disease Molecular Genetics and Metabolism. 114
Kovac V, Yund BD, Ahmed A, et al. (2014) The development of brain and neurocognitive function in typically developing children ages 4-7 years Molecular Genetics and Metabolism. 111
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