نتایج جستجو برای: nephrocalcinosis

تعداد نتایج: 1865  

Journal: :Archives of Disease in Childhood - Fetal and Neonatal Edition 2006

Journal: :Archives of Disease in Childhood 1955

Journal: :International Journal of Health Sciences (IJHS) 2022

In this present study, Karpura shilajit, an Ayurvedic herbo-mineral, currently used in the clinical practice for various ailments, was investigated chemically and pharmacologically.To screen anti-lithiatic activity of shilajit against sodium oxalate (70 mg/kg, i.p) 7 days vitro by nucleation-aggregation assay. Cystone (500 p.o.)used as a standard drug study.Nephrolithiasis may also be associate...

Journal: :Journal of Diagnostic Medical Sonography 2013

Journal: :Kidney & blood pressure research 2015
Tilman Jobst-Schwan Andrea Pannes Karl Peter Schlingmann Kai-Uwe Eckardt Bodo B Beck Michael S Wiesener

BACKGROUND/AIMS Hypercalcemia can result in nephrocalcinosis/nephrolithiasis and may lead to renal failure. Idiopathic infantile hypercalcemia is caused by mutations of the CYP24A1 gene, which regulates vitamin D activity. Classically infants present with hypercalcemia. Recently, a number of individuals have been reported with late onset clinical manifestation or late diagnosis in adulthood. Al...

Journal: :Srpski arhiv za celokupno lekarstvo 2010
Amira Peco-Antić Martin Konrad Gordana Milosevski-Lomić Nikola Dimitrijević

INTRODUCTION Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis (FHHNC) is a rare autosomal recessive disease characterized by excessive renal magnesium and calcium wasting, bilateral nehrocalcinosis and progressive renal failure. This is the first report of FHHNC of four patients in Serbia. OUTLINE OF CASES The first three patients were siblings from the same family. The index...

Journal: :Nefrologia : publicacion oficial de la Sociedad Espanola Nefrologia 2013
Laura Escobar Natalia Mejía Helena Gil Fernando Santos

Distal renal tubular acidosis (dRTA) or RTA type I is characterised by reduced H+ hydrogen ions and ammonium urinary excretion. In children affected by dRTA there is stunted growth, vomiting, constipation, loss of appetite, polydipsia and polyuria, nephrocalcinosis, weakness and muscle paralysis due to hypokalaemia. This work summarises progress made in dRTA genetic studies in populations ...

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