Zobrazeno 1 - 10
of 52
pro vyhledávání: '"Ahmad, Tamaddoni"'
Publikováno v:
Caspian Journal of Internal Medicine, Vol 14, Iss 1, Pp 10-15 (2023)
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
Externí odkaz:
https://doaj.org/article/d6b7dab015fb4d0b8fa5aab552ba4d4b
Publikováno v:
Caspian Journal of Internal Medicine, Vol 13, Iss 4, Pp 765-771 (2022)
Background: Due to anemia in thalassemia major (TM) and thalassemia intermedia (TI) patients, bone changes occur, especially in the broad bones like jaw and skull, which are the main sites of hematopoiesis. Therefore, the dentist should be aware of t
Externí odkaz:
https://doaj.org/article/9b85a066e1634c58acbd8b5d3b97c74f
Autor:
Hadi Sorkhi, Mohamadreza esmaeilidooki, Maryam Nikpour, Mohsen Mohammadi, Ali Mohammadpour-Mir, Masood Kiani, Sanaz Mehrabani, Sahar Sadr Moharerpour, Morteza Alijanpour, Kazem Babazadeh, Hassan Mahmoodi-Nesheli, Mohamadreza Tabatabaie, Ahmad Tamaddoni, Mohammadreza Salehiomran, Paiam Payandeh, Iraj Mohammadzadeh, Sareh Hosseinpour
Publikováno v:
Caspian Journal of Internal Medicine, Vol 13, Iss Covid 19 Supplement 2, Pp 193-198 (2022)
Background: The New coronavirus (SARS COV-2) can cause acute respiratory disease and also multiorgan dysfunction. There is insufficient data about kidney involvement in children. So, this study was done on children with COVID-19 to evaluate nephrolog
Externí odkaz:
https://doaj.org/article/fa2ad6e4c7494e7285c6dc125703a3ce
Autor:
Ahmad Tamaddoni, Morteza Alijanpour
Publikováno v:
Journal of Mazandaran University of Medical Sciences, Vol 30, Iss 185, Pp 51-60 (2020)
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
Externí odkaz:
https://doaj.org/article/e47dc6d16c84409686ee7069281a61f0
Publikováno v:
Journal of Education and Health Promotion, Vol 11, Iss 1, Pp 37-37 (2022)
BACKGROUND: Caring for the children suffering from thalassemia is a stressful experience with various aspects making the mothers face various challenges. Thus, the present study aimed to explain the psychosocial challenges of mothers with thalassemia
Externí odkaz:
https://doaj.org/article/61170a8580f741048fec1297445b64d7
Publikováno v:
Caspian Journal of Pediatrics, Vol 4, Iss 2, Pp 316-319 (2018)
Background: Tumor lysis syndrome (TLS) which mostly occurs in lymphoproliferative malignancies after the start of chemotherapy is an oncologic emergency. Manifestations of metabolic imbalance including increasing hyperkalemia, hyperphosphatemia, hype
Externí odkaz:
https://doaj.org/article/96fd5479914b4858b29db4601f5648d6
Publikováno v:
Caspian Journal of Pediatrics, Vol 4, Iss 1, Pp 290-293 (2018)
Background: Kikuchi disease is a rare, benign, self-limited disease characterized primarily by fever and cervical lymphadenopathy. Diagnosis is based on excisional biopsy and pathologic study. We report a case of an atypical axillary lymph node enlar
Externí odkaz:
https://doaj.org/article/3e2e47d3dcf24024a3acb458ab74200f
Autor:
Mohammad Zamani, Amin Vahedi, Ahmad Tamaddoni, Ali Bijani, Mojgan Bagherzade, Javad Shokri-Shirvani
Publikováno v:
Caspian Journal of Internal Medicine, Vol 9, Iss 1, Pp 54-59 (2018)
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 patie
Externí odkaz:
https://doaj.org/article/e1f4b294c34e478bb69acb4d2d400ef1
Publikováno v:
Caspian Journal of Pediatrics, Vol 1, Iss 2, Pp 65-72 (2015)
Background: The prevalence of obesity is increasing and many countries are struggling with its high rate and serious complications. As a result of distinct diet in obese children, they may be susceptible to nutritional deficiencies in particular, iro
Externí odkaz:
https://doaj.org/article/944c321dfb024119a546e17c47120b24
Publikováno v:
Majallah-i Dānishgāh-i ̒Ulūm-i Pizishkī-i Bābul, Vol 16, Iss 11, Pp 22-27 (2014)
Objective:Thalassemia is the most common genetic disorder of hemoglobin synthesis by reducing alpha or beta globin chains is determined. The main symptoms of the disease include bone deformities, especially in the skull, maxilla and zygoma and dental
Externí odkaz:
https://doaj.org/article/85ea5ae04e744a54ad191caa4a14e25e