Results 81 to 90 of about 2,403 (210)
Journal of Cellular and Molecular Medicine, Volume 28, Issue 7, April 2024.Abstract Kidney stone, one of the oldest known diseases, has plagued humans for centuries, consistently imposing a heavy burden on patients and healthcare systems worldwide due to their high incidence and recurrence rates. Advancements in endoscopy, imaging, genetics, molecular biology and bioinformatics have led to a deeper and more comprehensive ...
Caitao Dong +9 more
wiley +1 more source
Metabolic evaluation in patients with recurrent calcium oxalate stones
Urology Research and Practice, 2019 Objective: This study aimed to evaluate the metabolic changes in patients with recurrent calcium oxalate stones. Materials and methods: We evaluated 143 patients with recurrent oxalate stones and measured serum calcium, phosphate, creatinine, urate ...
Mustafa Kıraç +3 more
doaj +2 more sources
International Brazilian Journal of Urology, 2011 OBJECTIVE: To evaluate the preventive effects of alkaline citrate on stone recurrence as well as stone growth post-ESWL or PCNL in patients with calcium-containing stones.
B Lojanapiwat +7 more
doaj +1 more source
Analysis of metabolism associated risk factors of hypocitrateuria in patients with kidney stone [PDF]
Jichu yixue yu linchuang, 2021 Objective To retrospectively analyze metabolism associated risk factors of hypocitrateuria in kidney stone patients. Methods Totally 92 kidney stone patients with qualified data from metabolic evaluation database of Peking Union Medical College ...
QIAO Yi, XIAO He, FAN Xiao-hong, SHI Bing-bing, JI Zhi-gang
doaj
Safety of topiramate for treating migraines. [PDF]
, 2014 INTRODUCTION: Migraine is a very common medical disorder characterized by attacks of moderate-severe headache, nausea and disability. Topiramate is an effective, popular prophylactic migraine treatment, which is approved for use in adults and adolescents.
Marmura, Michael J
core +2 more sources
Annals of Human Genetics, Volume 88, Issue 1, Page 58-75, January 2024.Abstract Autosomal recessive polycystic kidney disease is an early onset inherited hepatorenal disorder affecting around 1 in 20,000 births with no approved specific therapies. The disease is almost always caused by variations in the polycystic kidney and hepatic disease 1 gene, which encodes fibrocystin (FC), a very large, single‐pass transmembrane ...
Travis A K Bannell, Joseph J B Cockburn
wiley +1 more source
Metabolic and Physico-chemical Urolithiasis Parameters in the First Morning Urine [PDF]
, 2009 The 24-hour urine is golden standard for metabolic assessment of stone formers. However, due to the difficulties in collecting almost 1/3 of the samples can not be used for the analysis. Therefore, we analyzed first morning urine and calculated different
Ines Bilić-]určić +5 more
core +1 more source
Long Term Sequela of Pediatric Bladder Reconstruction [PDF]
, 2015 Children with refractory neurogenic bladder (NGB) who have failed maximal medical management are presented with options for bladder reconstruction. It is critical to understand the long-term sequela of bladder augmentation and bladder neck reconstruction
Cain, Mark +3 more
core +1 more source
Recurrent Urolithiasis Revealing Primary Hyperparathyroidism in a Nephrology Department
Case Reports in Nephrology, Volume 2024, Issue 1, 2024.Background. Urinary lithiasis constitutes a recurrent pathology affecting a relatively young population. The risk of progression to chronic renal failure and the cost of treatment are the most important issues. Primary hyperparathyroidism (PHPT) is responsible for urolithiasis and nephrocalcinosis in 7% of patients, and it represents the 7th cause of ...
Hajji Meriam +6 more
wiley +1 more source
Biochemical Risk Factors for Stone Formation in Healthy School Children
Acta Medica Iranica, 2012 Prevalence of urolithiasis in childhood is increasing. The wide geographic variation in the incidence of lithiasis in childhood is related to climatic, dietary, and socioeconomic factors. Many children with stone disease have a metabolic abnormality.
Mohsen Akhavan-Sepahi +4 more
doaj +2 more sources