A5028783631- Dialysis and Renal Disease Management
- Chronic Kidney Disease and Diabetes
- Neurogenetic and Muscular Disorders Research
- Renal and Vascular Pathologies
- RNA modifications and cancer
- Blood Pressure and Hypertension Studies
- Electrolyte and hormonal disorders
- Magnesium in Health and Disease
- Vascular anomalies and interventions
- Muscle and Compartmental Disorders
- Congenital Anomalies and Fetal Surgery
- Neurological and metabolic disorders
- Parathyroid Disorders and Treatments
- Chronic Disease Management Strategies
- Nutrition and Health in Aging
- Abdominal vascular conditions and treatments
- Hemodynamic Monitoring and Therapy
- Renal Diseases and Glomerulopathies
- Renal function and acid-base balance
- Restless Legs Syndrome Research
- Genetic and Kidney Cyst Diseases
- Pancreatic and Hepatic Oncology Research
- Multiple and Secondary Primary Cancers
- Iron Metabolism and Disorders
- Genomics and Rare Diseases
Ahvaz Jundishapur University of Medical Sciences
2012-2024
Sharif University of Technology
2023
Marymount University
2016
Universiti Sains Malaysia
2008-2014
Hospital Universiti Sains Malaysia
2009-2014
Islamic Azad University, Omidieh Branch
2012
Imam Khomeini Hospital
2011
Imam Hossein Hospital
2011
Background: Chronic kidney disease (CKD) is defined as damage or reduced function for three months more, regardless of the cause. Hemodialysis (HD) has become dominant renal replacement therapy in many parts world. Currently, due to absence definitive evidence on safety and efficacy, there no consensus optimal sodium concentration dialysis. Objectives: Considering importance regulation HD patients, we conducted a study impact low levels dialysis fluid hemodynamics chronic patients. Methods:...
Introduction: Malnutrition is a complex, multi-factorial and common problem in patients with end-stage renal disease (ESRD) undergoing hemodialysis that increases morbidity mortality rate them. Objectives: To assess the prevalence of malnutrition associated factors patients. Patients Methods: This cross-sectional study was conducted on 239 (162 males 77 females) referred to three dialysis centers Ahvaz, Iran 2018. The nutritional statuswas measured using subjective global assessment...
Tuberous sclerosis complex is an autosomal dominant neurocutaneous disorder affecting multiple organs. caused by mutation in either one of the two disease-causing genes, TSC1 or TSC2, encoding for hamartin and tuberin, respectively. TSC2/PKD1 contiguous gene deletion syndrome a very rare condition due to involving both TSC2 PKD1 genes. cannot be easily diagnosed since there no pathognomonic feature, although are consensus diagnostic criteria that. Mutation analysis useful plays important...
Implication for health policy/practice
Genetic diagnosis of spinal muscular atrophy (SMA) is complicated by the presence SMN2 gene as majority SMA patients show absence or deletion SMN1 gene. PCR may amplify both genes non selectively in high amount DNA. We evaluated whether allele-specific for diagnostic screening reliable genomic DNA, which commonly used when performing using restriction enzymes.A total 126 blood DNA samples were tested amounts ranging 80-200 ng, referred genetic conventional PCR-RFLP and PCR.The results from...
Background: Information on sitagliptin as a third line agent in combination with other antidiabetic agents is still lacking.This study evaluated the safety and efficacy of an add-on therapyin type 2 diabetes mellitus (T2DM) patients poorly controlled glucose control despite receiving optimum dose ofmetforminand sulphonylurea.Method: In 24-week, non-randomized, open-labeled trial study, T2DM (n=93) who were dosage metformin sulphonylurea additionally treated 100 mg daily.Primary end point was...
Diabetic nephropathy is a clinical syndrome characterized by persistent albuminuria and progressive impairment in renal function. Pentoxifylline non-specific inhibitor of phosphodiesterase with anti-inflammatory properties which may have therapeutic potency patients diabetic kidney disease.
Background: End-stage renal disease patients on maintenance hemodialysis (ESRD-HD) are at very high risk for COVID-19 infections due to their older age and comorbidities such as diabetes hypertension. Objectives: This study aimed investigate the outcomes of in ESRD-HD patients. Methods: was a retrospective conducted aged 18 years who were referred Razi Hospitals Ahvaz from February 2020 May 2021 diagnosed with COVID-19. Patient information extracted retrospectively medical records. Results:...
Implication for health policy/practice/research/medical educationHypermagnesemia is also not a prominent feature among patients with chronic kidney disease, in the absence of increased magnesium administration, however renal failure mostly at its final stages most common cause hypermagnesemia.