Erythrocyte Na+ and K+ transport systems in children with Bartter syndrome: Increase in passive sodium permeability. Na+ and K+ intracellular content was studied in five children with Bartter syndrome and their age and race-paired controls. Na+ and K+ pump (ouabain sensitive) fluxes, Na+-K+ co-transport (furosemide sensitive), and rate constants of passive Na+ and K+ permeability were determined in each patient and control and also in six parents. The results show that in Bartter syndrome, there is a significant increase in the rate constant of passive Na+ permeability without any change in passive K+ permeability. This increase in the rate constant of passive permeability might explain at least partially the increased intracellular Na+ con...
The present study was designed to investigate the role of abnormalities in red blood cell sodium-pot...
Several sodium transport abnormalities have been reported in erythrocytes from essential hyperten-si...
Bartter Syndrome (BS) is a rare, inherited renal tubulopathy characterised by hypokalaemic, hypochlo...
The basic tubular alteration present in Bartter's syndrome is still a subject of controversy. The po...
The basic tubular alteration present in Bartter's syndrome is still a subject of controversy. The po...
Erythrocyte Na+ and K+ transport systems in children with Bartter syndrome: Increase in passive sodi...
PRELIMINARY RESULTS CONCERNING KINETIC AND GENETIC ASPECTS OF SODIUM MEMBRANE TRANSPORT SYSTEMS IN E...
Bartter's syndrome is a disorder that has been linked to mutations in one of three ion transporter p...
transport) were measured in whole blood of 16 normotensive and 19 hypertensive white male subjects, ...
Established essential HTA is considered to result from the influence of both heredity and environmen...
1. The maximal rate of activity of sodium extrusion by the sodium pump, Na+--K+ outward cotransport,...
A kinetic study of cation transport from uremic patients. We previously described in red blood cells...
Sodium transport in red blood cells from dialyzed uremic patients. Studies on red blood cell (RBC) s...
Erythrocyte sodium-lithium countertransport was evaluated in three adult patients with Bartter's syn...
Clinical profiles and erythrocyte Na+ transport abnormalities of four major types of primary hyperte...
The present study was designed to investigate the role of abnormalities in red blood cell sodium-pot...
Several sodium transport abnormalities have been reported in erythrocytes from essential hyperten-si...
Bartter Syndrome (BS) is a rare, inherited renal tubulopathy characterised by hypokalaemic, hypochlo...
The basic tubular alteration present in Bartter's syndrome is still a subject of controversy. The po...
The basic tubular alteration present in Bartter's syndrome is still a subject of controversy. The po...
Erythrocyte Na+ and K+ transport systems in children with Bartter syndrome: Increase in passive sodi...
PRELIMINARY RESULTS CONCERNING KINETIC AND GENETIC ASPECTS OF SODIUM MEMBRANE TRANSPORT SYSTEMS IN E...
Bartter's syndrome is a disorder that has been linked to mutations in one of three ion transporter p...
transport) were measured in whole blood of 16 normotensive and 19 hypertensive white male subjects, ...
Established essential HTA is considered to result from the influence of both heredity and environmen...
1. The maximal rate of activity of sodium extrusion by the sodium pump, Na+--K+ outward cotransport,...
A kinetic study of cation transport from uremic patients. We previously described in red blood cells...
Sodium transport in red blood cells from dialyzed uremic patients. Studies on red blood cell (RBC) s...
Erythrocyte sodium-lithium countertransport was evaluated in three adult patients with Bartter's syn...
Clinical profiles and erythrocyte Na+ transport abnormalities of four major types of primary hyperte...
The present study was designed to investigate the role of abnormalities in red blood cell sodium-pot...
Several sodium transport abnormalities have been reported in erythrocytes from essential hyperten-si...
Bartter Syndrome (BS) is a rare, inherited renal tubulopathy characterised by hypokalaemic, hypochlo...