SwePub
Sök i SwePub databas

  Utökad sökning

Träfflista för sökning "WFRF:(Heijbel Jan) "

Sökning: WFRF:(Heijbel Jan)

  • Resultat 1-3 av 3
Sortera/gruppera träfflistan
   
NumreringReferensOmslagsbildHitta
1.
  • Heijbel, H, et al. (författare)
  • Anaesthetic gas monitoring comparison between two side-stream monitors.
  • 2010
  • Ingår i: J Clin Monit Comput. - : Springer Science and Business Media LLC. - 1573-2614 .- 1387-1307. ; 24:2, s. 169-72
  • Tidskriftsartikel (övrigt vetenskapligt/konstnärligt)abstract
    • End-tidal gas monitoring has become standard of care during inhaled general anaesthesia. We studied the performance of a new side stream gas monitor the ISA multi-gas monitor. The performance was studied at constant low flow of calibration gas and end-tidal anaesthetic measure was studied during routine day case anaesthesia. Pair wise readings of end-tidal halogenated anaesthetic concentration were recorded during low flow anaesthesia. Performance was found to be high; all calibration gas measures were within 0.1 vol% deviation. During routine anaesthesia mean bias was -0.036 vol% and 93 out of 97 pair-wise readings were within the agreement limits as compared to the reference Datex instrument.
  •  
2.
  •  
3.
  • Holmberg, Monica, et al. (författare)
  • Localization of autosomal dominant cerebellar ataxia associated with retinal degeneration and anticipation to chromosome 3p12-p21.1
  • 1995
  • Ingår i: Human Molecular Genetics. - : Oxford University Press (OUP). - 0964-6906 .- 1460-2083. ; 4:8, s. 1441-1445
  • Tidskriftsartikel (refereegranskat)abstract
    • We present linkage analysis on a large Swedish five-generation family of 15 affected individuals with autosomal dominant cerebellar ataxia (ADCA) associated with retinal degeneration and anticipation, Common clinical signs in this family include ataxia, dysarthria and severely impaired vision with the phenotype ADCA type II, Different subtypes of ADCA have proven difficult to classify clinically due to extensive phenotypic variability within and between families. Genetic analysis of a number of ADCA type I families shows that heterogeneity exists also genetically, During the last few years several types of ADCA type I have been localized and to date six genetically distinct forms have been identified including SCA1 (6p), SCA2 (12q), SCA3 and Machado-Joseph disease (MJD) (14q), SCA4 (16q), and finally SCA5 (11), We performed a genome-wide search of the Swedish ADCA type II family using a total of 270 microsatellite markers, Positive lod scores were obtained with a number of microsatellite markers located on chromosome 3p12-p21.1. Three markers gave lod scores over 3 with a maximum lod score of 4.53 achieved with the marker D3S1600. The ADCA type II gene could be restricted to a region of 32 cM by the markers D3S1547 and D3S1274.
  •  
Skapa referenser, mejla, bekava och länka
  • Resultat 1-3 av 3

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Stäng

Kopiera och spara länken för att återkomma till aktuell vy