Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Fatemeh Saffari"'
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
Autor:
Fatemeh Saffari, Banafsheh Arad
Publikováno v:
Journal of Pediatrics Review, Vol 10, Iss 1, Pp 67-72 (2022)
Background: 11beta-hydroxylase deficiency (11βOHD) is clinically presented with external genitalia virilization in girls and precocious puberty in boys. Low renin hypertension occurs in both sexes. Early diagnosis and treatment of hypertension can p
Externí odkaz:
https://doaj.org/article/43a7ded4693b40f2ba238e123ed3ed74
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:
Shabnam Jalilolghadr, Fatemeh Saffari, Mehdi Alizadeh, AliReza Taremiha, Marjan Ghodsi, Mersedeh Ghodsi
Publikováno v:
Clinical Case Reports, Vol 11, Iss 2, Pp n/a-n/a (2023)
Abstract Alstrom syndrome is a rare genetic disorder with an autosomal recessive mutation in the ALMS1 gene. The disease's manifestations include ophthalmic problems, hearing loss, obesity, and cardiovascular disorders. In addition, medical cases inc
Externí odkaz:
https://doaj.org/article/9ce4a8b2d77d4d80995ba16a3f91d4d1
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
Publikováno v:
پژوهش در نظامهای آموزشی, Vol 14, Iss ویژه نامه, Pp 27-36 (2020)
The purpose of the present study is to deduce the aims, principles and principles of justice in the teaching of Islam based on Islamic teachings. To achieve this goal, a qualitative research method was used by applying the reconstructed Frankenza inf
Externí odkaz:
https://doaj.org/article/c4b68a4add5f4ff79ddc38da19a88e54
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:
Foroogh Namjoyan, Fatemeh Kiashi, Zahra Beigom Moosavi, Fatemeh Saffari, Behzad Sharif Makhmalzadeh
Publikováno v:
Journal of Traditional and Complementary Medicine, Vol 6, Iss 1, Pp 37-40 (2016)
The blood-red sap of Dragon's blood has been used in folk medicine for fractures, wounds, inflammation, gastrointestinal disorders, rheumatism, blood circulation dysfunctions, and cancer. Existing in vitro and in vivo bioactivity of this herb on diff
Externí odkaz:
https://doaj.org/article/0412da5fdf1a4ccdaf75c8c0ba7344d8