User profiles for Maury Pinsk
 | Maury PinskProfessor, University of Manitoba Verified email at hsc.mb.ca Cited by 1486 |
Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities
Hypertension affects one billion people and is a principal reversible risk factor for
cardiovascular disease. Pseudohypoaldosteronism type II (PHAII), a rare Mendelian syndrome …
cardiovascular disease. Pseudohypoaldosteronism type II (PHAII), a rare Mendelian syndrome …
Canadian society of nephrology commentary on the kidney disease improving global outcomes 2017 clinical practice guideline update for the diagnosis, evaluation …
Purpose of review: (1) To provide commentary on the 2017 update to the Kidney Disease
Improving Global Outcomes (KDIGO) 2017 Clinical Practice Guideline Update for the Diagnosis…
Improving Global Outcomes (KDIGO) 2017 Clinical Practice Guideline Update for the Diagnosis…
Canadian Society of Nephrology Commentary on the 2012 KDIGO clinical practice guideline for glomerulonephritis: management of nephrotic syndrome in children
…, M Zappitelli, A Dart, C Mammen, M Pinsk… - American Journal of …, 2014 - Elsevier
The KDIGO (Kidney Disease: Improving Global Outcomes) clinical practice guideline for
management of glomerulonephritis was recently released. The Canadian Society of Nephrology …
management of glomerulonephritis was recently released. The Canadian Society of Nephrology …
Epidemiologic characteristics of acute kidney injury during cisplatin infusions in children treated for cancer
…, GDE Cuvelier, C Mammen, M Pinsk… - JAMA network …, 2020 - jamanetwork.com
Importance Few multicenter pediatric studies have comprehensively described the
epidemiologic characteristics of cisplatin-associated acute kidney injury using standardized …
epidemiologic characteristics of cisplatin-associated acute kidney injury using standardized …
Monitoring dialysis adequacy: history and current practice
L Ding, J Johnston, MN Pinsk - Pediatric Nephrology, 2021 - Springer
Dialysis adequacy for pediatric patients has largely followed the trends in adult dialysis by
judging the success or adequacy of peritoneal or hemodialysis with urea kinetic modeling. …
judging the success or adequacy of peritoneal or hemodialysis with urea kinetic modeling. …
A variant in a cis‐regulatory element enhances claudin‐14 expression and is associated with pediatric‐onset hypercalciuria and kidney stones
…, A Ramesh, S Rehman, C Morgan, M Pinsk… - Human …, 2017 - Wiley Online Library
The greatest risk factor for kidney stones is hypercalciuria, the etiology of which is largely
unknown. A recent genome‐wide association study (GWAS) linked hypercalciuria and kidney …
unknown. A recent genome‐wide association study (GWAS) linked hypercalciuria and kidney …
[HTML][HTML] A rational approach to guide cost-effective de novo donor-specific antibody surveillance with tacrolimus immunosuppression
…, D Pochinco, A Goldberg, P Birk, M Pinsk… - American Journal of …, 2023 - Elsevier
De novo donor-specific antibody (dnDSA) after renal transplantation has been shown to
correlate with antibody-mediated rejection and allograft loss. However, the lack of proven …
correlate with antibody-mediated rejection and allograft loss. However, the lack of proven …
Canadian Society of Nephrology Commentary on the 2012 KDIGO clinical practice guideline for glomerulonephritis: management of glomerulonephritis in adults
…, M Zappitelli, A Dart, C Mammen, M Pinsk… - American Journal of …, 2014 - Elsevier
The KDIGO (Kidney Disease: Improving Global Outcomes) clinical practice guideline for
management of glomerulonephritis was recently released. The Canadian Society of Nephrology …
management of glomerulonephritis was recently released. The Canadian Society of Nephrology …
Acute myelogenous leukemia and glycogen storage disease 1b
M Pinsk, J Burzynski, M Yhap, RB Fraser… - Journal of pediatric …, 2002 - journals.lww.com
Glycogen storage disease 1b (GSD 1b) is caused by a deficiency of glucose-6-phosphate
translocase and the intracellular accumulation of glycogen. The disease presents with failure …
translocase and the intracellular accumulation of glycogen. The disease presents with failure …
Deletions in 16q24. 2 are associated with autism spectrum disorder, intellectual disability and congenital renal malformation
Background The contribution of copy-number variation (CNV) to disease has been highlighted
with the widespread adoption of array-based comparative genomic hybridisation (aCGH) …
with the widespread adoption of array-based comparative genomic hybridisation (aCGH) …