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Biallelic SQSTM1 mutations in early-onset, variably progressive neurodegeneration.
Neurology. 2018 Jul 24;91(4):e319-e330. doi: 10.1212/WNL.0000000000005869. Epub 2018 Jun 29.
Neurology. 2018.
PMID: 29959261
Free PMC article.
Expression changes of serotonin receptor gene subtype 5HT3a in peripheral blood mononuclear cells from schizophrenic patients treated with haloperidol and Olanzapin.
Shariati GR, Ahangari G, Hossein-nezhad A, Asadi SM, Pooyafard F, Ahmadkhaniha HR.
Shariati GR, et al.
Iran J Allergy Asthma Immunol. 2009 Sep;8(3):135-9.
Iran J Allergy Asthma Immunol. 2009.
PMID: 20124604
Free article.
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Novel Homozygous Missense Mutation in RYR1 Leads to Severe Congenital Ptosis, Ophthalmoplegia, and Scoliosis in the Absence of Myopathy.
Dilaver N, Mazaheri N, Maroofian R, Zeighami J, Seifi T, Zamani M, Sedaghat A, Shariati GR, Galehdari H.
Dilaver N, et al. Among authors: shariati gr.
Mol Syndromol. 2017 Dec;9(1):25-29. doi: 10.1159/000481897. Epub 2017 Nov 15.
Mol Syndromol. 2017.
PMID: 29456480
Free PMC article.
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