Biblio

Author Title Type [ Year(Desc)]
Filters: Author is Uchiyama, Yuri  [Clear All Filters]
2022
Uchino K, Kanasugi J, Enomoto M, Kitamura F, Tsuchida N, Uchiyama Y, Maeda A, Kirino Y, Matsumoto N, Takami A. VEXAS syndrome. Int J Hematol. 2022.
2023
Kunimoto H, Miura A, Maeda A, Tsuchida N, Uchiyama Y, Kunishita Y, Nakajima Y, Takase-Minegishi K, Yoshimi R, Miyazaki T, et al. Clinical and genetic features of Japanese cases of MDS associated with VEXAS syndrome. Int J Hematol. 2023.
Tsuchida N, Uchiyama Y, Maeda A, Horita N, Kirino Y, Matsumoto N. Comment on: Efficient detection of somatic UBA1 variants and clinical scoring system predicting patients with variants in VEXAS syndrome: reply. Rheumatology (Oxford). 2023.
Maeda A, Tsuchida N, Uchiyama Y, Horita N, Kobayashi S, Kishimoto M, Kobayashi D, Matsumoto H, Asano T, Migita K, et al. Efficient detection of somatic UBA1 variants and clinical scoring system predicting patients with variants in VEXAS syndrome. Rheumatology (Oxford). 2023.
Miyoshi Y, Kise T, Morita K, Okada H, Imadome K-I, Tsuchida N, Maeda A, Uchiyama Y, Kirino Y, Matsumoto N, et al. Long-term remission of VEXAS syndrome achieved by a single course of CHOP therapy: A case report. Mod Rheumatol Case Rep. 2023.
Li D, Wang Q, Bayat A, Battig MR, Zhou Y, Bosch DGm, van Haaften G, Granger L, Petersen AK, Pérez-Jurado LA, et al. Spliceosome malfunction causes neurodevelopmental disorders with overlapping features. J Clin Invest. 2023.