Samaneh Vojdani
Overview
Explore the profile of Samaneh Vojdani including associated specialties, affiliations and a list of published articles.
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Articles
7
Citations
35
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0
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Recent Articles
1.
Abbaskhani H, Seifati S, Salmani T, Vojdani S, Al-Rubaye S, Yaseen R, et al.
Nucleosides Nucleotides Nucleic Acids
. 2022 Jun;
41(9):891-899.
PMID: 35737431
Unexplained recurrent pregnancy loss (RPL) composed almost half of all diagnosed miscarriage cases. As the apoptosis pathway is involved in the pregnancy process the present investigation aimed to assess the...
2.
Vojdani S, Ghaderian S, Zali A, Rakhshan A, Oraee Yazdani S, Poursheikhani A, et al.
Exp Mol Pathol
. 2021 Jun;
121:104655.
PMID: 34062187
Objective: Glioblastoma multiform (GBM) is the most prevalent and invasive brain malignancy in adults. There are ongoing researches to introduce novel and non-invasive potential biomarkers for the early detection of...
3.
Al-Rubaye S, Ghaderian S, Salehpour S, Salmani T, Vojdani S, Yaseen R, et al.
Gynecol Endocrinol
. 2021 Mar;
37(7):660-664.
PMID: 33719810
Aims: Recurrent pregnancy loss (RPL), with unknown causes, is one of the most common challenges facing pregnancy. Apoptotic signaling pathways are involved in the normal and abnormal pregnancy process. Despite...
4.
Jafarzadeh-Esfehani R, Vojdani S, Hashemian S, Mirinezhad M, Pourafshar M, Forouzanfar N, et al.
J Pediatr Endocrinol Metab
. 2020 Feb;
33(3):355-359.
PMID: 32069237
Background Phenylketonuria (PKU) is a common metabolic disorder with great burden if left untreated or undiagnosed. Genetic variations in the phenylalanine hydroxylase (PAH) gene may be widely varied across different...
5.
Vojdani S, Esfehani R, Iranmanesh V, Davari H, Amini N, Jaripour M, et al.
Iran J Otorhinolaryngol
. 2019 Apr;
31(103):109-113.
PMID: 30989077
Introduction: Hearing impairment is a complex medical disorder which has genetic and non-genetic causes. Gap Junction Protein Beta 2 (GJB2) gene variant is a well-known disease-causing gene among patients with...
6.
Vojdani S, Amirsalari S, Milanizadeh S, Molaei F, Ajalloueyane M, Khosravi A, et al.
Fetal Pediatr Pathol
. 2019 Apr;
38(4):273-281.
PMID: 30942114
: Jervell and Lange-Nielsen syndrome (JLNS) is an autosomal recessive genetic disease with deafness and QT prolongation. Mutations in KCNQ1 and KCNE1 genes are a cause of JLNS. Our objective...
7.
Parizadeh S, Jafarzadeh-Esfehani R, Hassanian S, Parizadeh S, Vojdani S, Ghandehari M, et al.
Int J Biochem Cell Biol
. 2019 Mar;
110:75-83.
PMID: 30818083
Colorectal cancer is one of the most common cancers globally. A large portion of colorectal cancer patients who are treated with conventional chemotherapy eventually develop local recurrence or metastases. The...