Margit Serban
Overview
Explore the profile of Margit Serban including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
22
Citations
153
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Ursu C, Serban M, Patrascu J, Coriu D, Jr J, Ionita I, et al.
Life (Basel)
. 2024 Sep;
14(9).
PMID: 39337955
Despite the controversies regarding the appropriateness and justification of simultaneous bi- and multi-concomitant surgical procedures, this operative technique is increasingly undertaken for economic reasons. This paper discusses three cases of...
2.
Blag C, Serban M, Ursu C, Popa C, Traila A, Jinca C, et al.
J Clin Med
. 2023 Dec;
12(23).
PMID: 38068488
A coincidental occurrence of severe haemophilia A and Turner syndrome in a female person is extremely rare (less than 10 cases published). In such challenging cases, a multidisciplinary approach based...
3.
Brinza M, Grigore A, Dragomir M, Jardan D, Jardan C, Balanescu P, et al.
Medicina (Kaunas)
. 2023 Oct;
59(10).
PMID: 37893540
: Despite the vast heterogeneity in the genetic defects causing hemophilia A (HA), large intron inversions represent a major cause of disease, accounting for almost half of the cases of...
4.
Tigu A, Hotea I, Drula R, Zimta A, Dirzu N, Santa M, et al.
J Cell Mol Med
. 2023 Jun;
27(13):1790-1796.
PMID: 37317065
Acquired haemophilia (AH) is a rare disorder characterized by bleeding in patients with no personal or family history of coagulation/clotting-related diseases. This disease occurs when the immune system, by mistake,...
5.
Abolhassani H, Avcin T, Bahceciler N, Balashov D, Bata Z, Bataneant M, et al.
Front Immunol
. 2023 Jan;
13:1032358.
PMID: 36605210
Introduction: The J Project (JP) physician education and clinical research collaboration program was started in 2004 and includes by now 32 countries mostly in Eastern and Central Europe (ECE). Until...
6.
Boeriu E, Arghirescu T, Serban M, Patrascu J, Boia E, Jinca C, et al.
J Clin Med
. 2022 Jun;
11(12).
PMID: 35743393
(1) Background: Mild and moderate hemophilia, synonymous with non-severe hemophilia (NSH), are of constant interest for the clinicians. Bleeding occurs usually after trauma, injury, surgery, or inhibitor development, sometimes leading...
7.
Dirzu N, Hotea I, Jitaru C, Brinza M, Urian L, Peters M, et al.
Front Med (Lausanne)
. 2021 Aug;
8:711973.
PMID: 34447770
The management of patients with hemophilia has evolved significantly since the first treatment attempts were made in the late 1930s. Since then, each new step in the treatment of patients...
8.
Hotea I, Brinza M, Blag C, Zimta A, Dirzu N, Burzo C, et al.
Ann Transl Med
. 2021 Aug;
9(13):1091.
PMID: 34423003
Hemophilia A (HA) and hemophilia B (HB) are rare disorders, being caused by the total lack or under-expression of two factors from the coagulation cascade coded by genes of the...
9.
Zimta A, Hotea I, Brinza M, Blag C, Iluta S, Constantinescu C, et al.
Front Med (Lausanne)
. 2021 May;
8:654197.
PMID: 33968959
Hemophilia type A (HA) is the most common type of blood coagulation disorder. While the vast majority of cases are inherited and caused by mutations in the gene, recent data...
10.
Primary autoimmune neutropenia of infancy and childhood in a cohort of patients from western Romania
Jinca C, Serban M, Ursu E, Munteanu A, Arghirescu S
Exp Ther Med
. 2021 Feb;
21(3):280.
PMID: 33603887
Neutropenia is commonly diagnosed in pediatric clinics. Due to the special vulnerability of neutropenic patients, the assessment of the etiopathogenic background of neutropenia is mandatory. In this retrospective cross-sectional cohort...