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Konrad, Martin; Hou, Jianghui; Weber, Stefanie; Dötsch, Jörg; Kari, Jameela A; Seeman, Tomas; Kuwertz-Bröking, Eberhard; Peco-Antic, Amira; Tasic, Velibor; Dittrich, Katalin; Alshaya, Hammad O; von Vigier, Rodo O; Gallati, Sabina; Goodenough, Daniel A; Schaller, André (2008). CLDN16 genotype predicts renal decline in familial hypomagnesemia with hypercalciuria and nephrocalcinosis. Journal of the American Society of Nephrology, 19(1), pp. 171-81. Hagerstown, Md.: Lippincott Williams & Wilkins 10.1681/ASN.2007060709
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, G D; Konrad, M (2006). [Examination of urine in the child]. Therapeutische Umschau, 63(9), pp. 579-84. Bern: Huber 10.1024/0040-5930.63.9.579
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
Pressler, Carsten A; Heinzinger, Jolanta; Jeck, Nikola; Waldegger, Petra; Pechmann, Ulla; Reinalter, Stephan; Konrad, Martin; Beetz, Rolf; Seyberth, Hannsjörg W; Waldegger, Siegfried (2006). Late-onset manifestation of antenatal Bartter syndrome as a result of residual function of the mutated renal Na+-K+-2Cl- co-transporter. Journal of the American Society of Nephrology, 17(8), pp. 2136-42. Hagerstown, Md.: Lippincott Williams & Wilkins 10.1681/ASN.2005101071
Kutluturk, Faruk; Temel, Berna; Uslu, Bora; Aral, Ferihan; Azezli, Adil; Orhan, Yusuf; Konrad, Martin; Ozbey, Nese (2006). An unusual patient with hypercalciuria, recurrent nephrolithiasis, hypomagnesemia and G227R mutation of Paracellin-1. An unusual patient with hypercalciuria and hypomagnesemia unresponsive to thiazide diuretics. Hormone research, 66(4), pp. 175-81. Basel: Karger 10.1159/000094253
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
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
Zimmermann, Bettina; Plank, Christian; Konrad, Martin; Stöhr, Wolfgang; Gravou-Apostolatou, Chara; Rascher, Wolfgang; Dötsch, Jörg (2006). Hydrochlorothiazide in CLDN16 mutation. Nephrology, dialysis, transplantation, 21(8), pp. 2127-32. Oxford: Oxford University Press 10.1093/ndt/gfl144
von Schnakenburg, Christian; Feneberg, Reinhard; Plank, Christian; Zimmering, Miriam; Arbeiter, Klaus; Bald, Martin; Fehrenbach, Henry; Griebel, Martin; Licht, Christoph; Konrad, Martin; Timmermann, Kirsten; Kemper, Markus J (2006). Percutaneous endoscopic gastrostomy in children on peritoneal dialysis. Peritoneal dialysis international, 26(1), pp. 69-77. Toronto: Multimed
Gorgojo, Juan José; Donnay, Sergio; Jeck, Nikola; Konrad, Martin (2006). A Spanish founder mutation in the chloride channel gene, CLCNKB, as a cause of atypical Bartter syndrome in adult age. Hormone research, 65(2), pp. 62-8. Basel: Karger 10.1159/000090601
