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Monica-Cristina Panzaru

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Articles 11
Citations 47
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Recent Articles
1.
Balinisteanu I, Panzaru M, Caba L, Ungureanu M, Florea A, Grigore A, et al.
Biomedicines . 2023 Aug; 11(8). PMID: 37626640
Cancer predisposition syndromes are entities determined especially by germinal pathogenic variants, with most of them autosomal dominantly inherited. The risk of a form of cancer is variable throughout life and...
2.
Butnariu L, Gorduza E, Tarca E, Panzaru M, Popa S, Stoleriu S, et al.
Diagnostics (Basel) . 2023 Jul; 13(14). PMID: 37510094
Atherogenic dyslipidemia plays a critical role in the development of metabolic syndrome (MetS), being one of its major components, along with central obesity, insulin resistance, and hypertension. In recent years,...
3.
Ciobanu C, Nuca I, Popescu R, Antoci L, Caba L, Ivanov A, et al.
Int J Mol Sci . 2023 Jun; 24(11). PMID: 37298158
The diagnosis and management of fragile X syndrome (FXS) have significantly improved in the last three decades, although the current diagnostic techniques are not yet able to precisely identify the...
4.
Panzaru M, Florea A, Caba L, Gorduza E
World J Clin Cases . 2023 May; 11(12):2604-2620. PMID: 37214584
Osteogenesis imperfecta (OI) is a genetically heterogeneous monogenic disease characterized by decreased bone mass, bone fragility, and recurrent fractures. The phenotypic spectrum varies considerably ranging from prenatal fractures with lethal...
5.
Gavril E, Nuca I, Panzaru M, Ivanov A, Mihai C, Antoci L, et al.
Genes (Basel) . 2023 Feb; 14(2). PMID: 36833393
Materials And Methods: In this study we analyzed nine newly diagnosed cases with 2q37 deletion (3 male/6 female, aged between 2 and 30 years old), and followed up at the...
6.
Zob D, Augustin I, Caba L, Panzaru M, Popa S, Popa A, et al.
Int J Mol Sci . 2023 Jan; 24(1). PMID: 36614156
Melanoma is a common and aggressive tumor originating from melanocytes. The increasing incidence of cutaneous melanoma in recent last decades highlights the need for predictive biomarkers studies. Melanoma development is...
7.
Gavril E, Popescu R, Nuca I, Ciobanu C, Butnariu L, Rusu C, et al.
Genes (Basel) . 2022 Nov; 13(11). PMID: 36360320
Methods: We conducted a retrospective study of 59 22q11.2SD cases, with the aim of highlighting phenotype-genotype correlations. All cases were tested using MLPA combined kits: SALSA MLPA KIT P245 and...
8.
Panzaru M, Popa S, Lupu A, Gavrilovici C, Lupu V, Gorduza E
Front Genet . 2022 Oct; 13:958570. PMID: 36246626
The corpus callosum is the largest white matter structure connecting the two cerebral hemispheres. Agenesis of the corpus callosum (ACC), complete or partial, is one of the most common cerebral...
9.
Panzaru M, Caba L, Florea L, Braha E, Gorduza E
Diagnostics (Basel) . 2022 Jun; 12(6). PMID: 35741135
Epidermolysis bullosa is a heterogeneous group of rare genetic disorders characterized by mucocutaneous fragility and blister formation after minor friction or trauma. There are four major epidermolysis bullosa types based...
10.
Popescu R, Gramescu M, Caba L, Panzaru M, Butnariu L, Braha E, et al.
Genes (Basel) . 2021 Dec; 12(12). PMID: 34946906
We present a complex chromosomal anomaly identified using cytogenetic and molecular methods. The child was diagnosed during the neonatal period with a multiple congenital anomalies syndrome characterized by: flattened occipital...