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Improving the likelihood of neurology patients being examined using patient feedback.
Appleton JP, Ilinca A, Lindgren A, Puschmann A, Hbahbih M, A Siddiqui K, de Silva R, Jones M, Butterworth R, Willmot M, Hayton T, Lunn M, Nicholl D. Appleton JP, et al. Among authors: ilinca a, a siddiqui k. BMJ Qual Improv Rep. 2015 Nov 5;4(1):u209610.w4063. doi: 10.1136/bmjquality.u209610.w4063. eCollection 2015. BMJ Qual Improv Rep. 2015. PMID: 26734445 Free PMC article.
New generation genetic testing entering the clinic.
Gorcenco S, Ilinca A, Almasoudi W, Kafantari E, Lindgren AG, Puschmann A. Gorcenco S, et al. Among authors: ilinca a. Parkinsonism Relat Disord. 2020 Apr;73:72-84. doi: 10.1016/j.parkreldis.2020.02.015. Epub 2020 Mar 2. Parkinsonism Relat Disord. 2020. PMID: 32273229 Free article. Review.
Throat-Clearing Vocalizations in Primary Brain Calcification Syndromes.
Mulroy E, Ilinca A, Gonzalez-Robles C, Magrinelli F, Puschmann A, Bhatia KP. Mulroy E, et al. Among authors: ilinca a. Mov Disord Clin Pract. 2021 Mar 13;8(4):627-630. doi: 10.1002/mdc3.13175. eCollection 2021 May. Mov Disord Clin Pract. 2021. PMID: 33981802 Free PMC article. No abstract available.
Exonic trinucleotide repeat expansions in ZFHX3 cause spinocerebellar ataxia type 4: A poly-glycine disease.
Wallenius J, Kafantari E, Jhaveri E, Gorcenco S, Ameur A, Karremo C, Dobloug S, Karrman K, de Koning T, Ilinca A, Landqvist Waldö M, Arvidsson A, Persson S, Englund E, Ehrencrona H, Puschmann A. Wallenius J, et al. Among authors: ilinca a. Am J Hum Genet. 2024 Jan 4;111(1):82-95. doi: 10.1016/j.ajhg.2023.11.008. Epub 2023 Nov 29. Am J Hum Genet. 2024. PMID: 38035881 Free PMC article.
A stroke gene panel for whole-exome sequencing.
Ilinca A, Samuelsson S, Piccinelli P, Soller M, Kristoffersson U, Lindgren AG. Ilinca A, et al. Eur J Hum Genet. 2019 Feb;27(2):317-324. doi: 10.1038/s41431-018-0274-4. Epub 2018 Oct 24. Eur J Hum Genet. 2019. PMID: 30356112 Free PMC article.
32 results