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Ozlu, Ferda; Yapicio¿lu, Hacer; Satar, Mehmet; Narli, Nejat; Ozcan, Kenan; Buyukcelik, Mithat; Konrad, Martin; Demirhan, Osman (2006). Barttin mutations in antenatal Bartter syndrome with sensorineural deafness. Pediatric nephrology, 21(7), pp. 1056-7. Berlin: Springer 10.1007/s00467-006-0108-4
Konrad, Martin; Schaller, André; Seelow, Dominik; Pandey, Amit Vikram; Waldegger, Siegfried; Lesslauer, Annegret; Vitzthum, Helga; Suzuki, Yoshiro; Luk, John M; Becker, Christian; Schlingmann, Karl P; Schmid, Marcel; Rodriguez-Soriano, Juan; Ariceta, Gema; Cano, Francisco; Enriquez, Ricardo; Juppner, Harald; Bakkaloglu, Sevcan A; Hediger, Matthias A; Gallati, Sabina; ... (2006). Mutations in the tight-junction gene claudin 19 (CLDN19) are associated with renal magnesium wasting, renal failure, and severe ocular involvement. American journal of human genetics, 79(5), pp. 949-57. New York, N.Y.: Cell Press 10.1086/508617
Simonetti, Giacomo D; von Vigier, Rodo O; Konrad, Martin; Rizzi, Mattia; Fossali, Emilio; Bianchetti, Mario G (2006). Candesartan cilexetil in children with hypertension or proteinuria: preliminary data. Pediatric nephrology, 21(10), pp. 1480-2. Berlin: Springer 10.1007/s00467-006-0144-0
Türkmen, Mehmet; Kasap, Belde; Soylu, Alper; Böber, Ece; Konrad, Martin; Kavukçu, Salih (2006). Paracellin-1 gene mutation with multiple congenital abnormalities. Pediatric nephrology, 21(11), pp. 1776-8. Berlin: Springer 10.1007/s00467-006-0247-7
Schönfelder, EM; Knüppel, T; Tasic, V; Miljkovic, P; Konrad, M; Wühl, E; Antignac, C; Bakkaloglu, A; Schaefer, F; Weber, S; ESCAPE, Trial Group (2006). Mutations in Uroplakin IIIA are a rare cause of renal hypodysplasia in humans. American Journal of Kidney Diseases, 47(6), pp. 1004-12. Philadelphia, Pa.: W.B. Saunders 10.1053/j.ajkd.2006.02.177
