M Kleanthous
Overview
Explore the profile of M Kleanthous including associated specialties, affiliations and a list of published articles.
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Articles
13
Citations
154
Followers
0
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Recent Articles
1.
Fanis P, Skordis N, Frangos S, Christopoulos G, Spanou-Aristidou E, Andreou E, et al.
J Endocrinol Invest
. 2018 Feb;
41(10):1149-1157.
PMID: 29396759
Purpose: Multiple endocrine neoplasia type 2 (MEN2) affects patients with RET proto-oncogene mutations. This cohort study refers to patients who were diagnosed with familial medullary thyroid carcinoma (MTC) and underwent...
2.
Egea J, Fabregat I, Frapart Y, Ghezzi P, Gorlach A, Kietzmann T, et al.
Redox Biol
. 2017 Nov;
14:694-696.
PMID: 29107648
No abstract available.
3.
Voskou S, Aslan M, Fanis P, Phylactides M, Kleanthous M
Redox Biol
. 2015 Aug;
6:226-239.
PMID: 26285072
Sickle cell disease and β-thalassaemia are inherited haemoglobinopathies resulting in structural and quantitative changes in the β-globin chain. These changes lead to instability of the generated haemoglobin or to globin...
4.
Christodoulou I, Patsali P, Stephanou C, Antoniou M, Kleanthous M, Lederer C
Gene Ther
. 2015 Jul;
23(1):113-8.
PMID: 26202078
Lentiviruses are the vectors of choice for many preclinical studies and clinical applications of gene therapy. Accurate measurement of biological vector titre before treatment is a prerequisite for vector dosing,...
5.
Kyrri A, Felekis X, Kalogerou E, Christopoulos G, Makariou C, Loizidou D, et al.
Hemoglobin
. 2002 Jan;
25(4):421-4.
PMID: 11791876
No abstract available.
6.
Old J, Khan S, Verma I, Fucharoen S, Kleanthous M, Ioannou P, et al.
Hemoglobin
. 2002 Jan;
25(4):397-407.
PMID: 11791873
The spectrum of the beta-thalassemia mutations of Thailand, Pakistan, India, Sri Lanka, Mauritius and Syria has been further characterized by a multi-center study of 1,235 transfusion-dependent patients, and the mutations...
7.
Kleanthous M, Kyriacou K, Kyrri A, Kalogerou E, Vassiliades P, Drousiotou A, et al.
Prenat Diagn
. 2001 May;
21(5):413-7.
PMID: 11360286
In Cyprus all couples carrying alpha0-thalassaemia mutations are detected in the course of the thalassaemia carrier screening program and prenatal diagnosis is offered to all of them. Prenatal diagnosis for...
8.
Feleki X, Najmabadi H, Christopoulos G, Kleanthous M
Hemoglobin
. 2001 Feb;
24(4):319-21.
PMID: 11186262
No abstract available.
9.
Kyriacou K, Kyrri A, Kalogirou E, Vasiliades P, Angastiniotis M, Ioannou P, et al.
Hemoglobin
. 2000 Sep;
24(3):171-80.
PMID: 10975437
The purpose of this study was to examine the frequency of alpha-thalassemia in the population of Cyprus using cord blood samples. The levels of Hb Bart's were compared with the...
10.
Kyriacou K, Al Quobaili F, Pavlou E, Christopoulos G, Ioannou P, Kleanthous M
Hemoglobin
. 2000 Mar;
24(1):1-13.
PMID: 10722110
This study concerns the determination of beta-thalassemia alleles and other hemoglobin variants in 82 patients from Syria. We have characterized 146 chromosomes and found 17 different beta-thalassemia mutations, and one...