Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Nasrollah Saleh-Gohari"'
Autor:
Nasrollah Saleh-gohari, molok torabi, Reihaneh Saleh Gohari, Elham Abbaszadeh, Malihe Saleh-gohari
Publikováno v:
Journal of Kerman University of Medical Sciences, Vol 30, Iss 5, Pp 290-295 (2023)
Background: Oral lichen planus (OLP) is a chronic inflammatory disease that affects 0.1% to 4% of the population. The disease causes lesions in the buccal mucosa, gingiva, and rarely in the palate. In this study, the relationship between OLP and TNF
Externí odkaz:
https://doaj.org/article/05b330c873964b8cac624c5459854714
Publikováno v:
Iranian Journal of Public Health, Vol 49, Iss 4 (2020)
Background: β-thalassemia is characterized by reduced synthesis of the hemoglobin beta chain that results in microcytic hypochromic anemia and reduced amounts of hemoglobin A (HbA) on hemoglobin analysis. β-thalassemias are caused by mutations in t
Externí odkaz:
https://doaj.org/article/f43fba7f31bb407781aff7e960770ad3
Publikováno v:
Novelty in Biomedicine, Vol 6, Iss 3, Pp 147-151 (2018)
Background: Hepatitis viruses are one of the serious medical problems and Hepatitis B is one of the chief transferable disease via blood and its products. Nowadays, 11 genotypes of hepatitis B have known over the world by the genome sequencing. Hepat
Externí odkaz:
https://doaj.org/article/c6599765160747b1a3ad080f9cf41bd2
Publikováno v:
Journal of Kerman University of Medical Sciences, Vol 24, Iss 5, Pp 414-419 (2017)
Background & Aims:Thromboembolism is an acute cardiovascular disease that ranges from clinically unimportant to massive embolism. Both acquired and hereditary risk factors contribute to the disease. We aimed to determine the prevalence of two heredit
Externí odkaz:
https://doaj.org/article/d40f4600ca0c4368a7701bf48e8cbe4d
Publikováno v:
Journal of Kerman University of Medical Sciences, Vol 23, Iss 5, Pp 572-584 (2016)
Background & Aims: Preeclampsia is one of the complications of pregnancy and a major cause of maternal mortality. Since, hypercoagulation is one of the risk factors, defined polymorphisms of V and II coagulation factors (G1691A and G20210A) may incre
Externí odkaz:
https://doaj.org/article/bb5dac42547d405ab3f9e70b167339d7
Publikováno v:
Basic and Clinical Neuroscience, Vol 4, Iss 1, Pp 88-90 (2013)
Congenital insensitivity to pain with anhidrosis is a rare disease of the nervous system which causes one to lose his/her feeling of pain. The disease is subtype four of hereditary sensory and autonomic neuropathy (HSAN IV) that results from NTRK1 ge
Externí odkaz:
https://doaj.org/article/bb8286fe478e408d98ddd70483abf2ae
Autor:
Alireza Haghighi, Amit Tiwari, Niloofar Piri, Gudrun Nürnberg, Nasrollah Saleh-Gohari, Amirreza Haghighi, John Neidhardt, Peter Nürnberg, Wolfgang Berger
Publikováno v:
PLoS ONE, Vol 9, Iss 11, p e112747 (2014)
The aim of this study was to identify the genetic basis of a chorioretinal dystrophy with high myopia of unknown origin in a child of a consanguineous marriage. The proband and ten family members of Iranian ancestry participated in this study. Linkag
Externí odkaz:
https://doaj.org/article/afbd01504d2446b8a8aa0f2edc0b89d7
Publikováno v:
Neurological Sciences. 42:5077-5085
Progressive myoclonic epilepsy-4 with or without renal failure (EPM4) is a rare neurological autosomal recessive disorder caused by mutations in SCARB2 gene. In this study, we described clinical features and genetic causes of an Iranian family with t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01d70785479bfc4491447074f996d196
https://doi.org/10.1007/s10072-021-05196-0
https://doi.org/10.1007/s10072-021-05196-0
Publikováno v:
Pregnancy Hypertension. 16:75-78
MicroRNAs (miRNAs, miRs) are small regulatory non-coding RNAs that regulate gene expression by incomplete complementary attachment to the 3′UTR, 5′UTR, ORF and promoter regions of target mRNAs. We compared plasma levels of miR-210-3p and miR-517c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0a3cd520af0aa8d3a7ba70e21afa3ce
https://doi.org/10.1016/j.preghy.2019.03.004
https://doi.org/10.1016/j.preghy.2019.03.004
Autor:
Fatemeh Hashemi, Nasrollah Saleh-Gohari, Ali Mousavi, Abolfazl Yari, Arezoo Afzalli, Kolsoum Saeidi
Publikováno v:
Gene Reports. 27:101621
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ed1cca4d2666b91c0a1d0b6322094d23
https://doi.org/10.1016/j.genrep.2022.101621
https://doi.org/10.1016/j.genrep.2022.101621