Zobrazeno 1 - 10
of 76
pro vyhledávání: '"Fatemeh Sayarifard"'
Autor:
Hamidreza Mianesaz, Safoura Ghalamkari, Farzaneh Abbasi, Maryam Razzaghy‐Azar, Fatemeh Sayarifard, Rahim Vakili, Maryam Sedghi, Samaneh Noroozi Asl, Sousan Hosseini, Mahsa M Amoli, Hanieh Yaghootkar
Publikováno v:
Journal of Diabetes Investigation, Vol 15, Iss 10, Pp 1390-1402 (2024)
ABSTRACT Introduction Neonatal diabetes mellitus (NDM) is a rare non‐immunological monogenic disorder characterized by hyperglycemic conditions primarily occurring within the first 6 months of life. The majority of cases are attributed to pathogeni
Externí odkaz:
https://doaj.org/article/d5d59eee454645a18bc1d5fc7a3c602b
Publikováno v:
Clinical Case Reports, Vol 11, Iss 9, Pp n/a-n/a (2023)
Key Clinical Message Infantile liver failure type 2 is described as repeated attacks of liver dysfunction with remission. This syndrome should be considered in the differential diagnosis of any child with symptoms of recurrent hepatic encephalopathy.
Externí odkaz:
https://doaj.org/article/7d751b1cc5e247b9b1ffb9b1b6b584bf
Autor:
Aria Setoodeh, Samareh Panjeh-Shahi, Fariba Bahmani, Fatemeh Vand-Rajabpour, Nazanin Jalilian, Fatemeh Sayarifard, Farzaneh Abbasi, Azadeh Sayarifard, Parastoo Rostami, Nima Parvaneh, Haleh Akhavan-Niaki, Mohamadreza Ahmadifard, Mina Tabrizi
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-9 (2022)
Abstract Objective Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED) is a rare autosomal recessive systemic autoimmune disease caused by mutations in the autoimmune regulator (AIRE) gene. Incidence of this genetic disor
Externí odkaz:
https://doaj.org/article/5b6db6f799634bb7b7a4fc7d2be757a3
Publikováno v:
Bihdād, Vol 9, Iss 1, Pp 91-94 (2020)
Introduction: Myopathy and rhabdomyolysis are not common in children and, if not detected and do not treated it will be associated with high mortality and morbidity rate. The causes of rhabdomyolysis include hypokalemia, trauma, viral myositis, poiso
Externí odkaz:
https://doaj.org/article/6450200147e04113a0ada84c4b0df961
Autor:
Soheila Hoseinzadeh Moghadam, Masood Ghahvechi, Fatemeh Mozafari, Fatemeh Sayarifard, Mahdieh-Sadat Mousavi, Reza Rostami, Vahid Ziaee
Publikováno v:
Acta Medica, Vol 62, Iss 4, Pp 161-165 (2020)
Mucopolysaccharidoses (MPS) are a subgroup of lysosomal storage disorders. The underlying mechanism of MPS disorders are deficiency in specific enzymes which leads to accumulation of partially degraded glycosaminoglycans (GAGs) in various tissues. A
Externí odkaz:
https://doaj.org/article/b96520769dd24b62848a7304563e7880
Autor:
Mahdieh Soveizi, Nejat Mahdieh, Aria Setoodeh, Fatemeh Sayarifard, Farzaneh Abbasi, Himangshu S. Bose, Bahareh Rabbani, Ali Rabbani
Publikováno v:
International Journal of Endocrinology, Vol 2020 (2020)
Premature pubarche (PP) is the appearance of sexual hair in children before puberty. The PP phenotype may attribute to nonclassic congenital adrenal hyperplasia (NC-CAH). In this study, we investigated the role of CYP21A2 gene variants in patients wi
Externí odkaz:
https://doaj.org/article/844d86afe4b9423ab70c051cb8a1d006
Autor:
Fatemeh Sayarifard, Fereshteh Bakhshi Imcheh, Shirinsadat Badri, Toktam Faghihi, Mostafa Qorbani, Mania Radfar
Publikováno v:
Journal of Research in Pharmacy Practice, Vol 6, Iss 1, Pp 40-43 (2017)
Objective: One of the main problems facing public health providers and administrators in many countries is ensuring the rational use of high-cost drugs. In this regard, on-going process of medication use evaluation can be considered as a useful tool.
Externí odkaz:
https://doaj.org/article/6a9fc0ffcfc54563863a255bbcf3231f
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 35:709-726
Background Registries are considered valuable data sources for identification of pediatric conditions treated with growth hormone (GH), and their follow-up. Currently, there is no systematic literature review on the scope and characteristics of pedia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f87bb745276d35e537253a4e5b0aea13
https://doi.org/10.1515/jpem-2022-0045
https://doi.org/10.1515/jpem-2022-0045
Autor:
Nima Rezaei, Reihaneh Mohsenipour, Parisa Tajdini, Fatemeh Sayarifard, Hamid Reza Khoramkhorshid, Sedigheh Madani
Publikováno v:
Endocrine, Metabolic & Immune Disorders - Drug Targets. 21:2296-2299
Background: In Congenital Disorder of Glycosylation (CDG) type Ia, homozygous mutations of the PMM2 gene cause phosphomannomutase 2 dysfunction. Case presentation: Herein, a 10-month-old girl is presented with severe hypotonia along with inappropriat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::08fc92b86c3772f9b89ec607e63f8294
https://doi.org/10.2174/1871530321666210415105917
https://doi.org/10.2174/1871530321666210415105917
Autor:
Aria Setoodeh, Ali Rabbani, Fatemeh Sayarifard, Zahra Haghshenas, Azadeh Sayarifard, Parastoo Rostami, Farzaneh Abbasi, Mohadeseh Bayat, Sima Amini, Reza Tavakolizadeh
Publikováno v:
Iranian Journal of Pediatrics. 32
Background: The purpose of this study was to compare the effectiveness of once-daily versus twice-daily insulin detemir injection in children with type 1 diabetes mellitus (T1DM). Methods: In this randomized 4-month clinical trial, 60 children aged 3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4bb0cee9b2c50607e843e1ed1f94bc8c
https://doi.org/10.5812/ijp-116461
https://doi.org/10.5812/ijp-116461