Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Morteza Alijanpour Aghamaleki"'
Autor:
Morteza Alijanpour Aghamaleki, Masoomeh Rezapour, Kazem Babazadeh, Hassan Zamani, Faeze Aghajanpour
Publikováno v:
Journal of Pediatrics Review, Vol 7, Iss 1, Pp 55-60 (2019)
Background: Methylmalonate-semialdehyde Dehydrogenase Deficiency (MMSDHD) is an uncommon autosomal recessive disorder. MMSDH is an enzyme encoded by the protein coding gene ALDH6A1 in humans. Case Presentation: We present a 4-year-old boy with elevat
Externí odkaz:
https://doaj.org/article/26ca4b30d8424ee6aad818c0eace429d
Autor:
Morteza Alijanpour Aghamaleki, Mohammad Reza Esmaeili Dooki, Leila Moslemi, Masomeh Rezapour, Robab Chypaz, Faeze Aghajanpour
Publikováno v:
Caspian Journal of Pediatrics, Vol 3, Iss 1, Pp 205-208 (2017)
Background: Type 1 diabetes mellitus (T1DM) as an autoimmune disorder is associated with other autoimmune diseases such as autoimmune thyroid (AIT) disease. The aim of this study was to determine the prevalence of AIT in children who were referred to
Externí odkaz:
https://doaj.org/article/1c893e0415d1499b9a0ee32d7aa42479
Autor:
Morteza Alijanpour Aghamaleki, Zohreh Shabanzadeh, Masomeh Rezapour, Ali Bijani, Faeze Aghajanpour
Publikováno v:
Caspian Journal of Pediatrics, Vol 2, Iss 2, Pp 142-147 (2016)
Background: Diabetic ketoacidosis (DKA) is the final consequence and life-threatening complication of severe insulin deficiency in type 1 diabetes with occurrence of 20-40%. The aim of this study was to investigate the incidence and predisposing fact
Externí odkaz:
https://doaj.org/article/0c9b2234f8a74a0b9243f4f3a61aa6d0
Autor:
Morteza Alijanpour Aghamaleki, Mahmoud Hajiahmadi, Mohammad Pornasrollah, Zahra Oruji, Faeze Aghajanpour
Publikováno v:
International Journal of Pediatrics, Vol 7, Iss 2, Pp 8977-8984 (2019)
Background Considering the increasing prevalence of type 1 diabetes mellitus (T1DM) as an autoimmune disease in recent years and the positive effects of vitamin D (VD) on this disease, especially the preventive effect of VD on progressive reduction o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::92c9f67474b66de37206a5011b70d810
http://ijp.mums.ac.ir/article_11332_faca26563f4e229c1f108681aa8fa8a9.pdf
http://ijp.mums.ac.ir/article_11332_faca26563f4e229c1f108681aa8fa8a9.pdf
Autor:
Hassan Ali Zamani, Faeze Aghajanpour, Kazem Babazadeh, Morteza Alijanpour Aghamaleki, Masoomeh Rezapour
Publikováno v:
Journal of Pediatrics Review, Vol 7, Iss 1, Pp 55-60 (2019)
Background: Methylmalonate-semialdehyde Dehydrogenase Deficiency (MMSDHD) is an uncommon autosomal recessive disorder. MMSDH is an enzyme encoded by the protein coding gene ALDH6A1 in humans. Case Presentation: We present a 4-year-old boy with elevat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5ba50fccefca3182c68cd78c97bf596
http://jpr.mazums.ac.ir/browse.php?a_code=A-10-285-1&slc_lang=en&sid=1
http://jpr.mazums.ac.ir/browse.php?a_code=A-10-285-1&slc_lang=en&sid=1
Autor:
Hassan Mahmoodi Nesheli, Motahareh Amouzadeh Samakoush, Mahmoud Hajiahmadi, Faeze Aghajanpour, Ahmad Tamaddoni, Morteza Alijanpour Aghamaleki
Publikováno v:
Iranian Journal of Pediatric Hematology & Oncology.
Background: Thalassemia major (TM) is one of the most common hereditary anemia with multiple endocrinopathies (especially hypogonadism). So, we evaluated the rate of delayed puberty (DP) and its relation with serum ferritin level in patients. Materia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::82c5a418fde435923fe4c385ff75dad4
https://doi.org/10.18502/ijpho.v9i1.294
https://doi.org/10.18502/ijpho.v9i1.294
Autor:
Seyed Reza Hosseini, Mohammad Pournasrollah, Leila Moslemi, Negar Noushiravani, Mahmoud Hajiahmadi, Morteza Alijanpour Aghamaleki, Mohammadreza Esmaeili Dooki
Publikováno v:
J Diabetes Metab Disord
OBJECTIVES: This study aimed to investigate the association between Helicobacter pylori infection with diabetes mellitus type one and the effect of infected Helicobacter pylori on glycemic control. METHODS: This case control study was conducted on ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9bc76d33fe799b553b7f210d197a0156
https://pubmed.ncbi.nlm.nih.gov/32550173
https://pubmed.ncbi.nlm.nih.gov/32550173
Autor:
Mahdi Pouramir, Morteza Alijanpour Aghamaleki, Ali Bijani, Sohrab Kazemi, Mohammad Pornasrollah, Mohammadreza Esmaeili Dooki, Hassan Ashrafianamiri, Ali Akbar Moghadamnia, Leila Moslemi, Hajighorban Nooreddini
Publikováno v:
Pediatric research. 84(5)
To evaluate the efficacy of stoss therapy using fortified biscuit for vitamin D-deficient children. A total of 108 children aged 30–72 months with vitamin D deficiency were studied in a randomized single-blind clinical trial. The deficient children
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5378a61c05b6993679e88fb4d155edda
https://pubmed.ncbi.nlm.nih.gov/30120406
https://pubmed.ncbi.nlm.nih.gov/30120406
Autor:
Mohammadreza, Esmaeili Dooki, Leila, Moslemi, Ali Akbar, Moghadamnia, Morteza, Alijanpour Aghamaleki, Ali, Bijani, Mohammad, Pornasrollah, Hassan, Ashrafianamiri, Haji-Ghorban, Nooreddin
Publikováno v:
Archives of Iranian medicine. 21(12)
Rickets is failure in mineralization of growing bone and cartilage due to extreme vitamin D deficiency (VDD). The study aimed to identify rickets among vitamin D deficient children and determine any relationship between clinical findings and paraclin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::32d5d1c57a32ad3396f5524078c7af99
https://pubmed.ncbi.nlm.nih.gov/30634857
https://pubmed.ncbi.nlm.nih.gov/30634857