Ryan E - Search Results

1

Clinical evaluation of sibling pairs with gaucher disease discordant for parkinsonism.

Lopez G, Steward A, Ryan E, Groden C, Wiggs E, Segalà L, Monestime GM, Tayebi N, Sidransky E. Lopez G, et al. Among authors: ryan e. Mov Disord. 2020 Feb;35(2):359-365. doi: 10.1002/mds.27916. Epub 2019 Nov 30. Mov Disord. 2020. PMID: 31785030

2

Recent advances in the diagnosis and management of Gaucher disease.

Gary SE, Ryan E, Steward AM, Sidransky E. Gary SE, et al. Among authors: ryan e. Expert Rev Endocrinol Metab. 2018 Mar;13(2):107-118. doi: 10.1080/17446651.2018.1445524. Epub 2018 Mar 12. Expert Rev Endocrinol Metab. 2018. PMID: 30058864 Free PMC article.

3

GBA1-associated parkinsonism: new insights and therapeutic opportunities.

Ryan E, Seehra G, Sharma P, Sidransky E. Ryan E, et al. Curr Opin Neurol. 2019 Aug;32(4):589-596. doi: 10.1097/WCO.0000000000000715. Curr Opin Neurol. 2019. PMID: 31188151 Review.

4

Five-parameter evaluation of dysphagia: A novel prognostic scale for assessing neurological decline in Gaucher disease type 2.

Seehra G, Solomon B, Ryan E, Steward AM, Roshan Lal T, Tanima Y, Lopez G, Sidransky E. Seehra G, et al. Among authors: ryan e. Mol Genet Metab. 2019 Jul;127(3):191-199. doi: 10.1016/j.ymgme.2019.06.002. Epub 2019 Jun 8. Mol Genet Metab. 2019. PMID: 31256856 Free PMC article.

5

Mutations, modifiers and epigenetics in Gaucher disease: Blurred boundaries between simple and complex disorders.

Ryan E, Seehra GK, Sidransky E. Ryan E, et al. Mol Genet Metab. 2019 Sep-Oct;128(1-2):10-13. doi: 10.1016/j.ymgme.2019.08.006. Epub 2019 Aug 20. Mol Genet Metab. 2019. PMID: 31474515 No abstract available.

6

Variation in cognitive function over time in Gaucher disease type 3.

Steward AM, Wiggs E, Lindstrom T, Ukwuani S, Ryan E, Tayebi N, Roshan Lal T, Lopez G, Schiffmann R, Sidransky E. Steward AM, et al. Among authors: ryan e. Neurology. 2019 Dec 10;93(24):e2272-e2283. doi: 10.1212/WNL.0000000000008618. Epub 2019 Nov 12. Neurology. 2019. PMID: 31719137 Free PMC article.

7

The natural history of type 2 Gaucher disease in the 21st century: A retrospective study.

Roshan Lal T, Seehra GK, Steward AM, Poffenberger CN, Ryan E, Tayebi N, Lopez G, Sidransky E. Roshan Lal T, et al. Among authors: ryan e. Neurology. 2020 Oct 13;95(15):e2119-e2130. doi: 10.1212/WNL.0000000000010605. Epub 2020 Aug 6. Neurology. 2020. PMID: 32764102 Free PMC article.

8

Parkinsonism in Patients with Neuronopathic (Type 3) Gaucher Disease: A Case Series.

Ryan E, Amato D, MacKenzie JJ, Sidransky E, Lopez G. Ryan E, et al. Mov Disord Clin Pract. 2020 Aug 17;7(7):834-837. doi: 10.1002/mdc3.13031. eCollection 2020 Oct. Mov Disord Clin Pract. 2020. PMID: 33043079 Free PMC article.

9

EEG abnormalities in patients with chronic neuronopathic Gaucher disease: A retrospective review.

Poffenberger CN, Inati S, Tayebi N, Stubblefield BK, Ryan E, Schiffmann R, Sidransky E, Lopez G. Poffenberger CN, et al. Among authors: ryan e. Mol Genet Metab. 2020 Nov;131(3):358-363. doi: 10.1016/j.ymgme.2020.10.010. Epub 2020 Oct 20. Mol Genet Metab. 2020. PMID: 33183916 Free PMC article.

10

Gaucher Disease and Heart Failure of Unknown Origin.

Ryan E, Nguyen ML, Lopez G, Mitchell K, Lowery M, Singh S, Cholewa A, Bandettini WP, Moore C, Sidransky E. Ryan E, et al. Am J Med. 2021 Jun;134(6):745-748. doi: 10.1016/j.amjmed.2020.11.020. Epub 2021 Jan 14. Am J Med. 2021. PMID: 33359772 No abstract available.

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