同: Muckle-Wells syndrome

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the 13th letter of the Roman alphabet (同)m

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Mach number / mark[s] / Monsieur

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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2016/02/08 10:34:38」(JST)

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1. アミロイド疾患の遺伝的要因 genetic factors in the amyloid diseases
2. 閉経後のホルモン療法と乳癌リスク postmenopausal hormone therapy and the risk of breast cancer
3. クリオピリン関連周期性発熱症候群および関連疾患 cryopyrin associated periodic syndromes and related disorders
4. 先天性巨大結腸症（ヒルシュスプルング病） congenital aganglionic megacolon hirschsprung disease
5. 尿毒症毒素 uremic toxins

English Journal

Prevalence and correlates of major depressive disorder among rural-to-urban migrant workers in Shenzhen, China.

Zhong BL1, Liu TB2, Chan SS1, Jin D2, Hu CY2, Dai J2, Chiu HF3.
Journal of affective disorders.J Affect Disord.2015 Sep 1;183:1-9. doi: 10.1016/j.jad.2015.04.031. Epub 2015 Apr 27.
BACKGROUND: In China, rural-to-urban migrant workers (MWs) are a large and vulnerable population that may be at high risk for depression, but previous studies focused on depressive symptoms of MWs and no study has investigated the epidemiology of major depressive disorder (MDD). The objective of thi
PMID 25989590

Impact of IL-1 inhibition on fatigue associated with Autoinflammatory syndromes.

Efthimiou P, Yadlapati S.
Modern rheumatology / the Japan Rheumatism Association.Mod Rheumatol.2015 Jul 3:1-22. [Epub ahead of print]
Cryopyrin associated periodic syndromes (CAPS) is a rare group of autoinflammatory disorders that includes familial cold autoinflammatory syndrome (FCAS), Muckle-wells syndrome (MWS), and Neonatal onset multisystemic inflammatory disease (NOMID) . CAPS is caused by a mutation in the NLRP3 (NOD like
PMID 26140469

Clinical spectrum of eye malformations in four patients with Mowat-Wilson syndrome.

Bourchany A1, Giurgea I2, Thevenon J3, Goldenberg A4, Morin G5, Bremond-Gignac D6, Paillot C7, Lafontaine PO7, Thouvenin D8, Massy J9, Duncombe A9, Thauvin-Robinet C3, Masurel-Paulet A3, Chehadeh SE3, Huet F1, Bron A7, Creuzot-Garcher C7, Lyonnet S10, Faivre L3.
American journal of medical genetics. Part A.Am J Med Genet A.2015 Jul;167(7):1587-92. doi: 10.1002/ajmg.a.36898. Epub 2015 Apr 21.
Mowat-Wilson syndrome (MWS) is a rare genetic syndrome characterized by a specific facial gestalt, intellectual deficiency, Hirschsprung disease and multiple congenital anomalies. Heterozygous mutations or deletions in the zinc finger E-box-binding homeobox2 gene (ZEB2) cause MWS. ZEB2 encodes for S
PMID 25899569

Japanese Journal

脳卒中片麻痺患者における歩行周期変動の歩行・バランス能力及び下肢筋力との関連

伊藤優也,佐々木誠,佐川貢一,ITO Yuya,SASAKI Makoto,SAGAWA Koichi
秋田大学大学院医学系研究科保健学専攻紀要 21(2), 125-130, 2013-10-31
… Attach to target 41 people stroke hemiplegic patients, was measured STV, Functional Ambulation Classification (FAC), 10m Maximum Walking Speed (10MWS), Berg Balance Scale (BBS), the paralyzed side and non-paralyzed side leg strength. … Significant differences in STV in walking non-independence group and independence group, showed a significant correlation between STV and FAC, 10MWS, BBS, and the paralyzed side leg strength. …
NAID 120005348743

地域健常高齢者におけるFour Square Step Test の有用性

若狭正彦,齊藤明,津軽谷恵,石川隆志,小原千絵,WAKASA Masahiko,SAITO Akira,TSUGARUYA Megumi,ISHIKAWA Takashi,OBARA Chie
秋田大学大学院医学系研究科保健学専攻紀要 21(1), 31-36, 2013-03-31
… 評価項目はFour Square Step Test (FSST) の他,その他の身体運動機能評価項目として, 膝伸展筋群筋力(LES), 長座位体前屈距離(FFD), 片脚立位保持時間(SLS), Timed Up and Go test (TUG), 10ｍ最大歩行速度(10MWS) を計測した. …
NAID 120005348734

P4-10 Muckle-Wells症候群におけるNLRP3体細胞モザイク変異の検討

中川権史,西小森隆太,井澤和司,河合朋樹,八角高裕,河合利尚,梅林宏明,武井修治,小林法元,小原收,Eva Gonzalez-Roca,Arostegui Juan I.,平家俊男
日本臨床免疫学会会誌 36(5), 390b-390b, 2013
… Cryopyrin-associated periodic syndrome（CAPS）は，NLRP3遺伝子の機能獲得型変異によりIL-1βの過剰産生が惹起され，炎症を生じる自己炎症性疾患である．CAPSには，家族性寒冷蕁麻疹（FCAS），Muckle-Wells症候群（MWS），CINCA症候群/NOMIDが含まれる．これら3つの疾患は，遺伝子型と表現型にある程度の相関が見られ，軽症型のFCASから最重症であるCINCA症候群/NOMIDへと一連の症状群として捉えることができる．近年我々は，NLRP3遺伝子に …
NAID 130003383102

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