Mahdieh Taghizadeh
Overview
Explore the profile of Mahdieh Taghizadeh including associated specialties, affiliations and a list of published articles.
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7
Citations
17
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0
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Recent Articles
1.
Karimzade P, Eghbali A, Keramatipour M, Shiari R, Golchehre Z, Taghizadeh M, et al.
Case Reports Immunol
. 2024 Aug;
2024:4380689.
PMID: 39161369
Background: Adenosine deaminase deficiency 2 (DADA2) is an autoinflammatory disorder, caused by the gene mutation. The major clinical manifestations include recurrent vasculitis, neurological disorders such as stroke, hematologic abnormalities, and...
2.
Nourmohammadi P, Asadollahi M, Karamzade A, Eshaghkhani Y, Babaei M, Golchehre Z, et al.
J Genet
. 2023 Sep;
102.
PMID: 37674283
Vanishing of white matter (VWM) is a hereditary heterogeneous brain disorder that most often affects children. However, the onset of the disease varies from childhood to adulthood. VWM is caused...
3.
Eshaghkhani Y, Mohamadifar A, Asadollahi M, Taghizadeh M, Karamzade A, Saberi M, et al.
Rep Biochem Mol Biol
. 2021 Oct;
10(2):280-287.
PMID: 34604417
Background: Dilated cardiomyopathy (DCM) is a progressive heart condition characterized by left ventricular chamber enlargement associated with systolic heart failure and prolonged action potential duration. Genetic variations in genes that...
4.
Majidzadeh-A K, Zarinfam S, Abdoli N, Yadegari F, Esmaeili R, Farahmand L, et al.
Fam Cancer
. 2021 Mar;
21(2):137-142.
PMID: 33754277
BRCA1 and BRCA2 are two prominent genes that account for about 20-40% of inherited breast cancer. Mutations in these genes are often associated with clustering of especially early-onset cancers in...
5.
Taghizadeh M, Noruzinia M
Cell J
. 2017 Apr;
19(1):50-64.
PMID: 28367417
Objective: The stem cell theory in the endometriosis provides an advanced avenue of targeting these cells as a novel therapy to eliminate endometriosis. In this regard, studies showed that lovastatin...
6.
Atri Barzanjeh S, Behshid M, Hosseini M, Ezari M, Taghizadeh M, Dastgiri S
Genet Res Int
. 2013 Jan;
2012:129575.
PMID: 23304526
The aim of the study was to report a description of the primary, secondary, and tertiary level services available for genetic disorders in Iran. For the purpose of this study,...
7.
Dastgiri S, Taghizadeh M, Heidarzadeh M
Cardiol Young
. 2011 Jan;
21(2):194-6.
PMID: 21205405
Considerable numbers of congenital cardiac anomalies are missed at the time of delivery. Study reports show that congenital cardiac anomalies are the second most common birth defect in many countries....