Found: 686
Select item for more details and to access through your institution.
Posttransplant Nephrocalcinosis Is Associated with Poor Renal Allograft Function: A Single-Center Experience.
- Published in:
- Ochsner Journal, 2015, v. 15, n. 1, p. 25
- By:
- Publication type:
- Article
Tophi as first manifestation of gout.
- Published in:
- Indian Journal of Dermatology, Venereology & Leprology, 2010, v. 76, n. 4, p. 393, doi. 10.4103/0378-6323.66593
- By:
- Publication type:
- Article
In silico analysis and verification of critical genes related to vascular calcification in multiple diseases.
- Published in:
- Cell Biochemistry & Function, 2023, v. 41, n. 8, p. 1242, doi. 10.1002/cbf.3858
- By:
- Publication type:
- Article
First Report of a Novel Missense CLDN19 Mutations Causing Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis in a Chinese Family.
- Published in:
- Calcified Tissue International, 2015, v. 96, n. 4, p. 265, doi. 10.1007/s00223-014-9951-7
- By:
- Publication type:
- Article
Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis (FHHNC): A Cross-sectional Study from Malaysia.
- Published in:
- Asian Journal of Pediatric Nephrology, 2024, v. 7, n. 1, p. 3, doi. 10.4103/ajpn.ajpn_19_23
- By:
- Publication type:
- Article
Medullary Nephrocalcinosis: The Role of Genetic Analysis.
- Published in:
- Asian Journal of Pediatric Nephrology, 2022, v. 5, n. 2, p. 91, doi. 10.4103/ajpn.ajpn_10_22
- By:
- Publication type:
- Article
Massive thrombosis in an infant with suspected nephrocalcinosis: case report and literature review.
- Published in:
- Central European Journal of Immunology, 2020, v. 45, n. 3, p. 355, doi. 10.5114/ceji.2020.101268
- By:
- Publication type:
- Article
Hypertensive emergency due to a delayed dialysis modality transition in a patient with familial hypomagnesemia with hypercalciuria and nephrocalcinosis: a case report.
- Published in:
- European Review for Medical & Pharmacological Sciences, 2024, v. 28, n. 9, p. 3313
- By:
- Publication type:
- Article
Single-Cell Gene Expression Analysis in Patients with Medullary Sponge Kidney and a Retrospective Study.
- Published in:
- BioMed Research International, 2022, v. 2022, p. 1, doi. 10.1155/2022/7688947
- By:
- Publication type:
- Article
Dent's Disease: A Cause of Monogenic Kidney Stones and Nephrocalcinosis.
- Published in:
- Journal of Personalized Medicine, 2024, v. 14, n. 6, p. 623, doi. 10.3390/jpm14060623
- By:
- Publication type:
- Article
The effect of intracrystalline and surface-bound osteopontin on the attachment of calcium oxalate dihydrate crystals to Madin-Darby canine kidney (MDCK) cells in ultrafiltered human urine.
- Published in:
- BJU International, 2012, v. 109, n. 7, p. 1100, doi. 10.1111/j.1464-410X.2011.10530.x
- By:
- Publication type:
- Article
Laterality of nephrocalcinosis in kidney stone formers with severe hypocitraturia.
- Published in:
- BJU International, 2011, v. 107, n. 1, p. 106, doi. 10.1111/j.1464-410X.2010.09492.x
- By:
- Publication type:
- Article
Nephrocalcinosis in Premature Infants.
- Published in:
- Journal of Perinatology, 1999, v. 19, n. 7, p. 498, doi. 10.1038/sj.jp.7200263
- By:
- Publication type:
- Article
Bilateral slipped capital femoral epiphysis in a male adolescent with familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC), chronic renal failure, and severe hyperparathyroidism.
- Published in:
- European Journal of Pediatrics, 2013, v. 172, n. 11, p. 1551, doi. 10.1007/s00431-013-1979-6
- By:
- Publication type:
- Article
Chronic renal failure in a boy with classic Bartter's syndrome due to a novel mutation in CLCNKB coding for the chloride channel.
- Published in:
- 2009
- By:
- Publication type:
- journal article
Nephrocalcinosis in glucose-galactose malabsorption: nephrocalcinosis and proximal tubular dysfunction in a young infant with a novel mutation of SGLT1.
- Published in:
- 2008
- By:
- Publication type:
- journal article
Medullary sponge kidney associated with distal renal tubular acidosis in a 5-year-old girl.
- Published in:
- 2006
- By:
- Publication type:
- journal article
Bilateral urinary calculi after treatment with a silicate-containing milk thickener.
- Published in:
- European Journal of Pediatrics, 2004, v. 163, n. 4/5, p. 239, doi. 10.1007/s00431-004-1400-6
- By:
- Publication type:
- Article
Urinary lithogenic and inhibitory factors in preterm neonates receiving either total parenteral nutrition or milk formula.
- Published in:
- European Journal of Pediatrics, 2003, v. 162, n. 7/8, p. 481, doi. 10.1007/s00431-003-1209-8
- By:
- Publication type:
- Article
Nephrocalcinosis and urolithiasis in carbonic anhydrase II deficiency syndrome.
- Published in:
- European Journal of Pediatrics, 1997, v. 156, n. 12, p. 957, doi. 10.1007/s004310050751
- By:
- Publication type:
- Article
Primary hyperoxaluria type 2.
- Published in:
- 1997
- By:
- Publication type:
- journal article
Primary hyperoxaluria type 2.
- Published in:
- European Journal of Pediatrics, 1997, v. 156, n. 7, p. 509, doi. 10.1007/s004310050649
- By:
- Publication type:
- Article
OGT-Mediated KEAP1 Glycosylation Accelerates NRF2 Degradation Leading to High Phosphate-Induced Vascular Calcification in Chronic Kidney Disease.
- Published in:
- Frontiers in Physiology, 2020, v. 11, p. N.PAG, doi. 10.3389/fphys.2020.01092
- By:
- Publication type:
- Article
Compounded Effervescent Magnesium for Familial Hypomagnesemia: A Case Report.
- Published in:
- Pharmaceuticals (14248247), 2023, v. 16, n. 6, p. 785, doi. 10.3390/ph16060785
- By:
- Publication type:
- Article
Different Potent Glucocorticoids, Different Routes of Exposure but the Same Result: Iatrogenic Cushing's Syndrome and Adrenal Insufficiency.
- Published in:
- Journal of Clinical Research in Pediatric Endocrinology, 2020, v. 12, n. 4, p. 383, doi. 10.4274/jcrpe.galenos.2020.2019.0220
- By:
- Publication type:
- Article
Nationwide Turkish Cohort Study of Hypophosphatemic Rickets.
- Published in:
- Journal of Clinical Research in Pediatric Endocrinology, 2020, v. 12, n. 2, p. 150, doi. 10.4274/jcrpe.galenos.2019.2019.0098
- By:
- Publication type:
- Article
CYP24A1 Mutation in a Girl Infant with Idiopathic Infantile Hypercalcemia.
- Published in:
- Journal of Clinical Research in Pediatric Endocrinology, 2018, v. 10, n. 1, p. 83, doi. 10.4274/jcrpe.4841
- By:
- Publication type:
- Article
Childhood Sustained Hypercalcemia: A Diagnostic Challenge.
- Published in:
- Journal of Clinical Research in Pediatric Endocrinology, 2017, v. 9, n. 4, p. 315, doi. 10.4274/jcrpe.4247
- By:
- Publication type:
- Article
Preliminary Observations of Urinary Calcium and Osteopontin Excretion in Premature Infants, Term Infants and Adults.
- Published in:
- Neonatology (16617800), 2008, v. 93, n. 4, p. 241, doi. 10.1159/000111103
- By:
- Publication type:
- Article
WT1 mutation and steroid-resistant nephrotic syndrome associated with cortical nephrocalcinosis.
- Published in:
- 2010
- By:
- Publication type:
- Case Study
Chronic hypokalaemia and nephrocalcinosis.
- Published in:
- NDT Plus, 2009, v. 2, n. 4, p. 314, doi. 10.1093/ndtplus/sfp047
- By:
- Publication type:
- Article
Pathognomonic oral profile of Enamel Renal Syndrome (ERS) caused by recessive FAM20A mutations.
- Published in:
- 2014
- By:
- Publication type:
- journal article
Ultrasound imaging of the kidneys.
- Published in:
- British Journal of Hospital Medicine (17508460), 2008, v. 69, n. 4, p. M52, doi. 10.12968/hmed.2008.69.Sup4.38891
- By:
- Publication type:
- Article
CDC42 promotes vascular calcification in chronic kidney disease.
- Published in:
- Journal of Pathology, 2019, v. 249, n. 4, p. 461, doi. 10.1002/path.5334
- By:
- Publication type:
- Article
FAM20A Mutations Associated with Enamel Renal Syndrome.
- Published in:
- Journal of Dental Research, 2014, v. 93, n. 1, p. 42, doi. 10.1177/0022034513512653
- By:
- Publication type:
- Article
Incidence of Complications in 25 Adult Patients With X-linked Hypophosphatemia.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Do the Heterozygous Carriers of a CYP24A1 Mutation Display a Different Biochemical Phenotype Than Wild Types?
- Published in:
- 2021
- By:
- Publication type:
- journal article
Nephrocalcinosis, Renal Dysfunction, and Calculi in Patients With Primary Hypoparathyroidism on Long-Term Conventional Therapy.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Multiple myeloma as a cause of chylothorax.
- Published in:
- Journal of the Royal Society of Medicine, 1986, v. 79, n. 1, p. 49, doi. 10.1177/014107688607900117
- By:
- Publication type:
- Article
Targeting a Silent Disease: Vascular Calcification in Chronic Kidney Disease.
- Published in:
- International Journal of Molecular Sciences, 2022, v. 23, n. 24, p. 16114, doi. 10.3390/ijms232416114
- By:
- Publication type:
- Article
Vitamin D and Calcium Supplementation Accelerate Vascular Calcification in a Model of Pseudoxanthoma Elasticum.
- Published in:
- International Journal of Molecular Sciences, 2022, v. 23, n. 4, p. 2302, doi. 10.3390/ijms23042302
- By:
- Publication type:
- Article
Lanthionine, a Novel Uremic Toxin, in the Vascular Calcification of Chronic Kidney Disease: The Role of Proinflammatory Cytokines.
- Published in:
- International Journal of Molecular Sciences, 2021, v. 22, n. 13, p. 6875, doi. 10.3390/ijms22136875
- By:
- Publication type:
- Article
Nephrocalcinosis: A Review of Monogenic Causes and Insights They Provide into This Heterogeneous Condition.
- Published in:
- International Journal of Molecular Sciences, 2020, v. 21, n. 1, p. 369, doi. 10.3390/ijms21010369
- By:
- Publication type:
- Article
Pseudoxanthoma Elasticum, Kidney Stones and Pyrophosphate: From a Rare Disease to Urolithiasis and Vascular Calcifications.
- Published in:
- International Journal of Molecular Sciences, 2019, v. 20, n. 24, p. 6353, doi. 10.3390/ijms20246353
- By:
- Publication type:
- Article
Nephrocalcinosis: Biochemical Evaluation and Genetic Analysis.
- Published in:
- 2020
- By:
- Publication type:
- Editorial
Etiological Profile of Nephrocalcinosis in Children from Southern India.
- Published in:
- Indian Pediatrics, 2020, v. 57, n. 5, p. 415, doi. 10.1007/s13312-020-1814-x
- By:
- Publication type:
- Article
Childhood Sarcoidosis Presenting as Recurrent Facial Palsy.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
Significant associations between bone mineral density and vascular calcification in patients with different stages of chronic kidney disease.
- Published in:
- 2022
- By:
- Publication type:
- journal article
Dent-2 disease with a Bartter-like phenotype caused by the Asp631Glu mutation in the OCRL gene.
- Published in:
- 2022
- By:
- Publication type:
- journal article
Serum uric acid is associated with coronary artery calcification in early chronic kidney disease: a cross-sectional study.
- Published in:
- BMC Nephrology, 2021, v. 22, n. 1, p. 1, doi. 10.1186/s12882-021-02463-2
- By:
- Publication type:
- Article