Pages that link to "Q68832596"

The following pages link to Hyperkalemia, acidosis, and short stature associated with a defect in renal potassium excretion (Q68832596):

Displaying 22 items.

• Renal tubular acidosis in childhood (Q34276772) (← links)
• Hereditary disorders of potassium homeostasis (Q35612242) (← links)
• Heritable forms of hypertension (Q36890057) (← links)
• Renal tubular hyperkalaemia in childhood (Q39611440) (← links)
• Investigations into the mechanisms of hyperkalemia following renal transplantation (Q40801335) (← links)
• A patient with pseudohypoaldosteronism type II complicated by congenital hypopituitarism carrying a KLHL3 mutation (Q41497831) (← links)
• Pseudohypoaldosteronism: case report and discussion of the syndrome (Q41564697) (← links)
• Familial Hyperkalemic Hypertension: A New Early-onset Pediatric Case (Q43120944) (← links)
• Hyporeninemic hypoaldosteronism in a child with lactic acidosis, deafness, and mental retardation (Q52098695) (← links)
• Mineralocorticoid-resistant renal hyperkalemia without salt wasting (type II pseudohypoaldosteronism): role of increased renal chloride reabsorption. (Q54535930) (← links)
• "Chloride-shunt" syndrome: an overlooked cause of renal hypercalciuria (Q69320526) (← links)
• Use of furosemide in the evaluation of renal tubular acidosis (Q69965226) (← links)
• The Spitzer-Weinstein syndrome: one form of type IV renal tubular acidosis and its response to hydrochlorothiazide (Q70024423) (← links)
• The syndrome of hypertension and hyperkalaemia with normal glomerular function (Gordon's syndrome). A pathophysiological study (Q70074246) (← links)
• Primary hypoaldosteronism, pseudo-hypoaldosteronism and distal tubular acidosis (Q70383485) (← links)
• Renal tubular acidosis (Q70426575) (← links)
• Furosemide versus thiazide in Gordon syndrome (Q71589768) (← links)
• Neonatal presentation of Gordon syndrome (Q71686336) (← links)
• [Primary hypoaldosteronism and secondary pseudo-hypoaldosteronism] (Q72394325) (← links)
• Diagnosis and Treatment of Renal Tubular Disorders in Children (Q72946188) (← links)
• Familial hyperkalemic hypertension: phenotypic analysis in a large family with the WNK1 deletion mutation (Q73343837) (← links)
• Familial or Genetic Primary Aldosteronism and Gordon Syndrome (Q84085493) (← links)