Popescu R - Search Results

1

Different Types of Deletions Created by Low-Copy Repeats Sequences Location in 22q11.2 Deletion Syndrome: Genotype-Phenotype Correlation.

Gavril EC, Popescu R, Nucă I, Ciobanu CG, Butnariu LI, Rusu C, Pânzaru MC. Gavril EC, et al. Among authors: popescu r. Genes (Basel). 2022 Nov 10;13(11):2083. doi: 10.3390/genes13112083. Genes (Basel). 2022. PMID: 36360320 Free PMC article.

2

[Improvement of genetic diagnostic strategy in velo-cardio-facial syndrome].

Pânzaru M, Rusu C, Voloşciuc M, Braha E, Butnariu L, Ivanov I, Grămescu M, Popescu R, Caba L, Sireteanu A, Macovei M, Covic M, Gorduza EV. Pânzaru M, et al. Among authors: popescu r. Rev Med Chir Soc Med Nat Iasi. 2011 Jul-Sep;115(3):756-61. Rev Med Chir Soc Med Nat Iasi. 2011. PMID: 22046783 Romanian.

3

[Clopidogrel resistance--risk factor in patients with acute coronary syndromes].

Costache Il, Rusu C, Ivanov I, Popescu R, Petriş A. Costache Il, et al. Among authors: popescu r. Rev Med Chir Soc Med Nat Iasi. 2012 Apr-Jun;116(2):383-8. Rev Med Chir Soc Med Nat Iasi. 2012. PMID: 23077924 Romanian.

4

Impact of clopidogrel response on the clinical evolution in patients with acute coronary syndromes.

Costache II, Rusu C, Ivanov I, Popescu R, Petriş A. Costache II, et al. Among authors: popescu r. Rev Med Chir Soc Med Nat Iasi. 2012 Oct-Dec;116(4):962-7. Rev Med Chir Soc Med Nat Iasi. 2012. PMID: 23700873 Clinical Trial.

5

Ring autosomes: some unexpected findings.

Caba L, Rusu C, Plăiaşu 5th, Gug G, Grămescu M, Bujoran C, Ochiană D, Voloşciuc M, Popescu R, Braha E, Pânzaru M, Butnariu L, Sireteanu A, Covic M, Gorduza E. Caba L, et al. Among authors: popescu r. Balkan J Med Genet. 2012 Dec;15(2):35-46. doi: 10.2478/bjmg-2013-0005. Balkan J Med Genet. 2012. PMID: 24052730 Free PMC article.

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: popescu r. 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

Genotype- phenotype correlation in trisomy X: a retrospective study of a selected group of 36 patients and review of literature.

Butnariu L, Rusu C, Caba L, Pânzaru M, Braha E, Grămescu M, Popescu R, Bujoranu C, Gorduza EV. Butnariu L, et al. Among authors: popescu r. Rev Med Chir Soc Med Nat Iasi. 2013 Jul-Sep;117(3):714-21. Rev Med Chir Soc Med Nat Iasi. 2013. PMID: 24502039 Review.

8

Inverted duplication deletion of 8P: characterization by standard cytogenetic and SNP array analyses.

Sireteanu A, Braha E, Popescu R, Gramescu M, Gorduza EV, Rusu C. Sireteanu A, et al. Among authors: popescu r. Rev Med Chir Soc Med Nat Iasi. 2013 Jul-Sep;117(3):731-4. Rev Med Chir Soc Med Nat Iasi. 2013. PMID: 24502041

9

Mutations of filament-aggregating protein gene in Romanian children diagnosed with atopic dermatitis.

Chiriac AE, Popescu R, Butnariu L, Murgu A, Foia L, Azoicai D. Chiriac AE, et al. Among authors: popescu r. Exp Ther Med. 2020 Dec;20(6):212. doi: 10.3892/etm.2020.9343. Epub 2020 Oct 15. Exp Ther Med. 2020. PMID: 33149776 Free PMC article.

10

Genetics of Hearing Impairment in North-Eastern Romania-A Cost-Effective Improved Diagnosis and Literature Review.

Resmerita I, Cozma RS, Popescu R, Radulescu LM, Panzaru MC, Butnariu LI, Caba L, Ilie OD, Gavril EC, Gorduza EV, Rusu C. Resmerita I, et al. Among authors: popescu r. Genes (Basel). 2020 Dec 15;11(12):1506. doi: 10.3390/genes11121506. Genes (Basel). 2020. PMID: 33333757 Free PMC article. Review.

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