Hereditary angioneurotic oedema: characterization of plasma kinin and vascular permeability-enhancing activities.

Autor: Shoemaker, L. R.¹, Schurman, S. J.¹, Donaldson, V. H.¹, Davis, A. E.¹

Publikováno v: Clinical & Experimental Immunology. Jan1994, Vol. 95 Issue 1, p22-28. 7p.

Contrasting Phenotypes of Children with Different Bartter's Syndrome (BS) Gene Defects † 483

Autor: Schurman, S J, Bergstrom, W H, Shoemaker, L R, Simon, D B

Publikováno v: Pediatric Research; April 1998, Vol. 43 Issue: 1, Number 1 Supplement 4 p85-85, 1p

Genotype/phenotype observations in African Americans with Bartter syndrome.

Autor: Schurman SJ; Department of Pediatrics, Divisions of Nephrology and Genetics, University of South Florida College of Medicine and All Children's Hospital, St Petersburg, Florida, USA., Perlman SA, Sutphen R, Campos A, Garin EH, Cruz DN, Shoemaker LR

Publikováno v: The Journal of pediatrics [J Pediatr] 2001 Jul; Vol. 139 (1), pp. 105-10.

Urea kinetic analysis of automated peritoneal dialysis allows calculation of a CAPD-equivalent Kt/V(urea).

Autor: Schurman SJ; Department of Pediatrics, Division of Nephrology, University of South Florida College of Medicine and All Children's Hospital, St. Petersburg, Florida, USA. schurman@allkids.org, Shoemaker LR, Warady BA

Publikováno v: Kidney international [Kidney Int] 2000 Sep; Vol. 58 (3), pp. 1318-24.

Conjunctive effects of fibroblast growth factor and glycosaminoglycan on bone metabolism in neonatal bartter syndrome.

Autor: Williams WJ; Department of Pediatrics, SUNY Health Science Center, Syracuse 13210, USA., Shoemaker LR, Schurman SJ, Welch TR, Bergstrom WH

Publikováno v: Pediatric research [Pediatr Res] 1999 May; Vol. 45 (5 Pt 1), pp. 726-32.