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D B Simon

Showing results (21-30 of 31) with videos related to

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Pediatric Nephrology (Berlin, Germany)|September 7, 2000
Bartter syndrome and focal segmental glomerulosclerosis: a possible link between two diseasesI H Su, R Frank, B G Gauthier, et al.
International Journal of Cardiology|March 28, 2003
Can we predict which patients with implantable cardioverter defibrillators receive appropriate shock therapy? A study of 155 patientsC Aldo Rinaldi, Ron D B Simon, Artur Baszko, et al.
Pacing and Clinical Electrophysiology : PACE|July 25, 2003
A randomized prospective study of single coil versus dual coil defibrillation in patients with ventricular arrhythmias undergoing implantable cardioverter defibrillator therapyC Aldo Rinaldi, Ron D B Simon, Peter Geelen, et al.
Hypertension (Dallas, Tex. : 1979)|June 16, 2001
Mutations in the Na-Cl cotransporter reduce blood pressure in humansD N Cruz, D B Simon, C Nelson-Williams, et al.
Nature Genetics|October 1, 1996
Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMKD B Simon, F E Karet, J Rodriguez-Soriano, et al.
The International Journal of Cardiovascular Imaging|July 2, 2003
Three- and four-dimensional reconstruction of intra-cardiac anatomy from two-dimensional magnetic resonance imagesM E Miquel, D L G Hill, E J Baker, et al.
Nature Genetics|June 1, 1997
Multilocus linkage of familial hyperkalaemia and hypertension, pseudohypoaldosteronism type II, to chromosomes 1q31-42 and 17p11-q21T A Mansfield, D B Simon, Z Farfel, et al.
Science (New York, N.Y.)|July 3, 1999
Paracellin-1, a renal tight junction protein required for paracellular Mg2+ resorptionD B Simon, Y Lu, K A Choate, et al.
Nature Genetics|January 1, 1996
Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporterD B Simon, C Nelson-Williams, M J Bia, et al.
Science (New York, N.Y.)|August 11, 2001
Human hypertension caused by mutations in WNK kinasesF H Wilson, S Disse-Nicodème, K A Choate, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
Pediatric Nephrology (Berlin, Germany)|September 7, 2000
Bartter syndrome and focal segmental glomerulosclerosis: a possible link between two diseasesI H Su, R Frank, B G Gauthier, et al.
International Journal of Cardiology|March 28, 2003
Can we predict which patients with implantable cardioverter defibrillators receive appropriate shock therapy? A study of 155 patientsC Aldo Rinaldi, Ron D B Simon, Artur Baszko, et al.
Pacing and Clinical Electrophysiology : PACE|July 25, 2003
A randomized prospective study of single coil versus dual coil defibrillation in patients with ventricular arrhythmias undergoing implantable cardioverter defibrillator therapyC Aldo Rinaldi, Ron D B Simon, Peter Geelen, et al.
Hypertension (Dallas, Tex. : 1979)|June 16, 2001
Mutations in the Na-Cl cotransporter reduce blood pressure in humansD N Cruz, D B Simon, C Nelson-Williams, et al.
Nature Genetics|October 1, 1996
Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMKD B Simon, F E Karet, J Rodriguez-Soriano, et al.
The International Journal of Cardiovascular Imaging|July 2, 2003
Three- and four-dimensional reconstruction of intra-cardiac anatomy from two-dimensional magnetic resonance imagesM E Miquel, D L G Hill, E J Baker, et al.
Nature Genetics|June 1, 1997
Multilocus linkage of familial hyperkalaemia and hypertension, pseudohypoaldosteronism type II, to chromosomes 1q31-42 and 17p11-q21T A Mansfield, D B Simon, Z Farfel, et al.
Science (New York, N.Y.)|July 3, 1999
Paracellin-1, a renal tight junction protein required for paracellular Mg2+ resorptionD B Simon, Y Lu, K A Choate, et al.
Nature Genetics|January 1, 1996
Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporterD B Simon, C Nelson-Williams, M J Bia, et al.
Science (New York, N.Y.)|August 11, 2001
Human hypertension caused by mutations in WNK kinasesF H Wilson, S Disse-Nicodème, K A Choate, et al.
Pageof 4