Cargando…

Predicting autosomal dominant polycystic kidney disease progression: review of promising Serum and urine biomarkers

Autosomal dominant polycystic kidney disease (ADPKD) is one of the leading causes of end-stage renal disease. In spite of the recent tremendous progress in the understanding of ADPKD pathogenesis, the molecular mechanisms of the disease remain incompletely understood. Considering emerging new target...

Descripción completa

Detalles Bibliográficos
Autores principales:	Sorić Hosman, Iva, Cvitković Roić, Andrea, Fištrek Prlić, Margareta, Vuković Brinar, Ivana, Lamot, Lovro
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2023
Materias:	Pediatrics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10667601/ https://www.ncbi.nlm.nih.gov/pubmed/38027263 http://dx.doi.org/10.3389/fped.2023.1274435

Ejemplares similares

Two sides of the same coin: a complex presentation of autosomal dominant tubulointerstitial kidney diseases: a literature review and case reports
por: Fistrek Prlic, Margareta, et al.
Publicado: (2023)

A Systematic Review of the (Un)known Host Immune Response Biomarkers for Predicting Recurrence of Urinary Tract Infection
por: Sorić Hosman, Iva, et al.
Publicado: (2022)

Typical course of cystinuria leading to untypical complications in pregnancy: A case report and review of literature
por: Ivandic, Ema, et al.
Publicado: (2023)

Serum Amyloid A in Inflammatory Rheumatic Diseases: A Compendious Review of a Renowned Biomarker
por: Sorić Hosman, Iva, et al.
Publicado: (2021)

Case report: Sevelamer-associated colitis—a cause of pseudotumor formation with colon perforation and life-threatening bleeding
por: Fistrek Prlic, Margareta, et al.
Publicado: (2023)

Clinical Trials in Pediatric Autosomal Dominant Polycystic Kidney Disease
por: Cadnapaphornchai, Melissa A.
Publicado: (2017)

Hemolytic uremic syndrome in the setting of COVID-19 successfully treated with complement inhibition therapy: An instructive case report of a previously healthy toddler and review of literature
por: Matošević, Matija, et al.
Publicado: (2023)

Is Autosomal Dominant Polycystic Kidney Disease Becoming a Pediatric Disorder?
por: De Rechter, Stéphanie, et al.
Publicado: (2017)

Cystatin C, renal resistance index, and kidney injury molecule-1 are potential early predictors of diabetic kidney disease in children with type 1 diabetes
por: Trutin, Ivana, et al.
Publicado: (2022)

Two novel variants in the lecithin:cholesterol acyltransferase gene resulted in classic LCAT deficiency
por: Fistrek Prlic, Margareta, et al.
Publicado: (2022)

The Genetic and Cellular Basis of Autosomal Dominant Polycystic Kidney Disease—A Primer for Clinicians
por: Cordido, Adrián, et al.
Publicado: (2017)

Urine proteome of autosomal dominant polycystic kidney disease patients
por: Bakun, Magda, et al.
Publicado: (2012)

Is It Ethical to Test Apparently “Healthy” Children for Autosomal Dominant Polycystic Kidney Disease and Risk Medicalizing Thousands?
por: Harris, Tess
Publicado: (2018)

Successful Treatment of Cyst Infection in an Infant With Autosomal Dominant Polycystic Kidney Disease Using Trimethoprim/Sulfamethoxazole
por: Yokoyama, Hiroki, et al.
Publicado: (2020)

A Case of New Familiar Genetic Variant of Autosomal Dominant Polycystic Kidney Disease-2: A Case Study
por: Litvinchuk, Tetiana, et al.
Publicado: (2015)

Serum Calprotectin Is a Valid Biomarker in Distinction of Bacterial Urinary Tract Infection From Viral Respiratory Illness in Children Under 3 Years of Age
por: Lamot, Mirta, et al.
Publicado: (2022)

Autosomal dominant polycystic kidney
por: Gudadhe, Rugaved Raghavendra, et al.
Publicado: (2022)

Urine Fetuin-A is a biomarker of autosomal dominant polycystic kidney disease progression
por: Piazzon, Nathalie, et al.
Publicado: (2015)

Early Urinary Biomarkers in Pediatric Autosomal Dominant Polycystic Kidney Disease (ADPKD): No Evidence in the Interest of Urinary Neutrophil Gelatinase-Associated Lipocalin (uNGAL)
por: Tsingos, Marianthi, et al.
Publicado: (2019)

Genetics of Autosomal Recessive Polycystic Kidney Disease and Its Differential Diagnoses
por: Bergmann, Carsten
Publicado: (2018)

Diagnosis and Management of Hepatobiliary Complications in Autosomal Recessive Polycystic Kidney Disease
por: Wehrman, Andrew, et al.
Publicado: (2017)

Hematuria as an Early Sign of Multisystem Inflammatory Syndrome in Children: A Case Report of a Boy With Multiple Comorbidities and Review of Literature
por: Generalić, Ana, et al.
Publicado: (2021)

Risk Factors for Neurocognitive Functioning in Children with Autosomal Recessive Polycystic Kidney Disease
por: Hooper, Stephen R.
Publicado: (2017)

Urinary Biomarkers in Monitoring the Progression and Treatment of Autosomal Dominant Polycystic Kidney Disease—The Promised Land?
por: Pana, Camelia, et al.
Publicado: (2023)

Case Report: Guanfacine and methylphenidate improved chronic lower back pain in autosomal dominant polycystic kidney disease with comorbid attention deficit hyperactivity disorder and autism spectrum disorder
por: Kasahara, Satoshi, et al.
Publicado: (2023)

Autosomal dominant polycystic kidney disease in Colombia
por: Camargo, Jessica T., et al.
Publicado: (2023)

Growth in Children with Autosomal Recessive Polycystic Kidney Disease in the CKiD Cohort Study
por: Hartung, Erum A., et al.
Publicado: (2016)

Transient Elastography for Detection of Liver Fibrosis in Children With Autosomal Recessive Polycystic Kidney Disease
por: Wicher, Dorota, et al.
Publicado: (2019)

Recent Progress of the ARegPKD Registry Study on Autosomal Recessive Polycystic Kidney Disease
por: Ebner, Kathrin, et al.
Publicado: (2017)

Prenatal MR imaging features of Caroli syndrome in association with autosomal recessive polycystic kidney disease
por: Rivas, Amanda, et al.
Publicado: (2018)

Gastrostomy Tube Insertion in Pediatric Patients With Autosomal Recessive Polycystic Kidney Disease (ARPKD): Current Practice
por: Burgmaier, Kathrin, et al.
Publicado: (2018)

Case report: Severe hypertension-induced priapism in an infant with unrecognized autosomal recessive polycystic kidney disease
por: Konopásek, Patrik, et al.
Publicado: (2023)

Developments in the management of autosomal dominant polycystic kidney disease
por: Masoumi, Amirali, et al.
Publicado: (2008)

Hypertension in autosomal-dominant polycystic kidney disease (ADPKD)
por: Sans-Atxer, Laia, et al.
Publicado: (2013)

Nephrotic syndrome and autosomal dominant polycystic kidney disease
por: Visciano, Bianca, et al.
Publicado: (2012)

Umbilical hernia in autosomal dominant polycystic kidney disease
por: Hattori, Yoshinari, et al.
Publicado: (2014)

Diagnostic Imaging of Autosomal Dominant Polycystic Kidney Disease
por: Gradzik, Monika, et al.
Publicado: (2016)

Obturator hernia in autosomal dominant polycystic kidney disease
por: Jung, Jong Hwan, et al.
Publicado: (2018)

Autosomal dominant polycystic kidney disease: updated perspectives
por: Rastogi, Anjay, et al.
Publicado: (2019)

Educational Case: Autosomal Dominant Polycystic Kidney Disease
por: Frazier, Ryan L., et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_7iv6ebru6vlhq4k4lgtn9hkkg8