[HTML][HTML] Ren. Nu, a dietary program for individuals with autosomal-dominant polycystic kidney disease implementing a sustainable, plant-focused, kidney-safe …
DM Bruen, JJ Kingaard, M Munits, CS Paimanta… - Kidney and …, 2022 - mdpi.com
Autosomal dominant polycystic kidney disease (ADPKD) is the most common inherited
cause of renal failure and has limited pharmacological treatment options. Disease …
cause of renal failure and has limited pharmacological treatment options. Disease …
[HTML][HTML] Caspase-1 and the inflammasome promote polycystic kidney disease progression
KI Swenson-Fields, CJ Ward, ME Lopez… - Frontiers in molecular …, 2022 - frontiersin.org
We and others have previously shown that the presence of renal innate immune cells can
promote polycystic kidney disease (PKD) progression. In this study, we examined the …
promote polycystic kidney disease (PKD) progression. In this study, we examined the …
Contribution of phosphate and FGF23 to CKD progression
Studies presented in this review highlight important scientific discoveries that have molded
our current understanding of the contribution of altered phosphate homeostasis to CKD …
our current understanding of the contribution of altered phosphate homeostasis to CKD …
[HTML][HTML] Hereditary Hypophosphatemic Rickets with Hypercalciuria Presenting with Enthesopathy, Renal Cysts, and High Serum c-Terminal FGF23: Single-Center …
MH Dodamani, SS Memon, M Karlekar, AR Lila… - Calcified Tissue …, 2024 - Springer
Hereditary hypophosphatemic rickets with hypercalciuria (HHRH) is a rare disorder of
phosphate homeostasis. We describe a single-center experience of genetically proven …
phosphate homeostasis. We describe a single-center experience of genetically proven …
Risk of Nephrolithiasis in adults heterozygous for SLC34A3 Ser192Leu in an unselected health system cohort
Homozygous or compound heterozygous mutations in solute carrier family 34, member 3
(SLC34A3), encoding the sodium-dependent inorganic phosphate cotransport proteins 2c …
(SLC34A3), encoding the sodium-dependent inorganic phosphate cotransport proteins 2c …
An update on clinical presentation and responses to therapy of patients with hereditary hypophosphatemic rickets with hypercalciuria (HHRH).
Z Zhu, BBR Ho, A Chen, J Amrhein, A Apetrei… - Kidney International, 2024 - Elsevier
Pathogenic variants in solute carrier family 34, member 3 (SLC34A3), the gene encoding the
sodium-dependent phosphate cotransporter 2c (NPT2c), cause hereditary …
sodium-dependent phosphate cotransporter 2c (NPT2c), cause hereditary …
Kidney stone formation in a novel murine model of polycystic kidney disease
HAL Riddle, S Zhang, F Qian… - American Journal …, 2022 - journals.physiology.org
Individuals with autosomal dominant polycystic kidney disease have a higher incidence of
stone formation than the general population. However, there are no cystic animal models …
stone formation than the general population. However, there are no cystic animal models …
Detecting Multiple Cysts in the Kidney with the Development of an Active Contour Method Based on Kidney Ultrasound (USG) Images
M Tajuddin - International Journal of Intelligent Systems and …, 2023 - ijisae.org
This study examined digital 2-Dimensional (2D) Ultrasonography (USG) images of human
kidneys. The ultrasound image was captured with an ultrasound instrument that locates …
kidneys. The ultrasound image was captured with an ultrasound instrument that locates …