A5022138818- Multiple Sclerosis Research Studies
- Cervical Cancer and HPV Research
- BRCA gene mutations in cancer
- Immunotherapy and Immune Responses
- Genomic variations and chromosomal abnormalities
- Genital Health and Disease
- Hepatitis B Virus Studies
- Blood Coagulation and Thrombosis Mechanisms
- Rheumatoid Arthritis Research and Therapies
- Nutrition, Genetics, and Disease
- Genetic factors in colorectal cancer
- Hemoglobinopathies and Related Disorders
- Cerebral Venous Sinus Thrombosis
- Long-Term Effects of COVID-19
- Cancer-related gene regulation
- Coronary Artery Anomalies
- Antiplatelet Therapy and Cardiovascular Diseases
- IL-33, ST2, and ILC Pathways
- SARS-CoV-2 and COVID-19 Research
- Intracerebral and Subarachnoid Hemorrhage Research
- Peripheral Neuropathies and Disorders
- Cancer Cells and Metastasis
- Glutathione Transferases and Polymorphisms
- Parvovirus B19 Infection Studies
- Kruppel-like factors research
Qom University of Medical Science and Health Services
2014-2023
Tehran University of Medical Sciences
2009-2017
Imam Khomeini Hospital
2017
Motamed Cancer Institute
2007-2012
University of Tehran
2008
Objective Based on the few population-based studies that have been conducted in Middle East, we determined incidence of stroke Qom, one central provinces Iran. Methods The Qom province includes an estimated at-risk population about 1 million. During a 12-month period (November 2018–November 2019), all first-ever strokes occurring target were registered. Hospitalized cases ascertained by discharge codes. Out-of-hospital prospective screening emergency medical services, departments, ambulances...
Introduction Familial Mediterranean fever (FMF) is a hereditary inflammatory disorder caused by mutation in MEFV, gene which encodes 781-amino acid protein called pyrin . The classic clinical picture consists of recurrent febrile episodes that are usually an acute onset, variable frequency, sometimes without recognized triggering factor, but often occurring with menstruation, emotional stress or strenuous physical activity FMF autosomal recessive disorder. disease affects populations origin:...
Introduction: Annually a considerable number of people die because breast cancer, common disease among women also in Iran. Identifying risk factors and susceptible can lead to prevention or at least early diagnosis. Among susceptibility risks, 5-10% patients have family history predisposing factor which influence the incidence family. Having registry program be more practical way screen high families for preventive planning. Method: Based on inclusion criteria, questionnaire was prepared...
Background: Gastric cancer is the second most common cause of death. It has a poor prognosis with only 5-10% hereditary etiology. If it diagnosed, could be helpful for screening other susceptible members family preventive procedures. Usually identified by symptoms such as presence in different family, some special type pathology diffused adenocarcinoma, having younger age and multiple syndromes. Hence, designing registry program can more practical way to screen high risk families program....
Background: Statins are widely used for the medical management of vascular conditions, including ischemic stroke. However, genetic factors and polymorphisms, SLCO1B1 388A>G single-nucleotide polymorphism (SNP), have shown significant effects in response to statin therapy. To best our knowledge, gender-gene interaction therapy, affected by 388 A>G SNP, has not been investigated yet. The current study describes therapeutic outcomes this variation terms clinical evaluations laboratory...
Context: Inherited thrombophilia is an abnormality of blood coagulation that increases the risk thromboembolic disease. During pregnancy, thrombogenic potential this inherited disorder enhanced because hypercoagulable state produced by normal pregnancy-associated changes in several factors. Aims: The purpose research was to find association polymorphisms and mutations Settings Design: This Study first comprehensive study genes Iranian population. Methods Material: current performed a group...
Background and Aim: A stroke is the rapid loss of brain function due to a disturbance in blood supply. Age major risk factor for stroke. Genetic influence may be more important younger patients. Patients with positive results should receive appropriate counseling. This study first comprehensively thrombophilia genes Iranian populations ischemic The purpose this was determine occurrence genetic mutations linked CVD individuals examine their correlation clinical parameters Markers...
The Clinical Profile and 1-Year Prognosis of Patients With Cerebral Venous Sinus Thrombosis: A Study in Qom Province, Iran
Background and Aim: COVID-19 is an emerging threat that could affect the cardiovascular system in setting of a cytokine storm syndrome. This study examines cardiac injury associated with patients Multiple Sclerosis (MS). Case Presentation: We analyzed 6 cases MS association who underwent evaluation during their hospitalization. The mean age our was 36.6 years. Two had Secondary Progressive (SPMS), one patient Primary (PPMS), rest Relapsing-Remitting (RRMS). Our were on both immunomodulatory...