Asieh Mosallanejad
Overview
Explore the profile of Asieh Mosallanejad including associated specialties, affiliations and a list of published articles.
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17
Citations
32
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Recent Articles
11.
Mosallanejad A, Alaei M, Ghaffari S, Rafati M, Saneifard H
Iran J Child Neurol
. 2020 Apr;
14(2):101-106.
PMID: 32256629
Mucopolysaccharidosis type VII (MPS VII) or Sly syndrome is a rare autosomal recessive disorder caused by deficiency of β-glucuronidase enzyme, which is involved in degradation of glycosaminoglycans. The lack of...
12.
Shakiba M, Alaei M, Saneifard H, Mosallanejad A
Iran J Child Neurol
. 2020 Apr;
14(2):27-39.
PMID: 32256622
Objectives: Dietary phenylalanine restriction is the main treatment of phenylketonuria (PKU, OMIM 261600). There are a number of studies which have demonstrated growth retardation in these patients, and some are...
13.
Jafari N, Mosallanejad A, Ghobadifar A, Karimzadeh P, Ghassemabadi R, Nasehi M, et al.
Iran J Child Neurol
. 2020 Feb;
14(1):123-132.
PMID: 32021636
Objectives: The current study aimed at identifying the role of seizure types and related clinical features in differentiation between neurometabolic disorders and other causes of seizure. Materials & Methods: The...
14.
Shabani Mirzaee H, Mosallanejad A, Rabbani A, Setoodeh A, Abbasi F, Sayarifard F, et al.
Iran J Pediatr
. 2017 Feb;
26(5):e5511.
PMID: 28203334
Background: There is limited data on sexual maturation among girls with intellectual, sensory, or physical disabilities. Objectives: The present cross-sectional study was conducted to assess the sexual maturation of girls...
15.
Mosallanejad A, Tabatabai S, Shakiba M, Alaei M, Saneifard H
J Clin Diagn Res
. 2017 Jan;
10(11):SD07-SD08.
PMID: 28050466
Ovarian hyperstimulation syndrome is a rare disease among preterm infants. This syndrome was first described in 1985 in four infants with a gestational age of <30 weeks. Several explanations for...
16.
Mosallanejad A, Sayarifard F, Hosseinverdi S, Abbasi F, Shabni Mirzaee H, Rezaei N
Acta Med Iran
. 2016 Jan;
53(12):782-4.
PMID: 26749236
There is a number of syndromes, associated with proptosis, micrognathia, low-set ear and chest deformity. Herein, we report a 9-year-old female with such phenotype who was presented with a vaginal...
17.
Movahedi M, Tavakol M, Hirbod-Mobarakeh A, Gharagozlou M, Aghamohammadi A, Tavakol Z, et al.
Iran J Allergy Asthma Immunol
. 2015 Mar;
14(2):222-7.
PMID: 25780889
Chronic urticaria is the most common skin diseases, characterized by chronic cutaneous lesions which severely debilitates patients in several aspects of their everyday life. Vitamin D is known to exert...
18.
Abbasi F, Azizi F, Javaheri M, Mosallanejad A, Ebrahim-Habibi A, Ghafouri-Fard S
Gene
. 2014 Dec;
557(1):103-5.
PMID: 25523092
Fanconi-Bickel syndrome (FBS) is a rare autosomal recessive disorder characterized by hepatorenal glycogen accumulation, proximal renal tubular dysfunction, impaired utilization of glucose and galactose, rickets, and severe short stature. It...