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

Year Number of Results
1980 4
1981 1
1982 1
1983 1
1984 3
1985 3
1986 6
1987 3
1988 1
1989 3
1995 2
1996 1
1999 2
2000 1
2001 3
2004 2
2005 1
2007 2
2009 4
2010 2
2011 5
2012 4
2013 3
2014 1
2015 1
2016 1
2017 2
2018 2
2019 2
2020 2
2021 1
2022 2
2024 0

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68 results

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Page 1
Consensus treatment recommendations for late-onset Pompe disease.
Cupler EJ, Berger KI, Leshner RT, Wolfe GI, Han JJ, Barohn RJ, Kissel JT; AANEM Consensus Committee on Late-onset Pompe Disease. Cupler EJ, et al. Among authors: leshner rt. Muscle Nerve. 2012 Mar;45(3):319-33. doi: 10.1002/mus.22329. Epub 2011 Dec 15. Muscle Nerve. 2012. PMID: 22173792 Free PMC article. Review.
Efficacy and Safety of Vamorolone in Duchenne Muscular Dystrophy: A 30-Month Nonrandomized Controlled Open-Label Extension Trial.
Mah JK, Clemens PR, Guglieri M, Smith EC, Finkel RS, Tulinius M, Nevo Y, Ryan MM, Webster R, Castro D, Kuntz NL, McDonald CM, Damsker JM, Schwartz BD, Mengle-Gaw LJ, Jackowski S, Stimpson G, Ridout DA, Ayyar-Gupta V, Baranello G, Manzur AY, Muntoni F, Gordish-Dressman H, Leinonen M, Ward LM, Hoffman EP, Dang UJ; NorthStar UK Network and CINRG DNHS Investigators. Mah JK, et al. JAMA Netw Open. 2022 Jan 4;5(1):e2144178. doi: 10.1001/jamanetworkopen.2021.44178. JAMA Netw Open. 2022. PMID: 35076703 Free PMC article. Clinical Trial.
Acute pediatric rhabdomyolysis.
Watemberg N, Leshner RL, Armstrong BA, Lerman-Sagie T. Watemberg N, et al. Among authors: leshner rl. J Child Neurol. 2000 Apr;15(4):222-7. doi: 10.1177/088307380001500404. J Child Neurol. 2000. PMID: 10805187
Intractable hiccups. (singultus).
Nathan MD, Leshner RT, Keller AP Jr. Nathan MD, et al. Among authors: leshner rt. Laryngoscope. 1980 Oct;90(10 Pt 1):1612-8. Laryngoscope. 1980. PMID: 7421372
Carpal tunnel syndrome.
Owen DS Jr, Leshner RT, McDowell CL. Owen DS Jr, et al. Among authors: leshner rt. Va Med. 1987 Nov;114(11):670-3. Va Med. 1987. PMID: 3424930 No abstract available.
TCTEX1D1 is a genetic modifier of disease progression in Duchenne muscular dystrophy.
Spitali P, Zaharieva I, Bohringer S, Hiller M, Chaouch A, Roos A, Scotton C, Claustres M, Bello L, McDonald CM, Hoffman EP; CINRG Investigators; Koeks Z, Eka Suchiman H, Cirak S, Scoto M, Reza M, 't Hoen PAC, Niks EH, Tuffery-Giraud S, Lochmüller H, Ferlini A, Muntoni F, Aartsma-Rus A. Spitali P, et al. Eur J Hum Genet. 2020 Jun;28(6):815-825. doi: 10.1038/s41431-019-0563-6. Epub 2020 Jan 2. Eur J Hum Genet. 2020. PMID: 31896777 Free PMC article.
Development of a model-based clinical trial simulation platform to optimize the design of clinical trials for Duchenne muscular dystrophy.
Lingineni K, Aggarwal V, Morales JF, Conrado DJ, Corey D, Vong C, Burton J, Larkindale J, Romero K, Schmidt S, Kim S; Cooperative International Neuromuscular Research Group investigators and Duchenne Regulatory Science Consortium members. Lingineni K, et al. CPT Pharmacometrics Syst Pharmacol. 2022 Mar;11(3):318-332. doi: 10.1002/psp4.12753. Epub 2022 Jan 3. CPT Pharmacometrics Syst Pharmacol. 2022. PMID: 34877803 Free PMC article.
68 results