1月の掲載論文・受賞
■腎臓グループ
Rohner K, Marlais M, Ahn YH, Ali A, Alsharief A, Novak AB, Brambilla M, Cakici EK, Candan C, Canpolat N, Yu-Hin Chan E, Decramer S, Didsbury M, Durao F, Durkan AM, Düzova A, Forbes T, Gracchi V, Güngör T, Horinouchi T, Demir BK, Kobayashi Y, Koskela M, Kurt-Sukur ED, La Scola C, Langan D, Li X, Malgieri G, Mastrangelo A, Min J, Mizerska-Wasiak M, Moussaoui N, Noyan A, Nuutinen M, O'Gormon J, Okamoto T, Oni L, Oosterveld M, Pańczyk-Tomaszewska M, Parmaksiz G, Pasini A, Rianthavorn P, Roelofs J, Shen Y, Sinha R, Topaloglu R, Torres DD, Udagawa T, Wennerström M, Yap YC, Tullus K.
Outcome of immunosuppression in children with IgA vasculitis-related nephritis.
Nephrol Dial Transplant. 2024 Jan 11.
doi: 10.1093/ndt/gfae009. Epub ahead of print. PMID: 38211969.
佐藤 泰征
小児科診療 87巻1号 （2024年1月発行）
特集 小児疾患におけるアフェレシス―治療法の1つの選択肢としての血液浄化療法―
Ⅱ．各論：各疾患に対するアフェレシス
感染症疾患に対するアフェレシス
■循環器グループ
Morita S, Nomura S, Azuma K, Chida-Nagai A, Furutani Y, Inai K, Inoue T, Niimi Y, Iizuka Y, Tsutsumi Y, Ishizaki R, Yamagishi H, Kawamata T, Akagawa H.
Functional characterization of variants found in Japanese patients with hereditary hemorrhagic telangiectasia.
Clin Genet. 2024 Jan 15.
doi: 10.1111/cge.14483. Epub ahead of print. PMID: 38225712.
Abe J, Tsubaki J, Shimura K, Hasegawa T.
A Pitfall of Adrenal Hypoplasia Congenita
Clin Pediatr (Phila). 2024:99228231222714.
doi: 10.1177/00099228231222714. Online ahead of print. PMID: 38279818
■新生児グループ
Honjo R, Cho K, Hashimoto K, Takeda K, Seto Y, Kaneshi Y, Furuse Y, Manabe A. Neonatal-onset pulmonary alveolar proteinosis is a phenotype associated with poor outcomes in surfactant protein-C disorder.
Early Hum Dev. 2024 Jan 4;189:105930.
doi: 10.1016/j.earlhumdev.2023.105930. Epub ahead of print. PMID: 38199047.