Zwischen Mitgestalten und Alltagsdruck: Herausforderungen zivilgesellschaftlich Engagierter zur (Wieder)belebung einer Kleinstadt in Ostdeutschland

by Kummel Olivia
Published 2020-05-01

Analyse der Auswirkungen des demografischen Wandels auf die Siedlungsentwässerung mit Hilfe des Realoptionsansatzes

by Gaitzsch, Gunnar
Published 2009

Erratum to “Endolymphatic Sac Enlargement in a Girl with a Novel Mutation for Distal Renal Tubular Acidosis and Severe Deafness”

by Nikki Rink, Martin Bitzan, Gus O'Gorman, Mato Nagel, Elena Torban, Paul Goodyer
Published 2013-01-01

Epilepsy, ataxia, sensorineural deafness, tubulopathy syndrome in a European child with mutations: A case report

by Antigone Papavasiliou, Katerina Foska, John Ioannou, Mato Nagel
Published 2017-07-01

A case report of Gitelman syndrome resulting from two novel mutations in SLC12A3 gene

by Wojciech Wolyniec, Sonia Kaniuka- Jakubowska, Mato Nagel, Zuzanna Wolyniec, Lukasz Obolonczyk, Renata Swiatkowska-Stodulska, Krzysztof Sworczak, Marcin Renke
Published 2016-05-01

A case report of Gitelman syndrome resulting from two novel mutations in SLC12A3 gene

by Wojciech Wolyniec, Sonia Kaniuka- Jakubowska, Mato Nagel, Zuzanna Wolyniec, Lukasz Obolonczyk, Renata Swiatkowska-Stodulska, Krzysztof Sworczak, Marcin Renke
Published 2016-05-01

Polymorphisms of the insertion / deletion ACE and M235T AGT genes and hypertension: surprising new findings and meta-analysis of data

by Zhu Ai- Ling, Liu Pengbo, Loh Marie, Mondry Adrian, Nagel Mato
Published 2005-01-01

Endolymphatic Sac Enlargement in a Girl with a Novel Mutation for Distal Renal Tubular Acidosis and Severe Deafness

by Rink Nikki, Bitzan Martin, O'Gorman Gus, Nagel Mato, Torban Elena, Goodyer Paul
Published 2012-01-01

Challenging Disease Ontology by Instances of Atypical PKHD1 and PKD1 Genetics

by Jonathan de Fallois, Ria Schönauer, Johannes Münch, Mato Nagel, Bernt Popp, Jan Halbritter
Published 2021-06-01

Kidney Injury by Variants in the <i>COL4A5</i> Gene Aggravated by Polymorphisms in Slit Diaphragm Genes Causes Focal Segmental Glomerulosclerosis

by Jenny Frese, Matthias Kettwig, Hildegard Zappel, Johannes Hofer, Hermann-Josef Gröne, Mato Nagel, Gere Sunder-Plassmann, Renate Kain, Jörg Neuweiler, Oliver Gross
Published 2019-01-01

The Hypomorphic Variant p.(Gly624Asp) in COL4A5 as a Possible Cause for an Unexpected Severe Phenotype in a Family With X-Linked Alport Syndrome

by Eva Pauline Macheroux, Matthias C. Braunisch, Matthias C. Braunisch, Stephanie Pucci Pegler, Robin Satanovskij, Robin Satanovskij, Korbinian M. Riedhammer, Korbinian M. Riedhammer, Roman Günthner, Roman Günthner, Oliver Gross, Mato Nagel, Lutz Renders, Julia Hoefele
Published 2019-11-01