Identification of Primary Hyperoxaluria Type III by Gas Chromatography/Mass Spectrometry-Based Urine Metabolomics. [PDF]
Kuhara T +4 more
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Global prevalence of urolithiasis: a meta-analysis accounting for methodological heterogeneity. [PDF]
Vera-Ponce VJ +5 more
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Rapid and accurate preoperative diagnosis of urinary tract infections in urolithiasis patients: clinical validation of the HB&L system. [PDF]
Chang Z +12 more
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Comprehensive diagnostic evaluation of urolithiasis and cystitis in K9 dogs in Iraq: Clinical, laboratory, and imaging correlates. [PDF]
Aldujaily AH, Abeed SA, Ameer NAHA.
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Metabolic abnormalities, recurrence risk, patient and stone characteristics in calcium-based pediatric stone formers: is there any association? [PDF]
Sobh AA +7 more
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Precision diagnosis of preoperative infection in urolithiasis: integrating targeted next-generation sequencing for enhanced accuracy-a multicenter cohort study. [PDF]
Chang Z +13 more
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Uroliths occur commonly in the bladder and/or urethra of dogs and cats and can be life-threatening if urethral obstruction occurs. The majority of uroliths are composed of struvite or calcium oxalate; however, other minerals such as urate and cystine occur. Uroliths may be composed of more than one mineral.
Joseph W, Bartges, Amanda J, Callens
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Urolithiasis is the most common urinary problem in male ruminants, and one of the most common emergencies in male goats and sheep. This disease has substantial welfare implications because it causes severe pain and it has a high fatality rate. The expense associated with veterinary care and loss of affected animals has a strong economic impact on pet ...
Ricardo, Videla, Sarel, van Amstel
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There are few publications about urolithiasis of the new born baby and infant (UNI). The UNI represents 20% of the pediatric urolithiasis. The etiologies in this age group are chiefly dominated by the urinary-tract infections and metabolic abnormalities.
Jallouli, Mohamed +2 more
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Xanthine calculi are uncommonly encountered stones. When they occur, they typically do so in association with inborn metabolic disorders such as hereditary xanthinuria or Lesch-Nyhan syndrome. They may also occur in association with states of profound hyperuricemia such as myeloproliferative disease after treatment with allopurinol.
Vernon M, Pais +4 more
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