Bilaketaren emaitzak - Heiko Reutter
- Erakusten 1 - 20 emaitzak -- 32
- Go to Next Page
-
1
The Exstrophy-epispadias complex nork Anne‐Karoline Ebert, Heiko Reutter, Michael Ludwig, Wolfgang Rösch
Argitaratua 2009Revisão -
2
-
3
The components of arginine and methylarginine metabolism are indicative of altered kidney function in intrauterine growth-restricted neonates nork Lina Kleinebenne, Waldemar Röhrig, Fabian Ebach, Heiko Reutter, Alexander Pankraz, Katharina Monika Heuchel, Andreas Müller, Alina C. Hilger
Argitaratua 2024Artigo -
4
Oral health status in children with chronic kidney disease, kidney transplantation, and nephrotic syndrome: a cross-sectional study nork Anna Beyer, Fabian Ebach, Heiko Reutter, Katja Sauerstein, Alina C. Hilger, Tobias Krickau, Anja Tzschoppe, Joachim Woelfe, Matthias Galiano, Jan Schaefer
Argitaratua 2025Artigo -
5
Infancy-Onset T1DM, Short Stature, and Severe Immunodysregulation in Two Siblings With a Homozygous LRBA Mutation nork Felix Schreiner, Michaela Plamper, Gesche Düeker, Stefan Schoenberger, Laura Gámez‐Díaz, Bodo Grimbacher, Alina C. Hilger, Bettina Gohlke, Heiko Reutter, Joachim Woelfle
Argitaratua 2016Artigo -
6
-
7
-
8
Mild Recessive Mutations in Six Fraser Syndrome–Related Genes Cause Isolated Congenital Anomalies of the Kidney and Urinary Tract nork Stefan Kohl, Daw‐Yang Hwang, Gabriel C. Dworschak, Alina C. Hilger, Pawaree Saisawat, Asaf Vivante, Nataša Stajić, Radovan Bogdanović, Heiko Reutter, Elijah O. Kehinde, Velibor Tasić, Friedhelm Hildebrandt
Argitaratua 2014Artigo -
9
Mutations in 12 known dominant disease-causing genes clarify many congenital anomalies of the kidney and urinary tract nork Daw‐Yang Hwang, Gabriel C. Dworschak, Stefan Kohl, Pawaree Saisawat, Asaf Vivante, Alina C. Hilger, Heiko Reutter, Neveen A. Soliman, Radovan Bogdanović, Elijah O. Kehinde, Velibor Tasić, Friedhelm Hildebrandt
Argitaratua 2014Artigo -
10
An Approach to the Identification of Anomalies and Etiologies in Neonates with Identified or Suspected VACTERL (Vertebral Defects, Anal Atresia, Tracheo-Esophageal Fistula with Eso... nork Benjamin D. Solomon, Linda A. Baker, Kelly Bear, Bridget Cunningham, Philip F. Giampietro, Colleen Hadigan, Donald W. Hadley, Steven J. Harrison, Marc A. Levitt, Nickie Niforatos, Scott M. Paul, Cathleen Raggio, Heiko Reutter, Nicole Warren‐Mora
Argitaratua 2013Revisão -
11
Epidemiological Survey of 214 Families With Bladder Exstrophy-Epispadias Complex nork Lisa Gambhir, Tobias Höller, Martín Müller, G. Schott, Hannes Vogt, B. Detlefsen, A. Ebert, Margit Fisch, Sylvie Beaudoın, Raimund Stein, Simeon A. Boyadjiev, John P. Gearhart, Wolfgang Rösch, Boris Utsch, Thomas M. Boemers, Heiko Reutter, Michael Ludwig
Argitaratua 2008Artigo -
12
Yunis-Varón Syndrome Is Caused by Mutations in FIG4, Encoding a Phosphoinositide Phosphatase nork Philippe M. Campeau, Guy M. Lenk, James T. Lu, Yangjin Bae, Lindsay C. Burrage, Peter D. Turnpenny, Jorge Román Corona‐Rivera, Lucia Morandi, Marina Mora, Heiko Reutter, Anneke T. Vulto-van Silfhout, Laurence Faivre, Eric Haan, Richard A. Gibbs, Miriam H. Meisler, Brendan H. Lee
Argitaratua 2013Artigo -
13
Targeted Resequencing of 29 Candidate Genes and Mouse Expression Studies Implicate<i>ZIC3</i>and<i>FOXF1</i>in Human VATER/VACTERL Association nork Alina C. Hilger, Jan Halbritter, Tracie Pennimpede, Amelie van der Ven, Georgia Sarma, Daniela A. Braun, Jonathan D. Porath, Stefan Kohl, Daw‐Yang Hwang, Gabriel C. Dworschak, Bernhard G. Hermann, Anna Pavlova, Osman El‐Maarri, Markus M. Nöthen, Michael Ludwig, Heiko Reutter, Friedhelm Hildebrandt
Argitaratua 2015Artigo -
14
Genome-wide Association Study and Meta-Analysis Identify ISL1 as Genome-wide Significant Susceptibility Gene for Bladder Exstrophy nork Markus Draaken, Michael Knapp, Tracie Pennimpede, Johanna Magdalena Schmidt, Anne‐Karolin Ebert, Wolfgang Rösch, Raimund Stein, Boris Utsch, Karin Hirsch, Thomas M. Boemers, Elisabeth Mangold, Stefanie Heilmann‐Heimbach, Kerstin U. Ludwig, Ekkehart Jenetzky, Nadine Zwink, Susanne Moebus, Bernhard G. Herrmann, Manuel Mattheisen, Markus M. Nöthen, Michael Ludwig, Heiko Reutter
Argitaratua 2015Revisão -
15
Muscarinic Acetylcholine Receptor M3 Mutation Causes Urinary Bladder Disease and a Prune-Belly-like Syndrome nork Stefanie Weber, Hölger Thiele, Sevgı Mır, Mohammad R. Toliat, Betül Sözeri, Heiko Reutter, Markus Draaken, Michael Ludwig, Janine Altmüller, Peter Frommolt, Helen M. Stuart, Parisa Ranjzad, Neil A. Hanley, Rachel Jennings, William G. Newman, Duncan T. Wilcox, Uwe Thiel, Karl P. Schlingmann, Rolf Beetz, Peter F. Hoyer, Martin Konrad, Franz Schaefer, Peter Nürnberg, Adrian S. Woolf
Argitaratua 2011Artigo -
16
Cantú Syndrome Is Caused by Mutations in ABCC9 nork Bregje W.M. van Bon, Christian Gilissen, Dorothy K. Grange, Raoul C.M. Hennekam, Hülya Kayserili, Hartmut Engels, Heiko Reutter, John R. Østergaard, Éva Morava, Konstantinos Tsiakas, Bertrand Isidor, M Le Merrer, Metin Eser, Nienke Wieskamp, Petra de Vries, Marloes Steehouwer, Joris A. Veltman, Stephen P. Robertson, Han G. Brunner, Bert B.A. de Vries, Alexander Hoischen
Argitaratua 2012Artigo -
17
Research perspectives in the etiology of congenital anorectal malformations using data of the International Consortium on Anorectal Malformations: evidence for risk factors across... nork Charlotte H. W. Wijers, Ivo de Blaauw, Carlo Marcelis, René Wijnen, Han G. Brunner, Paola Midrio, Piergiorgio Gamba, Maurizio Clementi, Ekkehart Jenetzky, Nadine Zwink, Heiko Reutter, Enrika Bartels, Sabine Grasshoff‐Derr, Stefan Holland‐Cunz, Stuart Hosie, Stefanie Märzheuser, Eberhard Schmiedeke, Célia Cretolle, Sabine Sarnacki, Marc A. Levitt, Nine Knoers, Nel Roeleveld, Iris A.L.M. van Rooij
Argitaratua 2010Artigo -
18
Mutations of the SLIT2–ROBO2 pathway genes SLIT2 and SRGAP1 confer risk for congenital anomalies of the kidney and urinary tract nork Daw‐Yang Hwang, Stefan Kohl, Xueping Fan, Asaf Vivante, Stefanie Chan, Gabriel C. Dworschak, Julian Schulz, Albertien M. van Eerde, Alina C. Hilger, Heon Yung Gee, Tracie Pennimpede, Bernhard G. Herrmann, Glenn van de Hoek, Kirsten Y. Renkema, Christoph Schell, Tobias B. Huber, Heiko Reutter, Neveen A. Soliman, Nataša Stajić, Radovan Bogdanović, Elijah O. Kehinde, Richard P. Lifton, Velibor Tasić, Lu W, Friedhelm Hildebrandt
Argitaratua 2015Artigo -
19
Sequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft Palate nork Elisabeth Mangold, Anne C. Böhmer, Nina Ishorst, Ann‐Kathrin Hoebel, Pınar Gültepe, Hannah Schuenke, Johanna Klamt, Andrea Hofmann, Lina Gölz, Ruth Raff, Peter Teßmann, Stefanie Nowak, Heiko Reutter, Alexander Hemprich, Thomas Kreusch, Franz‐Josef Kramer, Bert Braumann, Rudolf H. Reich, Gül Schmidt, Andreas Jäger, Rudolf Reiter, Sibylle Brosch, Janis Stavusis, Miho Ishida, Rimante Seselgyte, Gudrun E. Moore, Markus M. Nöthen, Guntram Borck, Khalid Aldhorae, Baiba Lāce, Philip Stanier, Michael Knapp, Kerstin U. Ludwig
Argitaratua 2016Artigo -
20
Novel congenital disorder of <i>O</i>-linked glycosylation caused by GALNT2 loss of function nork Monica Zilmer, Andrew C. Edmondson, Sumeet A. Khetarpal, Viola Alesi, Maha S. Zaki, Kevin Rostásy, Charlotte Madsen, Francesca Romana Lepri, Lorenzo Sinibaldi, Raffaella Cusmai, Antonio Novelli, Mahmoud Y. Issa, Christina Fenger, Rami Abou Jamra, Heiko Reutter, Silvana Briuglia, Emanuele Agolini, Lars Hestbjerg Hansen, Ulla E. Petäjä‐Repo, John Hintze, Kimiyo Raymond, Kristen Liedtke, Valentina Stanley, Damir Musaev, Joseph G. Gleeson, Cecilia Vitali, William T. O’Brien, Elena Gardella, Guido Rubboli, Daniel J. Rader, Katrine T. Schjoldager, Rikke S. Møller
Argitaratua 2020Artigo
Bilaketa egiteko lanabesak:
Antzeko gaiak
Biology
Genetics
Gene
Medicine
Internal medicine
Mutation
Phenotype
Pathology
Exome sequencing
Kidney
Embryonic stem cell
Kidney development
Cancer research
Endocrinology
Kidney disease
Renal agenesis
Surgery
Atresia
Disease
Genome-wide association study
Genotype
Missense mutation
Pediatrics
Pregnancy
Single-nucleotide polymorphism
Ureteric bud
Urinary system
Anal atresia
Anatomy
Biochemistry