نتایج جستجو برای: 016

تعداد نتایج: 2468  

2013
V Messia M Pardeo R Nicolai C Bracaglia F De Benedetti A Insalaco

Introduction Chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature (CANDLE) syndrome is a newly described autoinflammatory disease, which had been recently reported in 9 patients. It is characterized by onset during the first year of life of recurrent fevers, purpuric skin lesions, arthralgia, progressive lipodystrophy, hypochromic or normocytic anemia, delayed ph...

Journal: :Newfoundland and Labrador studies 2022

Keith Mercer. Rough Justice: Policing, Crime, and the Origins of Newfoundland Constabulary, 1729–1871. St. John’s: Flanker Press, 2021. ISBN 978-1-77457-016-6. An article from journal Labrador Studies (Volume 36, Number 2, 2021, pp. 171-344), on Érudit.

1999

We report new direct measurements of the Z-lepton coupling asymmetry parameters Ae, A and A , with polarized Z 's collected by the SLD detector at the SLAC Linear Collider. The parameters are extracted from the measurement of the left-right-forward-backward asymmetries for each lepton species. The 1996, 1997 and 1998 SLD runs are included in this analysis and combined with published data from t...

2016
Anu Radha Sharma Padmalatha S Rai

The role of clopidogrel in disruption of platelet aggregation is well known. The variability in clopidogrel response is a well-documented phenomenon and has been widely addressed through pharmacogenomics. CYP2C19 has been considered as genetic predictor of clopidogrel response. Owing to the inter-individual variations, CPIC (Clinical Pharmacogenetics Implementation Consortium) had issued guidel...

2013
CD Rose R Cimaz C Thomee R Khubchandani G Espada R Russo M Harjacek B Bader-Meunier P Brissaud N Wulffraat S Vastert R Merino A Naranjo-Hernandez S Oliveira-Knupp F Mackensen J Arostegui J Anton J Fernandez-Martin C Wouters

Introduction Blau syndrome is an autosomal dominant monogenic granulomatous disease associated with gain of function mutations at or near the NACHT domain of NOD2; it is the only form of granulomatous arthritis with a known gene mutation. Although its phenotype has been amply described as a triad of arthritis, uveitis and dermatitis in case series and retrospective cohorts, prospective studies ...

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