مقالات در نشریات
- ۱. Mohammad Shariati و سایر،The prevalence of SMN gene deletion/duplication in spinal muscular atrophy families referred to neuro-genetic centers of Mashhad,Iran،Egyptian Journal of Medical Human Genetics،۲۰۲۴/۰۷/۳۱.
- ۲. Predictors of Health Literacy among Caregivers of Patients with Multiple Sclerosis: A Family-Centred Empowerment Approach،British Journal of Social Work،۲۰۲۲/۰۷/۰۴.
- ۳. Barbara Garavaglia a, Sadeq Vallian b, Luigi M. Romito c, Giulia Straccia c, Marianna Capecci d, Federica Invernizzi a, Elisa Andrenelli d, Arezu Kazemi b, Sylvia Boesch e, Robert Kopajtich f,g, Nahid Olfati h, Mohammad Shariati i,j, Ali Shoeibi i, Ariane،AOPEP variants as a novel cause of recessive dystonia: generalized dystonia and dystonia-parkinsonism،Parkinsonism and related disorders،۲۰۲۲/۰۳/۱۶.
- ۴. محمد شریعتی و سایر،Cell-based Treatment of Cerebral Palsy: Still a Long Way Ahead،Current Stem Cell Research & Therapy،۲۰۲۱/۱۲/۰۷.
- 5. مجید غیور مبرهن et al.,Beyond traditional metrics: evaluating the triglyceride-total cholesterol-body weight index (TCBI) in cardiovascular risk assessment,BMC Cardiovascular Disorders,25/01/2025.
- 6. Unveiling Parry-Romberg Syndrome With Native Demyelinating Etiology as the Underlying Cause,Acta Medica Iranica,2023/11/11.
- 7. محمد رضا سیدتقیا et al.,Copy number analysis from whole-exome sequencing data revealed a novel homozygous deletion in PARK7 leads to severe,Heliyon,2023/04/08.
- 8. رضا جعفرزاده اصفهانی , محمدشریعتی , آریانه صدرنبوی , حمیدرضابیدخوری,Evaluation of COVID-19 Trend in Iran; Population Response to the Recent Pandemic Overtime,International Journal of Preventive Medicine,2022/01/19.
- 9. Michael Zech et.al.,Scoring Algorithm-Based Genomic Testing in Dystonia: A Prospective Validation Study,Movement Disorders,2021/05/05.
نمایش ۱ تا ۹ مورد از کل ۹ مورد.