Regina Gamirova

Dr. Regina Gamirova

Independent Researcher, San Salvador, El Salvador
orcid

Research Focus & Metrics

Academic Career Length

9Years (2018-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
22 November 2023 in Journal of Human Genetics
Verified
Journal Article
Closed access
PDF file
RGRegina Gamirova
Regina Gamirova
ESElena Shagimardanova
Elena Shagimardanova
TSTakehiro Sato
Takehiro Sato
TKTakayuki Kannon
Takayuki Kannon
RGRimma Gamirova
Rimma Gamirova
Atsushi TajimaAtsushi Tajima
Atsushi Tajima

18 January 2018 in BioNanoScience
Verified
Journal Article
Closed access
PDF file
RGRinat Gamirov
Rinat Gamirov
LKLudmila Komarova
Ludmila Komarova
RKRustem Khasanov
Rustem Khasanov
RGRegina Gamirova
Regina Gamirova

1 October 2021 in Journal of the Neurological Sciences
Verified
Journal Article
Closed access
RGRimma Gamirova
Rimma Gamirova
ATArtur Tutarov
Artur Tutarov
RSRoza Shajmardanova
Roza Shajmardanova
RGRegina Gamirova
Regina Gamirova

1 June 2024 in The Bulletin of Contemporary Clinical Medicine
Verified
Journal Article
Closed access
KUKazan Federal University
Kazan Federal University
ASAlina A. Sokolova
Alina A. Sokolova
EGElena A. Gorobets
Elena A. Gorobets
RGRegina Gamirova
Regina Gamirova
Introduction. Juvenile myoclonic epilepsy is the most common form of genetic generalized epilepsy, which is included in the group of idiopathic generalized epilepsies. The etiology of drug-resistant forms of juvenile myoclonic epilepsy, which represent a serious clinical problem, is currently a controversial issue. Aim. To reveal the most significant risk factors of resistance in juvenile myoclonic epilepsy. Materials and Methods. The observational retrospective study included 56 patients, 46 (82%) women and 10 (18%) men. Inclusion criteria: patients diagnosed with juvenile myoclonic epilepsy based on the criteria of the International League Against Epilepsy, treatment for at least 2 years. The type and frequency of epileptic seizures, the onset and course of the disease, concomitant diseases, family history, all available results of 1-2 hours video electroencephalographic monitoring with sleep, and magnetic resonance imaging results were analyzed. Depending on the treatment effect, all patients were divided into two groups: 1 – without seizures, 2 – with seizures. Lack of complete seizure control for at least 2 years was considered intractable epilepsy. Risk ratios as outcomes for dichotomous variables in two compared groups for various characteristics and their confidence intervals were calculated using the Review Manager program (v5.3). Differences were considered significant at P<0.05. Results and Discussion. As a result, there were obtained data on the resistance of juvenile myoclonic epilepsy depending on the age of disease onset, the type of epileptic seizures, changes in the electroencephalogram, and the type of antiepileptic treatment. Conclusions. The most significant risk factors of resistance in juvenile myoclonic epilepsy have been identified: frequent generalized tonic-clonic seizures (more than 5 times a year) accompanying the basic disease, depression, anxiety, and lack of response to the treatment with valproic acid. At the same time, non-compliance, sleep disturbances, consumption of alcohol and energy drinks during therapy are factors that can be controlled during the physician’s individual work with the patient aimed at the explanation and prevention of risks in treatment.