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1 . Academic Journal
PKD2 mutation in an Iranian autosomal dominant polycystic kidney disease family with misleading linkage analysis data
저자
by
Entezam, Mona
;
Khatami, Mohammad Reza
;
Saddadi, Fereshteh
;
Ayati, Mohsen
;
Roozbeh, Jamshid
, et al.
소스
Kidney Research and Clinical Practice
. 35(2):96-101
View Record (KoreaMed)
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7 . Academic Journal
Replication of TCF7L2 rs7903146 association with type 2 diabetes in an Iranian population
저자
by
Amoli, Mahsa M.
;
Amiri, Parvin
;
Tavakkoly-Bazzaz, Javad
;
Charmchi, Elham
;
Hafeziyeh, Jila
, et al.
소스
Genetics and Molecular Biology
. January 2010 33(3)
Open Access (SciELO)
Web of Science
Scopus
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7 . Academic Journal
Exome sequencing reveals novel rare variants in Iranian familial multiple sclerosis: The importance of POLD2 in the disease pathogenesis
저자
by
Salehi, Zahra
;
Keramatipour, Mohammad
;
Talebi, Saeed
;
Arab, Seyed Shahriar
;
Naser Moghadasi, Abdorreza
, et al.
소스
In
Genomics
July 2021 113(4):2645-2655
Full Text (ScienceDirect)
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7 . Academic Journal
First report of Klein-Waardenburg Syndrome in Iran and a novel pathogenic splice site variant in PAX3 gene
저자
by
Saberi, Mohammad
;
Golchehre, Zahra
;
Salmani, Hamzeh
;
Karamzade, Arezou
;
Tabatabaie, Seyed Ziaeddin
, et al.
소스
In
International Journal of Pediatric Otorhinolaryngology
October 2018 113:229-233
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7 . Academic Journal
Targeted next generation sequencing identified a novel mutation in MYO7A causing Usher syndrome type 1 in an Iranian consanguineous pedigree
저자
by
Kooshavar, Daniz
;
Razipour, Masoumeh
;
Movasat, Morteza
;
Keramatipour, Mohammad
.
소스
In
International Journal of Pediatric Otorhinolaryngology
January 2018 104:10-13
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6 . Academic Journal
A novel missense variant in EIF2B5 identified in a consanguineous Iranian family with vanishing white matter disease and a brief review of the literature.
저자
by
Nourmohammadi, Parisa
;
Asadollahi, Mostafa
;
Karamzade, Arezou
;
Eshaghkhani, Yeganeh
;
Babaei, Meisam
, et al.
소스
Journal of Genetics
. Dec2023, Vol. 102 Issue 2, p1-8. 8p.
Web of Science
Scopus
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7 . Academic Journal
APOA II genotypes frequency and their interaction with saturated fatty acids consumption on lipid profile of patients with type 2 diabetes
저자
by
Noorshahi, Neda
;
Sotoudeh, Gity
;
Djalali, Mahmoud
;
Eshraghian, Mohamad Reza
;
Keramatipour, Mohammad
, et al.
소스
In
Clinical Nutrition
August 2016 35(4):907-911
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7 . Academic Journal
Effect of DHA-rich fish oil on PPARγ target genes related to lipid metabolism in type 2 diabetes: A randomized, double-blind, placebo-controlled clinical trial
저자
by
Mansoori, Anahita
;
Sotoudeh, Gity
;
Djalali, Mahmoud
;
Eshraghian, Mohammad-Reza
;
Keramatipour, Mohammad
, et al.
소스
In
Journal of Clinical Lipidology
November-December 2015 9(6):770-777
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7 . Academic Journal
Clinical, Immunological, and Genetic Findings in Iranian Patients with MHC-II Deficiency: Confirmation of c.162delG RFXANK Founder Mutation in the Iranian Population.
저자
by
Mousavi Khorshidi, Mohadese Sadat
;
Seeleuthner, Yoann
;
Chavoshzadeh, Zahra
;
Behfar, Maryam
;
Hamidieh, Amir Ali
, et al.
소스
Journal of Clinical Immunology
. Nov2023, Vol. 43 Issue 8, p1941-1952. 12p.
Web of Science
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7 . Academic Journal
Intestinal hypomagnesemia in an Iranian patient with a novel TRPM6 variant: a case report and review of the literature.
저자
by
Kamali, Farnaz
;
Jamee, Mahnaz
;
Sayer, John A.
;
Sadeghi-Bojd, Simin
;
Golchehre, Zahra
, et al.
소스
CEN Case Reports; Nov2023, Vol. 12 Issue 4, p413-418, 6p
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