Yousef Shafeghati
Overview
Explore the profile of Yousef Shafeghati including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
26
Citations
337
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Alamatsaz M, Jalalypour F, Hashemi M, Shafeghati Y, Nasr-Esfahani M, Ghaedi K
J Cell Biochem
. 2021 May;
PMID: 33955040
The peroxisome is responsible for a variety of vital pathways in primary metabolism, including the very long-chain fatty-acid oxidation and plasmalogen lipid biosynthesis. Autosomal recessive disorder of the Zellweger spectrum...
2.
Valilou S, Alavi A, Pashaei M, Ghasemi Firouzabadi S, Shafeghati Y, Nozari A, et al.
Mol Syndromol
. 2020 Jul;
11(2):62-72.
PMID: 32655337
Autism spectrum disorder (ASD) is characterized by 3 core symptoms with impaired social communication, repetitive behavior, and/or restricted interests in early childhood. As a complex neurodevelopmental disorder (NDD), the phenotype...
3.
Mohammadzadeh A, Akbaroghli S, Aghaei-Moghadam E, Mahdieh N, Badv R, Jamali P, et al.
Cell J
. 2019 Jun;
21(3):337-349.
PMID: 31210441
Objective: Major birth defects are inborn structural or functional anomalies with long-term disability and adverse impacts on individuals, families, health-care systems, and societies. Approximately 20% of birth defects are due...
4.
Colombo E, Mutlu-Albayrak H, Shafeghati Y, Balasar M, Piard J, Gentilini D, et al.
Front Pediatr
. 2019 Jun;
7:210.
PMID: 31192177
Baller-Gerold (BGS, MIM#218600) and Roberts (RBS, MIM#268300) syndromes are rare autosomal recessive disorders caused, respectively, by biallelic alterations in (MIM603780) and (MIM609353) genes. Common features are severe growth retardation, limbs...
5.
Noguchi M, Honsho M, Abe Y, Toyama R, Niwa H, Sato Y, et al.
J Hum Genet
. 2014 May;
59(7):387-92.
PMID: 24849933
Rhizomelic chondrodysplasia punctata (RCDP) is an autosomal recessive disorder due to the deficiency in ether lipid synthesis. RCDP type 1, the most prominent type, is caused by the dysfunction of...
6.
Behjati F, Ghasemi Firouzabadi S, Sajedi F, Kahrizi K, Najafi M, Ebrahimizade Ghasemlou B, et al.
Iran Red Crescent Med J
. 2014 Apr;
15(10):e8221.
PMID: 24693374
Background: Mental retardation/Developmental delay (MR/DD) is present in 1 - 3% of the general population (1, 2). MR is defined as a significant impairment of both cognitive (IQ < 70)...
7.
Hadipour Z, Shafeghati Y, Hadipour F
Acta Med Iran
. 2014 Mar;
52(1):85-7.
PMID: 24658994
The Yunis-Varón syndrome represents a rare autosomal recessive syndrome of easy recognition characterized by defective growth of the cranial bone along with complete or partial absence of the clavicles (cleidocranial...
8.
Hadipour F, Shafeghati Y, Bagherizadeh E, Behjati F, Hadipour Z
Acta Med Iran
. 2014 Jan;
51(12):907-9.
PMID: 24442548
49,XXXXY is rare chromosomal pattern and these patients have mental retardation, small penis, cryptorchidism and skeletal anomalies. We reported a 10 month-old boy who has hypotonia, microcephaly, hypertelorism, depressed nasal...
9.
Hadipour F, Sarkheil P, Noruzinia M, Hadipour Z, Baghdadi T, Shafeghati Y
Indian J Hum Genet
. 2013 Aug;
19(1):84-6.
PMID: 23901198
Fanconi-Bickel syndrome is an extremely rare hereditary metabolic disease, characterized by hepatomegaly due to glycogen storage, refractory hypophosphatemic rickets, marked growth retardation and proximal renal tubular acidosis. Recurrent bone fractures...
10.
Hajikhan Mirzaei M, Noruzinia M, Karbassian H, Shafeghati Y, Keyhanee M, Bidmeshki-Pour A
Cell J
. 2013 Apr;
14(1):19-24.
PMID: 23626933
Objective: Breast cancer is one of the most common malignancies in women worldwide. It is caused by a number of genetic and epigenetic factors. Aberrant hypermethylation of the promoter regions...