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A Comprehensive Overview of NF1 Mutations in Iranian Patients.
Neuromolecular Med. 2024 Jul 2;26(1):28. doi: 10.1007/s12017-024-08790-5.
Neuromolecular Med. 2024.
PMID: 38954284
Elejalde syndrome - A neuroectodermal melanolysosomal disease: A case report.
Noohi AH, Shojaaldini Ardakani H, Khashayar K, Najafi L.
Noohi AH, et al. Among authors: shojaaldini ardakani h.
Caspian J Intern Med. 2024 Winter;15(1):193-198. doi: 10.22088/cjim.15.1.24.
Caspian J Intern Med. 2024.
PMID: 38463909
Free PMC article.
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Hereditary Autonomic Neuropathy of the Oral Cavity and its Management.
Esmaeilzadeh N, Ashrafi MR, Shojaaldini Ardakani H, Seraj B, Aref P.
Esmaeilzadeh N, et al. Among authors: shojaaldini ardakani h.
Iran J Child Neurol. 2022 Winter;16(1):135-142. doi: 10.22037/ijcn.v15i4.32016. Epub 2022 Jan 1.
Iran J Child Neurol. 2022.
PMID: 35222664
Free PMC article.
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A novel pathogenic variant of BRAT1 gene causes rigidity and multifocal seizure syndrome, lethal neonatal.
Pourahmadiyan A, Heidari M, Shojaaldini Ardakani H, Noorian S, Savad S.
Pourahmadiyan A, et al. Among authors: shojaaldini ardakani h.
Int J Neurosci. 2021 Sep;131(9):875-878. doi: 10.1080/00207454.2020.1759589. Epub 2020 Apr 29.
Int J Neurosci. 2021.
PMID: 32345087
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