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Prof. Dr. Martin Konrad

Current affiliations

University Children's Hospital - Department for General Paediatrics

Publications

Systematic review of outcomes reported in clinical research on nephronophthisis: how do they align with SONG Kids priorities? Dahmer-Heath, Mareike; Optenhövel, Sven; Hechler, Tanja; Konrad, Martin; König, Jens (2025) In: Pediatric Nephrology, 40. doi:10.1007/s00467-025-06912-0 Review article (journal) \| Peer reviewed \| Published
Systematic evaluation of olfaction in patients with hereditary cystic kidney diseases/renal ciliopathies Dahmer-Heath, M., V. Schriever, S. Kollmann, C. Schleithoff, A. Titieni, M. Cetiner, L. Patzer, B. Tönshoff, M. Hansen, P. Pennekamp, J. Gerß, M. Konrad and J. König (2021) In: Journal of Medical Genetics, 58(9), 629-636. doi:10.1136/jmedgenet-2020-107192 Research article (journal) \| Peer reviewed \| Published
First reported nosocomial outbreak of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in a pediatric dialysis unit Schwierzeck V, König JC, Kühn J, Mellmann A, Correa-Martinez CL, Omran H, Konrad M, Kaiser T, Kampmeier S (2020) In: ((Bitte Journal prüfen)), 72(2), 265-270. doi:10.1093/cid/ciaa491 Research article (journal) \| Peer reviewed \| Published
Immunosuppression and Renal Outcome in Congenital and Pediatric Steroid-Resistant Nephrotic Syndrome (vol 5, pg 2075, 2010) Buescher AK, Kranz B, Buescher R, Hildebrandt F, Dworniczak B, Pennekamp P, Kuwertz-Broeking E, Wingen A-M, John U, Kemper M, Monnens L, Hoyer PF, Weber S, Konrad M (2012) In: Clinical Journal of the American Society of Nephrology, 7(8), 1372-1374. Research article (journal) \| Peer reviewed \| Published
Three different causes of hypercalciuria. Skalova S, Konrad M, Kutilek S (2011) In: Klinische Pädiatrie, 223(5), 287-289. doi:10.1055/s-0031-1273750 Research article (journal) \| Peer reviewed \| Published

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Projects

Neocyst, Network for early onset Cystic Kidney Disease (NEOCYST) Duration: 01/09/2016 - 31/08/2022 Type of project: Own resources project
Hereditäre Glomerulopathien - Identifizierung eines neuen Gens für eine autosomal-rezessive Form des nephrotischen Syndroms mit fokal-segmentaler… Duration: 01/01/2011 - 31/01/2012 Funded by: Foundations / Trusts Type of project: Individual project
Hereditäre Magnesiumverlusterkrankungen - Bedeutung der Hypomagnesiämie für die Entstehung eines metabolischen Syndroms/einer Nephrotoxizität bei Patienten… Duration: 01/12/2007 - 30/11/2008 Funded by: Foundations / Trusts Type of project: Individual project