Maryam Hosseini Moghadam

Mutational Spectrum of LDLR and PCSK9 Genes Identified in Iranian Patients With Premature Coronary Artery Disease and Familial Hypercholesterolemia

N. Seidah, S. Mowla, Zahra Ghaemmaghami, 2021, Frontiers in Genetics.

SURVEY THE MUTATION OF FGB (BETA FIBRINOGEN) AND FV (FACTOR V LEIDEN), FACTOR XIII AND FACTOR II (PROTHROMBIN), IN PATIENTS WITH RECURRENT ABORTIONS ALONG WITH NORMAL KARYOTYPE

J. Panahi, A. Shakoori, Pegah Larki, 2017 .

Megalencephalic Leukoencephalopathy with Subcortical Cysts: Presentation of an Asymptomatic Patient and Review of Literature

M. Barzegar, N. Mahdieh, B. Rabbani, 2019, Iranian Journal of Pediatrics.

Chromosome 9 Inversion: Pathogenic or Benign? A Comprehensive Systematic Review of all Clinical Reports.

M. Maleki, Niloofar Naderi, Samira Kalayinia, 2021, Current molecular medicine.

Exploring TTN variants as genetic insights into cardiomyopathy pathogenesis and potential emerging clues to molecular mechanisms in cardiomyopathies

Niloofar Naderi, Samira Kalayinia, Maryam Hosseini Moghadam, 2024, Scientific reports.

Correction to: High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy Registry

M. Garshasbi, Ali Hosseini Bereshneh, M. Rohani, 2023, neurogenetics.

High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy Registry

M. Barzegar, M. Garshasbi, Ali Hosseini Bereshneh, 2023, neurogenetics.