谷内江昭宏.
【家族性腫瘍学-家族性腫瘍の最新研究動向-】症候群 Autoimmune lymphoproliferative syndrome(ALPS)(自己免疫性リンパ増殖症候群).
日本臨床 2015; 73: 53-58.

谷内江昭宏.
【原発性免疫不全症候群 アップデート】原発性免疫不全症 総論.
アレルギー・免疫 2015; 22: 1172-1178.

清水正樹.
【小児リウマチ性疾患の最新治療】若年性特発性関節炎 マクロファージ活性化症候群の治療.
小児科診療 2015; 78: 1063-1067.

Hashida Y, Wada T, Saito T, Ohta K, Kasahara Y, Yachie A.
Early diagnosis of Danon disease: Flow cytometric detection of lysosome-associated membrane protein-2-negative leukocytes.
J Cardiol. 2015; 66: 168-74. doi: 10.1016/j.jjcc.2014.09.011.

Ohta K, Hashida Y, Wada T, Saito T, Kasahara Y, Yachie A.
Author’s reply: To PMID 25458169.
J Cardiol. 2015; 66: 89-90. doi: 10.1016/j.jjcc.2015.01.005.

Wada T, Akagi T, Muraoka M, Toma T, Kaji K, Agematsu K, Koeffler HP, Yokota T, Yachie A.
A Novel In-Frame Deletion in the Leucine Zipper Domain of C/EBPε Leads to Neutrophil-Specific Granule Deficiency.
J Immunol. 2015; 195: 80-6. doi: 10.4049/jimmunol.1402222.

Kuroda M, Shimizu M, Inoue N, Ikeno I, Nakagawa H, Yokoi A, Niida Y, Konishi M, Kaneda H, Igarashi N, Yamahana J, Taneichi H, Kanegane H, Ito M, Saito S, Furuichi K, Wada T, Nakagawa M, Yokoyama H, Yachie A.
Serum tau protein as a marker of disease activity in enterohemorrhagic Escherichia coli O111-induced hemolytic uremic syndrome.
Neurochem Int. 2015; 85-86: 24-30. doi: 10.1016/j.neuint.2015.04.003.

Yasunami M, Nakamura H, Agematsu K, Nakamura A, Yazaki M, Kishida D, Yachie A, Toma T, Masumoto J, Ida H, Koga T, Kawakami A, Eguchi K, Furukawa H, Nakamura T, Nakamura M, Migita K.
Identification of Disease-Promoting HLA Class I and Protective Class II Modifiers in Japanese Patients with Familial Mediterranean Fever.
PLoS One. 2015; 10: e0125938. doi: 10.1371/ journal.pone.0125938.

Shimizu M, Sakai S, Ohta K, Miyamoto M, Yachie A.
Uterus didelphys with obstructed hemivagina and contralateral multicystic dysplastic kidney.
CEN Case Rep. 2015; 4: 61-64. doi: 10.1007/s13730- 014-0139-9.

Ueno K, Shimizu M, Yokoyama T, Ishikawa S, Tasaki Y, Inoue N, Sugimoto N, Ohta K, Yachie A.
Urinary neopterin: an immune activation marker in mesangial proliferative glomerulonephritis.
Clin Exp Nephrol. 2015; 19: 264-70. doi: 10.1007/s10157-014-0984-z.

Yang X, Hoshino A, Taga T, Kunitsu T, Ikeda Y, Yasumi T, Yoshida K, Wada T, Miyake K, Kubota T, Okuno Y, Muramatsu H, Adachi Y, Miyano S, Ogawa S, Kojima S, Kanegane H.
A female patient with incomplete hemophagocytic lymphohistiocytosis caused by a heterozygous XIAP mutation associated with non-random X-chromosome inactivation skewed towards the wild-type XIAP allele.
J Clin Immunol. 2015; 35: 244-8. doi: 10.1007/s10875-015-0144-6.

Kato T, Crestani E, Kamae C, Honma K, Yokosuka T, Ikegawa T, Nishida N, Kanegane H, Wada T, Yachie A, Ohara O, Morio T, Notarangelo LD, Imai K, Nonoyama S.
RAG1 deficiency may present clinically as selective IgA deficiency.
J Clin Immunol. 2015; 35: 280-8. doi: 10.1007/s10875-015-0146-4.

清水正樹.
腸管出血性大腸菌による溶血性尿毒症症候群とサイトカイン.
日本小児腎臓病学会雑誌 2015; 28: 6-11.

太田邦雄.
【小児科医のための「小児救急」UP DATE】院外心停止を科学する.
小児科 2015; 56: 399- 404.

清水正樹.
【症例から学ぶ川崎病の診断・治療・管理のエッセンス】急性期の診断のエッセンス 膠原病とまぎらわしい例を鑑別する.
小児科診療 2015; 78: 323-327.

Tsuma Y, Imamura T, Ichise E, Sakamoto K, Ouchi K, Osone S, Ishida H, Wada T, Hosoi H.
Successful treatment of idiopathic colitis related to XIAP deficiency with allo-HSCT using reduced- intensity conditioning.
Pediatr Transplant. 2015; 19: E25-8. doi: 10.1111/petr.12405.

清水正樹.
【アフェレシス療法の新しい展開】免疫・リウマチ性疾患とアフェレシス療法 血球貪食性 リンパ組織球症・マクロファージ活性化症候群に対するアフェレシス治療.
腎と透析 2015; 78: 205-208.

清水正樹，井上なつみ，田﨑優子，谷内江昭宏.
Henoch-Schoenlein紫斑病罹患後に遷延する腹痛を呈した線維筋痛症の1例.
小児科 2015; 56: 199-202.

Yokoyama T, Sugimoto N, Kato E, Ohta K, Ishikawa S, Ueno K, Shimizu M, Yachie A.
Rotavirus gastroenteritis-associated urinary ammonium acid urate crystals.
Pediatr Int. 2015; 57: 158-60. doi: 10.1111/ped.12405.

Vu QV, Wada T, Tran TT, Ngo DN, Van Dinh T, Nguyen CH, Le HT, Yachie A, Nguyen SN.
Severe congenital neutropenia caused by the ELANE gene mutation in a Vietnamese boy with misdiagnosis of tuberculosis and autoimmune neutropenia: a case report.
BMC Hematol. 2015; 15: 2. doi: 10.1186/ s12878-015-0020-x.