Saeid Sadeghian

发表

Clinical non-penetrance associated with biallelic mutations in the RNase H2 complex

Y. Crow, M. Zamani, G. Rice, 2023, Journal of Clinical Immunology.

COVID‐19 in a case with Kikuchi‐Fujimoto disease

N. Rezaei, S. Sadeghian, K. Jaseb, 2021, Clinical case reports.

IN VITRO SEMI-QUANTITATIVE DETERMINATAION OF HUMAN GAMMA-INTERFERON EXPRESSION BY RT-PCR

A. Zamani, J. Nasiri, Saeid Sadeghian, 2007 .

Putative founder effect of Arg338* AP4M1 (SPG50) variant causing severe intellectual disability, epilepsy and spastic paraplegia: Report of three families

H. Galehdari, M. Abramowicz, G. Lefort, 2022, Clinical genetics.

Central nervous system manifestations in COVID‐19 patients: A systematic review and meta‐analysis

H. Ebadi, S. Dalvand, A. Azari Jafari, 2020, medRxiv.

Novel homozygous variants in PRORP expand the genotypic spectrum of combined oxidative phosphorylation deficiency 54

W. Yue, H. Galehdari, R. O’Keefe, 2023, European Journal of Human Genetics.

Biallelic MED27 variants lead to variable ponto-cerebello-lental degeneration with movement disorders

J. Lupski, S. Lalani, Matteo P. Ferla, 2023, Brain : a journal of neurology.

Global, regional, and national incidence of six major immune-mediated inflammatory diseases: findings from the global burden of disease study 2019

Sathish Kumar Jayapal, Vijay Kumar Chattu, Colin Simpson, 2023, EClinicalMedicine.

Global, regional, and national burden of disorders affecting the nervous system, 1990–2021: a systematic analysis for the Global Burden of Disease Study 2021

Sathish Kumar Jayapal, Tilahun Ferede Asena, Vijay Kumar Chattu, 2024, The Lancet Neurology.

ZSCAN10 deficiency causes a neurodevelopmental disorder with characteristic oto-facial malformations

Tzung-Chien Hsieh, S. Efthymiou, R. Maroofian, 2024, Brain : a journal of neurology.