Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Aazam Ahmadi Shadmehri"'
Autor:
Aliasgar Mohammadi, Aazam Ahmadi Shadmehri, Mahnaz Taghavi, Gholamhossein Yaghoobi, Mohammad Reza Pourreza, Mohammad Amin Tabatabaiefar
Publikováno v:
Iranian Journal of Basic Medical Sciences, Vol 23, Iss 8, Pp 1020-1027 (2020)
Objective(s): Granular and lattice corneal dystrophies (GCDs & LCDs) are autosomal dominant inherited disorders of the cornea. Due to genetic heterogeneity and large genes, unraveling the mutation is challenging.Materials and Methods: Patients underw
Externí odkaz:
https://doaj.org/article/5de735399d734e05aa45e541be2fe93c
Publikováno v:
Journal of Research in Applied and Basic Medical Sciences, Vol 6, Iss 1, Pp 14-17 (2020)
Carriers of structural chromosomal rearrangements such as Robertsonian or reciprocal translocations have an increased risk of spontaneous abortion and producing offspring with genetic abnormalities. Robertsonian translocations are present in 0.1% of
Externí odkaz:
https://doaj.org/article/5ad80fa027404f5ea25f8f56f7ab2bb2
Publikováno v:
Majallah-i Dānishgāh-i ’Ulūm-i Pizishkī-i Īlām, Vol 26, Iss 3, Pp 1-6 (2018)
Introduction: Edwards’s syndrome is a chromosomal disorder caused due to the presence of an extra chromosome 18. This syndrome was first reported in 1960 by Edward. The prevalence of this disease is approximately 1:6000 live births, and its preva
Externí odkaz:
https://doaj.org/article/23a0c5538ce046159312996393475308
Publikováno v:
Journal of Kerman University of Medical Sciences, Vol 22, Iss 5, Pp 524-532 (2015)
Background & Aims: Toxoplasmosis in one of the most prevalent parasitic infections that could result in abortion or miscarriage in the pregnant women. The main objective of this research was to determine seroepidemioligy of toxoplasmosis infection am
Externí odkaz:
https://doaj.org/article/f50b33a49ba64e5ca1d402862dc699fc
Publikováno v:
Gene, Cell and Tissue. 8
Introduction: Congenital ichthyosiform erythroderma (CIE) is a subtype of autosomal recessive congenital ichthyosis (ARCI), a group of ineffective keratinization disorders, which mainly results from missense mutations in the transglutaminase 1 (TGM1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::45c943a165892a783ac4a9d3792e7236
https://doi.org/10.5812/gct.109321
https://doi.org/10.5812/gct.109321
Publikováno v:
Majallah-i Dānishgāh-i ’Ulūm-i Pizishkī-i Īlām, Vol 26, Iss 3, Pp 1-6 (2018)
Introduction: Edwards’s syndrome is a chromosomal disorder caused due to the presence of an extra chromosome 18. This syndrome was first reported in 1960 by Edward. The prevalence of this disease is approximately 1:6000 live births, and its preva
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2d78a734ca4f81205080a49f95778c9
http://sjimu.medilam.ac.ir/browse.php?a_code=A-10-3469-1&slc_lang=en&sid=1
http://sjimu.medilam.ac.ir/browse.php?a_code=A-10-3469-1&slc_lang=en&sid=1
Autor:
Aazam Ahmadi Shadmehri, Hossein Safarpour, Ebrahim Miri-Moghaddam, Negin Parsamanesh, Shokoofe Etesam
Publikováno v:
Journal of molecular neuroscience : MN. 69(4)
Intellectual disability (ID) is characterized by limited mental ability and adaptive behavior that imposes a heavy burden on the patients’ families and the health care system. This study was aimed at determining the molecular aspect of nonsyndromic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8da0a4be4de0c946e673fc2376844c87
https://pubmed.ncbi.nlm.nih.gov/31414351
https://pubmed.ncbi.nlm.nih.gov/31414351