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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1988 1
1993 2
1994 2
1995 1
1997 1
1999 1
2000 2
2001 2
2002 3
2003 3
2004 1
2005 2
2006 2
2007 2
2009 1
2011 1
2012 4
2013 3
2014 4
2015 3
2016 3
2017 2
2019 1
2021 1
2022 2
2023 1
2024 1

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44 results

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Page 1
Eteplirsen for the treatment of Duchenne muscular dystrophy.
Mendell JR, Rodino-Klapac LR, Sahenk Z, Roush K, Bird L, Lowes LP, Alfano L, Gomez AM, Lewis S, Kota J, Malik V, Shontz K, Walker CM, Flanigan KM, Corridore M, Kean JR, Allen HD, Shilling C, Melia KR, Sazani P, Saoud JB, Kaye EM; Eteplirsen Study Group. Mendell JR, et al. Ann Neurol. 2013 Nov;74(5):637-47. doi: 10.1002/ana.23982. Epub 2013 Sep 10. Ann Neurol. 2013. PMID: 23907995 Free article. Clinical Trial.
Neonatal hypotonia.
Sparks SE. Sparks SE. Clin Perinatol. 2015 Jun;42(2):363-71, ix. doi: 10.1016/j.clp.2015.02.008. Clin Perinatol. 2015. PMID: 26042909 Review.
Congenital muscular dystrophies.
Sparks SE, Escolar DM. Sparks SE, et al. Handb Clin Neurol. 2011;101:47-79. doi: 10.1016/B978-0-08-045031-5.00004-9. Handb Clin Neurol. 2011. PMID: 21496624 Review.
Congenital Disorders of N-Linked Glycosylation and Multiple Pathway Overview.
Sparks SE, Krasnewich DM. Sparks SE, et al. 2005 Aug 15 [updated 2017 Jan 12]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2005 Aug 15 [updated 2017 Jan 12]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301507 Free Books & Documents. Review.
Integrative spatiotemporal map of nucleocytoplasmic transport.
Raveh B, Eliasian R, Rashkovits S, Russel D, Hayama R, Sparks SE, Singh D, Lim R, Villa E, Rout MP, Cowburn D, Sali A. Raveh B, et al. Among authors: sparks se. bioRxiv [Preprint]. 2024 Jan 2:2023.12.31.573409. doi: 10.1101/2023.12.31.573409. bioRxiv. 2024. PMID: 38260487 Free PMC article. Preprint.
Congenital protein hypoglycosylation diseases.
Sparks SE. Sparks SE. Appl Clin Genet. 2012 Jul 5;5:43-54. doi: 10.2147/TACG.S18673. Print 2012. Appl Clin Genet. 2012. PMID: 23776380 Free PMC article.
Measurement Properties of 2 Novel PROs, the Pompe Disease Symptom Scale and Pompe Disease Impact Scale, in the COMET Study.
Dimachkie MM, Kishnani PS, Ivanescu C, Flore G, Gwaltney C, van der Beek NAME, Hamed A, An Haack K, Pollissard L, Baranowski E, Sparks SE, DasMahapatra P; for COMET Study Group. Dimachkie MM, et al. Among authors: sparks se. Neurol Clin Pract. 2023 Oct;13(5):e200181. doi: 10.1212/CPJ.0000000000200181. Epub 2023 Aug 8. Neurol Clin Pract. 2023. PMID: 37559825 Free PMC article.
Motor Responses in Pediatric Pompe Disease in the ADVANCE Participant Cohort.
Duong T, Kishnani PS, An Haack K, Foster MC, Gibson JB, Wilson C, Hahn SH, Hillman R, Kronn D, Leslie ND, Peña LDM, Sparks SE, Stockton DW, Tanpaiboon P, Day JW; Pompe ADVANCE Study Consortium. Duong T, et al. Among authors: sparks se. J Neuromuscul Dis. 2022;9(6):713-730. doi: 10.3233/JND-210784. J Neuromuscul Dis. 2022. PMID: 36214004 Free PMC article.
Cardiac responses in paediatric Pompe disease in the ADVANCE patient cohort.
Byrne BJ, Colan SD, Kishnani PS, Foster MC, Sparks SE, Gibson JB, An Haack K, Stockton DW, Peña LDM, Hahn SH, Johnson J, Tanpaiboon PX, Leslie ND, Kronn D, Hillman RE, Wang RY; Pompe ADVANCE Study Consortium. Byrne BJ, et al. Among authors: sparks se. Cardiol Young. 2022 Mar;32(3):364-373. doi: 10.1017/S1047951121002079. Epub 2021 Aug 23. Cardiol Young. 2022. PMID: 34420548 Clinical Trial.
44 results