Kahani SM

References (2)

Title : Expression assay of the COLQ in a family with congenital myasthenic syndrome and symptomatic carriers - Mohammadi_2023_Clin.Case.Rep_11_e8062
Author(s) : Mohammadi MF , Fateh ST , Aghajani H , Bahramy A , Zaheryani SMS , Behroozi J , Kahani SM , Mohammadi P , Garshasbi M
Ref : Clin Case Rep , 11 :e8062 , 2023
Abstract :
PubMedSearch : Mohammadi_2023_Clin.Case.Rep_11_e8062
PubMedID: 37881193

Title : Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patients - Dehnavi_2023_Orphanet.J.Rare.Dis_18_177
Author(s) : Dehnavi AZ , Bemanalizadeh M , Kahani SM , Ashrafi MR , Rohani M , Toosi MB , Heidari M , Hosseinpour S , Amini B , Zokaei S , Rezaei Z , Aryan H , Amanat M , Vahidnezhad H , Mohammadi P , Garshasbi M , Tavasoli AR
Ref : Orphanet J Rare Dis , 18 :177 , 2023
Abstract :
PubMedSearch : Dehnavi_2023_Orphanet.J.Rare.Dis_18_177
PubMedID: 37403138