M. Zaniew

发表

Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens

Murim Choi, R. Lifton, M. Salvadori, 2014, Nature Genetics.

Characterization of 28 novel patients expands the mutational and phenotypic spectrum of Lowe syndrome

F. Anglani, V. Tasic, M. Litwin, 2015, Pediatric Nephrology.

A classic twin study of lower urinary tract obstruction: Report of 3 cases and literature review

M. Zaniew, B. Hoppe, M. Feldkötter, 2019, Lower urinary tract symptoms.

Still diagnosed too late and under-recognized? A first comprehensive report on primary hyperoxaluria from Poland.

M. Zaniew, B. Hoppe, M. Myślak, 2020, Polish archives of internal medicine.

Dent disease in Poland: what we have learned so far?

M. Zaniew, M. Mizerska-Wasiak, K. Pawlaczyk, 2017, International Urology and Nephrology.

Treatment and long-term outcome in primary distal renal tubular acidosis.

F. Trepiccione, G. Gambaro, Z. Gucev, 2019, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Long-term renal outcome in children with OCRL mutations: retrospective analysis of a large international cohort

Se Jin Park, F. Anglani, J. Moczko, 2016, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Hyperuricemia Is an Early and Relatively Common Feature in Children with HNF1B Nephropathy but Its Utility as a Predictor of the Disease Is Limited

M. Zaniew, P. Adamczyk, M. Szczepańska, 2021, Journal of clinical medicine.

Hypomagnesemia is underestimated in children with HNF1B mutations

M. Zaniew, K. Pawlaczyk, J. Walkowiak, 2020, Pediatric Nephrology.

Risk Factors for Early Dialysis Dependency in Autosomal Recessive Polycystic Kidney Disease

A. Anarat, S. Schmidt, S. Testa, 2018, The Journal of pediatrics.

Retrospective cohort study of familial hypomagnesaemia with hypercalciuria and nephrocalcinosis due to CLDN16 mutations.

M. Zaniew, M. Szczepańska, M. Konrad, 2015, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Intracellular cytokines of peripheral blood lymphocytes in nephrotic syndrome

M. Zaniew, J. Maciejewski, W. Bobkowski, 2002, Pediatric Nephrology.

Abnormal Cytokine Synthesis as a Consequence of Increased Intracellular Oxidative Stress in Children Treated with Dialysis

M. Zaniew, M. Lewandowska-Stachowiak, D. Runowski, 2005, Nephron Clinical Practice.

Copy Number Variant Analysis and Genome-wide Association Study Identify Loci with Large Effect for Vesicoureteral Reflux.

Craig S. Wong, H. Hakonarson, C. Willer, 2021, Journal of the American Society of Nephrology : JASN.

Distinct characteristics of multisystem inflammatory syndrome in children in Poland

M. Zaniew, D. Cysewski, B. Werner, 2021, Scientific Reports.

Diverse ancestry whole-genome sequencing association study identifies TBX5 and PTK7 as susceptibility genes for posterior urethral valves

C. D. Voinescu, A. Woolf, M. Zaniew, 2022, eLife.

Genome-wide association study in patients with posterior urethral valves

L. Kiemeney, I. V. van Rooij, M. Zaniew, 2022, Frontiers in Pediatrics.

Rare Variants in BNC2 Are Implicated in Autosomal-Dominant Congenital Lower Urinary-Tract Obstruction

I. V. van Rooij, G. Kristiansen, W. Newman, 2019, American journal of human genetics.

A questionnaire survey of radiological diagnosis and management of renal dysplasia in children

V. Tasic, A. Woolf, M. Zaniew, 2017, Journal of Nephrology.

Th1/Th2 balance and CD45-positive T cell subsets in primary nephrotic syndrome

M. Zaniew, J. Maciejewski, C. Barth, 2000, Pediatric Nephrology.

X-linked variations in SHROOM4 are implicated in congenital anomalies of the urinary tract and the anorectal, cardiovascular and central nervous systems

I. Thiffault, T. Pastinen, A. Bayat, 2022, Journal of Medical Genetics.

Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations.

D. Goldstein, S. Mane, G. Ardissino, 2017, American journal of human genetics.

Decreased antioxidant activity in hypercholesterolemic children with nephrotic syndrome.

M. Zaniew, J. Maciejewski, W. Bobkowski, 2003, Medical science monitor : international medical journal of experimental and clinical research.

Beneficial in vitro effect of N-acetyl-cysteine on oxidative stress and apoptosis

M. Zaniew, W. Bobkowski, D. Ostalska-Nowicka, 2005, Pediatric Nephrology.

Interest of URS-L in the Treatment of Ureterolithiasis in Preschool Children

M. Zaniew, A. Haliński, H. Steyaert, 2019, Front. Pediatr..

Clinical profile of a Polish cohort of children and young adults with cystinuria

M. Zaniew, M. Tkaczyk, Katarzyna Gadomska-Prokop, 2020, Renal failure.

GWAS defines pathogenic signaling pathways and prioritizes drug targets for IgA nephropathy

F. Kronenberg, P. Gregersen, C. Wijmenga, 2021, medRxiv.

Exome sequencing implicates a novel heterozygous missense variant in DSTYK in autosomal dominant lower urinary tract dysfunction and mild hereditary spastic paraparesis

M. Zaniew, H. Thiele, H. Reutter, 2021, Molecular and Cellular Pediatrics.

Mixed ancestry analysis of whole-genome sequencing identifies TBX5 and PTK7 as susceptibility genes for posterior urethral valves

W. Newman, A. Woolf, M. Zaniew, 2021 .

Mixed ancestry analysis of whole-genome sequencing reveals common, rare, and structural variants associated with posterior urethral valves

W. Newman, A. Woolf, M. Zaniew, 2021, medRxiv.

The copy number variation landscape of congenital anomalies of the kidney and urinary tract

Craig S. Wong, H. Hakonarson, A. Latos-Bieleńska, 2018, Nature Genetics.

Copy-number disorders are a common cause of congenital kidney malformations.

Stephan J Sanders, V. Jobanputra, W. Chung, 2012, American journal of human genetics.

Genetic Drivers of Kidney Defects in the DiGeorge Syndrome

Craig S. Wong, E. Zackai, H. Hakonarson, 2017, The New England journal of medicine.

Apoptosis and antioxidant defense in the nephrotic syndrome

M. Zaniew, W. Bobkowski, M. Lewandowska-Stachowiak, 2003, Pediatric Nephrology.

[Resistance to therapy in primary nephrotic syndrome: effect of MDR1 gene activity].

M. Zaniew, C. Zanker, J. Maciejewski, 2000, Polski merkuriusz lekarski : organ Polskiego Towarzystwa Lekarskiego.

[Intracellular synthesis of cytokines as the index of function of peripheral blood lymphocytes and monocytes in children with first relapse of nephrotic syndrome].

M. Zaniew, J. Maciejewski, W. Bobkowski, 2003, Polski merkuriusz lekarski : organ Polskiego Towarzystwa Lekarskiego.

Increased apoptosis of peripheral blood lymphocytes in children with nephrotic syndrome

M. Zaniew, G. Dworacki, J. Maciejewski, 2002, Pediatric Nephrology.

Whole-Exome Sequencing in Adults With Chronic Kidney Disease

V. Jobanputra, V. D’Agati, C. Antignac, 2018, Annals of Internal Medicine.

Genome-wide identification of disease-causing copy number variations in 450 individuals with anorectal malformations

A. Buness, S. Heilmann-Heimbach, M. Lacher, 2022, European Journal of Human Genetics.

Is it the right time to subject children with acute kidney injury to rasburicase trials?

M. Zaniew, D. Runowski, Joanna Tousty, 2012, Pediatric Nephrology.

[New, successful treatment of urinary tract infection caused by Pseudomonas aeruginosa].

M. Zaniew, A. Siwińska, J. Zachwieja, 2006, Przeglad lekarski.

Regulation of post-Golgi LH3 trafficking is essential for collagen homeostasis

M. Girolami, A. Lyne, W. Heywood, 2016, Nature Communications.

Abstracts of the 51st Annual ESPN Meeting, Antalya, October 2018

Carmine, Pape, W. Newman, 2018, Pediatric nephrology (Berlin, West).

HNF1B nephropathy has a slow-progressive phenotype in childhood—with the exception of very early onset cases: results of the German Multicenter HNF1B Childhood Registry

N. Ortiz-Brüchle, L. Weber, B. Tönshoff, 2019, Pediatric Nephrology.

Dent disease in children: diagnostic and therapeutic considerations.

M. Zaniew, M. Mizerska-Wasiak, K. Pawlaczyk, 2015, Clinical Nephrology.

Vitamin D status and bone density in steroid-treated children with glomerulopathies: effect of cholecalciferol and calcium supplementation.

M. Zaniew, T. Jarmoliński, 2012, Advances in medical sciences.

Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations.

D. Goldstein, S. Mane, G. Ardissino, 2017, American journal of human genetics.

Hypertensive nephropathy in children – do we diagnose early enough?

M. Zaniew, A. Musielak, J. Zachwieja, 2012, Blood pressure.

Genome-Wide Survey for Microdeletions or -Duplications in 155 Patients with Lower Urinary Tract Obstructions (LUTO)

M. Zaniew, S. Herms, M. Szczepańska, 2021, Genes.

Genome-wide association analyses define pathogenic signaling pathways and prioritize drug targets for IgA nephropathy

F. Kronenberg, P. Gregersen, C. Wijmenga, 2023, Nature Genetics.

Erratum : Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations (The American Journal of Human Genetics (2017) 101(5) (789–802) (S0002929717303877) (10.1016/j.ajhg.2017.09.018))

D. Goldstein, S. Mane, G. Ardissino, 2017 .

A report from the European Hyperoxaluria Consortium (OxalEurope) Registry on a large cohort of patients with primary hyperoxaluria type 3.

M. Zaniew, J. Bacchetta, B. Hoppe, 2021, Kidney international.

Rare Single Nucleotide and Copy Number Variants and the Etiology of Congenital Obstructive Uropathy: Implications for Genetic Diagnosis

A. Latos-Bieleńska, J. McKiernan, Shrikant Mane, 2023, Journal of the American Society of Nephrology : JASN.

UNM Digital Repository UNM Digital Repository

H. Hakonarson, I. Ionita-Laza, A. Latos-Bieleńska, 2022 .

Accidentally detected nephrocalcinosis in a boy with a homozygous R396W mutation in the CYP24A1 gene – 7-year follow-up

M. Zaniew, A. Maćkowska, J. Nowicki, 2023, Pediatria Polska.

Renal and Extrarenal Phenotypes in Patients With HNF1B Variants and Chromosome 17q12 Microdeletions

B. Tönshoff, M. Zaniew, D. Mekahli, 2024, Kidney international reports.

UNM Digital Repository UNM Digital Repository

C. Willer, I. Ionita-Laza, A. Latos-Bieleńska, 2022 .