Einträge von Ludwig, Michael auf dem Publikationsserver
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Anzahl der Einträge: 14.
2023
Merkel, Daniel, Züllich, Tim Felix, Schneider, Christoph, Yousefzada, Masuod, Beer, Diana, Ludwig, Michael, Weimer, Andreas, Künzel, Julian, Kloeckner, Roman und Weimer, Johannes Matthias
(2023)
Prospective Comparison of Handheld Ultrasound Devices from Different Manufacturers with Respect to B-Scan Quality and Clinical Significance for Various Abdominal Sonography Questions.
Diagnostics 13 (24), S. 3622.
Volltext nicht vorhanden.
Weimer, Johannes, Dionysopoulou, Anna, Strelow, Kai-Uwe, Buggenhagen, Holger, Weinmann-Menke, Julia, Dirks, Klaus, Weimer, Andreas, Künzel, Julian, Börner, Norbert, Ludwig, Michael, Yang, Yang, Lorenz, Liv, Ille, Carlotta und Müller, Lukas
(2023)
Undergraduate ultrasound training: prospective comparison of two different peer assisted course models on national standards.
BMC Medical Education 23 (1).
Volltext nicht vorhanden.
2022
Mingardo, Enrico, Beaman, Glenda, Grote, Philip
, Nordenskjöld, Agneta, Newman, William
, Woolf, Adrian S.
, Eckstein, Markus
, Hilger, Alina C., Dworschak, Gabriel C.
, Rösch, Wolfgang, Ebert, Anne-Karolin, Stein, Raimund, Brusco, Alfredo, Di Grazia, Massimo, Tamer, Ali, Torres, Federico M., Hernandez, Jose L., Erben, Philipp, Maj, Carlo, Olmos, Jose M.
, Riancho, Jose A., Valero, Carmen, Hostettler, Isabel C., Houlden, Henry, Werring, David J.
, Schumacher, Johannes, Gehlen, Jan, Giel, Ann-Sophie, Buerfent, Benedikt C., Arkani, Samara, Åkesson, Elisabeth
, Rotstein, Emilia, Ludwig, Michael, Holmdahl, Gundela, Giorgio, Elisa, Berettini, Alfredo, Keene, David, Cervellione, Raimondo M., Younsi, Nina, Ortlieb, Melissa, Oswald, Josef, Haid, Bernhard, Promm, Martin, Neissner, Claudia, Hirsch, Karin, Stehr, Maximilian, Schäfer, Frank-Mattias, Schmiedeke, Eberhard, Boemers, Thomas M., van Rooij, Iris A. L. M., Feitz, Wouter F. J., Marcelis, Carlo L. M., Lacher, Martin, Nelson, Jana, Ure, Benno, Fortmann, Caroline, Gale, Daniel P., Chan, Melanie M. Y., Ludwig, Kerstin U., Nöthen, Markus M., Heilmann, Stefanie, Zwink, Nadine, Jenetzky, Ekkehart, Odermatt, Benjamin, Knapp, Michael und Reutter, Heiko
(2022)
A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy.
Communications Biology 5 (1).
Volltext nicht vorhanden.
, Nordenskjöld, Agneta, Newman, William
, Woolf, Adrian S.
, Eckstein, Markus
, Hilger, Alina C., Dworschak, Gabriel C.
, Rösch, Wolfgang, Ebert, Anne-Karolin, Stein, Raimund, Brusco, Alfredo, Di Grazia, Massimo, Tamer, Ali, Torres, Federico M., Hernandez, Jose L., Erben, Philipp, Maj, Carlo, Olmos, Jose M.
, Riancho, Jose A., Valero, Carmen, Hostettler, Isabel C., Houlden, Henry, Werring, David J.
, Schumacher, Johannes, Gehlen, Jan, Giel, Ann-Sophie, Buerfent, Benedikt C., Arkani, Samara, Åkesson, Elisabeth
, Rotstein, Emilia, Ludwig, Michael, Holmdahl, Gundela, Giorgio, Elisa, Berettini, Alfredo, Keene, David, Cervellione, Raimondo M., Younsi, Nina, Ortlieb, Melissa, Oswald, Josef, Haid, Bernhard, Promm, Martin, Neissner, Claudia, Hirsch, Karin, Stehr, Maximilian, Schäfer, Frank-Mattias, Schmiedeke, Eberhard, Boemers, Thomas M., van Rooij, Iris A. L. M., Feitz, Wouter F. J., Marcelis, Carlo L. M., Lacher, Martin, Nelson, Jana, Ure, Benno, Fortmann, Caroline, Gale, Daniel P., Chan, Melanie M. Y., Ludwig, Kerstin U., Nöthen, Markus M., Heilmann, Stefanie, Zwink, Nadine, Jenetzky, Ekkehart, Odermatt, Benjamin, Knapp, Michael und Reutter, Heiko
(2022)
A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy.
Communications Biology 5 (1).
Volltext nicht vorhanden.
2020
Rieke, Johanna Magdalena, Zhang, Rong, Braun, Doreen, Yilmaz, Öznur, Japp, Anna S., Lopes, Filipa M., Pleschka, Michael, Hilger, Alina C., Schneider, Sophia, Newman, William G., Beaman, Glenda M., Nordenskjöld, Agneta, Ebert, Anne-Karoline, Promm, Martin, Rösch, Wolfgang H., Stein, Raimund, Hirsch, Karin, Schäfer, Frank-Mattias, Schmiedeke, Eberhard, Boemers, Thomas M., Lacher, Martin, Kluth, Dietrich, Gosemann, Jan-Hendrik, Anderberg, Magnus, Barker, Gillian, Holmdahl, Gundela, Läckgren, Göran, Keene, David, Cervellione, Raimondo M., Giorgio, Elisa, Di Grazia, Massimo, Feitz, Wouter F. J., Marcelis, Carlo L. M., Van Rooij, Iris A. L. M., Bökenkamp, Arend, Beckers, Goedele M. A., Keegan, Catherine E., Sharma, Amit
, Dakal, Tikam Chand, Wittler, Lars, Grote, Phillip
, Zwink, Nadine, Jenetzky, Ekkehart, Brusco, Alfredo, Thiele, Holger
, Ludwig, Michael, Schweizer, Ulrich
, Woolf, Adrian S.
, Odermatt, Benjamin und Reutter, Heiko
(2020)
SLC20A1 Is Involved in Urinary Tract and Urorectal Development.
Frontiers in Cell and Developmental Biology 8.
Volltext nicht vorhanden.
, Dakal, Tikam Chand, Wittler, Lars, Grote, Phillip
, Zwink, Nadine, Jenetzky, Ekkehart, Brusco, Alfredo, Thiele, Holger
, Ludwig, Michael, Schweizer, Ulrich
, Woolf, Adrian S.
, Odermatt, Benjamin und Reutter, Heiko
(2020)
SLC20A1 Is Involved in Urinary Tract and Urorectal Development.
Frontiers in Cell and Developmental Biology 8.
Volltext nicht vorhanden.
2016
von Lowtzow, Catharina, Hofmann, Andrea, Zhang, Rong, Marsch, Florian, Ebert, Anne-Karoline, Rösch, Wolfgang, Stein, Raimund, Boemers, Thomas M., Hirsch, Karin, Marcelis, Carlo, Feitz, Wouter F. J., Brusco, Alfredo
, Migone, Nicola, Di Grazia, Massimo, Moebus, Susanne, Nöthen, Markus M., Reutter, Heiko, Ludwig, Michael und Draaken, Markus
(2016)
CNV analysis in 169 patients with bladder exstrophy-epispadias complex.
BMC Medical Genetics 17 (1).
Volltext nicht vorhanden.
, Migone, Nicola, Di Grazia, Massimo, Moebus, Susanne, Nöthen, Markus M., Reutter, Heiko, Ludwig, Michael und Draaken, Markus
(2016)
CNV analysis in 169 patients with bladder exstrophy-epispadias complex.
BMC Medical Genetics 17 (1).
Volltext nicht vorhanden.
2014
Reutter, Heiko, Draaken, Markus
, Pennimpede, Tracie, Wittler, Lars, Brockschmidt, Felix F., Ebert, Anne-Karolin, Bartels, Enrika, Rösch, Wolfgang, Boemers, Thomas M., Hirsch, Karin, Schmiedeke, Eberhard, Meesters, Christian, Becker, Tim, Stein, Raimund, Utsch, Boris, Mangold, Elisabeth, Nordenskjöld, Agneta, Barker, Gillian, Kockum, Christina Clementsson, Zwink, Nadine, Holmdahl, Gundula, Läckgren, Göran, Jenetzky, Ekkehart, Feitz, Wouter F.J., Marcelis, Carlo, Wijers, Charlotte H.W., Van Rooij, Iris A.L.M., Gearhart, John P., Herrmann, Bernhard G., Ludwig, Michael, Boyadjiev, Simeon A., Nöthen, Markus M. und Mattheisen, Manuel
(2014)
Genome-wide association study and mouse expression data identify a highly conserved 32 kb intergenic region between WNT3 and WNT9b as possible susceptibility locus for isolated classic exstrophy of the bladder.
Human Molecular Genetics 23 (20), S. 5536-5544.
Volltext nicht vorhanden.
, Pennimpede, Tracie, Wittler, Lars, Brockschmidt, Felix F., Ebert, Anne-Karolin, Bartels, Enrika, Rösch, Wolfgang, Boemers, Thomas M., Hirsch, Karin, Schmiedeke, Eberhard, Meesters, Christian, Becker, Tim, Stein, Raimund, Utsch, Boris, Mangold, Elisabeth, Nordenskjöld, Agneta, Barker, Gillian, Kockum, Christina Clementsson, Zwink, Nadine, Holmdahl, Gundula, Läckgren, Göran, Jenetzky, Ekkehart, Feitz, Wouter F.J., Marcelis, Carlo, Wijers, Charlotte H.W., Van Rooij, Iris A.L.M., Gearhart, John P., Herrmann, Bernhard G., Ludwig, Michael, Boyadjiev, Simeon A., Nöthen, Markus M. und Mattheisen, Manuel
(2014)
Genome-wide association study and mouse expression data identify a highly conserved 32 kb intergenic region between WNT3 and WNT9b as possible susceptibility locus for isolated classic exstrophy of the bladder.
Human Molecular Genetics 23 (20), S. 5536-5544.
Volltext nicht vorhanden.
2013
Qi, Lihong, Wang, Mei, Yagnik, Garima, Mattheisen, Manuel
, Gearhart, John P., lakshmanan, Yegappan, Ebert, Anne‐Karolin, Rösch, Wolfgang, Ludwig, Michael, Draaken, Markus
, Reutter, Heiko und Boyadjiev, Simeon A.
(2013)
Candidate gene association study implicates p63 in the etiology of nonsyndromic bladder‐exstrophy‐epispadias complex.
Birth Defects Research Part A: Clinical and Molecular Teratology 97 (12), S. 759-763.
Volltext nicht vorhanden.
, Gearhart, John P., lakshmanan, Yegappan, Ebert, Anne‐Karolin, Rösch, Wolfgang, Ludwig, Michael, Draaken, Markus
, Reutter, Heiko und Boyadjiev, Simeon A.
(2013)
Candidate gene association study implicates p63 in the etiology of nonsyndromic bladder‐exstrophy‐epispadias complex.
Birth Defects Research Part A: Clinical and Molecular Teratology 97 (12), S. 759-763.
Volltext nicht vorhanden.
2012
Wittler, Lars, Hilger, Alina, Proske, Judith, Pennimpede, Tracie, Draaken, Markus
, Ebert, Anne-Karoline, Rösch, Wolfgang, Stein, Raimund, Nöthen, Markus M., Reutter, Heiko und Ludwig, Michael
(2012)
Murine expression and mutation analyses of the prostate androgen-regulated mucin-like protein 1 (Parm1) gene, a candidate for human epispadias.
Gene 506 (2), S. 392-395.
Volltext nicht vorhanden.
, Ebert, Anne-Karoline, Rösch, Wolfgang, Stein, Raimund, Nöthen, Markus M., Reutter, Heiko und Ludwig, Michael
(2012)
Murine expression and mutation analyses of the prostate androgen-regulated mucin-like protein 1 (Parm1) gene, a candidate for human epispadias.
Gene 506 (2), S. 392-395.
Volltext nicht vorhanden.
2011
Reutter, Heiko, Boyadjiev, Simeon A., Gambhir, Lisa, Ebert, Anne-Karoline, Rösch, Wolfgang H., Stein, Raimund, Schröder, Annette, Boemers, Thomas M., Bartels, Enrika, Vogt, Hannes, Utsch, Boris
, Müller, Martin, Detlefsen, Birte, Zwink, Nadine, Rogenhofer, Sebastian, Gobet, Rita, Beckers, Goedele M.A.
, Bökenkamp, Arend, Kajbafzadeh, Abdol-Mohammad, Jaureguizar, Enrique, Draaken, Markus
, Lakshmanan, Yegappan, Gearhart, John P., Ludwig, Michael, Nöthen, Markus M. und Jenetzky, Ekkehart
(2011)
Phenotype Severity in the Bladder Exstrophy-Epispadias Complex: Analysis of Genetic and Nongenetic Contributing Factors in 441 Families from North America and Europe.
The Journal of Pediatrics 159 (5), 825-831.e1.
Volltext nicht vorhanden.
, Müller, Martin, Detlefsen, Birte, Zwink, Nadine, Rogenhofer, Sebastian, Gobet, Rita, Beckers, Goedele M.A.
, Bökenkamp, Arend, Kajbafzadeh, Abdol-Mohammad, Jaureguizar, Enrique, Draaken, Markus
, Lakshmanan, Yegappan, Gearhart, John P., Ludwig, Michael, Nöthen, Markus M. und Jenetzky, Ekkehart
(2011)
Phenotype Severity in the Bladder Exstrophy-Epispadias Complex: Analysis of Genetic and Nongenetic Contributing Factors in 441 Families from North America and Europe.
The Journal of Pediatrics 159 (5), 825-831.e1.
Volltext nicht vorhanden.
2010
Draaken, Markus
, Reutter, Heiko, Schramm, Charlotte, Bartels, Enrika, Boemers, Thomas M., Ebert, Anne-Karoline, Rösch, Wolfgang, Schröder, Annette, Stein, Raimund, Moebus, Susanne, Stienen, Dietlinde, Hoffmann, Per
, Nöthen, Markus M. und Ludwig, Michael
(2010)
Microduplications at 22q11.21 are associated with non-syndromic classic bladder exstrophy.
European Journal of Medical Genetics 53 (2), S. 55-60.
Volltext nicht vorhanden.
, Reutter, Heiko, Schramm, Charlotte, Bartels, Enrika, Boemers, Thomas M., Ebert, Anne-Karoline, Rösch, Wolfgang, Schröder, Annette, Stein, Raimund, Moebus, Susanne, Stienen, Dietlinde, Hoffmann, Per
, Nöthen, Markus M. und Ludwig, Michael
(2010)
Microduplications at 22q11.21 are associated with non-syndromic classic bladder exstrophy.
European Journal of Medical Genetics 53 (2), S. 55-60.
Volltext nicht vorhanden.
2009
Reutter, Heiko, Bökenkamp, Arend, Ebert, Anne-Karolin, Rösch, Wolfgang, Boemers, Thomas M., Nöthen, Markus M. und Ludwig, Michael
(2009)
Possible association of Down syndrome and exstrophy–epispadias complex: report of two new cases and review of the literature.
European Journal of Pediatrics 168 (7), S. 881-883.
Volltext nicht vorhanden.
Ebert, Anne-Karoline, Reutter, Heiko, Ludwig, Michael und Rösch, Wolfgang H
(2009)
The Exstrophy-epispadias complex.
Orphanet Journal of Rare Diseases 4 (1).
Volltext nicht vorhanden.
2006
Reutter, Heiko, Thauvin-Robinet, Christel, Boemers, Thomas M., Rösch, Wolfgang H. und Ludwig, Michael
(2006)
Bladder exstrophy–epispadias complex: Investigation of suppressor of variegation, enhancer of zeste and Trithorax (SET) as a candidate gene in a large cohort of patients.
Scandinavian Journal of Urology and Nephrology 40 (3), S. 221-224.
Volltext nicht vorhanden.
Reutter, Heiko, Becker, Tim, Ludwig, Michael, Schäfer, Niklas, Detlefsen, Birte, Beaudoin, Sylvie, Fisch, Margit, Ebert, Anne‐Karoline, Rösch, Wolfgang, Nöthen, Markus M., Boemers, Thomas M. und Betz, Regina C.
(2006)
Family‐based association study of the MTHFR polymorphism C677T in the bladder‐exstrophy‐epispadias‐complex.
American Journal of Medical Genetics Part A 140A (22), S. 2506-2509.
Volltext nicht vorhanden.
(2006)
Family‐based association study of the MTHFR polymorphism C677T in the bladder‐exstrophy‐epispadias‐complex.
American Journal of Medical Genetics Part A 140A (22), S. 2506-2509.
Volltext nicht vorhanden.
