Zobrazeno 1 - 10
of 675
pro vyhledávání: '"E. Schwinger"'
Levosimendan is a positive inotrope with vasodilating properties (inodilator) indicated for decompensated heart failure (HF) patients with low cardiac output. Accumulated evidence supports several pleiotropic effects of levosimendan beyond inotropy,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::630c96c95f04847f8856acf93e41b8eb
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3100765
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3100765
Autor:
Ch. Rittner, E. Schwinger
Publikováno v:
Clinical Genetics. 4:398-406
Two series of 88 and 53 patients with Down's syndrome and 91 other mentally retarded patients were investigated for various blood, serum and enzyme groups. No association of trisomy 21 and the following systems and factors was found: ABO, Rh(D), MNSs
Publikováno v:
Gynäkologische Endokrinologie. 3:40-44
Die Ursachen habitueller Aborte sind sehr vielfaltig und in unterschiedlichsten Bereichen zu suchen. Einen wichtigen Aspekt stellen die chromosomalen Fehlverteilungen oder die strukturellen Chromosomenveranderungen dar. Im vorliegenden Beitrag werden
Publikováno v:
Andrologia. 37:1-9
Male infertility as a result of isolated congenital bilateral absence of the vas deferens (CBAVD) is one primary genital form of cystic fibrosis (CF) and occurs in 1-2% of infertile men. Assisted fertilization in patients with CBAVD increases the ris
Autor:
S.M. White, R. Mollicone, M. Rozek, Z. Tümer, T. Opiola, J.-J. Candelier, C.R. Bonvicino, H. Winking, A. Hebinck, H. Kuiper, Ch. Zühlke, H. Yasue, J.M. Perez de la Lastra, S. Kiuchi, A. Pienkowska, N. Arnal, B. Gläser, C. Ngo, H. Mehenni, C. Steinlein, P.S. D’Andrea, R.P.M.A. Crooijmans, A. Eggen, C. Zijlstra, M. Yerle, U. Butzmann, S.E. Antonarakis, Y.E. Shahein, E. Anton, R. Korstanje, D.F. de Andres-Cara, N.A. de Haan, R. Heilig, B. Brenig, J. Egozcue, C. Delcros, M. Østergaard, G.F. Gillissen, A. Wandall, R. Kreutz, R.J. McKinlay Gardner, F. Piumi, M. Mahony, A. Robic, C. Ozouf-Costaz, N. Tommerup, T. Haaf, C. Rodellar, C. Szpirer, F. Vidal, P.A. Ioannou, P.M. Kroisel, C. Drögemüller, K. Buchet-Poyau, Y. Takagaki, T.L. Harboe, C. Wilhelm, F. Porto-Foresti, J. Barciszewski, A.C.M. Bonné, M.T. Roldan-Arjona, C. Rogel-Gaillard, H. Hiraiwa, Y. Muneta, M. Grzmil, P. Zaragoza, C. Bonillo, H.A. van Lith, J. Kunz, A. Dalski, O. Distl, F. Laccone, D. Milan, C. Windpassinger, T. Awata, H. Uenishi, J. Szpirer, R. Fries, A.A. Bosma, F. Foresti, M.F.Z. Daniel-Silva, H. Hayes, R. Roy, H. Omran, P. Pinton, S. Schlickum, E. Petek, E. Schwinger, L. Li, P. Coullin, C. Knorr, L.F.M. van Zutphen, J. Blanco, H.P. Klinger, A. Volz, J. Mißbach, I.B. Otazu, E. Northrop, C. Andersen, P. Burfeind, M. Den Bieman, M. Meins, R. Melkaoui, J. Beck, U. Radhakrishna, M. Gautier, R. Oriol, L.F. Almeida-Toledo, I. Nanda, K. Wagner, F. Habermann, V. Petrovic, M. Schmid, R. Yamamoto, P. Moore, P. van Vooren, G. Hauke, H. Zürcher, F. Hildebrandt, C.G. Ziegler, J. Koch, P. Laurent, J.L. Williams, M.A.M. Groenen, J.J. Garrido, C. Schelling, S. Yadav, C. Kosan, H.R. Slater
Publikováno v:
Cytogenetic and Genome Research. 97:261-275
Publikováno v:
Cytogenetic and Genome Research. 95:28-33
The centromeric α-satellite DNA subfamilies from chromosomes 13 and 21 are almost identical in sequence. So far it has proven difficult to discriminate between sequence variations in the chromosome 13 and 21 α-satellite regions using in situ techni
Autor:
F. Pelliccia, M. Gerbault-Seureau, J. Daut, C. Denning, T. Meitinger, G. Fakis, K. Kikuchi, A. Dalski, H.G. Nothwang, N. Vogt, Y. Liu, M. Breen, P. Lichter, B. Malfoy, K.-H. Grzeschik, A. Rocchi, D. Incarnato, H.M. Mitchison, I. Papet, A.L. Loudon, C. Rossier, S. Schneider, B. Pedersen, D. Vogt, E. Chung, C. Menzel, L. Chen, G.A. Wittert, J. Perret, F. Willeke, L. Ferrara, Y. Watanabe, B. Ugele, W. Engel, V. Buckle, K.J. Fowler, S.E. Antonarakis, M.L. Ramírez-Dueñas, S.I. Anderson, M.E. Delany, R. Swanson, H. Turnbull, D. Sheer, T.E. Whitmore, F. Wei, M. Meeks, P. B. Bennett, H. Engel, A. Perucatti, J. Bonfils, A.C. Jelmberg, S.M. van der Maarel, K. Masuda, S. Lok, P.J. Hope, Y. Matsuda, L. French, R. Hawken, Ch. Zühlke, A. Hebinck, T. Lehnert, D.B. Zimonjic, R.H. Martin, E. Schwinger, R.M. Gardiner, M.L. Ayala-Madrigal, F. Liners, J.-P. Fryns, T.M. Skinner, T. Haaf, S.W. Scherer, M.M. Miller, E. Chevret, L. Rießelmann, R. Blevins, M.L. Watson, I.M. Adham, C.S. Haley, G.C. Webb, R. Shamsadin, M. Parmentier, L. Bartoloni, J. Koch, C. Gehrig, H. Hayes, S. Spiden, A.W.I. Lo, M.Z. Limongi, S. Ohl, S. Kollers, J.-L. Blouin, E. McKenna, A.B. Krupkin, J. Bernardino, D.S. Haines, J.L. Holloway, H.H. Ropers, R.M. Hope, C.E. Lofton-Day, A.R. Zinn, J. Wirth, S. Joos, N.C. Popescu, C. Lindbjerg Andersen, C.D. DeLozier-Blanchet, E.P. Cribiu, M. Østergaard, B. Brenig, E.V. Volpi, L. Schibler, B. Hinzmann, A. Krempler, M. Faure, M. Payton, N.K. Moschonas, A. Niveleau, N. Inoue, H.F. Otto, L. De Moerlooze, Q. Shi, B. Nielsen, P. Deloukas, K.H.A. Choo, M.F. Seldin, M. Otaño-Joos, C. Derst, D. Lefrançois, A. Schröer, I. Hansmann, P. Kalitsis, M.F. Maurer, R. Fries, M.T. Boyd, T.J. Quinton, A. Vilain, J.B. Vincent, K.K. Wilgenbus, G. von Beust, G.P. Di Meo, B. Dutrillaux, L. Gaddini, W. Scheurlen, G. Mechtersheimer, S. Doerr, A.L. Archibald, L. Iannuzzi, E. Sim, K. Regemann, R. Athwal, S. Kübart, A. Rosenthal, D.J. Figueroa, N. Tommerup, M.-G. Mattei, H. Shima, D.F.S. Longmuir, A.K. Maiti, J. Williamson, N.L. Lopez-Corrales, S. Boukouvala, C.P. Austin
Publikováno v:
Cytogenetic and Genome Research. 90:154-168
Autor:
E. Schwinger, K. Bcczkowski
Publikováno v:
Clinical Genetics. 4:447-449
The Y-body was studied in 36 patients with complete or partial androgen deficiency. In all cases a 46, XY karyotype was established. The frequency and size of the Y-body in the patients was similar to that observed in normal men. Thus it would seem t
Publikováno v:
Scandinavian Journal of Clinical and Laboratory Investigation. 55:263-266
It has been suggested that the delta F508 deletion, the most common mutation in the cystic fibrosis (CF) gene, might be linked to chronic bronchial hypersecretion. We investigated whether such an association could be found in chronic bronchitis, sinc