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Development of a quasi time stretch technology for indoor positioning system based on pulse modulated ultra high frequency radio.

• Authors : Xiong, Renhai; van Waasen, S.; Schelten, J.

• Source: 2015 IEEE SENSORS; 2015, p1-4, 4p

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Raspberry Pi based testbed verifying TrueTime network model parameters for application in distributed active turbulent flow control.

• Authors : Dueck, M.; Schloesser, M.; Kaparaki, M.

• Source: 2014 Proceedings of the SICE Annual Conference (SICE); 2014, p1970-1975, 6p

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Automated electrical stimulation and recording for retina implant research by LabVIEW configured standalone data acquisition device.

• Authors : Heil, R.; Schloesser, M.; Offenhausser, A.

• Source: 2014 Proceedings of the SICE Annual Conference (SICE); 2014, p1662-1667, 6p

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Reevaluation of the Incidence of Thromboembolic Complications in Congenital Factor XII Deficiency

• Authors : Zeerleder, S.; Schloesser, M.; Redondo, M.

• Source: Thrombosis and Haemostasis; April 1999, Vol. 81 Issue: 4 p1240-1246, 7p

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Precise Transfer Measurement of the Magnetic Axis to Outside Monuments.

• Authors : Holler, Y.; Krause, B.; Petrov, A.

Subjects: METHODOLOGY; MAGNETICS; QUADRUPOLE moments

• Source: IEEE Transactions on Applied Superconductivity; Jun2008, Vol. 18 Issue 2, p1645-1647, 3p, 3 Black and White Photographs, 1 Chart

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A novel 5′-upstream mutation in the factor XII gene is associated with a Taq I restriction site in an Alu repeat in factor XII-deficient patients

• Authors : Hofferbert, Sigrun; Müller, Jens; Köstering, Heinz

• Source: Human Genetics; June 1996, Vol. 97 Issue: 6 p838-841, 4p

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A cystic fibrosis patient with the nonsense mutation G542X and the splice site mutation 1717-1.

• Authors : Schloesser, M; Arleth, S; Lenz, U

• Source: Journal of Medical Genetics; Dec1991, Vol. 28 Issue 12, p878-880, 3p

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A cystic fibrosis patient homozygous for the nonsense mutation R553X.

• Authors : Bal, J; Stuhrmann, M; Schloesser, M

• Source: Journal of Medical Genetics; Oct1991, Vol. 28 Issue 10, p715-717, 3p

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Homozygous factor V Leiden mutation in a woman with multiple adverse pregnancy outcomes.

• Authors : Pauer, H.-U.; Neesen, J.; Schloesser, M.

Subjects: FETAL death; DEATH; PREGNANCY complications

• Source: Archives of Gynecology & Obstetrics; Nov2000, Vol. 264 Issue 3, p164-165, 2p

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Two cystic fibrosis patients with the genotype G542X/G551D.

• Authors : Reiss, J.; Ellermeyer, U.; Schloesser, M.

• Source: Human Genetics; 1993, Vol. 91 Issue 1, p78-79, 2p

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