Sanaz Attaripour Isfahani
Overview
Explore the profile of Sanaz Attaripour Isfahani including associated specialties, affiliations and a list of published articles.
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5
Citations
119
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Recent Articles
1.
Cif L, Cif L, Demailly D, Demailly D, Lin J, Lin J, et al.
ArXiv
. 2025 Feb;
PMID: 39990802
Heterozygous mutations in are associated with an early-onset, progressive and often complex dystonia (DYT28). Key characteristics of typical disease include focal motor features at disease presentation, evolving through a caudocranial...
2.
Isfahani S, McGurrin P, Vial F, Hallett M
Exp Brain Res
. 2025 Feb;
243(3):73.
PMID: 39982468
The goal of this study was to investigate the decision making process for choosing what movements to make. We used electroencephalography (EEG) to investigate patterns of the contingent negative variation...
3.
Vittayawacharin P, Sy M, Isfahani S, Karnes W, Kongtim P, Ciurea S
Am J Hematol
. 2023 Sep;
98(10):1659-1662.
PMID: 37676996
Level of autoantibodies after autologous hematopoietic stem cell transplantation. AGA, antigliadin antibody; AHSCT, autologous hematopoietic stem cell transplantation; Anti-GAD65, Ab anti-glutamic acid decarboxylase epitope 65 antibody; Anti-TPO, anti-thyroid peroxidase antibody;...
4.
Cif L, Demailly D, Lin J, Barwick K, Sa M, Abela L, et al.
Brain
. 2020 Nov;
143(11):3242-3261.
PMID: 33150406
Heterozygous mutations in KMT2B are associated with an early-onset, progressive and often complex dystonia (DYT28). Key characteristics of typical disease include focal motor features at disease presentation, evolving through a...
5.
Kletenik I, Sillau S, Isfahani S, LaFaver K, Hallett M, Berman B
Mov Disord Clin Pract
. 2020 Feb;
7(2):177-181.
PMID: 32071936
Background: The prevalence of functional movement disorders is 2 to 3 times higher in women than in men. Trauma and adverse life events are important risk factors for developing functional...
6.
Isfahani S, Dougherty M, Gliebus G
SAGE Open Med Case Rep
. 2017 Dec;
5:2050313X17744482.
PMID: 29276596
Creutzfeldt-Jakob disease accounts for more than 90% of all sporadic prion disease cases. The molecular MM2 genotype has been divided into cortical and thalamic subtypes based on structures involved and...
7.
Savli M, Bauer A, Mitterhauser M, Ding Y, Hahn A, Kroll T, et al.
Neuroimage
. 2012 Jul;
63(1):447-59.
PMID: 22789740
The highly diverse serotonergic system with at least 16 different receptor subtypes is implicated in the pathophysiology of most neuropsychiatric disorders including affective and anxiety disorders, obsessive compulsive disorder, post-traumatic...