Items where Author is "Hoseinzadeh, M."

Article

(2025) Evaluation of pathogenic variant in WFS1 in a patient with Wolfram syndrome. Egyptian Journal of Medical Human Genetics. p. 8. ISSN 1110-8630

(2024) Identification of novel likely pathogenic variant in CDH23 causing non-syndromic hearing loss, and a novel variant in OTOGL in an extended Iranian family. Egyptian Journal of Medical Human Genetics. p. 8. ISSN 1110-8630

(2023) Characterization of a novel androgen receptor gene variant identified in an Iranian family with complete androgen insensitivity syndrome (CAIS): a molecular dynamics simulation study. Journal of Biomolecular Structure & Dynamics. pp. 9850-9864. ISSN 1538-0254 (Electronic) 0739-1102 (Linking)

(2023) New molecular insights into the A218V variant impact on the steroidogenic acute regulatory protein (STAR) associated with 46, XY disorders of sexual development. Molecular Genetics and Genomics. pp. 693-708. ISSN 1617-4615

(2023) A Novel Homozygous Pathogenic Variant in CYP11B1 in a Female Iranian Patient with 11B Hydroxylase Deficiency. Laboratory Medicine. pp. 439-446. ISSN 1943-7730 (Electronic) 0007-5027 (Linking)

(2023) Nudging oral habits; application of behavioral economics in oral health promotion: a critical review. Frontiers in Public Health. p. 12.

(2016) Prebiotics for the management of hyperbilirubinemia in preterm neonates. Journal of Maternal-Fetal & Neonatal Medicine. pp. 3009-3013. ISSN 1476-7058

(2016) The effect of neutral oligosaccharides on fecal microbiota in premature infants fed exclusively with breast milk: A randomized clinical trial. Journal of Research in Pharmacy Practice. pp. 27-34. ISSN 2319-9644