Reference material for the validation of all types of hemoximeters : hemoxitrol : Oxygène et co-oxymétrieMAAS, B. H. A.RBM. Revue européenne de biotechnologie médicale. 1995, Vol 17, Num 7, pp 218-220, issn 0222-0776Article

Compatibility of amsacrine (Amsidyl®) concentrate for infusion with polypropylene syringesKRÄMER, I; MAAS, B.Pharmazie. 1999, Vol 54, Num 7, pp 538-541, issn 0031-7144Article

Stereoisomeric flavour compounds LXIX: Stereodifferentiation of δ(γ)-lactones C₈-C₁₈ in dairy products, margarine and coconutLEHMANN, D; MAAS, B; MOSANDL, A et al.Zeitschrift für Lebensmittel-Untersuchung und -Forschung. 1995, Vol 201, Num 1, pp 55-61, issn 0044-3026Article

Stabilität von Bendamusqtinhydrochlorid in Infusionslösungen = Stability of bendamustine hydrochloride in infusionsMAAS, B; HUBER, C; KRÄMER, I et al.Pharmazie. 1994, Vol 49, Num 10, pp 775-777, issn 0031-7144Article

Collection of enantiomer separation factors obtained by capillary gas chromatography on chiral stationary phasesMAAS, B; DIETRICH, A; MOSANDL, A et al.HRC. Journal of high resolution chromatography. 1994, Vol 17, Num 3, pp 169-173, issn 0935-6304Article

Allergische Kontaktdermatitis auf Asteraceae (Kompositen) Kreuzreaktion mit Liatris spicata = Dermatite de contact allergique aux asteraceae réaction croisée avec Liatris spicata = Allergic contact dermatitis to asteraceae. Cross reaction with Liatris spicataGOERZ, G; WIRTH, G; MAAS, B et al.Dermatosen in Beruf und Umwelt. 1985, Vol 33, Num 3, pp 95-98, issn 0343-2432Article

Diluted modified cyclodextrins as chiral stationary phases : influence of the polysiloxane solvent : heptakis(2,3-di-O-acetyl-6-O-tert-butyldimethylsilyl)-β-cyclodextrinDIETRICH, A; MAAS, B; MOSANDL, A et al.HRC. Journal of high resolution chromatography. 1995, Vol 18, Num 3, pp 152-156, issn 0935-6304Conference Paper

Multi-rail barrel design and performanceMAAS, B. L; BAUER, D. P; CHALLITA, A et al.IEEE transactions on magnetics. 1993, Vol 29, Num 1, pp 467-471, issn 0018-9464, 2Conference Paper

Spectroscopie gamma et étude microscopique de noyaux superdéformés de nombre de masse A ∼ 150 = Gamma-ray spectroscopy and microscopic study of superdeformed nucleiwith a number of mass A ∼ 150Rigollet, Catherine; Maas, B.1996, 159 p.Thesis

Steroisomeric flavor compounds. LXXII: Stereoisomeric distribution of some chiral sulfur-containing trace components of yellow passion fruitsWEBER, B; MAAS, B; ARMIN MOSANDL et al.Journal of agricultural and food chemistry (Print). 1995, Vol 43, Num 9, pp 2438-2441, issn 0021-8561Article

Collection of enantiomer separation factors obtained by capillary gas chromatography on chiral stationary phasesMAAS, B; DIETRICH, A; MOSANDL, A et al.HRC. Journal of high resolution chromatography. 1994, Vol 17, Num 2, pp 109-115, issn 0935-6304Article

Short pulse, peak current ratings of diodesMAAS, B. L; CLEMENTS, N. D; RINALDI, V et al.IEEE transactions on magnetics. 1993, Vol 29, Num 1, pp 1017-1020, issn 0018-9464, 2Conference Paper

A multiple armature railgun launcherCHALLITA, A; MAAS, B. L; BAUER, D. P et al.IEEE transactions on magnetics. 1993, Vol 29, Num 1, pp 763-768, issn 0018-9464, 2Conference Paper

Residual plasma property control for hypervelocity railgun performanceBAUER, D. P; KNOTH, E. A; MAAS, B. L et al.IEEE transactions on magnetics. 1993, Vol 29, Num 1, pp 745-750, issn 0018-9464, 2Conference Paper

Stereoisomer flavour compounds. LXVI: Enantiomeric distribution of the chiral sulphur-containing alcohols by yellow and purple passion fruitsWEBER, B; DIETRICH, A; MAAS, B et al.Zeitschrift für Lebensmittel-Untersuchung und -Forschung. 1994, Vol 199, Num 1, pp 48-50, issn 0044-3026Article

Stereoisomeric flavor compounds XLI : new applications of permethylated β-cyclodextrin phase in chiral CGC analysisMOSANDL, A; RETTINGER, K; FISCHER, K et al.HRC. Journal of high resolution chromatography. 1990, Vol 13, Num 5, pp 382-385, issn 0935-6304, 4 p.Article

Synthesis and evaluation of radiolabeled antagonists for imaging of β-adrenoceptors in the brain with PETDOZE, P; ELSINGA, P. H; MAAS, B et al.Neurochemistry international. 2002, Vol 40, Num 2, pp 145-155, issn 0197-0186Article

Stereoisomeric flavor compounds. LX: Diluted modified cyclodextrins as chiral stationary phases : the influence of the polysiloxane solventDIETRICH, A; MAAS, B; BRAND, G et al.HRC. Journal of high resolution chromatography. 1992, Vol 15, Num 11, pp 769-772, issn 0935-6304Article

A comparative bioavailability study of carbamazepine tablets and a chewable tablet formulationMAAS, B; GARNETT, W. R; PELLOCK, J. M et al.Therapeutic drug monitoring. 1987, Vol 9, Num 1, pp 28-33, issn 0163-4356Article

Stereoisomeric flavor compounds. LV: Stereodifferentiation of some chiral volatiles on heptakis(2,3-di-O-acetyl-6-O-tert-butyldimethylsilyl)-β-cyclodextrinDIETRICH, A; MAAS, B; KARL, V et al.HRC. Journal of high resolution chromatography. 1992, Vol 15, Num 3, pp 176-179, issn 0935-6304Article

Chiral compounds of essential oils. X : The role of linalool in the origin evaluation of essential oilsHENER, U; BRAUNSDORF, R; KREIS, P et al.Chemie, Mikrobiologie, Technologie der Lebensmittel. 1992, Vol 14, Num 5-6, pp 129-133, issn 0366-7154Article