Results 61 to 70 of about 4,884 (208)
PTH and 1.25 vitamin D response to a low-calcium diet is associated with bone mineral density in renal stone formers [PDF]
Background. Renal calcium stones and hypercalciuria are associated with a reduced bone mineral density (BMD). Therefore, the effect of changes in calcium homeostasis is of interest for both stones and bones. We hypothesized that the response of calciuria,
Bonny, Olivier +4 more
core
Effect of calcium intake on urinary oxalate excretion in calcium stone-forming patients [PDF]
Dietary calcium lowers the risk of nephrolithiasis due to a decreased absorption of dietary oxalate that is bound by intestinal calcium. The aim of the present study was to evaluate oxaluria in normocalciuric and hypercalciuric lithiasic patients under ...
Heilberg, Ita Pfeferman +4 more
core +3 more sources
An Unusual Presentation of Barakat Syndrome: Gene Deletion at Chromosome 10p15
Barakat syndrome, also known as HDR syndrome (HDRS), is an autosomal dominant genetic disease classically characterized by hypoparathyroidism (H), deafness (D), and renal disease (R). Less than 200 patients have been reported in the literature since it was first described in 1977 and has meanwhile been shown to have considerable genotypic variability ...
Matthew Satariano +4 more
wiley +1 more source
Mechanisms of human kidney stone formation [PDF]
The precise mechanisms of kidney stone formation and growth are not completely known, even though human stone disease appears to be one of the oldest diseases known to medicine.
Coe, Fredric L. +4 more
core +1 more source
Evaluation of Compliance With International Guidelines During the Follow‐Up of Hypoparathyroidism
Aims: Hypoparathyroidism is a disorder that causes renal complications, bone disease, an increased risk of cardiovascular diseases, neuromuscular complications, and ocular findings. In this study, we aimed to determine how well the existing guidelines were followed in the follow‐up of patients with hypoparathyroidism.
Beril Turan Erdogan +8 more
wiley +1 more source
Objective Idiopathic infantile hypercalcemia (IIH) is a rare disorder of PTH-independent hypercalcemia. CYP24A1 and SLC34A1 gene mutations cause two forms of hereditary IIH.
Qiao Wang +7 more
doaj +1 more source
Drug‐ and Vaccine‐Induced Cutaneous T‐Cell Lymphoma: A Systematic Review of the Literature
Cutaneous T‐cell lymphomas (CTCLs) are a type of non‐Hodgkin lymphoma that usually involves the skin. It has different subtypes including mycosis fungoides (MFs), Sézary syndrome (SS), primary cutaneous anaplastic large lymphoma (PC‐ALCL), lymphomatoid papulosis (LyP), and subcutaneous panniculitis–like T‐cell lymphoma (SPTCL).
Ifa Etesami +13 more
wiley +1 more source
Juvenile onset IIH and CYP24A1 mutations
The term Idiopathic infantile hypercalcemia (IIH) was first introduced almost 70 years ago when symptomatic hypercalcemia developed in children after receiving high doses of vitamin D for the prevention of rickets. The underlying pathophysiology remained
Karl P. Schlingmann +2 more
doaj +1 more source
Epidemiology of paediatric renal stone disease: a 22-year single centre experience in the UK [PDF]
BACKGROUND: Whilst still rare, the incidence of paediatric stone disease is increasing in developed countries and it is important to evaluate the aetiology.
Bockenhauer, D +5 more
core +1 more source
ABSTRACT The prevalence of hypercalciuria in children is 3%–10% globally and up to 35% in the United States. Hypercalciuria in children has many presentations; it causes different metabolic disorders and can negatively affect a child's growth. It also increases the risk of low bone mineral density and urinary tract infections.
Izat MohammadKhawajah +4 more
wiley +1 more source

