トピックス

1月の掲載論文・受賞

・免疫グループ
Recurrence of juvenile dermatomyositis 8 years after remission.
Muramatsu K, Ujiie H, Yokozeki M, Tsukinaga I, Ito M, Shikano T, Suzuki A, Tozawa Y, Kobayashi I:
JAAD Case Rep 26: 29-32, 2016

Low T Cell Numbers Resembling T-B+ SCID in a Patient with Wiskott-Aldrich Syndrome and the Outcome of Two Hematopoietic Stem Cell Transplantations.
Cagdas D, Aytac S, Kuskonmaz B, Ariga T, van der Burg M, Cetinkaya DU, Sanal Ö, Tezcan İ.
J Clin Immunol. 2016 Nov 30. [Epub ahead of print]

Anasarca as the initial symptom in a Japanese girl with Sjögren’s syndrome.
Ueki M, Kobayashi I, Tozawa Y, Konishi S, Takezaki S, Yamada M, Ariga T.
Modern Rheumatology in press

・循環器グループ
Point catheter ablation of macro-re-entrant ventricular tachycardia in a patient after surgical repair for double-outlet right ventricle.
Izumi G, Yokoshiki H, Takeda A.
Cardiol Young. 2017 Jan 12:1-4. doi: 10.1017/S1047951116002717. [Epub ahead of print]

Significance of right atrial tension for the development of complications in patients after atriopulmonary connection Fontan procedure: potential indicator for Fontan conversion.
Izumi G, Senzaki H, Takeda A, Yamazawa H, Takei K, Furukawa T, Inai K, Shinohara T, Nakanishi T.
Heart Vessels. 2017 Jan 7. doi: 10.1007/s00380-016-0941-8. [Epub ahead of print]

・遺伝グループ
SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome.
Shaw ND, Brand H, Kupchinsky ZA, Bengani H, Plummer L, Jones TI, Erdin S, Williamson KA, Rainger J, Stortchevoi A, Samocha K, Currall BB, Dunican DS, Collins RL, Willer JR, Lek A, Lek M, Nassan M, Pereira S, Kammin T, Lucente D, Silva A, Seabra CM, Chiang C, An Y, Ansari M, Rainger JK, Joss S, Smith JC, Lippincott MF, Singh SS, Patel N, Jing JW, Law JR, Ferraro N, Verloes A, Rauch A, Steindl K, Zweier M, Scheer I, Sato D, Okamoto N, Jacobsen C, Tryggestad J, Chernausek S, Schimmenti LA, Brasseur B, Cesaretti C, García-Ortiz JE, Buitrago TP, Silva OP, Hoffman JD, Mühlbauer W, Ruprecht KW, Loeys BL, Shino M, Kaindl AM, Cho CH, Morton CC, Meehan RR, van Heyningen V, Liao EC, Balasubramanian R, Hall JE, Seminara SB, Macarthur D, Moore SA, Yoshiura KI, Gusella JF, Marsh JA, Graham JM Jr, Lin AE, Katsanis N, Jones PL, Crowley WF Jr, Davis EE, FitzPatrick DR, Talkowski ME.
Nat Genet. 2017 Feb;49(2):238-248. doi: 10.1038/ng.3743. Epub 2017 Jan 9.