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.

Wada T, Matsuda Y, Muraoka M, Toma T, Yachie A.
Fecal eosinophil-derived neurotoxin in cow’s milk-sensitive enteropathy: a case report.
Allergol Int. 2015; 64: 99-100. doi: 10.1016/j.alit.2014.11.001.

Takahara T, Shimizu M, Nakagishi Y, Kinjo N, Yachie A.
Serum IL-18 as a potential specific marker for differentiating systemic juvenile idiopathic arthritis from incomplete Kawasaki disease.
Rheumatol Int. 2015; 35: 81-4. doi: 10.1007/s00296-014-3059-2.

和田泰三.
原発性免疫不全症におけるRevertant somatic mosaicism.
日本臨床免疫学会会誌 2014; 37: 447-453.

Okumura A, Ozaki M, Niida Y.
Development of a practical NF1 genetic testing method through the pilot analysis of five Japanese families with neurofibromatosis type 1.
Brain Dev. 2015; 37: 677-89. doi: 10.1016/j.braindev.2014.11.002.

谷内江昭宏.
【周産期感染症2014】新生児からみた周産期感染症 基礎編 胎児・新生児の免疫系の発達とその機能 獲得免疫系.
周産期医学 2014; 44: 257-262.

Shimizu M, Nakagishi Y, Yoshida A, Yachie A.
Serum interleukin 18 as a diagnostic remission criterion in systemic juvenile idiopathic arthritis.
J Rheumatol. 2014; 41: 2328-30. doi: 10.3899/ jrheum.140025.

Shimizu M, Ueno K, Ishikawa S, Tokuhisa Y, Inoue N, Yachie A.
Treatment of refractory polyarticular juvenile idiopathic arthritis with tacrolimus.
Rheumatology (Oxford). 2014; 53: 2120-2. doi: 10.1093/rheumatology/keu297.

井上雅之, 吉尾里夏, 藤澤裕子, 谷内江昭宏.
造影CTにより咽後膿瘍と鑑別しえた不全型川崎病の1例.
小児科臨床 2014; 67: 2165-2170.

清水正樹, 山田恵子, 小西道雄, 袖本衣代, 谷内江昭宏.
目で見る小児科 出血性膿疱/水疱を呈したHenoch-Schoenlein紫斑病の1例.
小児科 2014; 55: 1811-1812.