Klinik für Pädiatrie mit Schwerpunkt Nephrologie

Publikationen

Thumfart J, Jung S, Amasheh S, Kraemer S, Peters H, Sommer K, Biber J, Murer H, Meij I, Querfeld U, Wagner CA, Muller D. Magnesium stimulates renal phosphate reabsorption. Am J Physiol Renal Physiol 2008; 295: F1126-33.

Müller-Berghaus J, Kemper MJ, Hoppe B, Querfeld U, Müller-Wiefel DE, Morahan G, Schadendorf D, Tenbrock K. The clinical course of steroid-sensitive childhood nephrotic syndrome is associated with a functional IL12B promoter polymorphism. Nephrol Dial Transplant 2008; 23: 3841-4.

Briese S, Claus M, Querfeld U. Arterial stiffness in children after renal transplantation. Pediatr Nephrol 2008; 23: 2241-5.

Müller D, Zimmering M, Chan CT, McFarlane PA, Pierratos A, Querfeld U. Intensified hemodialysis regimens: neglected treatment options for children and adolescents. Pediatr Nephrol 2008; 23: 1729-36.

Nissel R, Faraj S, Sommer K, Henning L, van der Giet M, Querfeld U. Oxidative stress markers in young hemodialysis patients – a pilot study. Clin Nephrol 2008; 70:135-143.

Thumfart J, Gellermann J, Querfeld U. Therapie der arteriellen Hypertonie im Kindesalter. Monatsschr Kinderheilkd 2008; 156: 1121-1131.

Offner G, Toenshoff B, Höcker B, Krauss M, Bulla M, Cochat P, Fehrenbach H, Fischer W, Foulard M, Hoppe B, Hoyer PF, Jungraithmayr TC, Klaus G, Latta K, Leichter H, Mihatsch MJ, Misselwitz J, Montoya C, Müller-Wiefel DE, Neuhaus TJ, Pape L, Querfeld U, Plank C, Schwarke D, Wygoda S, Zimmerhackl LB. Efficacy and safety of basiliximab in pediatric renal transplant patients receiving cyclosporine, mycophenolate mofetil, and steroids. Transplantation 2008; 86: 1241-8.

Will C, Fromm M, Müller D. Claudin Tight Junction Proteins – Novel Aspects in paracellular transport. Perit Dial Int 2008; 28: 577-84.

Günzel D, Haisch L, Pfaffenbach S, Krug S, Milatz S, Amasheh S, Hunziker W, Müller D. Claudin function in the thick ascending limb of Henle’s loop. Ann N Y Acad Sci 2009; 1165: 152-62.

Thumfart J, Müller D. Hämolytisch-urämisches Syndrom im Kindesalter. Nephrologe 2008; 3: 297–307.

Gambhir L, Höller T, Müller M, Schott G, Vogt H, Detlefsen B, Ebert AK, Fisch M, Beaudoin S, Stein R, Boyadjiev SA, Gearhart JP, Rösch W, Utsch B, Boemers TM, Reutter H, Ludwig M. Epidemiological survey of 214 families with bladder exstrophy-epispadias complex. J Urol 2008; 179: 1539-43.

Fischer DC, Jacoby U, Pape L, Ward CJ, Kuwertz-Broeking E, Renken C, Nizze H, Querfeld U, Rudolph B, Mueller-Wiefel DE, Bergmann C, Haffner D. Activation of the AKT/mTOR pathway in autosomal recessive polycystic kidney disease (ARPKD). Nephrol Dial Transplant 2009; 24:1819-27.

Gimpel C, Wühl E, Arbeiter K, Drozdz D, Trivelli A, Charbit M, Gellermann J, Dusek J, Jankauskiene A, Emre S, Schaefer F; ESCAPE Trial Group. Superior consistency of ambulatory blood pressure monitoring in children: implications for clinical trials. J Hypertens 2009; 27: 1568-74.

Tabatabaeifar M, Schlingmann KP, Litwin M, Emre S, Bakkaloglu A, Mehls O, Antignac C, Schaefer F, Weber S; ESCAPE Trial Group. Functional analysis of BMP4 mutations identified in pediatric CAKUT patients. Pediatr Nephrol 2009; 24: 2361-8.

ESCAPE Trial Group, Wühl E, Trivelli A, Picca S, Litwin M, Peco-Antic A, Zurowska A, Testa S, Jankauskiene A, Emre S, Caldas-Afonso A, Anarat A, Niaudet P, Mir S, Bakkaloglu A, Enke B, Montini G, Wingen AM, Sallay P, Jeck N, Berg U, Caliskan S, Wygoda S, Hohbach-Hohenfellner K, Dusek J, Urasinski T, Arbeiter K, Neuhaus T, Gellermann J, Drozdz D, Fischbach M, Möller K, Wigger M, Peruzzi L, Mehls O, Schaefer F. Strict blood-pressure control and progression of renal failure in children. N Engl J Med 2009; 361: 1639-50.

Utsch B, Brun-Heath I, Gravou-Apostolatou C, Karle S, Jacobs U, Ludwig M, Zenker M, Dörr HG, Rascher W, Mornet E, Dötsch J. Infantile hypophosphatasia due to a new compound heterozygous TNSALP mutation – functional evidence for a hydrophobic side-chain? Exp Clin Endocr Diab 2009; 117: 28-33.

Otto EA, Tory K, Attanasio M, Zhou W, Chaki M, Paruchuri Y, Wise EL, Wolf MT, Utsch B, Becker C, Nürnberg G, Nürnberg P, Nayir A, Saunier S, Antignac C, Hildebrandt F. Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11). J Med Genet 2009 ; 46: 663-670.

Günzel D, Stuiver M, Kausalya PJ, Haisch L, Hunziker W, Krug S, Meij IC, Fromm M, Müller D. Identification and characterization of six novel Claudin-10 splice variants. J Cell Sci 2009; 122: 1507-17.

Raile K, Klopocki E, Holder M, Wessel T, Galler A, Deiss D, Müller D, Riebel T, Horn D, Maringa M, Weber J, Ullmann R, Grüters A. Expanded clinical spectrum in HNF1B-MODY. J Clin Endocrinol Metab 2009; 94: 2658-64.

Raile K, Klopocki E, Wessel T, Deiss D, Horn D, Müller D, Ullmann R, Grüters A. HNF1B abnormality (MODY5) in children and adolescents: high prevalence in autoantibody-negative type 1 diabetes with kidney defects. Diabetes Care 2008; 31: e83.

Heeringa SF, Vlangos CN, Chernin G, Hinkes B, Gbadegesin R, Liu J, Hoskins BE, Ozaltin F, Hildebrandt F. Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome; Members of the APN Study Group. Nephrol Dial Transplant 2008; 23: 3527-3533.

Devuyst O, Meij I, Jeunemaitre X, Ronco P, Antignac C, Christensen EI, Knoers NV, Levtchenko EN, Deen PM, Müller D, Wagner CA, Rampoldi L, Van't Hoff WG. EUNEFRON, the European Network for the Study of Orphan Nephropathies. Nephrol Dial Transplant 2009; 24: 2011-5.

Müller D, Müller DN. Battle against the renin-angiotensin system: Help from an unexpected party. Nephrol Dial Transplant 2009; 24: 1110-2.

Zebger-Gong H, Kampmann J, Kong L, Roigas J, Sommer K, Krämer S, Peters H, Müller D, Dragun D, Querfeld U. Decreased Transplant Arteriosclerosis in Endothelial Nitric Oxide Synthase-Deficient Mice. Transplantation 2010; 89: 518-26.

Will C, Breiderhoff T, Thumfart J, Stuiver M, Kopplin K, Sommer K, Günzel D, Querfeld U, Meij IC, Shan Q, Bleich M, Willnow TE, Müller D. Targeted deletion of murine Cldn16 identifies extra- and intrarenal compensatory mechanisms of Ca2+ and Mg2+ wasting. Am J Physiol Renal 2010, in press.

Zipfel PF, Mache C, Müller D, Licht C, Wigger M, Skerka C. How Deficiency of CFHR1 and CFHR3 Plasma Proteins and Autoantibodies to Factor H Contribute Hemolytic Uremic Syndrome: THE DEAP HUS Subtype-Form. Pediatr Nephrol 2010, in press.