Kinga Kozma - Search Results

Year	Number of Results
2011	1
2014	1
2017	2
2018	3
2020	1
2021	2
2022	2
2023	2
2024	0

1

Jurcă MC, Ivaşcu ME, Jurcă AA, Kozma K, Magyar I, Şandor MI, Jurcă AD, Zaha DC, Albu CC, Pantiş C, Bembea M, Petcheşi CD. Jurcă MC, et al. Among authors: kozma k. Rom J Morphol Embryol. 2020 Oct-Dec;61(4):1039-1049. doi: 10.47162/RJME.61.4.06. Rom J Morphol Embryol. 2020. PMID: 34171053 Free PMC article.

2

Greig Cephalopolysyndactyly Contiguous Gene Syndrome: Case Report and Literature Review.

Kozma K, Bembea M, Jurca CM, Ioana M, Streață I, Şoşoi SŞ, Pirvu A, Petchesi CD, Szilágyi A, Sava CN, Jurca A, Ujfalusi A, Szűcs Z, Szakszon K. Kozma K, et al. Genes (Basel). 2021 Oct 23;12(11):1674. doi: 10.3390/genes12111674. Genes (Basel). 2021. PMID: 34828280 Free PMC article. Review.

3

Survey of patient satisfaction after bilateral cataract surgery.

Kinga K, Ursula HK. Kinga K, et al. Rom J Ophthalmol. 2022 Jan-Mar;66(1):36-40. doi: 10.22336/rjo.2022.9. Rom J Ophthalmol. 2022. PMID: 35531447 Free PMC article.

4

Tuberous Sclerosis, Type II Diabetes Mellitus and the PI3K/AKT/mTOR Signaling Pathways-Case Report and Literature Review.

Jurca CM, Kozma K, Petchesi CD, Zaha DC, Magyar I, Munteanu M, Faur L, Jurca A, Bembea D, Severin E, Jurca AD. Jurca CM, et al. Among authors: kozma k. Genes (Basel). 2023 Feb 8;14(2):433. doi: 10.3390/genes14020433. Genes (Basel). 2023. PMID: 36833359 Free PMC article. Review.

5

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. Among authors: kozma k. Genes (Basel). 2022 Aug 4;13(8):1392. doi: 10.3390/genes13081392. Genes (Basel). 2022. PMID: 36011303 Free PMC article. Review.

6

Anatomic variants in Dandy-Walker complex.

Jurcă MC, Kozma K, Petcheşi CD, Bembea M, Pop OL, MuŢiu G, Coroi MC, Jurcă AD, Dobjanschi L. Jurcă MC, et al. Among authors: kozma k. Rom J Morphol Embryol. 2017;58(3):1051-1055. Rom J Morphol Embryol. 2017. PMID: 29250689 Free article.

7

Cardiofaciocutaneous syndrome - a longitudinal study of a case over 33 years: case report and review of the literature.

Jurcă MC, Iuhas OA, Puiu M, Chiriţă-Emandi A, Andreescu NI, Petcheşi CD, Jurcă AD, Magyar I, Jurcă SI, Kozma K, Severin EM, Bembea M. Jurcă MC, et al. Among authors: kozma k. 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.

8

Clinical and genetic diversity of congenital hyperammonemia.

Jurcă AD, Jurcă MC, Bembea M, Kozma K, Budişteanu M, Gug C. Jurcă AD, et al. Among authors: kozma k. Rom J Morphol Embryol. 2018;59(3):945-948. Rom J Morphol Embryol. 2018. PMID: 30534838 Free article.

9

Morphological and genetic abnormalities in a Jacobsen syndrome.

Jurcă AD, Kozma K, Ioana M, Streaţă I, Petcheşi CD, Bembea M, Jurcă MC, Cuc EA, Vesa CM, Buhaş CL. Jurcă AD, et al. Among authors: kozma k. Rom J Morphol Embryol. 2017;58(4):1531-1534. Rom J Morphol Embryol. 2017. PMID: 29556653 Free article.

10

PAH Pathogenic Variants and Clinical Correlations in a Group of Hyperphenylalaninemia Patients from North-Western Romania.

Iuhas A, Jurca C, Kozma K, Riza AL, Streață I, Petcheși C, Dan A, Sava C, Balmoș A, Marinău C, Niulaș L, Ioana M, Bembea M. Iuhas A, et al. Among authors: kozma k. Diagnostics (Basel). 2023 Apr 20;13(8):1483. doi: 10.3390/diagnostics13081483. Diagnostics (Basel). 2023. PMID: 37189584 Free PMC article.

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