Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Kiavash Khashayar"'
Publikováno v:
Caspian Journal of Internal Medicine, Vol 15, Iss 1, Pp 193-198 (2024)
Background: Elejalde syndrome is a rare neuroectodermal melanolysosomal disease with an autosomal recessive heredity. Patients usually present with silvery-gray hair, neurological abormalities, diffuse skin hypopigmentation and suntanned skin color.
Externí odkaz:
https://doaj.org/article/969098d0b0cc40dca4932103ed5b00e1
Autor:
Farimah Fayyaz, Kiavash Khashayar, Mina Rasmi, Ehsan Shahrestanaki, Hamid Asayesh, Marzieh Tavakol, Mostafa Qorbani
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 21, Iss 4 (2022)
This study is a part of the Global Asthma Network (GAN) phase I project to assess asthma symptoms in children, adolescents, and their parents in Karaj, Iran. The present cross-sectional study was conducted in 2019-2020 in Karaj, Iran, in alignment wi
Externí odkaz:
https://doaj.org/article/fff866da8163462cb37224252d654695
Autor:
Farimah Fayyaz, Kiavash Khashayar, Mina Rasmi, Ehsan Shahrestanaki, Hamid Asayesh, Marzieh Tavakol, Mostafa Qorbani
Publikováno v:
Iranian journal of allergy, asthma, and immunology. 21(4)
This study is a part of the Global Asthma Network (GAN) phase I project to assess asthma symptoms in children, adolescents, and their parents in Karaj, Iran. The present cross-sectional study was conducted in 2019-2020 in Karaj, Iran, in alignment wi