Results 31 to 40 of about 2,591 (165)
Saudi Journal of Kidney Diseases and Transplantation, 2017 Overactive bladder is a stressful condition which affects around 15%—20% of 5- year-old and up to 2% of young adults. One of the most common causes of overactive bladder is hypercalciuria.
Parsa Yousefichaijan +4 more
doaj +1 more source
Cancer Medicine, Volume 15, Issue 3, March 2026.ABSTRACT Introduction The European Summary of Product Characteristics (SmPC) for 5‐FU warns of significant granulocyte decline when combined with thiazides, cyclophosphamide, or methotrexate, based on a 1981 cohort of 14 patients. Despite limited evidence, drug‐interaction checkers still flag this risk.
Gerard Ronda‐Roca +5 more
wiley +1 more source
ALPL Mutations With Dominant‐Negative Effect in Infantile Hypophosphatasia Monozygotic Twins
Human Mutation, Volume 2026, Issue 1, 2026.Background and Aims Hypophosphatasia (HPP) is a rare inborn error of metabolism caused by ALPL gene mutations, resulting in deficient tissue‐nonspecific alkaline phosphatase (ALP) activity. We investigated genotype–phenotype correlations in a monozygotic female twin pair with infantile HPP.
Luna Hao +8 more
wiley +1 more source
The idiopathic hypercalciuria reviewed. Metabolic abnormality or disease?
Nefrología (English Edition), 2019 Idiopathic hypercalciuria (IH) is defined as that clinical situation in which an increase in urinary calcium excretion is observed, in the absence of hypercalcemia and other known causes of hypercalciuria.
Víctor M. García Nieto +4 more
doaj +1 more source
Phosphate in Physiological and Pathological Mineralization: Important yet Often Unheeded
MedComm, Volume 6, Issue 7, July 2025.Phosphate serves as a building block for physiological mineralization, and as a signaling molecule that regulates the activity of mineralizing cells. The disturbance in these processes could induce a series of pathological mineralization, with abnormal mineralization of hard tissues and ectopic mineralization of soft tissues being the most ...
Wen Qin +8 more
wiley +1 more source
Nefrología (English Edition), 2022 Objective: To assess the effects of pharmacological interventions in patients with idiopathic hypercalciuria. Methods: We performed a search of multiple databases, trial registries, grey literature and conference proceedings up to October 2019.
Natalia Ferre +6 more
doaj +1 more source
Human asthenozoospermia: Update on genetic causes, patient management, and clinical strategies
Andrology, Volume 13, Issue 5, Page 1044-1064, July 2025.Abstract Background In mammals, sperm fertilization potential relies on efficient progression within the female genital tract to reach and fertilize the oocyte. This fundamental property is supported by the flagellum, an evolutionarily conserved organelle, which contains dynein motor proteins that provide the mechanical force for sperm propulsion and ...
Emma Cavarocchi +5 more
wiley +1 more source
Silicosarcoidosis: Histologic and Clinical Features of an Occupational Granulomatous Disease
American Journal of Industrial Medicine, Volume 68, Issue 6, Page 491-507, June 2025.ABSTRACT Sarcoidosis is a multisystem inflammatory disease of unknown etiology. Growing evidence indicates that occupational exposure to respirable crystalline silica (RCS) is associated with an increased incidence of sarcoidosis. Yet a diagnosis of sarcoidosis rarely prompts investigation to identify preventable exposures.
Jeremy T. Hua +11 more
wiley +1 more source
Urology Journal, 2010 Purpose: Our aim was to determine association of vesicoureteral reflux (VUR) and idiopathic hypercalciuria in children with recurrent and single episode of urinary tract infection (UTI).Materials and Methods: The study group consisted of 45 children with
Hashem Mahmoodzadeh
doaj
Isolated hypercalciuria with mutation in CLCN5: Relevance to idiopathic hypercalciuria [PDF]
Kidney International, 2000 Isolated hypercalciuria with mutation in CLCN5: Relevance to idiopathic hypercalciuria.Idiopathic hypercalciuria (IH) is the most common risk factor for kidney stones and often has a genetic component. Dent's disease (X-linked nephrolithiasis) is associated with mutations in the CLCN5 chloride channel gene, and low molecular weight (LMW) proteinuria ...
Scheinman, S +11 more
openaire +3 more sources