Gorduza EV - Search Results

1

Intrapartum diagnostic of Roberts syndrome - case presentation.

Socolov RV, Andreescu NI, Haliciu AM, Gorduza EV, Dumitrache F, Balan RA, Puiu M, Dobrescu MA, Socolov DG. Socolov RV, et al. Among authors: gorduza ev. Rom J Morphol Embryol. 2015;56(2):585-8. Rom J Morphol Embryol. 2015. PMID: 26193234 Free article.

2

Prenatal diagnosis of gonosomal anomalies: limitations of the FISH method and genetic counseling difficulties in 15 cases.

Braha E, Martiniuc V, Panzaru M, Caba L, Butnariu L, Onofriescu M, Socolov D, Grigore M, Nemescu D, Mihălceanu E, Iliev G, Gorduza EV. Braha E, et al. Among authors: gorduza ev. Rev Med Chir Soc Med Nat Iasi. 2013 Apr-Jun;117(2):450-6. Rev Med Chir Soc Med Nat Iasi. 2013. PMID: 24340530

3

CHARGE syndrome associated with de novo (I1460Rfs^*15) frameshift mutation of CHD7 gene in a patient with arteria lusoria and horseshoe kidney.

Gug C, Gorduza EV, Lăcătuşu A, Vaida MA, Bîrsăşteanu F, Puiu M, Stoicănescu D. Gug C, et al. Among authors: gorduza ev. Exp Ther Med. 2020 Jul;20(1):479-485. doi: 10.3892/etm.2020.8683. Epub 2020 Apr 23. Exp Ther Med. 2020. PMID: 32509017 Free PMC article.

4

Rare splicing mutation in COL1A1 gene identified by whole exomes sequencing in a patient with osteogenesis imperfecta type I followed by prenatal diagnosis: A case report and review of the literature.

Gug C, Caba L, Mozos I, Stoian D, Atasie D, Gug M, Gorduza EV. Gug C, et al. Among authors: gorduza ev. Gene. 2020 May 30;741:144565. doi: 10.1016/j.gene.2020.144565. Epub 2020 Mar 10. Gene. 2020. PMID: 32165296

5

A Case of Inherited t(4;10)(q26;q26.2) Chromosomal Translocation Elucidated by Multiple Chromosomal and Molecular Analyses. Case Report and Review of the Literature.

Popescu R, Grămescu M, Caba L, Pânzaru MC, Butnariu L, Braha E, Popa S, Rusu C, Cardos G, Zeleniuc M, Martiniuc V, Gug C, Păduraru L, Stamatin M, Diaconu CC, Gorduza EV. Popescu R, et al. Among authors: gorduza ev. Genes (Basel). 2021 Dec 7;12(12):1957. doi: 10.3390/genes12121957. Genes (Basel). 2021. PMID: 34946906 Free PMC article. Review.

6

Phenotypic variability in Patau syndrome.

Caba L, Rusu C, Butnariu L, Panzaru M, Braha E, Volosciuc M, Popescu R, Gramescu M, Bujoran C, Martiniuc V, Covic M, Gorduza EV. Caba L, et al. Among authors: gorduza ev. Rev Med Chir Soc Med Nat Iasi. 2013 Apr-Jun;117(2):321-7. Rev Med Chir Soc Med Nat Iasi. 2013. PMID: 24340511

7

Holt-Oram Syndrome With Multiple Cardiac Abnormalities.

Spiridon MR, Petris AO, Gorduza EV, Petras AS, Popescu R, Caba L. Spiridon MR, et al. Among authors: gorduza ev. Cardiol Res. 2018 Oct;9(5):324-329. doi: 10.14740/cr767w. Epub 2018 Oct 7. Cardiol Res. 2018. PMID: 30344832 Free PMC article.

8

Pallister-Killian Syndrome versus Trisomy 12p-A Clinical Study of 5 New Cases and a Literature Review.

Arghir A, Popescu R, Resmerita I, Budisteanu M, Butnariu LI, Gorduza EV, Gramescu M, Panzaru MC, Papuc SM, Sireteanu A, Tutulan-Cunita A, Rusu C. Arghir A, et al. Among authors: gorduza ev. Genes (Basel). 2021 May 26;12(6):811. doi: 10.3390/genes12060811. Genes (Basel). 2021. PMID: 34073526 Free PMC article. Review.

9

Heterogeneity in combined immunodeficiencies with associated or syndromic features (Review).

Caba L, Gug C, Gorduza EV. Caba L, et al. Among authors: gorduza ev. Exp Ther Med. 2021 Jan;21(1):84. doi: 10.3892/etm.2020.9517. Epub 2020 Nov 26. Exp Ther Med. 2021. PMID: 33363595 Free PMC article. Review.

10

[Importance of genetic factors in the pathogenesis of gonadal and postgonadal human infertility].

Gorduza EV, Stoica O, Covic M. Gorduza EV, et al. Rev Med Chir Soc Med Nat Iasi. 2003 Apr-Jun;107(2):261-7. Rev Med Chir Soc Med Nat Iasi. 2003. PMID: 14755926 Review. Romanian.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

52 results

Search Page