Publikationen

Ataia I, Casaulta C, von Vigier RO, Pfammatter JP, Brekenfeld C, Sauvain MJ, Steinlin M: Vasculitis as a reason of chronic headache. Praxis (Bern 1994). 2008; 97: 322-5

Bergmann M, Corigliano T, Ataia I, Renella R, Simonetti GD, Bianchetti MG, von Vigier RO: Childhood extraordinary daytime urinary frequency- a case series and a systematic literature review. Pediatr Nephrol. 2009; 24: 89-95

Borsari AG, Bucher B, Brazzola P, Simonetti GD, Dolina M, Bianchetti MG: Susceptibility of Escherichia coli strains isolated in children with community-acquired urinary tract infection in Southern Switzerland. Clin Ther. 2008; 30: 2090-2095

Fiore E, Bernasconi M, Simonetti GD, Rizzi M, Bianchetti MG: Kidney disease in acute hemorrhagic edema of young children. Turk J Pediatr. 2008; 50: 512

Fiore E, Rizzi M, Ragazzi M, Vanoni F, Bernasconi M, Bianchetti MG, Simonetti GD: Acute hemorrhagic edema of young children (cockade purpura and edema) - A case series and a systematic review. J Am Acad Dermatol. 2008; 59 4): 684-95

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

Konrad M, Hou j, Weber S, Dötsch J, Kari JA, Seeman T, Kuwertz-Bröking E, Peco-Antic A, Tasic V, Dittrich K, Alshaya HO, von Vigier RO, Gallati S, Goodenough DA, Schaller A: CLDN16 genotype predicts renal decline in familial hypomagnesemia with hypercalciuria and nephrocalcinosis J Am Soc Nephrol. 2008; 19: 171-81

Konrad M, von Vigier RO, Waldegger S: Hereditary disorders of the thick ascending limb and distal convoluted tubule In: Mount DB, Pollak MR (eds.): Molecular and genetic basis of renal disease – A companion to Brenner & Rector’s The Kidney. 1st ed. Philadelphia, Saunders Elsevier, 2008, pp 229-249

Simonetti GD, Eisenberger U, Bergmann IP, Frey FJ, Mohaupt MG: Pulse Contour Analysis: A Valid Assessment of Central Arterial Stiffness in Children? Pediatr Nephrol. 2008; 23: 439-444

Simonetti GD, Raio L, Surbek D, Nelle M, Frey FJ, Mohaupt MG: Salt sensitivity of children with low birth weight. Hypertension 2008; 52: 625-30

Simonetti GD, von Vigier RO, Wühl E, Mohaupt MG: Ambulatory arterial stiffness index is increased in hypertensive childhood disease. Pediatr Res. 2008; 64: 303-7

Simonetti GD, Wühl E, Schaefer F: Population-based hypertension screening in preschool children. Kardiovaskuläre Medizin 2008; 11 (9): 290–292

Simonetti GD: Häusliche Selbstmessung des Blutdruckes. Der Nephrologe. 2008; 3 (2): 136-138

Sweeney WE Jr, von Vigier RO, Frost P, Avner ED: Src inhibition ameliorates autosomal recessive polycystic kidney disease. J Am Soc Nephrol. 2008; 19: 1331-41

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. 2008;117:28-33