Steven A. Moore - Search Results

Year	Number of Results
2002	8
2003	3
2004	5
2005	4
2006	5
2007	1
2008	7
2009	8
2010	4
2011	2
2012	7
2013	11
2014	10
2015	11
2016	3
2017	6
2018	9
2019	11
2020	6
2021	6
2022	8
2023	4
2024	0

1

Thirty-Year Follow-Up of Early Onset Amyotrophic Lateral Sclerosis with a Pathogenic Variant in SPTLC1.

Ajjarapu A, Feely SME, Shy ME, Trout C, Zuchner S, Moore SA, Mathews KD. Ajjarapu A, et al. Among authors: moore sa. Case Rep Neurol. 2023 Jun 12;15(1):146-152. doi: 10.1159/000530974. eCollection 2023 Jan-Dec. Case Rep Neurol. 2023. PMID: 37497262 Free PMC article.

2

A De Novo Sequence Variant in Barrier-to-Autointegration Factor Is Associated with Dominant Motor Neuronopathy.

Marcelot A, Rodriguez-Tirado F, Cuniasse P, Joiner ML, Miron S, Soshnev AA, Fang M, Pufall MA, Mathews KD, Moore SA, Zinn-Justin S, Geyer PK. Marcelot A, et al. Among authors: moore sa. Cells. 2023 Mar 9;12(6):847. doi: 10.3390/cells12060847. Cells. 2023. PMID: 36980188 Free PMC article.

3

DUX4 double whammy: The transcription factor that causes a rare muscular dystrophy also kills the precursors of the human nose.

Inoue K, Bostan H, Browne MR, Bevis OF, Bortner CD, Moore SA, Stence AA, Martin NP, Chen SH, Burkholder AB, Li JL, Shaw ND. Inoue K, et al. Among authors: moore sa. Sci Adv. 2023 Feb 17;9(7):eabq7744. doi: 10.1126/sciadv.abq7744. Epub 2023 Feb 17. Sci Adv. 2023. PMID: 36800423 Free PMC article.

4

Ventriculus terminalis cyst in an infant: a case report.

Menezes AH, Sato Y, Dlouhy BJ, Jones KA, Moore SA. Menezes AH, et al. Among authors: moore sa. J Med Case Rep. 2023 Jan 23;17(1):22. doi: 10.1186/s13256-023-03759-7. J Med Case Rep. 2023. PMID: 36683067 Free PMC article.

5

Development and Validation of a Western Blot Method to Quantify Mini-Dystrophin in Human Skeletal Muscle Biopsies.

Soderstrom CI, Larsen J, Owen C, Gifondorwa D, Beidler D, Yong FH, Conrad P, Neubert H, Moore SA, Hassanein M. Soderstrom CI, et al. Among authors: moore sa. AAPS J. 2022 Dec 20;25(1):12. doi: 10.1208/s12248-022-00776-0. AAPS J. 2022. PMID: 36539515 Free PMC article.

6

Miyoshi Muscular Dystrophy Due to Novel Splice Site Variants in DYSF Gene.

Bryant G, Moore SA, Nix JS, Rice G, Gokden M, Veerapandiyan A. Bryant G, et al. Among authors: moore sa. Child Neurol Open. 2022 Nov 16;9:2329048X221140298. doi: 10.1177/2329048X221140298. eCollection 2022 Jan-Dec. Child Neurol Open. 2022. PMID: 36419651 Free PMC article.

7

Sphingosine Phosphate Lyase Is Upregulated in Duchenne Muscular Dystrophy, and Its Inhibition Early in Life Attenuates Inflammation and Dystrophy in Mdx Mice.

De la Garza-Rodea AS, Moore SA, Zamora-Pineda J, Hoffman EP, Mistry K, Kumar A, Strober JB, Zhao P, Suh JH, Saba JD. De la Garza-Rodea AS, et al. Among authors: moore sa. Int J Mol Sci. 2022 Jul 8;23(14):7579. doi: 10.3390/ijms23147579. Int J Mol Sci. 2022. PMID: 35886926 Free PMC article.

8

Limb-Girdle Muscular Dystrophy R9 due to a Novel Complex Insertion/Duplication Variant in FKRP Gene.

Willis E, Moore SA, Cox MO, Stefans V, Aravindhan A, Gokden M, Veerapandiyan A. Willis E, et al. Among authors: moore sa. Child Neurol Open. 2022 Apr 28;9:2329048X221097518. doi: 10.1177/2329048X221097518. eCollection 2022 Jan-Dec. Child Neurol Open. 2022. PMID: 35557983 Free PMC article.

9

Intron mutations and early transcription termination in Duchenne and Becker muscular dystrophy.

Waldrop MA, Moore SA, Mathews KD, Darbro BW, Medne L, Finkel R, Connolly AM, Crawford TO, Drachman D, Wein N, Habib AA, Krzesniak-Swinarska MA, Zaidman CM, Collins JJ, Jokela M, Udd B, Day JW, Ortiz-Guerrero G, Statland J, Butterfield RJ, Dunn DM, Weiss RB, Flanigan KM. Waldrop MA, et al. Among authors: moore sa. Hum Mutat. 2022 Apr;43(4):511-528. doi: 10.1002/humu.24343. Epub 2022 Mar 7. Hum Mutat. 2022. PMID: 35165973 Free PMC article.

10

The inflammatory pathology of dysferlinopathy is distinct from calpainopathy, Becker muscular dystrophy, and inflammatory myopathies.

Becker N, Moore SA, Jones KA. Becker N, et al. Among authors: moore sa. Acta Neuropathol Commun. 2022 Feb 8;10(1):17. doi: 10.1186/s40478-022-01320-z. Acta Neuropathol Commun. 2022. PMID: 35135626 Free PMC article.

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