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

Year Number of Results
1979 2
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1981 3
1982 2
1983 1
1986 1
1987 2
1993 1
1995 1
1997 1
2003 2
2007 1
2008 1
2010 1
2011 6
2012 7
2013 7
2014 12
2015 4
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2017 2
2018 6
2019 5
2020 7
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122 results

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Page 1
A randomized double-blind clinical trial on safety and efficacy of tauroursodeoxycholic acid (TUDCA) as add-on treatment in patients affected by amyotrophic lateral sclerosis (ALS): the statistical analysis plan of TUDCA-ALS trial.
Lombardo FL, Spila Alegiani S, Mayer F, Cipriani M, Lo Giudice M, Ludolph AC, McDermott CJ, Corcia P, Van Damme P, Van den Berg LH, Hardiman O, Nicolini G, Vanacore N, Dickie B, Albanese A, Puopolo M; TUDCA-ALS Study Group. Lombardo FL, et al. Trials. 2023 Dec 5;24(1):792. doi: 10.1186/s13063-023-07638-w. Trials. 2023. PMID: 38053196 Free PMC article. Clinical Trial.
Clinical trials in amyotrophic lateral sclerosis: a systematic review and perspective.
Wong C, Stavrou M, Elliott E, Gregory JM, Leigh N, Pinto AA, Williams TL, Chataway J, Swingler R, Parmar MKB, Stallard N, Weir CJ, Parker RA, Chaouch A, Hamdalla H, Ealing J, Gorrie G, Morrison I, Duncan C, Connelly P, Carod-Artal FJ, Davenport R, Reitboeck PG, Radunovic A, Srinivasan V, Preston J, Mehta AR, Leighton D, Glasmacher S, Beswick E, Williamson J, Stenson A, Weaver C, Newton J, Lyle D, Dakin R, Macleod M, Pal S, Chandran S. Wong C, et al. Among authors: chaouch a. Brain Commun. 2021 Oct 23;3(4):fcab242. doi: 10.1093/braincomms/fcab242. eCollection 2021. Brain Commun. 2021. PMID: 34901853 Free PMC article. Review.
The use of genetic testing in amyotrophic lateral sclerosis (ALS): a practical approach.
Chaouch A, Crook A, Douglas AGL, McDermott CJ, Al-Chalabi A, McNeill A, Bedford J, Howard J, MacLeod R. Chaouch A, et al. Amyotroph Lateral Scler Frontotemporal Degener. 2025 Aug 8:1-7. doi: 10.1080/21678421.2025.2539895. Online ahead of print. Amyotroph Lateral Scler Frontotemporal Degener. 2025. PMID: 40779613 Free article. Review.
Fibronectin is a serum biomarker for Duchenne muscular dystrophy.
Cynthia Martin F, Hiller M, Spitali P, Oonk S, Dalebout H, Palmblad M, Chaouch A, Guglieri M, Straub V, Lochmüller H, Niks EH, Verschuuren JJ, Aartsma-Rus A, Deelder AM, van der Burgt YE, 't Hoen PA. Cynthia Martin F, et al. Among authors: chaouch a. Proteomics Clin Appl. 2014 Apr;8(3-4):269-78. doi: 10.1002/prca.201300072. Epub 2014 Mar 11. Proteomics Clin Appl. 2014. PMID: 24458521
A recurrent homozygous LMNA missense variant p.Thr528Met causes atypical progeroid syndrome characterized by mandibuloacral dysostosis, severe muscular dystrophy, and skeletal deformities.
Saadi A, Navarro C, Ozalp O, Lourenco CM, Fayek R, Da Silva N, Chaouch A, Benahmed M, Kubisch C, Munnich A, Lévy N, Roll P, Pacha LA, Chaouch M, Lessel D, De Sandre-Giovannoli A. Saadi A, et al. Among authors: chaouch a. Am J Med Genet A. 2023 Sep;191(9):2274-2289. doi: 10.1002/ajmg.a.63335. Epub 2023 Jun 30. Am J Med Genet A. 2023. PMID: 37387251
[Physiology of nociception].
Besson JM, Guilbaud G, Abdelmoumene M, Chaouch A. Besson JM, et al. Among authors: chaouch a. J Physiol (Paris). 1982;78(1):7-107. J Physiol (Paris). 1982. PMID: 6290651 Review. French. No abstract available.
[An unusual etiology of acute pancreatitis].
Ouni M, Rokbani S, Chaouch A, Chahed H, Bouzidi H. Ouni M, et al. Among authors: chaouch a. Ann Biol Clin (Paris). 2023 Nov 29;81(5). doi: 10.1684/abc.2023.1844. Online ahead of print. Ann Biol Clin (Paris). 2023. PMID: 38018825 French.
122 results