[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 …

[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 …

Contribution of phosphate and FGF23 to CKD progression

KP Jansson, SL Alan, JR Stubbs - Current opinion in nephrology …, 2022 - journals.lww.com
Studies presented in this review highlight important scientific discoveries that have molded
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 …

Risk of Nephrolithiasis in adults heterozygous for SLC34A3 Ser192Leu in an unselected health system cohort

C Nwachukwu, G Singh, B Moore… - Journal of the …, 2023 - journals.lww.com
Homozygous or compound heterozygous mutations in solute carrier family 34, member 3
(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 …

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 …

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 …