Mohammadreza Dehghani
Overview
Explore the profile of Mohammadreza Dehghani including associated specialties, affiliations and a list of published articles.
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37
Citations
206
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Recent Articles
11.
Eshaghi F, Dehghan Tezerjani M, Ghasemi N, Dehghani M
Int J Reprod Biomed
. 2022 Nov;
20(10):841-850.
PMID: 36381354
Background: Primary ovarian insufficiency (POI) is a rare disease clinically characterized by ovarian follicles depletion or dysfunction and menopause before the age of 40 yr as the cut-off age for...
12.
Christensen M, Levy A, Mohammadi N, Niceta M, Kaiyrzhanov R, Dentici M, et al.
Clin Genet
. 2022 May;
102(2):98-109.
PMID: 35616059
Biallelic variants of the gene encoding for the zinc-finger protein 142 (ZNF142) have recently been associated with intellectual disability (ID), speech impairment, seizures, and movement disorders in nine individuals from...
13.
Moudi M, Vahidi Mehrjardi M, Hozhabri H, Metanat Z, Kalantar S, Taheri M, et al.
J Clin Lab Anal
. 2022 Jan;
36(2):e24241.
PMID: 35019165
Background: Intellectual disability (ID) is a heterogeneous group of neurodevelopmental disorders that is characterized by significant impairment in intellectual and adaptive functioning with onset during the developmental period. Whole-exome sequencing...
14.
Hengel H, Hannan S, Dyack S, MacKay S, Schatz U, Fleger M, et al.
Am J Hum Genet
. 2021 May;
108(6):1069-1082.
PMID: 34022130
BCAS3 microtubule-associated cell migration factor (BCAS3) is a large, highly conserved cytoskeletal protein previously proposed to be critical in angiogenesis and implicated in human embryogenesis and tumorigenesis. Here, we established...
15.
Sisi S, Azarbayjani M, Vafaeenasab M, Peeri M, Dehghani M
Int J Reprod Biomed
. 2021 Apr;
19(3):283-292.
PMID: 33842825
Background: Menopause is the natural termination of menstruation which affects the quality and important aspects of women's life. Objective: To evaluate the effect of regular resistance training (Ex) with vitamin...
16.
Kaiyrzhanov R, Wortmann S, Reid T, Dehghani M, Vahidi Mehrjardi M, Alhaddad B, et al.
Brain
. 2021 Jan;
144(3):e30.
PMID: 33454747
No abstract available.
17.
Appelhof B, Wagner M, Hoefele J, Heinze A, Roser T, Koch-Hogrebe M, et al.
Eur J Hum Genet
. 2020 Nov;
29(3):411-421.
PMID: 33168985
Pontocerebellar hypoplasia (PCH) describes a group of rare heterogeneous neurodegenerative diseases with prenatal onset. Here we describe eight children with PCH from four unrelated families harboring the homozygous MINPP1 (NM_004897.4)...
18.
Hozhabri H, Talebi M, Mehrjardi M, De Luca A, Dehghani M
Am J Med Genet A
. 2020 Mar;
182(5):957-961.
PMID: 32162791
Warburg Micro syndrome and Martsolf syndrome are phenotypically overlapping autosomal recessive conditions characterized by multiple organ abnormalities involving the ocular, nervous, and endocrine systems. Warburg Micro syndrome, the more severe...
19.
Dehghani M, Zarch S, Vahidi Mehrjardi M, Nazari M, Babakhanzadeh E, Ghadimi H, et al.
Endocrinol Diabetes Nutr (Engl Ed)
. 2020 Jan;
67(7):454-460.
PMID: 31948856
Background: Type 2 diabetes mellitus (T2DM) is a progressive metabolic disorder whose prevalence is rising very fast across the world. Diagnosis of this disease in early stages (pre-diabetic stage) plays...
20.
Perenthaler E, Nikoncuk A, Yousefi S, Berdowski W, Alsagob M, capo I, et al.
Acta Neuropathol
. 2019 Dec;
139(3):415-442.
PMID: 31820119
Developmental and/or epileptic encephalopathies (DEEs) are a group of devastating genetic disorders, resulting in early-onset, therapy-resistant seizures and developmental delay. Here we report on 22 individuals from 15 families presenting...