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Toplam kayıt 5, listelenen: 1-5
A novel mutation c.2010delG of CLCN5 gene associated with Dent disease-1 in an 11-year-old male with nephrolithiasis and nephrocalcinosis
(2018)
Dent's disease-1 (CLCN5 gene) is a rare X-linked recessive tubulopathy characterized by low molecular weight proteinuria, hypercalciuria, nephrolcalcinosis or nephrolithiasis, proximal tubular dysfunction and renal failure ...
Renal Stone Composition Does not Affect The Outcome of Percutaneous Nephrolithotomy in Children
(2018)
Purpose We sought to investigate the association between renal stone composition and percutaneous nephrolithotomy outcomes in pediatric patients and define the characterization of the stone composition.
Methods The data ...
Factors Predicting Postoperative Febrile Urinary Tract Infection Following Percutaneous Nephrolithotomy in Prepubertal Children
(2018)
Predictive tables and scoring systems can predict stone clearance. However, there is a paucity of evidence regarding the prediction of complications during percutaneous nephrolithotomy (PCNL), particularly in children, ...
Hypomagnesemia in Pediatric Heart Transplant Patients Treated with Tacrolimus
(2018)
Objectives: We aimed to investigate the frequency of hypomagnesemia and urinary magnesium excretion in pediatric heart transplant recipients.
Materials and Methods: In this study, 22 pediatric patients who underwent ...
Post-traumatic Delayed Peripheral Facial Palsy
(2018)
Peripheral facial palsy in children is very rare in comparison to adults. The most common cause is idiopathic. Another rare cause of peripheral facial palsy in children is trauma. It occurs after head trauma, mostly due ...