Search Results - "Rauter, L"

Intrapartum acquired skull fracture as first sign of Menkes disease by Freidl, P, Rauter, L, Moser, R, Kerbl, R

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Factor V Leiden and prothrombin gene G 20210 A variant in children with ischemic stroke by Zenz, W, Bodó, Z, Plotho, J, Streif, W, Male, C, Bernert, G, Rauter, L, Ebetsberger, G, Kaltenbrunner, K, Kurnik, P, Lischka, A, Paky, F, Ploier, R, Höfler, G, Mannhalter, C, Muntean, W

“…To investigate if the factor V Leiden mutation (F-V-LM) and/or the prothrombin gene G 20210 A variant (P-G20210A-V) are risk factors for acute stroke in…”
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Nor-ursodeoxycholic acid improves biliary markers during normothermic machine perfusion by Dingfelder, J., Kollmann, D., Rauter, L., Pereyra, D., Kacar, S., Riha, M., Becker, N., Saffarian, T., Silberhumer, G., Salat, A., Soliman, T., Berlakovich, G., Györi, G.

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Rolle des Kinderarztes bei Lernstörungen und Schulproblemen by Rauter, L.

“…Zusammenfassung Mindestens 10 % der Kinder im Schulalter werden dem Pädiater wegen Problemen im Zusammenhang mit der Schule vorgestellt. Einen Großteil der…”
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Therapeutic application of norursodeoxycholic acid in normothermic machine perfusion reduces perfusate apoptosis markers in livers rejected for transplantation by Rauter, L., Kollmann, D., Dingfelder, J., Kacar, S., Pereyra, D., Riha, M., Becker, N., Saffarian, T., Mengrelis, K., Wahrmann, M., Salat, A., Silberhumer, G., Soliman, T., Berlakovich, G., Györi, G.

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Nachtschreck, Schlafwandeln und Albträume: Häufige Parasomnien im Kindes- und Jugendalter by Sauseng, W., Rauter, L., Kerbl, R.

“…Zusammenfassung Nachtschreck, Schlafwandeln und Albträume zählen zu den häufigsten Parasomnien im Kindes- und Jugendalter. Diese Parasomnien sind abnorme…”
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Menkes-Syndrom: Ein Fallbericht by Wolff, B, Naglis, R, Rauter, L, Ralph, G

“…Abstract only…”
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Direct coupling of fused silica columns to the ion source of a mass spectrometer applied to studies of arachidonic acid metabolism in human fibroblasts by Gleispach, H, Mayer, B, Rauter, L, Wurz, E

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Thymidinkinase-2-assoziiertes mitochondriales DNA-Depletionssyndrom: Erkrankung mit progredienter Muskelschwäche bei einem 2-jährigen Buben by Rauter, L., Kerbl, R., Bittner, R.

“…Zusammenfassung Mit dieser Fallpräsentation möchten wir die heutigen Möglichkeiten einer exakten Diagnosefindung bei Vorliegen einer so schwerwiegenden und für…”
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Molecular characterization of a 12q22-q24 deletion associated with congenital deafness: Confirmation and refinement of the DFNA25 locus by Petek, Erwin, Windpassinger, Christian, Mach, Monika, Rauter, Ludwig, Scherer, Stephen W., Wagner, Klaus, Kroisel, Peter M.

“…The DFNA25 locus for autosomal dominant nonsyndromic hereditary hearing loss has been mapped to 12q21‐q24 by linkage analysis. A de novo deletion in a…”
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Haemophilus influenzae meningitis 1983 to 1992--epidemiology and sequelae of the disease by Rauter, L, Mutz, I

“…During the ten-year period 1983-1992 40 children (16 girls and 24 boys) were treated for pyogenic meningitis caused by Haemophilus influenzae type b (Hib). The…”
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Molecular cytogenetics and phenotype characterization of a de novo pure partial trisomy 10(q24.33-qter) by Petek, E, Köstl, G, Rauter, L, Mutz, I, Wagner, K, Kroisel, P M

“…The molecular-cytogenetic characterization of a de novo pure partial trisomy 10(q24.33-qter) is described. This report provides information about the postnatal…”
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Determination of hydrogen in expiratory air of premature infants in suspected necrotizing enterocolitis by Rauter, L, Startinig, B, Mutz, I

“…Breath hydrogen (H2) analysis has been recommended for the differential diagnosis between necrotizing enterocolitis and transient feeding intolerance. We…”
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Characterization of lipoxygenase metabolites of arachidonic acid in cultured human skin fibroblasts by Mayer, B, Rauter, L, Zenzmaier, E, Gleispach, H, Esterbauer, H

“…Cultured human skin fibroblasts were incubated in the presence of [14C]arachidonic acid (50 microM; 1 m Ci/mmol) and the divalent cation ionophore A23187 at 37…”
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Should we recommend to Austrian physicians work in developing countries? by Rauter, L

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ASPECTS OF SURGERY IN UNDERDEVELOPED COUNTRIES. REPORT ON EXPERIENCES IN SOUTH PERSIA by RAUTER, L

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Molecular cytogenetics and phenotype characterization of a de novo pure partial trisomy 10(q24.33-qter) by Petek, E, Köstl, G, Rauter, L, Mutz, I, Wagner, K, Kroisel, P M

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Determination of prostaglandin F2 alpha and 6-oxo-prostaglandin F1 alpha in urine by gas chromatography--positive chemical ionisation-mass spectrometry using stable isotope dilutions with selected ion monitoring by Gleispach, H, Mayer, B, Rauter, L, Wurz, E

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