Vlad Dima
Overview
Explore the profile of Vlad Dima including associated specialties, affiliations and a list of published articles.
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Articles
18
Citations
58
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Recent Articles
11.
Demetrian M, Botezatu R, Gica N, Safta V, Grecu G, Dima V, et al.
Children (Basel)
. 2023 Jan;
10(1).
PMID: 36670617
We describe the case of a newborn with the antenatal onset of hepatic failure, which has been investigated for all etiologies that can cause liver damage: infectious, metabolic, genetic, and...
12.
Bohiltea R, Mihai B, Stanica C, Gheorghe C, Berceanu C, Dima V, et al.
J Clin Med
. 2022 Oct;
11(19).
PMID: 36233813
Background: Hysterosalpingo-foam sonography (HyFoSy) has gained popularity in the last decades, as it represents a feasible, well-tolerated, and minimally invasive method of evaluation of tubal patency in cases of infertility....
13.
Filip C, Zonda G, Vasilache I, Scripcariu I, Vicoveanu P, Dima V, et al.
Children (Basel)
. 2022 Aug;
9(8).
PMID: 36010072
(1) Background: Neonatal cerebral sinovenous thrombosis (CSVT) is a rare disorder, associated with long-term neurological sequelae. The aim of this study was to retrospectively evaluate the most commonly encountered perinatal...
14.
Mirea A, Leanca M, Onose G, Sporea C, Padure L, Shelby E, et al.
Front Biosci (Landmark Ed)
. 2022 Jun;
27(6):179.
PMID: 35748255
Introduction: Spinal muscular atrophy (SMA) is a progressive neurological disease with autosomal recessive transmission that affects motor neurons, causing their loss and resulting in muscle waste and motor deficiency. Nusinersen,...
15.
Bohiltea R, Pariza P, Stavarache I, Munteanu O, Dima V, Mihai B, et al.
Maedica (Bucur)
. 2022 Mar;
16(4):717-722.
PMID: 35261677
Double aortic arch represents a congenital vascular malformation that is characterized by the development of a complete vascular ring around the esophagus and trachea due to an anomaly in the...
16.
Bohiltea R, Ducu I, Mihai B, Iordache A, Dima V, Vladareanu E, et al.
Diagnostics (Basel)
. 2022 Feb;
12(2).
PMID: 35204464
Hemivertebra is a common cause of congenital scoliosis and results from a lack of formation of one-half of the vertebral body. This condition is very rare and can present as...
17.
Bohiltea R, Dima V, Ducu I, Iordache A, Mihai B, Munteanu O, et al.
Diagnostics (Basel)
. 2022 Feb;
12(2).
PMID: 35204327
Umbilical cord abnormalities are not rare, and are often associated with structural or chromosomal abnormalities, fetal intrauterine growth restriction, and poor pregnancy outcomes; the latter can be a result of...
18.
Bohiltea R, Varlas V, Dima V, Iordache A, Salmen T, Mihai B, et al.
J Clin Med
. 2022 Feb;
11(3).
PMID: 35160268
True umbilical knot (TUK), although not a commonly encountered pathology, hasan important psychological burden on the mother and obstetrician. It has an extremely low prenatal ultrasound diagnosis rate, despite its...
19.
Bohiltea R, Cioca A, Dima V, Ducu I, Grigoriu C, Varlas V, et al.
J Clin Med
. 2022 Jan;
11(1).
PMID: 35011954
Material And Methods: We conducted a retrospective observational analytical study, which included women with PPROM between 24 + 0 and 36 + 6 weeks. We divided the cohort into gestational...
20.
Mirea A, Shelby E, Axente M, Badina M, Padure L, Leanca M, et al.
J Clin Med
. 2021 Dec;
10(23).
PMID: 34884240
Background: Spinal muscular atrophy (SMA) is a neuromuscular progressive disease, characterized by decreased amounts of survival motor neuron (SMN) protein, due to an autosomal recessive genetic defect. Despite recent research,...