Detalhe da pesquisa
1.
Genomics and Epigenomics in the Molecular Biology of Melanoma-A Prerequisite for Biomarkers Studies.
Int J Mol Sci
; 24(1)2022 Dec 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-36614156
2.
The Genetic Architecture of Vascular Anomalies: Current Data and Future Therapeutic Perspectives Correlated with Molecular Mechanisms.
Int J Mol Sci
; 23(20)2022 Oct 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-36293054
3.
The Genetic Architecture of the Etiology of Lower Extremity Peripheral Artery Disease: Current Knowledge and Future Challenges in the Era of Genomic Medicine.
Int J Mol Sci
; 23(18)2022 Sep 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-36142394
4.
Genetic Counseling and Management: The First Study to Report NIPT Findings in a Romanian Population.
Medicina (Kaunas)
; 58(1)2022 Jan 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35056387
5.
Gorham-Stout Disease with Multiple Bone Involvement-Challenging Diagnosis of a Rare Disease and Literature Review.
Medicina (Kaunas)
; 57(7)2021 Jul 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34356962
6.
Polyploidy in First and Second Trimester Pregnancies in Romania - a Retrospective Study.
Clin Lab
; 66(4)2020 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32255304
7.
Rare Case of First Permanent Molar Primary Failure of Eruption with Agenesis of Premolars.
Children (Basel)
; 11(2)2024 Jan 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-38397264
8.
Modern Treatment of Valvulopathies in Patients with Congenital Hemophilia.
Life (Basel)
; 14(3)2024 Mar 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-38541679
9.
Classification of osteogenesis imperfecta: Importance for prophylaxis and genetic counseling.
World J Clin Cases
; 11(12): 2604-2620, 2023 Apr 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-37214584
10.
Cancer Predisposition Syndromes and Thyroid Cancer: Keys for a Short Two-Way Street.
Biomedicines
; 11(8)2023 Jul 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-37626640
11.
Hydatidiform Mole-Between Chromosomal Abnormality, Uniparental Disomy and Monogenic Variants: A Narrative Review.
Life (Basel)
; 13(12)2023 Dec 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-38137915
12.
Acute Myocardial Infarction in Patients with Hereditary Thrombophilia-A Focus on Factor V Leiden and Prothrombin G20210A.
Life (Basel)
; 13(6)2023 Jun 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-37374153
13.
Current Data and New Insights into the Genetic Factors of Atherogenic Dyslipidemia Associated with Metabolic Syndrome.
Diagnostics (Basel)
; 13(14)2023 Jul 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-37510094
14.
Genetic Heterogeneity in Bartter Syndrome: Clinical and Practical Importance.
Front Pediatr
; 10: 908655, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35722471
15.
Epidermolysis Bullosa-A Different Genetic Approach in Correlation with Genetic Heterogeneity.
Diagnostics (Basel)
; 12(6)2022 May 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-35741135
16.
Genetic heterogeneity in corpus callosum agenesis.
Front Genet
; 13: 958570, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36246626
17.
Monitoring and Management of Bardet-Biedl Syndrome: What the Multi-Disciplinary Team Can Do.
J Multidiscip Healthc
; 15: 2153-2167, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36193191
18.
Etiologic Puzzle of Coronary Artery Disease: How Important Is Genetic Component?
Life (Basel)
; 12(6)2022 Jun 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35743896
19.
Myocardial Ischemia Related to Common Cancer Therapy-Prevention Insights.
Life (Basel)
; 12(7)2022 Jul 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-35888122
20.
Heterogeneity in combined immunodeficiencies with associated or syndromic features (Review).
Exp Ther Med
; 21(1): 84, 2021 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-33363595