Results 91 to 100 of about 10,151 (205)

Nephrocalcinosis – latest reports on risk factors

Pediatria Polska
This review synthesises recent discoveries in the risk factors of nephrocalcinosis, with a particular focus on novel findings. Nephrocalcinosis, characterised by the deposition of calcium salts in the renal parenchyma, is linked to a variety of genetic ...
Tomasz Dudzik, Łucja Dudzik, Igor Domański, Aleksandra Kozieł, Paulina Wójcik, Natalia Kuderska   +5 more
doaj   +1 more source

Williams-Beuren syndrome associated with single kidney and nephrocalcinosis: a case report

The Pan African Medical Journal, 2015
Williams-Beuren syndrome is a rare neurodevelopmental disorder, characterized by congenital heart defects, abnormal facial features, mental retardation with specific cognitive and behavioral profile, growth hormone deficiency, renal and skeletal ...
Kamel Abidi, Manel Jellouli, Rania Ben Rabeh, Yousra Hammi, Tahar Gargah   +4 more
doaj   +1 more source

CHRONIC RENAL FAILURE DUE TO FAMILIAL HYPOMAGNESEMIC HYPERCALCIURIA (A CASE REPORT)

Turkish Journal of Nephrology, 2019
Familial Hypomagnesemia- hypercalciuria is a hereditary disease of unknown etiology characterized by persistant Hypomagnesemia, incomplete distal tubuler acidosis, hypercalciuria and nephrocalcinosis.
Ali Rıza ODABAŞ, Ramazan ÇETİNKAYA, Yılmaz SELÇUK, Hasan KAYA, Ünsal ÇOŞKUN   +4 more
doaj  

EZH2-mediated macrophage-to-myofibroblast transition contributes to calcium oxalate crystal-induced kidney fibrosis

Communications Biology
Long-term nephrocalcinosis leads to kidney injury, fibrosis, and even chronic kidney disease (CKD). Macrophage-to-myofibroblast transition (MMT) has been identified as a new mechanism in CKD, however, the effect of MMT in calcium oxalate (CaOx)-induced ...
Yuqi Xia, Zehua Ye, Bojun Li, Xinzhou Yan, Tianhui Yuan, Lei Li, Baofeng Song, Weimin Yu, Ting Rao, Jinzhuo Ning, Jiefu Zhu, Xing Li, Shuqin Mei, Zhiguo Mao, Xiangjun Zhou, Fan Cheng   +15 more
doaj   +1 more source

Efficacy and safety of lumasiran for infants and young children with primary hyperoxaluria type 1: 30-month analysis of the phase 3 ILLUMINATE-B trial

Frontiers in Pediatrics
BackgroundPrimary hyperoxaluria type 1 (PH1) is a genetic disorder resulting in overproduction of hepatic oxalate, potentially leading to recurrent kidney stones, nephrocalcinosis, chronic kidney disease, and kidney failure.
Yaacov Frishberg, Wesley Hayes, Hadas Shasha-Lavsky, Hadas Shasha-Lavsky, David J. Sas, Mini Michael, Anne-Laure Sellier-Leclerc, Julien Hogan, Richard Willey, John M. Gansner, Daniella Magen   +10 more
doaj   +1 more source

Nephrolithiasis Associated with Nephrocalcinosis Is Primarily Composed of Carbonate Apatite

Kidney & Blood Pressure Research
Introduction: This study was designed to determine the mineral composition of calculi in nephrocalcinosis with nephrolithiasis, diagnose the underlying disease, and monitor the course of renal function in patients with nephrocalcinosis-nephrolithiasis ...
Teresa Antonia Kiener, Elena Moré, Michael Franzen, Janne Cadamuro, Christoph Schwarz, Carsten Bergmann, Hermann Salmhofer   +6 more
doaj   +1 more source

Nephrocalcinosis Infantum [PDF]

Archives of Disease in Childhood, 1959
R A, SHANKS, A M, MACDONALD
openaire   +2 more sources

Familial hypomagnesemia with hypercalciuria and nephrocalcinosis

, 1995
Familial hypomagnesemia with hypercalciuria and nephrocalcinosis. Very few patients with familial hypomagnesemia, hypercalciuria and nephrocalcinosis have been described.
Vara, Julia, Alamo, Concepción, Praga, Manuel, Rodicio, José Luis, Araque, Alicia, González-Parra, Emilio, Ortiz, Arturo, Andrés, Amado   +7 more
core   +1 more source

A Prospective Study of Nephrocalcinosis in Very Preterm Infants: Incidence, Risk Factors and Vitamin D Intake in the First Month

Medicina
Background and objectives: Nephrocalcinosis (NC) is a common condition characterized by the deposition of calcium salts in the kidneys of very preterm infants due to tubular immaturity, intensive treatment and nutritional supplements.
Rasa Garunkstiene, Ruta Levuliene, Andrius Cekuolis, Rimante Cerkauskiene, Nijole Drazdiene, Arunas Liubsys   +5 more
doaj   +1 more source

The prevalence of the symptom of "hyperechoic pyramids" in children born with very low and extremely low body weight

Consilium Medicum
Aim. To determine the frequency and factors contributing to the formation of c-ma "hyperechoic pyramids" in children born with very low and extremely low body weight, as well as to assess kidney function in this contingent of children in a three-year ...
Alyona K. Mironova, Ismail M. Osmanov, Olga I. Potyanova   +2 more
doaj   +1 more source