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Expanding the phenotypic landscape of Gaucher disease type 3c with a novel entity - Transient neonatal cholestasis.
Bulut FD, Kor D, Kılavuz S, Şeker Yılmaz B, Kaplan İ, Ekinci F, Burgaç E, Varol İ, Köşeci B, Tuğ Bozdoğan S, Kara E, Demir F, Deniz A, Temiz F, Önenli Mungan N. Bulut FD, et al. Among authors: kaplan i. Eur J Med Genet. 2023 Jun;66(6):104764. doi: 10.1016/j.ejmg.2023.104764. Epub 2023 Apr 13. Eur J Med Genet. 2023. PMID: 37061027
Diagnostic Challenges in a Family with Dominant Dystrophic Epidermolysis Bullosa and Isolated Hereditary Nail Disorder: Paternal Gonosomal Mosaicism for COL7A1 Mutation and Maternal RSPO4 Variant.
Öktem A, Özaydın B, Gündüz K, Gökpınar İli E, Şanlı H, Kaplan İ, Yürür Kutlay N. Öktem A, et al. Among authors: kaplan i. Clin Exp Dermatol. 2024 Jun 3:llae215. doi: 10.1093/ced/llae215. Online ahead of print. Clin Exp Dermatol. 2024. PMID: 38828627
Nonpathogenic E. coli engineered to surface display cytokines as a new platform for immunotherapy.
Yang S, Sheffer M, Kaplan IE, Wang Z, Tarannum M, Dinh K, Abdulhamid Y, Shapiro R, Porter R, Soiffer R, Ritz J, Koreth J, Wei Y, Chen P, Zhang K, Márquez-Pellegrin V, Bonanno S, Joshi N, Guan M, Yang M, Li D, Bellini C, Chen J, Wu CJ, Barbie D, Li J, Romee R. Yang S, et al. Among authors: kaplan ie. Res Sq [Preprint]. 2024 Mar 22:rs.3.rs-4031911. doi: 10.21203/rs.3.rs-4031911/v1. Res Sq. 2024. PMID: 38562821 Free PMC article. Preprint.
857 results