Soheila Sadat Alyasin (Soheila Aleyasin, Soheila Alyasin)

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 7

Top Topics

Allergic Rhinitis

Chronic Obstructive Pulmonary Disease

Top Venues

Health science reports

Computational and mathematical methods in medicine

Pediatric pulmonology

Case reports in genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Soheila Sadat Alyasin, Fateme S Sadeghi, Forough Saki, Mohammad Hossein Dabbaghmanesh
Evaluation of vitamin D deficiency and low bone mass in children with asthma in fars province: A case-control study. Health science reports 7 (6) (2024)
Soheila Sadat Alyasin, Fateme S Sadeghi, Forough Saki, Mohammad Hossein Dabbaghmanesh
Evaluation of vitamin D deficiency and low bone mass in children with asthma in fars province: A case-control study. Health science reports 7 (6) (2024)
Zahra Kanannejad, Mohammad Shomali, Hossein Esmaeilzadeh, Sayyed Hesamedin Nabavizadeh, Koorosh Nikaein, Zahra Ghahramani, Mohammad Amin Ghatee, Soheila Sadat Alyasin
Geoclimatic risk factors for childhood asthma hospitalization in southwest of Iran. Pediatric pulmonology 57 (9) (2022)
Milad Mohkam, Nasim Golkar, Seyed Hesamodin Nabavizadeh, Hossein Esmaeilzadeh, Aydin Berenjian, Zahra Ghahramani, Ahmad Golami, Soheila Sadat Alyasin
In Silico Evaluation of Nonsynonymous SNPs in Human ADAM33: The Most Common Form of Genetic Association to Asthma Susceptibility. Computational and mathematical methods in medicine 2022 (2022)
Sayyed Hesamedin Nabavizadeh, Rafat Noeiaghdam, Leila Johari, Seyed Ali Hosseini, Hossein Esmaeilzadeh, Soheila Sadat Alyasin
A rare case of SRD5A3-CDG in a patient with ataxia and telangiectasia: A case report. Clinical case reports 10 (11) (2022)
Hossein Esmaeilzadeh, Rafat Noeiaghdam, Leila Johari, Seyed Ali Hosseini, Sayyed Hesamedin Nabavizadeh, Soheila Sadat Alyasin
Homozygous Autosomal Recessive DIAPH1 Mutation Associated with Central Nervous System Involvement and Aspergillosis: A Rare Case. Case reports in genetics 2022 (2022)
Mohsen Farvardin, Mohammad Hassan Jalalpour, Mohammad Reza Khalili, Golnoush Mahmoudinezhad, Fereshteh Mosavat, Soheila Sadat Alyasin, Hamidreza Jahanbani-Ardakani
Retinal Occlusive Vasculitis in a Patient with Hyperimmunoglobulin E Syndrome. Case reports in ophthalmological medicine 2021 (2021)