A Family With Novel X-Linked Recessive Homozygous Mutation in ANOS1 (c.628_629 del, p.1210fs∗) in Kallmann Syndrome Associated Unilateral Ptosis: Case Report and Literature Review...

por Noorian, Shahab, Savad, Shahram, Khavandegar, Armin, Jamee, Mahnaz
Publicado 2021

GCK Mutation in a Child with Maturity Onset Diabetes of the Young, Type 2

por Noorian, Shahab, Sayarifard, Fatemeh, Farhadi, Elham, Barbetti, Fabrizio, Rezaei, Nima
Publicado 2013

Late infantile form of multiple sulfatase deficiency

por Mohammadian Khonsari, Nami, Hakak-Zargar, Benyamin, Voth, Tessa, Noorian, Shahab
Publicado 2020

Associated factors to insulin adherence in type 1 diabetes in Tehran and Karaj, Iran

por Fayyaz, Farimah, Aghamahdi, Fatemeh, Noorian, Shahab, Tabatabaei-Malazy, Ozra, Qorbani, Mostafa
Publicado 2022

Reliability of Pubertal Self Assessment Method: An Iranian Study

por Rabbani, Ali, Noorian, Shahab, Fallah, Javad S., Setoudeh, Arya, Sayarifard, Fatemeh, Abbasi, Farzaneh
Publicado 2013

Dizygotic Twins Concordant for Down Syndrome: Implication for Establishing a National Birth Defect Registry in Iran

por SAVAD, Shahram, HAMZEHLOU, Sepideh, GHAFFOURIAN ABADI, Jila, MODARRESSI, Mohammad Hossein, NOORIAN, Shahab
Publicado 2016

The Role of Thyroid Function Tests in Diagnosing Allan-herndon-dudley Syndrome Revisited: A Novel Iran-based Mutation

por Noorian, Shahab, Hamzehlou, Sepideh, Rabbani, Ali, Sotoudeh, Arya, Pour Rostami, Kioumars, Savad, Shahram
Publicado 2021