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Rare Disease Day - at a glance.
Plaiasu V, Nanu M, Matei D. Plaiasu V, et al. Maedica (Bucur). 2010 Jan;5(1):65-6. Maedica (Bucur). 2010. PMID: 21977122 Free PMC article. No abstract available.
Update in genetics.
Plaiasu V. Plaiasu V. Maedica (Bucur). 2011 Jan;6(1):70. Maedica (Bucur). 2011. PMID: 21977200 Free PMC article. No abstract available.
X-Linked agammaglobulinemia in a child with Klinefelter's syndrome.
Cochino AV, Janda A, Ravcukova B, Plaiasu V, Ochiana D, Gherghina I, Freiberger T. Cochino AV, et al. Among authors: plaiasu v. J Clin Immunol. 2014 Feb;34(2):142-5. doi: 10.1007/s10875-013-9986-y. Epub 2014 Jan 30. J Clin Immunol. 2014. PMID: 24477949
The Role of Video-EEG Monitoring in Lesch-Nyhan Syndrome.
Roza E, Baloi AD, Plaiasu V, Teleanu RI. Roza E, et al. Among authors: plaiasu v. Maedica (Bucur). 2023 Jun;18(2):348-351. doi: 10.26574/maedica.2023.18.2.348. Maedica (Bucur). 2023. PMID: 37588833 Free PMC article.
Analyses of LMNA-negative juvenile progeroid cases confirms biallelic POLR3A mutations in Wiedemann-Rautenstrauch-like syndrome and expands the phenotypic spectrum of PYCR1 mutations.
Lessel D, Ozel AB, Campbell SE, Saadi A, Arlt MF, McSweeney KM, Plaiasu V, Szakszon K, Szőllős A, Rusu C, Rojas AJ, Lopez-Valdez J, Thiele H, Nürnberg P, Nickerson DA, Bamshad MJ, Li JZ, Kubisch C, Glover TW, Gordon LB. Lessel D, et al. Among authors: plaiasu v. Hum Genet. 2018 Dec;137(11-12):921-939. doi: 10.1007/s00439-018-1957-1. Epub 2018 Nov 19. Hum Genet. 2018. PMID: 30450527 Free PMC article.
16 results