WordNet

an infection caused by fungi of the genus Monilia or Candida (especially Candida albicans) (同)moniliasis, monilia disease

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1. 腹部および胸部のカンジダ感染症 candida infections of the abdomen and thorax
2. カンジダ感染症の概要 overview of candida infections
3. 成人におけるカンジダ菌血症および侵襲性カンジダ症 treatment of candidemia and invasive candidiasis in adults
4. 免疫不全患者における肺感染症 pulmonary infections in immunocompromised patients
5. 小児におけるカンジダ感染症：概要 candida infections in children an overview

Mometasone furoate (MF) improves lung function in pediatric asthma: A double-blind, randomized controlled dose-ranging trial of MF metered-dose inhaler.

Amar NJ1, Shekar T2, Varnell TA2, Mehta A2, Philip G2.
Pediatric pulmonology.Pediatr Pulmonol.2016 Oct 14. doi: 10.1002/ppul.23563. [Epub ahead of print]
OBJECTIVES: Mometasone furoate (MF), delivered via dry-powder inhaler (DPI) QD in the evening (PM), is a treatment option for pediatric patients with asthma. We evaluated MF delivered via a metered-dose inhaler (MDI), in children ages 5-11 years with persistent asthma.METHODS: This was a 12-week dou
PMID 27740721

Severe Early-Onset Combined Immunodeficiency due to Heterozygous Gain-of-Function Mutations in STAT1.

Baris S1, Alroqi F2, Kiykim A3, Karakoc-Aydiner E3, Ogulur I3, Ozen A3, Charbonnier LM2, Bakır M3, Boztug K4, Chatila TA2, Barlan IB3.
Journal of clinical immunology.J Clin Immunol.2016 Oct;36(7):641-8. doi: 10.1007/s10875-016-0312-3. Epub 2016 Jul 5.
PURPOSE: Loss and gain-of-function (GOF) mutations in human signal transducer and activator of transcription 1 (STAT1) lead to distinct phenotypes. Although recurrent infections are common to both types of STAT1 mutations, GOF mutations are distinguished by chronic mucocutaneous candidiasis and auto
PMID 27379765

Dual T cell- and B cell-intrinsic deficiency in humans with biallelic RLTPR mutations.

Wang Y1, Ma CS2, Ling Y1, Bousfiha A3, Camcioglu Y4, Jacquot S5, Payne K6, Crestani E7, Roncagalli R8, Belkadi A1, Kerner G1, Lorenzo L1, Deswarte C1, Chrabieh M1, Patin E9, Vincent QB1, Müller-Fleckenstein I10, Fleckenstein B10, Ailal F3, Quintana-Murci L9, Fraitag S11, Alyanakian MA12, Leruez-Ville M13, Picard C14, Puel A1, Bustamante J14, Boisson-Dupuis S15, Malissen M8, Malissen B8, Abel L1, Hovnanian A16, Notarangelo LD17, Jouanguy E15, Tangye SG2, Béziat V18, Casanova JL19.
The Journal of experimental medicine.J Exp Med.2016 Sep 19. pii: jem.20160576. [Epub ahead of print]
Combined immunodeficiency (CID) refers to inborn errors of human T cells that also affect B cells because of the T cell deficit or an additional B cell-intrinsic deficit. In this study, we report six patients from three unrelated families with biallelic loss-of-function mutations in RLTPR, the mouse
PMID 27647349