Zohreh Karamizadeh
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View article: Insulin Resistance Among Children and Adolescents with Subclinical Hypothyroidism: A Case-Control Study
Insulin Resistance Among Children and Adolescents with Subclinical Hypothyroidism: A Case-Control Study Open
Background: Subclinical hypothyroidism (SCH) is marked by elevated thyroid-stimulating hormone (TSH) levels while maintaining normal thyroxine levels. Although the link between insulin resistance (IR) and overt hypothyroidism is well-estab…
View article: Metabolic Nutri-Expert System: A Comprehensive Tool for Achieving Metabolic Control of Inborn Errors of Amino Acid Metabolism
Metabolic Nutri-Expert System: A Comprehensive Tool for Achieving Metabolic Control of Inborn Errors of Amino Acid Metabolism Open
The main aim of this study was to develop a comprehensive nutritional planning expert system for inborn errors of amino acid metabolism (IEAAM).Metabolic Nutri-Expert System, integrated in the electronic nutritional history record, was des…
View article: A Classic Case of Maple Syrup Urine Disease and a Novel Mutation in the BCKDHA Gene
A Classic Case of Maple Syrup Urine Disease and a Novel Mutation in the BCKDHA Gene Open
Background: Maple syrup urine disease (MSUD) is an inherited branched-chain amino acid metabolic disorder caused by the deficiency in the branched-chain alpha-keto acid dehydrogenase (BCKD) complex. In MSUD, elevation of the branched-chain…
View article: Comparison of Continuous Versus Intermittent Administration of Triptorelin on the Final Height of Girls with Idiopathic Precocious Puberty
Comparison of Continuous Versus Intermittent Administration of Triptorelin on the Final Height of Girls with Idiopathic Precocious Puberty Open
Background: It has long been reported that gonadotropin releasing hormone (GnRH) analogs can improve final height of patients with idiopathic precocious puberty (IPP). This study aimed at comparing 2 different doses of GnRH agonist, tripto…
View article: Evaluation of Metabolic Syndrome and Related Factors in Children Affected by Acute Lymphoblastic Leukemia.
Evaluation of Metabolic Syndrome and Related Factors in Children Affected by Acute Lymphoblastic Leukemia. Open
Being overweight is a complication of ALL treatment, which is associated with elevated blood leptin level and BMI Z-score. Therefore, MS criteria, such as BP, weight, and serum triglyceride level, should be taken into account in eac…
View article: ASCIA‐P69: A NOVEL <i>AICDA</i> MUTATION IN A CASE OF AUTOSOMAL RECESSIVE HYPER‐IGM SYNDROME, GROWTH HORMONE DEFICIENCY AND AUTOIMMUNITY
ASCIA‐P69: A NOVEL <i>AICDA</i> MUTATION IN A CASE OF AUTOSOMAL RECESSIVE HYPER‐IGM SYNDROME, GROWTH HORMONE DEFICIENCY AND AUTOIMMUNITY Open
The Hyper-immunoglobulin M syndromes (HIGM) or immunoglobulin class switch recombination (Ig-CSR) deficiencies are rare primary immunodeficiency (PID) disorders. A 9-year-old girl with recurrent ear infections and failure to thrive since t…
View article: A Case of Antley-Bixler Syndrome with New Genetic Study Result
A Case of Antley-Bixler Syndrome with New Genetic Study Result Open
Aims: Antley-Bixler syndrome (ABS) is a rare disease which is a complex of skeletal, visceral, extremity and genital anomalies and occasionally is associated with adrenal insufficiency due to P450-oxidoreductase deficiency.In this article …
View article: Complementary and Alternative Medicine to Treat Diabetes Mellitus Type 1 in Southern Iran
Complementary and Alternative Medicine to Treat Diabetes Mellitus Type 1 in Southern Iran Open
View article: Oral Therapy in a Diabetic Patient With History of Infantile Hyperinsulinism
Oral Therapy in a Diabetic Patient With History of Infantile Hyperinsulinism Open
Dear editor,
Hyperinsulinism is the most common cause of persistent hypoglycemia in early infancy (1). Loss of function mutation in HNF4A gene is an unusual cause of this disease (2). HNF4A protein is a homodimer nuclear transcription f…
View article: Zespół Brucka — rzadki zespół charakteryzujący się kruchością kości, przykurczami stawowymi i nowoodkrytą homozygotyczną mutacją FKBP10
Zespół Brucka — rzadki zespół charakteryzujący się kruchością kości, przykurczami stawowymi i nowoodkrytą homozygotyczną mutacją FKBP10 Open
Bruck syndrome is an autosomal recessive syndrome consisting of bone fragility and congenital joint contractures. According to the genotype, it has been classified into types 1 and 2. Recently, mutations in FKBP10, localised to chromosome …
View article: Critical Illness – Related Corticosteroid Insufficiency
Critical Illness – Related Corticosteroid Insufficiency Open
In some acute critical illnesses, the function of Hypothalamus-Pituitary-Adrenal axis can be impaired. This event is called "Critical Illness-Related Corticosteroid Insufficiency" (CIRCI). We conducted a study to determine which of the CIR…