Baty K - Search Results

Year	Number of Results
2014	2
2015	3
2017	2
2018	1
2019	2
2020	5
2021	2
2024	0

1

Perioperative Bridging Anticoagulation in Patients with Atrial Fibrillation.

Douketis JD, Spyropoulos AC, Kaatz S, Becker RC, Caprini JA, Dunn AS, Garcia DA, Jacobson A, Jaffer AK, Kong DF, Schulman S, Turpie AG, Hasselblad V, Ortel TL; BRIDGE Investigators. Douketis JD, et al. N Engl J Med. 2015 Aug 27;373(9):823-33. doi: 10.1056/NEJMoa1501035. Epub 2015 Jun 22. N Engl J Med. 2015. PMID: 26095867 Free PMC article. Clinical Trial.

2

Engineering of monosized lipid-coated mesoporous silica nanoparticles for CRISPR delivery.

Noureddine A, Maestas-Olguin A, Saada EA, LaBauve AE, Agola JO, Baty KE, Howard T, Sabo JK, Espinoza CRS, Doudna JA, Schoeniger JS, Butler KS, Negrete OA, Brinker CJ, Serda RE. Noureddine A, et al. Among authors: baty ke. Acta Biomater. 2020 Sep 15;114:358-368. doi: 10.1016/j.actbio.2020.07.027. Epub 2020 Jul 21. Acta Biomater. 2020. PMID: 32702530

3

A novel, pathogenic dinucleotide deletion in the mitochondrial MT-TY gene causing myasthenia-like features.

Lim AZ, McMacken G, Rastelli F, Oláhová M, Baty K, Hopton S, Falkous G, Töpf A, Lochmüller H, Marini-Bettolo C, McFarland R, Taylor RW. Lim AZ, et al. Among authors: baty k. Neuromuscul Disord. 2020 Aug;30(8):661-668. doi: 10.1016/j.nmd.2020.06.008. Epub 2020 Jun 24. Neuromuscul Disord. 2020. PMID: 32684384 Free PMC article.

4

Progressive external ophthalmoplegia due to a recurrent de novo m.15990C>T MT-TP (mt-tRNA^Pro) gene variant.

Joshi PR, Baty K, Hopton S, Cordts I, Falkous G, Schoser B, Blakely EL, Taylor RW, Deschauer M. Joshi PR, et al. Among authors: baty k. Neuromuscul Disord. 2020 Apr;30(4):346-350. doi: 10.1016/j.nmd.2020.02.020. Epub 2020 Mar 5. Neuromuscul Disord. 2020. PMID: 32305257 Free article.

5

A novel MT-CO2 variant causing cerebellar ataxia and neuropathy: The role of muscle biopsy in diagnosis and defining pathogenicity.

Baty K, Farrugia ME, Hopton S, Falkous G, Schaefer AM, Stewart W, Willison HJ, Reilly MM, Blakely EL, Taylor RW, Ng YS. Baty K, et al. Neuromuscul Disord. 2021 Nov;31(11):1186-1193. doi: 10.1016/j.nmd.2021.05.014. Epub 2021 Jun 4. Neuromuscul Disord. 2021. PMID: 34325999 Free PMC article.

6

Corrigendum to "Engineering of monosized lipid-coated mesoporous silica nanoparticles for CRISPR delivery" Acta Biomaterialia (2020), 114, 358-368.

Noureddine A, Maestas-Olguin A, Saada EA, LaBauve AE, Agola JO, Baty KE, Howard T, Sabo JK, Espinoza CRS, Doudna JA, Schoeniger JS, Butler KS, Negrete OA, Brinker CJ, Serda RE. Noureddine A, et al. Among authors: baty ke. Acta Biomater. 2021 Feb;121:764. doi: 10.1016/j.actbio.2020.11.038. Epub 2020 Dec 9. Acta Biomater. 2021. PMID: 33309186 Free article. No abstract available.

7

Chronic Progressive External Ophthalmoplegia due to a Rare de novo m.12334G>A MT-TL2 Mitochondrial DNA Variant1.

O'Donnell L, Blakely EL, Baty K, Alexander M, Bogdanova-Mihaylova P, Craig J, Walsh R, Brett F, Taylor RW, Murphy SM. O'Donnell L, et al. Among authors: baty k. J Neuromuscul Dis. 2020;7(3):355-360. doi: 10.3233/JND-200486. J Neuromuscul Dis. 2020. PMID: 32310184

8

A Novel Pathogenic Variant in MT-CO2 Causes an Isolated Mitochondrial Complex IV Deficiency and Late-Onset Cerebellar Ataxia.

Zierz CM, Baty K, Blakely EL, Hopton S, Falkous G, Schaefer AM, Hadjivassiliou M, Sarrigiannis PG, Ng YS, Taylor RW. Zierz CM, et al. Among authors: baty k. J Clin Med. 2019 Jun 4;8(6):789. doi: 10.3390/jcm8060789. J Clin Med. 2019. PMID: 31167410 Free PMC article.

9

A novel pathogenic m.4412G>A MT-TM mitochondrial DNA variant associated with childhood-onset seizures, myopathy and bilateral basal ganglia changes.

Lim AZ, Blakely EL, Baty K, He L, Hopton S, Falkous G, McWilliam K, Cozens A, McFarland R, Taylor RW. Lim AZ, et al. Among authors: baty k. Mitochondrion. 2019 Jul;47:18-23. doi: 10.1016/j.mito.2019.04.007. Epub 2019 Apr 22. Mitochondrion. 2019. PMID: 31022467 Free PMC article. Clinical Trial.

10

Pathogenic mitochondrial mt-tRNA(Ala) variants are uniquely associated with isolated myopathy.

Lehmann D, Schubert K, Joshi PR, Hardy SA, Tuppen HA, Baty K, Blakely EL, Bamberg C, Zierz S, Deschauer M, Taylor RW. Lehmann D, et al. Among authors: baty k. Eur J Hum Genet. 2015 Dec;23(12):1735-8. doi: 10.1038/ejhg.2015.73. Epub 2015 Apr 15. Eur J Hum Genet. 2015. PMID: 25873012 Free PMC article.

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