Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

253 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Therapeutic Approaches for Duchenne Muscular Dystrophy: Old and New.
Mackenzie SJ, Nicolau S, Connolly AM, Mendell JR. Mackenzie SJ, et al. Among authors: nicolau s. Semin Pediatr Neurol. 2021 Apr;37:100877. doi: 10.1016/j.spen.2021.100877. Epub 2021 Feb 11. Semin Pediatr Neurol. 2021. PMID: 33892842 Review.
Immune-Mediated Megaconial Myopathy: A Novel Subtype of Autoimmune Myopathy.
Santilli AR, Ni O, Milone M, Selcen D, Mehrabyan AC, Seth A, Hsieh C, Raslan WF, Alkhalifah MM, Alenezi RM, Nicolau S, Soontrapa P, Liewluck T. Santilli AR, et al. Among authors: nicolau s. Neurology. 2024 Nov 26;103(10):e210001. doi: 10.1212/WNL.0000000000210001. Epub 2024 Oct 30. Neurology. 2024. PMID: 39475687
Spinal Muscular Atrophy.
Nicolau S, Waldrop MA, Connolly AM, Mendell JR. Nicolau S, et al. Semin Pediatr Neurol. 2021 Apr;37:100878. doi: 10.1016/j.spen.2021.100878. Epub 2021 Feb 11. Semin Pediatr Neurol. 2021. PMID: 33892848 Review.
Cardiac Involvement in Facioscapulohumeral Muscular Dystrophy (FSHD).
Ducharme-Smith A, Nicolau S, Chahal CAA, Ducharme-Smith K, Rehman S, Jaliparthy K, Khan N, Scott CG, St Louis EK, Liewluck T, Somers VK, Lin G, Brady PA, Milone M. Ducharme-Smith A, et al. Among authors: nicolau s. Front Neurol. 2021 May 24;12:668180. doi: 10.3389/fneur.2021.668180. eCollection 2021. Front Neurol. 2021. PMID: 34108930 Free PMC article.
A form of muscular dystrophy associated with pathogenic variants in JAG2.
Coppens S, Barnard AM, Puusepp S, Pajusalu S, Õunap K, Vargas-Franco D, Bruels CC, Donkervoort S, Pais L, Chao KR, Goodrich JK, England EM, Weisburd B, Ganesh VS, Gudmundsson S, O'Donnell-Luria A, Nigul M, Ilves P, Mohassel P, Siddique T, Milone M, Nicolau S, Maroofian R, Houlden H, Hanna MG, Quinlivan R, Beiraghi Toosi M, Ghayoor Karimiani E, Costagliola S, Deconinck N, Kadhim H, Macke E, Lanpher BC, Klee EW, Łusakowska A, Kostera-Pruszczyk A, Hahn A, Schrank B, Nishino I, Ogasawara M, El Sherif R, Stojkovic T, Nelson I, Bonne G, Cohen E, Boland-Augé A, Deleuze JF, Meng Y, Töpf A, Vilain C, Pacak CA, Rivera-Zengotita ML, Bönnemann CG, Straub V, Handford PA, Draper I, Walter GA, Kang PB. Coppens S, et al. Among authors: nicolau s. Am J Hum Genet. 2021 May 6;108(5):840-856. doi: 10.1016/j.ajhg.2021.03.020. Epub 2021 Apr 15. Am J Hum Genet. 2021. PMID: 33861953 Free PMC article.
253 results