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Nephrocalcinosis and proximal tubulopathy in Sjögren's Syndrome
(Universidad Nacional de Córdoba, 2018-06)
Primary Sjögren´s syndrome is a systemic and chronic autoimmune disease. Renal involvement may occur in up to 30% of patients. The incidence of tubulopathies ranges from 2.6 to 33%. They are manifested by defects in the ...
Nephrocalcinosis induced by hyperoxaluria in rats
(2013-07-01)
Purpose: To investigate nephrocalcinosis due to hyperoxaluria induced by two different inducing agents in rats. Methods: Forty Sprague-Dawley male rats were randomly distributed into four groups: Group1 (Clinical control, ...
Nephrocalcinosis induced by hyperoxaluria in rats
(2013-07-01)
Purpose: To investigate nephrocalcinosis due to hyperoxaluria induced by two different inducing agents in rats. Methods: Forty Sprague-Dawley male rats were randomly distributed into four groups: Group1 (Clinical control, ...
Interstitial nephrocalcinosis and chronic glomerulonephritis in a bitchNefrocalcinosis intersticial y glomerulonefritis crónica en una perra
(Universidad Nacional Mayor de San Marcos, Facultad de Medicina Veterinaria, 2018)
Hiperparatiroidismo primario en el adolescente: Caso clínico
(Sociedad Médica de Santiago, 2008)
A novel mutation in the anion exchanger 1 gene is associated with familial distal renal tubular acidosis and nephrocalcinosis
(Amer Acad PediatricsElk Grove VillageEUA, 2003)
ClC-5 chloride channel and kidney stones : what is the link?
(2001-03)
Nephrolithiasis is one of the most common diseases in the Western world. The disease manifests itself with intensive pain, sporadic infections, and, sometimes, renal failure. The symptoms are due to the appearance of urinary ...
Enamel-renal Syndrome In 2 Patients With A Mutation In Fam20 A And Atypical Hypertrichosis And Hearing Loss Phenotypes
(Elsevier Science IncNew York, 2017)
Poor phenotype-genotype association in a large series of patients with Type III Bartter syndrome
(Public Library of Science, 2017)
Introduction: Type III Bartter syndrome (BS) is an autosomal recessive renal tubule disorder caused by loss-of-function mutations in the CLCNKB gene, which encodes the chloride channel protein ClC-Kb. In this study, we ...