King KE - Search Results

1

Issues of COVID-19-related distance learning for children with neuronopathic mucopolysaccharidoses.

Eisengart JB, Esler AN, Ellinwood NM, Hudock RL, King KE, Klein TL, Lee C, Morton J, Stephens K, Ziegler R, O'Neill C. Eisengart JB, et al. Among authors: king ke. Mol Genet Metab. 2021 Sep-Oct;134(1-2):68-76. doi: 10.1016/j.ymgme.2021.06.012. Epub 2021 Jul 6. Mol Genet Metab. 2021. PMID: 34247933 Free PMC article.

2

The Neurobehavioral Phenotype in Mucopolysaccharidosis Type IIIB: an Exploratory Study.

Shapiro E, King K, Ahmed A, Rudser K, Rumsey R, Yund B, Delaney K, Nestrasil I, Whitley C, Potegal M. Shapiro E, et al. Mol Genet Metab Rep. 2016 Mar 1;6:41-47. doi: 10.1016/j.ymgmr.2016.01.003. Mol Genet Metab Rep. 2016. PMID: 26918231 Free PMC article.

3

Association of somatic burden of disease with age and neuropsychological measures in attenuated mucopolysaccharidosis types I, II and VI.

Ahmed A, Shapiro E, Rudser K, Kunin-Batson A, King K, Whitley CB. Ahmed A, et al. Mol Genet Metab Rep. 2016 Apr 1;7:27-31. doi: 10.1016/j.ymgmr.2016.03.006. eCollection 2016 Jun. Mol Genet Metab Rep. 2016. PMID: 27114913 Free PMC article.

4

A longitudinal study of emotional adjustment, quality of life and adaptive function in attenuated MPS II.

Shapiro EG, Rudser K, Ahmed A, Steiner RD, Delaney KA, Yund B, King K, Kunin-Batson A, Eisengart J, Whitley CB. Shapiro EG, et al. Mol Genet Metab Rep. 2016 Apr 1;7:32-9. doi: 10.1016/j.ymgmr.2016.03.005. eCollection 2016 Jun. Mol Genet Metab Rep. 2016. PMID: 27114914 Free PMC article.

5

Infantile gangliosidoses: Mapping a timeline of clinical changes.

Jarnes Utz JR, Kim S, King K, Ziegler R, Schema L, Redtree ES, Whitley CB. Jarnes Utz JR, et al. Mol Genet Metab. 2017 Jun;121(2):170-179. doi: 10.1016/j.ymgme.2017.04.011. Epub 2017 Apr 29. Mol Genet Metab. 2017. PMID: 28476546 Free PMC article. Clinical Trial.

6

Attention and corpus callosum volumes in individuals with mucopolysaccharidosis type I.

King KE, Rudser KD, Nestrasil I, Kovac V, Delaney KA, Wozniak JR, Mueller BA, Lim KO, Eisengart JB, Mamak EG, Raiman J, Ali N, Cagle S, Harmatz P, Whitley CB, Shapiro EG. King KE, et al. Neurology. 2019 May 14;92(20):e2321-e2328. doi: 10.1212/WNL.0000000000007496. Epub 2019 Apr 12. Neurology. 2019. PMID: 30979856 Free PMC article.

7

Intrathecal enzyme replacement for Hurler syndrome: biomarker association with neurocognitive outcomes.

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. Eisengart JB, et al. Among authors: king ke. Genet Med. 2019 Nov;21(11):2552-2560. doi: 10.1038/s41436-019-0522-1. Epub 2019 Apr 25. Genet Med. 2019. PMID: 31019279 Free PMC article. Clinical Trial.

8

A longitudinal study of neurocognition and behavior in patients with Hurler-Scheie syndrome heterozygous for the L238Q mutation.

Ahmed A, Ou L, Rudser K, Shapiro E, Eisengart JB, King K, Chen A, Dickson P, Whitley CB. Ahmed A, et al. Mol Genet Metab Rep. 2019 Jun 27;20:100484. doi: 10.1016/j.ymgmr.2019.100484. eCollection 2019 Sep. Mol Genet Metab Rep. 2019. PMID: 31304092 Free PMC article.

9

Intrathecal enzyme replacement for cognitive decline in mucopolysaccharidosis type I, a randomized, open-label, controlled pilot study.

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. Chen AH, et al. Among authors: king ke. Mol Genet Metab. 2020 Feb;129(2):80-90. doi: 10.1016/j.ymgme.2019.11.007. Epub 2019 Nov 30. Mol Genet Metab. 2020. PMID: 31839529 Free PMC article. Clinical Trial.

10

The nature and impact of neurobehavioral symptoms in neuronopathic Hunter syndrome.

Eisengart JB, King KE, Shapiro EG, Whitley CB, Muenzer J. Eisengart JB, et al. Among authors: king ke. Mol Genet Metab Rep. 2019 Dec 20;22:100549. doi: 10.1016/j.ymgmr.2019.100549. eCollection 2020 Mar. Mol Genet Metab Rep. 2019. PMID: 31890590 Free PMC article.

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