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

Year Number of Results
1977 1
1986 1
1987 1
1988 4
1989 1
1990 1
1991 3
1992 3
1993 4
1994 4
1995 2
1997 2
2003 2
2004 2
2005 3
2007 6
2008 5
2009 1
2010 1
2011 1
2013 1
2015 1
2020 1
2021 3
2022 3
2024 1

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56 results

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Page 1
Intrathecal Gene Therapy for Giant Axonal Neuropathy.
Bharucha-Goebel DX, Todd JJ, Saade D, Norato G, Jain M, Lehky T, Bailey RM, Chichester JA, Calcedo R, Armao D, Foley AR, Mohassel P, Tesfaye E, Carlin BP, Seremula B, Waite M, Zein WM, Huryn LA, Crawford TO, Sumner CJ, Hoke A, Heiss JD, Charnas L, Hooper JE, Bouldin TW, Kang EM, Rybin D, Gray SJ, Bönnemann CG; GAN Trial Team. Bharucha-Goebel DX, et al. Among authors: charnas l. N Engl J Med. 2024 Mar 21;390(12):1092-1104. doi: 10.1056/NEJMoa2307952. N Engl J Med. 2024. PMID: 38507752
Current state of cardiac troponin testing in Duchenne muscular dystrophy cardiomyopathy: review and recommendations from the Parent Project Muscular Dystrophy expert panel.
Spurney CF, Ascheim D, Charnas L, Cripe L, Hor K, King N, Kinnett K, McNally EM, Sauer JM, Sweeney L, Villa C, Markham LW. Spurney CF, et al. Among authors: charnas l. Open Heart. 2021 Mar;8(1):e001592. doi: 10.1136/openhrt-2021-001592. Open Heart. 2021. PMID: 33762424 Free PMC article. Review.
Hematopoietic cell therapy for metabolic disease.
Orchard PJ, Blazar BR, Wagner J, Charnas L, Krivit W, Tolar J. Orchard PJ, et al. Among authors: charnas l. J Pediatr. 2007 Oct;151(4):340-6. doi: 10.1016/j.jpeds.2007.04.054. J Pediatr. 2007. PMID: 17889065 Review. No abstract available.
The oculocerebrorenal syndrome of Lowe.
Charnas LR, Gahl WA. Charnas LR, et al. Adv Pediatr. 1991;38:75-107. Adv Pediatr. 1991. PMID: 1927708 Review. No abstract available.
Neurologic profile in osteogenesis imperfecta.
Charnas LR, Marini JC. Charnas LR, et al. Connect Tissue Res. 1995;31(4):S23-6. doi: 10.3109/03008209509116828. Connect Tissue Res. 1995. PMID: 15612376
Novel approaches to analysis of the North Star Ambulatory Assessment (NSAA) in Duchenne muscular dystrophy (DMD): Observations from a phase 2 trial.
Muntoni F, Guglieri M, Mah JK, Wagner KR, Brandsema JF, Butterfield RJ, McDonald CM, Mayhew AG, Palmer JP, Marraffino S, Charnas L, Mercuri E. Muntoni F, et al. Among authors: charnas l. PLoS One. 2022 Aug 23;17(8):e0272858. doi: 10.1371/journal.pone.0272858. eCollection 2022. PLoS One. 2022. PMID: 35998119 Free PMC article. Clinical Trial.
Quantitative magnetic resonance imaging measures as biomarkers of disease progression in boys with Duchenne muscular dystrophy: a phase 2 trial of domagrozumab.
Sherlock SP, Palmer J, Wagner KR, Abdel-Hamid HZ, Bertini E, Tian C, Mah JK, Kostera-Pruszczyk A, Muntoni F, Guglieri M, Brandsema JF, Mercuri E, Butterfield RJ, McDonald CM, Charnas L, Marraffino S. Sherlock SP, et al. Among authors: charnas l. J Neurol. 2022 Aug;269(8):4421-4435. doi: 10.1007/s00415-022-11084-0. Epub 2022 Apr 8. J Neurol. 2022. PMID: 35396602 Free PMC article. Clinical Trial.
56 results