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New Presentation of CD27 Deficiency; Coronary Ectasia and COVID-19.
Golchehre Z, Sharafian S, Momtazmanesh N, Chavoshzadeh Z, Karimi A, Abolhassani H, Kazemi Aghdam M, Vahidshahi K, Hashemimoghaddam S, Kosari F, Khafafpour Z, Shamsian BS, Keramatipour M. Golchehre Z, et al. Iran J Allergy Asthma Immunol. 2023 Feb 20;22(1):110-118. doi: 10.18502/ijaai.v22i1.12013. Iran J Allergy Asthma Immunol. 2023. PMID: 37002625 Free article.
A Novel Mutation in SNX10 Gene Causes Malignant Infantile Osteopetrosis.
Amirfiroozy A, Hamidieh AA, Golchehre Z, Rezamand A, Yahyaei M, Beiranvandi F, Amirfiroozy S, Keramatipour M. Amirfiroozy A, et al. Among authors: golchehre z. Avicenna J Med Biotechnol. 2017 Oct-Dec;9(4):205-208. Avicenna J Med Biotechnol. 2017. PMID: 29090071 Free PMC article.
Whole-Exome Sequencing Identified a Novel Variant (C.405_422+39del) in DSP Gene in an Iranian Pedigree with Familial Dilated Cardiomyopathy.
Eshaghkhani Y, Mohamadifar A, Asadollahi M, Taghizadeh M, Karamzade A, Saberi M, Nourmohammadi P, Golchehre Z, Amin A, Keramatipour M. Eshaghkhani Y, et al. Among authors: golchehre z. Rep Biochem Mol Biol. 2021 Jul;10(2):280-287. doi: 10.52547/rbmb.10.2.280. Rep Biochem Mol Biol. 2021. PMID: 34604417 Free PMC article.
Next-generation sequencing identified novel truncating mutations in BBS9 causing Bardet Biedl syndrome in two Iranian consanguineous families.
Akbaroghli S, Kooshavar D, Golchehre Z, Karamzade A, Saberi M, Alaei MR, Abbasi Sadegh M, Asadollahi M, Keramatipour M. Akbaroghli S, et al. Among authors: golchehre z. Iran J Child Neurol. 2022 Winter;16(1):123-133. doi: 10.22037/ijcn.v16i1.31650. Epub 2022 Jan 1. Iran J Child Neurol. 2022. PMID: 35222663 Free PMC article.
18 results