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

Year Number of Results
1998 1
1999 3
2000 1
2001 1
2005 1
2006 1
2008 2
2009 2
2017 1
2020 2
2021 2
2023 1
2024 0

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15 results

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Page 1
Microcircuit failure in STXBP1 encephalopathy leads to hyperexcitability.
Dos Santos AB, Larsen SD, Guo L, Barbagallo P, Montalant A, Verhage M, Sørensen JB, Perrier JF. Dos Santos AB, et al. Among authors: barbagallo p. Cell Rep Med. 2023 Dec 19;4(12):101308. doi: 10.1016/j.xcrm.2023.101308. Epub 2023 Dec 11. Cell Rep Med. 2023. PMID: 38086378 Free PMC article.
Isolated homozygous R217X OPTN mutation causes knock-out of functional C-terminal optineurin domains and associated oligodendrogliopathy-dominant ALS-TDP.
Nolan M, Barbagallo P, Turner MR, Keogh MJ, Chinnery PF, Talbot K, Ansorge O. Nolan M, et al. Among authors: barbagallo p. J Neurol Neurosurg Psychiatry. 2021 Sep;92(9):1022-1024. doi: 10.1136/jnnp-2020-325803. Epub 2021 Mar 16. J Neurol Neurosurg Psychiatry. 2021. PMID: 33727253 Free PMC article. No abstract available.
Impairment of Mitochondrial Calcium Buffering Links Mutations in C9ORF72 and TARDBP in iPS-Derived Motor Neurons from Patients with ALS/FTD.
Dafinca R, Barbagallo P, Farrimond L, Candalija A, Scaber J, Ababneh NA, Sathyaprakash C, Vowles J, Cowley SA, Talbot K. Dafinca R, et al. Among authors: barbagallo p. Stem Cell Reports. 2020 May 12;14(5):892-908. doi: 10.1016/j.stemcr.2020.03.023. Epub 2020 Apr 23. Stem Cell Reports. 2020. PMID: 32330447 Free PMC article.
Thyroid hormones and lipid metabolism in a group of patients over seventy.
Maugeri D, Santangelo A, Barbagallo P, Bonanno MR, Malaguarnera M, Rizza I, Speciale S, Tomarchio M, Curasì MP, Panebianco P. Maugeri D, et al. Among authors: barbagallo p. Eur Rev Med Pharmacol Sci. 1999 Sep-Oct;3(5):211-6. Eur Rev Med Pharmacol Sci. 1999. PMID: 11075619 Clinical Trial.
Correction of amyotrophic lateral sclerosis related phenotypes in induced pluripotent stem cell-derived motor neurons carrying a hexanucleotide expansion mutation in C9orf72 by CRISPR/Cas9 genome editing using homology-directed repair.
Ababneh NA, Scaber J, Flynn R, Douglas A, Barbagallo P, Candalija A, Turner MR, Sims D, Dafinca R, Cowley SA, Talbot K. Ababneh NA, et al. Among authors: barbagallo p. Hum Mol Genet. 2020 Aug 3;29(13):2200-2217. doi: 10.1093/hmg/ddaa106. Hum Mol Genet. 2020. PMID: 32504093 Free PMC article.
C9orf72 and RAB7L1 regulate vesicle trafficking in amyotrophic lateral sclerosis and frontotemporal dementia.
Aoki Y, Manzano R, Lee Y, Dafinca R, Aoki M, Douglas AGL, Varela MA, Sathyaprakash C, Scaber J, Barbagallo P, Vader P, Mäger I, Ezzat K, Turner MR, Ito N, Gasco S, Ohbayashi N, El Andaloussi S, Takeda S, Fukuda M, Talbot K, Wood MJA. Aoki Y, et al. Among authors: barbagallo p. Brain. 2017 Apr 1;140(4):887-897. doi: 10.1093/brain/awx024. Brain. 2017. PMID: 28334866
15 results