Bastian AE - Search Results

1

Novel FHL1 mutation variant identified in a patient with nonobstructive hypertrophic cardiomyopathy and myopathy - a case report.

Giucă A, Mitu C, Popescu BO, Bastian AE, Capşa R, Mursă A, Rădoi V, Popescu BA, Jurcuţ R. Giucă A, et al. Among authors: bastian ae. BMC Med Genet. 2020 Sep 29;21(1):188. doi: 10.1186/s12881-020-01131-w. BMC Med Genet. 2020. PMID: 32993534 Free PMC article.

2

Discovery of a new mutation in the desmin gene in a young patient with cardiomyopathy and muscular weakness.

JurcuŢ RO, Bastian AE, Militaru S, Popa A, Manole E, Popescu BA, Tallila J, Popescu BO, Ginghină CD. JurcuŢ RO, et al. Among authors: bastian ae. Rom J Morphol Embryol. 2017;58(1):225-230. Rom J Morphol Embryol. 2017. PMID: 28523323 Free article.

3

Myokines as Possible Therapeutic Targets in Cancer Cachexia.

Manole E, Ceafalan LC, Popescu BO, Dumitru C, Bastian AE. Manole E, et al. Among authors: bastian ae. J Immunol Res. 2018 Oct 22;2018:8260742. doi: 10.1155/2018/8260742. eCollection 2018. J Immunol Res. 2018. PMID: 30426026 Free PMC article. Review.

4

Muscle involvement with pseudohypertrophy in systemic light chain amyloidosis: Case report.

Draghici M, Jercan A, Badelita SN, Irimia RM, Bastian AE, Dobrea C, Popescu M, Coriu D. Draghici M, et al. Among authors: bastian ae. Medicine (Baltimore). 2021 Dec 23;100(51):e28267. doi: 10.1097/MD.0000000000028267. Medicine (Baltimore). 2021. PMID: 34941106 Free PMC article.

5

A rare case of mitochondriopathy with autosomal dominant progressive external ophthalmoplegia diagnosed through skeletal muscle biopsy.

Bastian AE, Jugulete G, Manole E, Oprişan LA. Bastian AE, et al. Rom J Morphol Embryol. 2019;60(1):273-279. Rom J Morphol Embryol. 2019. PMID: 31263856 Free article.

6

Dermatomyositis and polyradiculoneuritis, a rare association.

Cojocaru IM, Socoliuc G, Sapira V, Bastian A, Alexianu M, Moldovan M. Cojocaru IM, et al. Rom J Intern Med. 2011;49(3):217-21. Rom J Intern Med. 2011. PMID: 22471104

7

Identification of GAA variants through whole exome sequencing targeted to a cohort of 606 patients with unexplained limb-girdle muscle weakness.

Johnson K, Töpf A, Bertoli M, Phillips L, Claeys KG, Stojanovic VR, Perić S, Hahn A, Maddison P, Akay E, Bastian AE, Łusakowska A, Kostera-Pruszczyk A, Lek M, Xu L, MacArthur DG, Straub V. Johnson K, et al. Among authors: bastian ae. Orphanet J Rare Dis. 2017 Nov 17;12(1):173. doi: 10.1186/s13023-017-0722-1. Orphanet J Rare Dis. 2017. PMID: 29149851 Free PMC article.

8

Sequential targeted exome sequencing of 1001 patients affected by unexplained limb-girdle weakness.

Töpf A, Johnson K, Bates A, Phillips L, Chao KR, England EM, Laricchia KM, Mullen T, Valkanas E, Xu L, Bertoli M, Blain A, Casasús AB, Duff J, Mroczek M, Specht S, Lek M, Ensini M, MacArthur DG; MYO-SEQ consortium; Straub V. Töpf A, et al. Genet Med. 2020 Sep;22(9):1478-1488. doi: 10.1038/s41436-020-0840-3. Epub 2020 Jun 11. Genet Med. 2020. PMID: 32528171 Free PMC article.

9

Role of Myokines in Myositis Pathogenesis and Their Potential to be New Therapeutic Targets in Idiopathic Inflammatory Myopathies.

Mageriu V, Manole E, Bastian AE, Staniceanu F. Mageriu V, et al. Among authors: bastian ae. J Immunol Res. 2020 Jul 24;2020:9079083. doi: 10.1155/2020/9079083. eCollection 2020. J Immunol Res. 2020. PMID: 32775472 Free PMC article. Review.

10

Histological findings in skeletal muscle of SARS-CoV2 infected patient.

Mageriu V, Zurac S, Bastian A, Staniceanu F, Manole E. Mageriu V, et al. J Immunoassay Immunochem. 2020 Nov 1;41(6):1000-1009. doi: 10.1080/15321819.2020.1863819. Epub 2020 Dec 22. J Immunoassay Immunochem. 2020. PMID: 33353460

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