A Challenging Case of Hypercalcemia Caused by a Novel Homozygous Variant Missense Mutation in the <i>CYP24A1</i> Gene. [PDF]
Ahsan T +4 more
europepmc +1 more source
Ten tips on the work-up and management of CKD patients with nephrolithiasis. [PDF]
Hawkins-van der Cingel G.
europepmc +1 more source
First Reported Use of Recombinant Parathyroid Hormone in Kenny-Caffey Syndrome Type 2: A Case Report and Literature Review. [PDF]
Djordjevic Milosevic M +11 more
europepmc +1 more source
Pseudohypoaldosteronism type II: The Relevance of A Challenging Diagnosis. [PDF]
Cruz D, Pintassilgo I.
europepmc +1 more source
Nephrolithiasis risk factors for obese patients on 24-hour urine collection metabolic evaluation. [PDF]
Sultan MI +8 more
europepmc +1 more source
Genetic and clinical phenotype of Dent disease in Chinese children and the etiological analysis of early - onset chronic kidney disease. [PDF]
Zhou L +7 more
europepmc +1 more source
Renal survival in hereditary urolithiasis: a monocentric cohort study from a Tunisian nephrology department. [PDF]
Bettaieb A +9 more
europepmc +1 more source
Índice calcio creatinina en el diagnóstico de la hipercalciuria en población pediátrica litiásica
Raymed A Bacallao Méndez +5 more
doaj

