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Cardiofaciocutaneous syndrome - a longitudinal study of a case over 33 years: case report and review of the literature.
Rom J Morphol Embryol. 2021 Apr-Jun;62(2):563-568. doi: 10.47162/RJME.62.2.23.
Rom J Morphol Embryol. 2021.
PMID: 35024745
Free PMC article.
Review.
Double autosomal trisomy with mosaicism 47,XY(+8)∕47,XY(+21). Morphological and genetic changes of a rare case.
Jurcă MC, Bembea M, Iuhas OA, Kozma K, Petcheşi CD, Jurcă AD, Szilágyi A, Dubău DL, Sava CN, Zaha DC, Cuc EA.
Jurcă MC, et al. Among authors: iuhas oa.
Rom J Morphol Embryol. 2018;59(3):985-988.
Rom J Morphol Embryol. 2018.
PMID: 30534844
Free article.
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Effects of Burosumab Treatment on Two Siblings with X-Linked Hypophosphatemia. Case Report and Literature Review.
Jurca CM, Iuhas O, Kozma K, Petchesi CD, Zaha DC, Bembea M, Jurca S, Paul C, Jurca AD.
Jurca CM, et al.
Genes (Basel). 2022 Aug 4;13(8):1392. doi: 10.3390/genes13081392.
Genes (Basel). 2022.
PMID: 36011303
Free PMC article.
Review.
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Ethnicity-related DMD Genotype Landscapes in European and Non-European Countries.
Selvatici R, Rossi R, Fortunato F, Trabanelli C, Sifi Y, Margutti A, Neri M, Gualandi F, Szabò L, Fekete B, Angelova L, Litvinenko I, Ivanov I, Vildan Y, Iuhas OA, Vintan M, Burloiu C, Lacramioara B, Visa G, Epure D, Rusu C, Vasile D, Sandu M, Vlodavets D, Mager M, Kyriakides T, Delin S, Lehman I, Fureš JS, Bojinova V, Militaru M, Guergueltcheva V, Burnyte B, Molnar MJ, Butoianu N, Bensemmane SD, Makri-Mokrane S, Herczegfalvi A, Panzaru M, Emandi AC, Lusakowska A, Potulska-Chromik A, Kostera-Pruszczyk A, Shatillo A, Khelladi DB, Dendane O, Fang M, Lu Z, Ferlini A.
Selvatici R, et al. Among authors: iuhas oa.
Neurol Genet. 2020 Dec 24;7(1):e536. doi: 10.1212/NXG.0000000000000536. eCollection 2021 Feb.
Neurol Genet. 2020.
PMID: 33376799
Free PMC article.
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