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Neonatal Screening in Europe Revisited: An ISNS Perspective on the Current State and Developments Since 2010.
Int J Neonatal Screen. 2021 Mar 5;7(1):15. doi: 10.3390/ijns7010015.
Int J Neonatal Screen. 2021.
PMID: 33808002
Free PMC article.
Newborn screening in southeastern Europe.
Groselj U, Tansek MZ, Smon A, Angelkova N, Anton D, Baric I, Djordjevic M, Grimci L, Ivanova M, Kadam A, Kotori VM, Maksic H, Marginean O, Margineanu O, Milijanovic O, Moldovanu F, Muresan M, Murko S, Nanu M, Lampret BR, Samardzic M, Sarnavka V, Savov A, Stojiljkovic M, Suzic B, Tincheva R, Tahirovic H, Toromanovic A, Usurelu N, Battelino T.
Groselj U, et al. Among authors: usurelu n.
Mol Genet Metab. 2014 Sep-Oct;113(1-2):42-5. doi: 10.1016/j.ymgme.2014.07.020. Epub 2014 Aug 1.
Mol Genet Metab. 2014.
PMID: 25174966
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Phenylketonuria screening and management in southeastern Europe - survey results from 11 countries.
Zerjav Tansek M, Groselj U, Angelkova N, Anton D, Baric I, Djordjevic M, Grimci L, Ivanova M, Kadam A, Kotori V, Maksic H, Marginean O, Margineanu O, Miljanovic O, Moldovanu F, Muresan M, Nanu M, Samardzic M, Sarnavka V, Savov A, Stojiljkovic M, Suzic B, Tincheva R, Tahirovic H, Toromanovic A, Usurelu N, Battelino T.
Zerjav Tansek M, et al. Among authors: usurelu n.
Orphanet J Rare Dis. 2015 May 30;10:68. doi: 10.1186/s13023-015-0283-0.
Orphanet J Rare Dis. 2015.
PMID: 26025111
Free PMC article.
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Untreated PKU Patients without Intellectual Disability: What Do They Teach Us?
van Vliet D, van Wegberg AMJ, Ahring K, Bik-Multanowski M, Casas K, Didycz B, Djordjevic M, Hertecant JL, Leuzzi V, Mathisen P, Nardecchia F, Powell KK, Rutsch F, Stojiljkovic M, Trefz FK, Usurelu N, Wilson C, van Karnebeek CD, Hanley WB, van Spronsen FJ.
van Vliet D, et al. Among authors: usurelu n.
Nutrients. 2019 Oct 25;11(11):2572. doi: 10.3390/nu11112572.
Nutrients. 2019.
PMID: 31731404
Free PMC article.
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Can untreated PKU patients escape from intellectual disability? A systematic review.
van Vliet D, van Wegberg AMJ, Ahring K, Bik-Multanowski M, Blau N, Bulut FD, Casas K, Didycz B, Djordjevic M, Federico A, Feillet F, Gizewska M, Gramer G, Hertecant JL, Hollak CEM, Jørgensen JV, Karall D, Landau Y, Leuzzi V, Mathisen P, Moseley K, Mungan NÖ, Nardecchia F, Õunap K, Powell KK, Ramachandran R, Rutsch F, Setoodeh A, Stojiljkovic M, Trefz FK, Usurelu N, Wilson C, van Karnebeek CD, Hanley WB, van Spronsen FJ.
van Vliet D, et al. Among authors: usurelu n.
Orphanet J Rare Dis. 2018 Aug 29;13(1):149. doi: 10.1186/s13023-018-0890-7.
Orphanet J Rare Dis. 2018.
PMID: 30157945
Free PMC article.
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No clinical utility of common polymorphisms in IGF1, IRS1, GCKR, PPARG, GCK1 and KCTD1 genes previously associated with insulin resistance in overweight children from Romania and Moldova.
Chirita-Emandi A, Munteanu D, Andreescu N, Tutac P, Paul C, Velea IP, Pusztai AM, Hlistun V, Boiciuc C, Sacara V, Vudu L, Usurelu N, Puiu M.
Chirita-Emandi A, et al. Among authors: usurelu n.
J Pediatr Endocrinol Metab. 2019 Jan 28;32(1):33-39. doi: 10.1515/jpem-2018-0288.
J Pediatr Endocrinol Metab. 2019.
PMID: 30864372
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Gaucher disease type 1: the first experience of enzyme replacement therapy in pediatric practice in Moldova - case report.
Uşurelu N, Blăniţă D, Boiciuc C, Hlistun V, Egorov V, Popovici E, Gnatcova E, Stamati A, Oglindă A, Revenco N, Gladun S, Ţurea V.
Uşurelu N, et al.
Med Pharm Rep. 2021 Aug;94(Suppl No 1):S57-S60. doi: 10.15386/mpr-2232. Epub 2021 Aug 10.
Med Pharm Rep. 2021.
PMID: 34527913
Free PMC article.
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Monitoring Methylmalonic Aciduria by NMR Urinomics.
Nicolescu A, Blanita D, Boiciuc C, Hlistun V, Cristea M, Rotaru D, Pinzari L, Oglinda A, Stamati A, Tarcomnicu I, Tutulan-Cunita A, Stambouli D, Gladun S, Revenco N, Uşurelu N, Deleanu C.
Nicolescu A, et al. Among authors: usurelu n.
Molecules. 2020 Nov 14;25(22):5312. doi: 10.3390/molecules25225312.
Molecules. 2020.
PMID: 33202577
Free PMC article.
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