تمدنی, احمد
مرکز تحقیقات بیماری های غیر واگیر کودکان، پژوهشکده سلامت، دانشگاه علوم پزشکی بابل، بابل، ایران
[ 1 ] - ارتباط عفونت هلیکو باکتر پیلوری با پورپورای ترومبو سیتو پنیک ایدیو پاتیک (ITP) در کودکان - بستری در بیمارستان کودکان امیرکلا
مقدمه: اخیرا مطالعات مختلفی شیوع بالای عفونت هلیکو باکتر پیلوری در بزرگسالان مبتلا به ITP را گزارش کرده اند علاوه بر این در این مطالعات افزایش شمارش پلاکتی در برخی از بیماران متعاقب درمان ریشه کن سازی این میکروب گزارش شده است که این مساله نقش احتمالی هلیکو باکتر پیلوری در بروز ITP بزرگسالان را مطرح می کند اما مطالعات صورت گرفته در این زمینه در گروه سنی کودکان بسیار محدود بوده است. هدف از این...
[ 2 ] - بررسی وضعیت سلامت دهان و کیفیت زندگی وابسته به آن در بیماران مبتلا به بتاتالاسمی ماژور
Background and purpose: This study aimed at determining the oral health condition and oral health-related quality of life in thalassemia major patients attending Amirkola Thalassemia Center. Materials and methods: In this cross-sectional study a total of 250 patients with beta thalassemia major, was evaluated for mucosa condition and dental health (DMFT index). Oral health-related quality of l...
[ 3 ] - Relationship between β-Thalassemia minor and Helicobacter pylori infection
Background: Until now, no study has been reported investigating the association between β-thalassemia minor and Helicobacter pylori (H. pylori) infection. This study was designed to compare H. pylori infection rate between β-thalassemia minor patients and healthy controls. Methods: A number of 100 β-thalassemia minor patients (50 males, 50 females) and 100 gender-matched healthy...
[ 4 ] - Isolated thrombocytopenia report of a rare presentation of childhood Systemic Lupus Erythematosus
Background: Systemic lupus erythematosus (SLE) has various presentations in children. Hematologic abnormalities is common in childhood onset of SLE, however, isolated thrombocytopenia is relatively rare. Thus, we present a child with isolated thrombocytopenia as a rare presentation of SLE. Case presentation: A 12-year-old boy with chief complaints of loss of appetite, weight loss, decrease...
[ 5 ] - رابطه ژنژیویت و پریودنتیت با بیماری β تالاسمی ماژور
سابقه و هدف: تالاسمی شایعترین اختلال ژنتیکی در سنتز هموگلوبین است که با کاهش زنجیره های آلفا و یا بتاگلوبین مشخص می شود. مهمترین نشانه های این بیماری شامل تغییرات استخوانی به ویژه در جمجمه، ماگزیلا و استخوان گونه و پوسیدگی های دندانی و بیماری پریودنتال می باشد. با توجه به شیوع بیشتر عوارض دهانی دندانی در این بیماران با تشخیص به موقع می توان به پیشگیری و درمان معضلات بیماران تالاسمیک اقدام کرد ل...
[ 6 ] - The incidence of hyperglycemia during the induction phase of chemotherapy in patients with acute lymphoblastic leukemia
Background: Hyperglycemia is one of the most complications of corticosteroid and asparaginase during induction phase of chemotherapy in children suffering from acute lymphoblastic leukemia (ALL). This study was carried out to evaluate the incidence of hyperglycemia and associated risk factors during chemotherapy induction phase at Amirkola Children's Hospital. Materials and Methods: In this c...
[ 7 ] - Therapeutic Effects of Recombinant Growth Hormone in Improving the Growth of Thalassemia Major Patients: A Retrospective Study
Background and purpose: Beta thalassemia major is one of the most common inherited blood diseases and patients with this condition require regular blood transfusions. The resulting iron overload deposition causes endocrine gland disorders, including growth hormone (GH) abnormality. In this study, we examined the effects of recombinant growth hormone (rGH) in these patients. Materials and metho...
[ 8 ] - Prevalence of HCVAb and HBsAg in Patients with Beta-thalassemia Major in Amirkola Thalassemia Center
Background and purpose: Beta-thalassemia major is a genetic disorder with known globin defect that leads to chronic hemolytic anemia. Due to the need for recurrent blood transfusion, the risk of infectious diseases such as hepatitis is higher in these patients. Materials and methods: This cross-sectional study recruited 518 patients with thalassemia major in Amirkola Thalassemia Center, 2013-2...
[ 9 ] - Complications of patients with hematologic malignancies in a selected Iranian population
Background: Hematologic malignancies in childhood and their treatments can cause dental anomalies and jaw bone abnormalities; therefore, the aim of this study was to assess the prevalence of these disorders in children. Methods: This cross-sectional study was conducted on all children diagnosed with hematologic malignancies that referred to in Amirkola Children’s Hospital from 2011 to 2018. Al...
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