Risultati della ricerca - Parham Nejati

A case study of a novel homozygous EDAR splice site variant in hypohidrotic ectodermal dysplasia with tooth agenesis: molecular dynamics insights di Parham Nejati, Teymoor Khosravi, Saba Lorestani, Morteza Oladnabi

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Combination of Myelin Basic Protein Gene Polymorphisms with HLA-DRB1*1501 in Iranian Patients with Multiple Sclerosis di Parham Nejati, Marzieh Attar, Maryam Rahimian, Davood Fathi, Majid Shahbazi

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Cytogenetic analysis of 570 couples with recurrent pregnancy loss: Reporting 11 years of experience di Reza Alibakhshi, Parham Nejati, Sara Hamani, Narges Mir-Ahadi, Nazanin Jalilian

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A novel Bi-Allelic pathogenic MCOLN1 variant underlying mucolipidosis type IV in an Iranian family: clinical, genetic, and molecular dynamics-based structural analysis di Mohaddese Mohsenipour, Parham Nejati, Teymoor Khosravi, Elham Alimoradi, Mohammad Salehi, Morteza Oladnabi, Reza Alibakhshi

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A novel compound heterozygous variant in LAMA2 gene in a family with merosin-deficient congenital muscular dystrophy di Parham Nejati, Nafiseh Falsafi, Elham Alimoradi, Teymoor Khosravi, Mohana Kamari, Morteza Oladnabi, Reza Alibakhshi

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Association between Genetic Variants of Nitric Oxide/cGMP Pathway and Susceptibility to Hypertension in Kermanshah Province di Parham Nejati, Saba Naseri, Maryam Eini, Reza Alibakhshi, Sousan Mahmoudi, Lida Haghnazari, Nazanin Jalilian

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Identification of a Novel Missense Homozygous Variant in LINS1 in Two Distinct Iranian Families With Consanguineous Marriage di Elham Alimoradi, Parham Nejati, Arash Salmaninejad, Nafiseh Falsafi, Fatemeh Molavi, Mohamad Javad Alibakhshi, Filippo Pinto e Vairo, Eric W. Klee, Reza Alibakhshi

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