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Pierre-Maurice Herr
Pierre-Maurice Herr
Technische Universität München
Nephrotic syndrome
Focal segmental glomerulosclerosis
Medicine
Intensive care medicine
Alport syndrome
2
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12
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Identification of disease-causing variants by comprehensive genetic testing with exome sequencing in adults with suspicion of hereditary FSGS.
2020
European Journal of Human Genetics
Matthias C. Braunisch
Korbinian M. Riedhammer
Pierre-Maurice Herr
Sarah Draut
Roman Günthner
Matias Wagner
Marc Weidenbusch
Adrian Lungu
Bader Alhaddad
Lutz Renders
Tim M. Strom
Uwe Heemann
Thomas Meitinger
Christoph Schmaderer
Julia Hoefele
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Heterozygous COL4A3 Variants in Histologically Diagnosed Focal Segmental Glomerulosclerosis
2018
Frontiers in Pediatrics
Matthias C. Braunisch
Maike Büttner-Herold
Roman Günthner
Robin Satanovskij
Korbinian Maria Riedhammer
Pierre-Maurice Herr
Hanns-Georg Klein
Dagmar Wahl
Claudius Küchle
Lutz Renders
Uwe Heemann
Christoph Schmaderer
Julia Hoefele
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Citations (11)
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