Violeta Martiniuc
Overview
Explore the profile of Violeta Martiniuc including associated specialties, affiliations and a list of published articles.
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7
Citations
17
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Recent Articles
1.
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...
2.
Gug C, Burada F, Ioana M, Riza A, Moldovan M, Mozos I, et al.
Clin Lab
. 2020 Apr;
66(4).
PMID: 32255304
Background: Polyploidy is a rare lethal cytogenetic anomaly in pregnancies, generally leading to pregnancy termination. This study aims to compare first and second trimester polyploidy in pregnancies and describe the...
3.
Socolov R, Ebner T, Gorduza V, Martiniuc V, Angioni S, Socolov D
Gynecol Endocrinol
. 2015 Jul;
31(7):529-30.
PMID: 26137987
A rare cause of infertility is the lack of fertilisation with the spontaneous activation of oocytes, leading to parthenogenesis. We present such a case. The patient was a G1P0 38-year-old...
4.
Braha E, Martiniuc V, Panzaru M, Caba L, Butnariu L, Onofriescu M, et al.
Rev Med Chir Soc Med Nat Iasi
. 2013 Dec;
117(2):450-6.
PMID: 24340530
Unlabelled: Prenatal diagnosis (PD) by FISH or cell culture is today an important tool for the prevention of chromosomal anomalies. A difficult issue is prenatal detection of gonosomal anomalies. Most...
5.
Caba L, Rusu C, Butnariu L, Panzaru M, Braha E, Volosciuc M, et al.
Rev Med Chir Soc Med Nat Iasi
. 2013 Dec;
117(2):321-7.
PMID: 24340511
Unlabelled: Patau syndrome has an incidence of 1/10.000-20.000, the clinical diagnosis being suggested by the triad cleft lip and palate, microphthalmia/anophthalmia and postaxial polydactyly. Most frequent cytogenetic abnormality is free...
6.
Avatajitei M, Moscalu M, Martiniuc V, Onofriescu M
Rev Med Chir Soc Med Nat Iasi
. 2012 Oct;
116(2):515-22.
PMID: 23077946
Unlabelled: In the last 10 years, several studies have been carried out on additional ultrasound markers in the first trimester of pregnancy in order to improve detection rate of fetal...
7.
Gorduza E, Onofriescu M, Martiniuc V, Grigore M, Mihalceanu E, Iliev G
Rev Med Chir Soc Med Nat Iasi
. 2008 Apr;
111(4):990-5.
PMID: 18389793
Unlabelled: Chromosomal disorders are severe and affect 0.9% of the newborns. In these conditions, prenatal diagnosis should be compulsory in every public medical system. Material And Method: Our study is...