Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Ali Homaei"'
Publikováno v:
JCRPE, Vol 15, Iss 3, Pp 318-323 (2023)
Osteoporosis-pseudoglioma syndrome (OPPG) is a rare autosomal recessive disorder characterized by severe osteoporosis and eye abnormalities that lead to vision loss. In this study, clinical findings and genetic study of two siblings with OPPG are pre
Externí odkaz:
https://doaj.org/article/9c98e735b5934989b20354e25a210a73
Publikováno v:
Journal of Pediatrics Review, Vol 10, Iss 1, Pp 61-66 (2022)
Background: We presented the clinical and genetic features of a male ambiguity due to 17-beta-hydroxysteroid dehydrogenase 3 (17B-HSD3) deficiency. Methods: The proposita was an 11-year-old girl and the first child of a consanguineous family. The ext
Externí odkaz:
https://doaj.org/article/a83f58b7e34f479ea511c9dc514f256e
Autor:
Ali Homaei
Publikováno v:
Chronic Diseases Journal, Vol 9, Iss 4, Pp 187-191 (2021)
BACKGROUND: Phenylketonuria (PKU) is a hereditary metabolic disorder and is inherited as autosomal recessive, so it is more likely to occur in consanguineous marriages. Early diagnosis is made by screening and timely treatment can prevent brain damag
Externí odkaz:
https://doaj.org/article/1f52659aec6446079a90eb92570205b2
Publikováno v:
Journal of Pediatrics Review, Vol 9, Iss 4, Pp 337-346 (2021)
Background: Puberty is an essential milestone in a person’s life. Studies show that precocious puberty is more common in girls than in boys. Objectives: The aim of this study was to survey the causes of precocious puberty in children referred to th
Externí odkaz:
https://doaj.org/article/f00a1517a64546469ccc22b3b632044a
Publikováno v:
The Journal of Qazvin University of Medical Sciences, Vol 25, Iss 2, Pp 85-92 (2021)
Background: Type 1 Diabetes (T1D) is an autoimmune condition, in which the pancreas produces little or no insulin. Nephropathy is a serious T1D microvascular complication that is associated with high mortality and morbidity. Objective: This study
Externí odkaz:
https://doaj.org/article/75f827fb41b7444a86580a39886dde40
Publikováno v:
مجله دانشکده پزشکی اصفهان, Vol 38, Iss 581, Pp 435-441 (2020)
Background: Type 1 diabetes mellitus (T1D) is the most common chronic endocrine-metabolic disorder of childhood and adolescence. Diabetic ketoacidosis (DKA) is one of the most important acute complications of T1D, and associated with significant morb
Externí odkaz:
https://doaj.org/article/37386ab55a1e45a2ad703b92b3b939ac
Autor:
Fatemeh Saffari, Mohammad Hassan Nikpendar, Neda Esmailzadehha, Sonia Oveisi, Ali Homaei, Shabnam Jalilolghadr
Publikováno v:
Iranian Journal of Neonatology, Vol 9, Iss 3, Pp 1-5 (2018)
Background: Congenital hypothyroidism increases the risk of sensorineural hearing loss (SNHL). Children with hearing impairment are prone to communication disorders. The present study aimed to determine the prevalence of SNHL in patients with congeni
Externí odkaz:
https://doaj.org/article/0fcd7f6c29a547d1864de99f5858a7e8
Autor:
Fatemeh Safari, Mohammad Hossein Ahmadi, Mehdi Azad, Neda Karami, Amirhosein Maali, Neda Mohammadi, Ali Homaei, Farshad Foroughi
Publikováno v:
Turkish Journal of Immunology. 11:17-22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4b04263e001035f7bfd6fdadeccf4f00
https://doi.org/10.4274/tji.galenos.2023.70883
https://doi.org/10.4274/tji.galenos.2023.70883
Publikováno v:
Journal of Pediatrics Review. 9:337-346
Background: Puberty is an essential milestone in a person’s life. Studies show that precocious puberty is more common in girls than in boys. Objectives: The aim of this study was to survey the causes of precocious puberty in children referred to th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ffd465644827d0ac059a17697dda072f
https://doi.org/10.32598/jpr.9.4.960.1
https://doi.org/10.32598/jpr.9.4.960.1
Publikováno v:
Journal of Comprehensive Pediatrics. 13
Background: Nonalcoholic fatty liver disease (NAFLD) is the most frequent form of liver disease in children, defined as the infiltration of fat into more than 5% of liver cells with metabolic syndrome consisting of dyslipidemia, insulin resistance, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2c8fcb09399aa30c991d3388194fb2a0
https://doi.org/10.5812/compreped-123944
https://doi.org/10.5812/compreped-123944