1. bookVolume 27 (2019): Issue 1 (January 2019)
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Journal
eISSN
2284-5623
First Published
08 Aug 2013
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4 times per year
Languages
English
access type Open Access

Do we really need genetic tests in current clinical practice?

Published Online: 01 Feb 2019
Page range: 9 - 14
Received: 27 Dec 2018
Accepted: 07 Jan 2019
Journal Details
License
Format
Journal
eISSN
2284-5623
First Published
08 Aug 2013
Publication timeframe
4 times per year
Languages
English

1. Jinca C, Petrescu CAM, Boeriu E, Oprisoni A, Balint-Gib L, Baica M, et al. The impact of immunological and biomolecular investigations on the outcome of children with acute lymphoblastic leukemia - experience of IIIrd Paediatric Clinic Timisoara. Rev Romana Med Lab. 2018;26(1):77-85. DOI: 10.1515/rrlm-2017-002910.1515/rrlm-2017-0029Open DOISearch in Google Scholar

2. Arber DA, Orazi A, Hasserjian R, Thiele J, Borowitz MJ, Le Beau MM, et al. The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia. Blood. 2016 May 19;127(20):2391–405. DOI: 10.1182/blood-2016-03-64354410.1182/blood-2016-03-643544Open DOISearch in Google Scholar

3. Döhner H, Estey E, Grimwade D, Amadori S, Appelbaum FR, Büchner T, et al. Diagnosis and management of AML in adults: 2017 ELN recommendations from an international expert panel. Blood. 2017 Jan 26;129(4):424–47 DOI: 10.1182/blood-2016-08-73319610.1182/blood-2016-08-733196Open DOISearch in Google Scholar

4. Berbec NP, Papuc SM, Tutulan-Cunita AC, Angelescu SM, Lupu AI, Arghir AA. Molecular characterization of complex chromosomal changes in de novo acute myeloid leukemia: a case report. Rev Romana Med Lab. 2013;21(1):59-65. DOI: 10.2478/rrlm-2013-001810.2478/rrlm-2013-0018Open DOISearch in Google Scholar

5. Crauciuc GA, Tripon F, Bogliş A, Făgărăşan A, Bănescu C. Multiplex ligation dependent probe amplification-A useful, fast and cost-effective method for identification of small supernumerary marker chromosome in children with developmental delay and congenital heart defect. Rev Romana Med Lab. 2018;26(4):461-70. DOI: 10.2478/rrlm-2018-003210.2478/rrlm-2018-0032Open DOISearch in Google Scholar

6. Drugan C, Drugan T, Caillaud C, Grigorescu-Sido P, Nistor T, Crăciun AM. Laboratory diagnosis and follow-up of Romanian Gaucher disease patients. Rev Romana Med Lab. 2017;25(3):275-85. DOI: 10.1515/rrlm-2017-001810.1515/rrlm-2017-0018Open DOISearch in Google Scholar

7. Sabin O, Bocșan IC, Trifa A, Major ZZ, Heghes SC, Brusturean Bota E, et al. Correlation between ABCB1 gene polymorphisms, antiepileptic drug concentrations and treatment response. Rev Romana Med Lab. 2018;26(4):479-87. DOI: 10.2478/rrlm-2018-001210.2478/rrlm-2018-0012Open DOISearch in Google Scholar

8. Muntean I, Şuteu C, Togănel R, Bănescu C. Association between MDR1 gene polymorphism and clinical course of pediatric pulmonary arterial hypertension. Rev Romana Med Lab. 2018;26(3):305-12. DOI: 10.2478/rrlm-2018-002510.2478/rrlm-2018-0025Search in Google Scholar

9. Negovan A, Iancu M, Moldovan V, Pantea M, Sarkany K, Bataga S, et al. Influence of MDR1 C3435T, CYP2C19*2 and CYP2C19*3 gene polymorphisms and clinical characteristics on the severity of gastric lesions: a case-control study. J Gastrointestin Liver Dis. 2016;25(2):258-60. DOI: 10.15403/jgld.2014.1121.252.mdr.10.15403/jgld.2014.1121.252.mdrSearch in Google Scholar

10. Georgescu AM, Bănescu C, Badea I, Moldovan V, Huțanu A, Voidăzan S, et al. IL-6 gene polymorphisms and sepsis in ICU adult Romanian patients: a prospective study. Rev Romana Med Lab. 2017;25(1):75-89. DOI: 10.1515/rrlm-2016-004410.1515/rrlm-2016-0044Search in Google Scholar

11. Negovan A, Iancu M, Moldovan V, Mocan S, Banescu C. The Interaction between GSTT1, GSTM1, and GSTP1 Ile105Val Gene Polymorphisms and Environmental Risk Factors in Premalignant Gastric Lesions Risk. Biomed Res Int. 2017;2017:7365080. DOI: 10.1155/2017/7365080.10.1155/2017/7365080Open DOISearch in Google Scholar

12. Mărginean A, Bănescu C, Moldovan V, Scridon A, Mărginean M, Bălaşa R, et al. The Impact of CYP2C19 Loss-of-Function Polymorphisms, Clinical, and Demographic Variables on Platelet Response to Clopidogrel Evaluated Using Impedance Aggregometry. Clin Appl Thromb Hemost. 2017;23(3):255-65. DOI: 10.1177/1076029616629211.10.1177/1076029616629211Open DOISearch in Google Scholar

13. Lazăr C, Popp R, Al-Khzouz C, Mihuț G, Grigorescu-Sido P. GJB2 and GJB6 genes mutations in children with non-syndromic hearing loss. Rev Romana Med Lab. 2017;25(1):37-46. DOI: 10.1515/rrlm-2017-000410.1515/rrlm-2017-0004Open DOISearch in Google Scholar

14. Bogliş A, Tripon F, Bănescu C. The utility of molecular genetic techniques in craniosynostosis cases associated with intellectual disability. Rev Romana Med Lab. 2018;26(4):471-7. DOI: 10.2478/rrlm-2018-003310.2478/rrlm-2018-0033Open DOISearch in Google Scholar

15. Goidescu IG, Eniu DT, Caracostea GV, Cruciat G, Stamatian F. Associations of pathogenic mutations responsible for breast cancer risk with histology and immunohistochemistry in Romanian population. Rev Romana Med Lab. 2018;26(2):165-75. DOI: 10.1515/rrlm-2017-003710.1515/rrlm-2017-0037Open DOISearch in Google Scholar

16. Maier D, Florea A, Tilinca MC, Zazgyva A, Cosgarea R. NIPAL4 mutation c.527C˃A identified in Romanian patients with autosomal recessive congenital ichthyosis. Rev Romana Med Lab. 2016;24(4):387-97. DOI: 10.1515/rrlm-2016-003410.1515/rrlm-2016-0034Open DOISearch in Google Scholar

17. Negura L, Negura A. Sanger sequencing of MMR genes in a one-plate system. Rev Romana Med Lab. 2018;26(2):153-63. DOI: 10.2478/rrlm-2018-000810.2478/rrlm-2018-0008Open DOISearch in Google Scholar

18. Coriu D, Jardan D, Jardan C, Tălmaci R, Dragomir M, Coliţă A. A new assay to identify recurrent mutations in acute myeloid leukemia using next-generation sequencing. Rev Romana Med Lab. 2014;22(1):93–9. DOI: 10.2478/rrlm-2014-000310.2478/rrlm-2014-0003Open DOISearch in Google Scholar

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