Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Simin Khayatzadeh Kakhki"'
Autor:
Ghazal Shariatpanahi, Simin Khayatzadeh Kakhki, Paniz Pourpashang, Parisa Ashournia, Malihe Rahimi, Masoumeh Ghasempour, Niloufar Ghanbari
Publikováno v:
Heliyon, Vol 10, Iss 24, Pp e40926- (2024)
The Ages and Stages Questionnaires: Social-Emotional, Second Edition (ASQ) is a parental-report tool designed to assess the social-emotional development of young children. Its adaptation and validation in diverse cultural contexts are vital for its e
Externí odkaz:
https://doaj.org/article/591f3e7a06d84a71b90aa5cf9e92dfe7
Autor:
Vahid Mansouri, Morteza Heidari, Maryam Bemanalizadeh, Reza Azizimalamiri, Shahriar Nafissi, Masood Ghahvechi Akbari, Mohammad Barzegar, Ali Reza Moayedi, Reza Shervin Badv, Mahmood Mohamadi, Ali Reza Tavasoli, Susan Amirsalari, Ali Khajeh, Soroor Inaloo, Farzad Fatehi, Sareh Hosseinpour, Meisam Babaei, Seyed Ahmad Hosseini, Seyyed Mohammad Mahdi Hosseiny, Afshin Fayyazi, Firoozeh Hosseini, Mehran Beiraghi Toosi, Nahid Khosroshahi, Homa Ghabeli, Habibeh Nejad Biglari, Simin Khayatzadeh Kakhki, Seyed Hossein Mirlohi, Elham Bidabadi, Bahram Mohammadi, Abdolmajid Omrani, Mostafa Sedighi, Mohammad Vafaee-Shahi, Maryam Rasulinezhad, Seyyed Mohamad Hoseini, Mojtaba Movahedinia, Zahra Rezaei, Parviz Karimi, Hossein Farshadmoghadam, Saeed Anvari, Omid Yaghini, Jafar Nasiri, Gholamreza Zamani, Mahmoud Reza Ashrafi
Publikováno v:
Journal of Neuromuscular Diseases. 10:211-225
Background: Insufficient amounts of survival motor neuron protein is leading to one of the most disabling neuromuscular diseases, spinal muscular atrophy (SMA). Before the current study, the detailed characteristics of Iranian patients with SMA had n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1050f12b1ad45d5c6285a65d7c6b2244
https://doi.org/10.3233/jnd-221614
https://doi.org/10.3233/jnd-221614
Publikováno v:
American Journal of Medical Case Reports. 9:65-66
Pancake or doughnut kidney is a very rare anatomical abnormality. It is subgroup of fusion anomaly. Most of the time, diagnosed incidentally because affected patients are asymptomatic. Here we repot Pancake kidney in Toddler boy with proteinuria and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5902149a5aa95268e05b96107bac770e
https://doi.org/10.12691/ajmcr-9-1-16
https://doi.org/10.12691/ajmcr-9-1-16