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)
Type of Publication: Research article (journal)

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)
Type of Publication: Research article (journal)

Mutations in CYP24A1 and idiopathic infantile hypercalcemia.

Schlingmann KP, Kaufmann M, Weber S, Irwin A, Goos C, John U, Misselwitz J, Klaus G, Kuwertz-Bröking E, Fehrenbach H, Wingen AM, Güran T, Hoenderop JG, Bindels RJ, Prosser DE, Jones G, Konrad M (2011)
In: New England Journal of Medicine, 365(5)
Type of Publication: Research article (journal)

Hypomagnesemia-hypercalciuria-nephrocalcinosis and ocular findings: a new claudin-19 mutation

Ekinci Z, Kayabey O, Konrad M (2011)
In: Pediatric Nephrology, 26(9)
Type of Publication: Research article (journal)

Accelerated kidney transplant rejection and hypertensive encephalopathy in a pediatric patient associated with antibodies against angiotensin type 1 receptor and HLA class II.

Kelsch R, Everding AS, Kuwertz-Bröking E, Brand E, Spriewald BM, Sibrowski W, Konrad M, Dragun D (2011)
In: Transplantation, 92(10)
Type of Publication: Research article (journal)

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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) Type of Publication: Research article (journal)
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: Clin. Infect. Dis., 72(2) Type of Publication: Research article (journal)
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) Type of Publication: Research article (journal)
Three different causes of hypercalciuria. Skalova S, Konrad M, Kutilek S (2011) In: Klinische Pädiatrie, 223(5) Type of Publication: Research article (journal)
Mutations in CYP24A1 and idiopathic infantile hypercalcemia. Schlingmann KP, Kaufmann M, Weber S, Irwin A, Goos C, John U, Misselwitz J, Klaus G, Kuwertz-Bröking E, Fehrenbach H, Wingen AM, Güran T, Hoenderop JG, Bindels RJ, Prosser DE, Jones G, Konrad M (2011) In: New England Journal of Medicine, 365(5) Type of Publication: Research article (journal)
Muscarinic Acetylcholine Receptor M3 Mutation Causes Urinary Bladder Disease and a Prune-Belly-like Syndrome. Weber S, Thiele H, Mir S, Toliat MR, Sozeri B, Reutter H, Draaken M, Ludwig M, Altmüller J, Frommolt P, Stuart HM, Ranjzad P, Hanley NA, Jennings R, Newman WG, Wilcox DT, Thiel U, Schlingmann KP, Beetz R, Hoyer PF, Konrad M, Schaefer F, Nürnberg P, Woolf AS (2011) In: American Journal of Human Genetics, 89(5) Type of Publication: Research article (journal)
Hypomagnesemia-hypercalciuria-nephrocalcinosis and ocular findings: a new claudin-19 mutation Ekinci Z, Kayabey O, Konrad M (2011) In: Pediatric Nephrology, 26(9) Type of Publication: Research article (journal)
CYP24A1 Mutations in Idiopathic Infantile Hypercalcemia REPLY Schlingmann KarlP, Jones Glenville, Konrad Martin (2011) In: New England Journal of Medicine, 365(18) Type of Publication: Research article (journal)
Accelerated kidney transplant rejection and hypertensive encephalopathy in a pediatric patient associated with antibodies against angiotensin type 1 receptor and HLA class II. Kelsch R, Everding AS, Kuwertz-Bröking E, Brand E, Spriewald BM, Sibrowski W, Konrad M, Dragun D (2011) In: Transplantation, 92(10) Type of Publication: Research article (journal)
Genotype/phenotype correlation in FHHNC caused by mutations in either CLDN16 or CLDN19: long-term follow-up in 125 patients Haisch L, Schlingmann KP, Tasic V, Al-Attrach I, Cochat P, Sikora P, Ariceta G, Kari J, Dittrich K, Konrad M (2011) In: Pediatric Nephrology, 26(9) Type of Publication: Research article (journal)