Cargando…

Mechanism of Chronic Kidney Disease Progression and Novel Biomarkers: A Metabolomic Analysis of Experimental Glomerulonephritis

While a complex network of cellular and molecular events is known to be involved in the pathophysiological mechanism of chronic kidney disease (CKD), the divergence point between reversal and progression and the event that triggers CKD progression are still unknown. To understand the different mecha...

Descripción completa

Detalles Bibliográficos
Autores principales:	Han, Kyoung Hee, Kim, Bora, Ji, Sang Chun, Kang, Hee Gyung, Cheong, Hae Il, Cho, Joo-Youn, Ha, Il-Soo
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2020
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7240957/ https://www.ncbi.nlm.nih.gov/pubmed/32344531 http://dx.doi.org/10.3390/metabo10040169

Ejemplares similares

Bilateral iliac and popliteal arterial thrombosis in a child with focal segmental glomerulosclerosis
por: Han, Kyoung Hee, et al.
Publicado: (2016)

Disseminated adenovirus infection in a 10-year-old renal allograft recipient
por: Lee, Bora, et al.
Publicado: (2018)

Recurrence and Treatment after Renal Transplantation in Children with FSGS
por: Kang, Hee Gyung, et al.
Publicado: (2016)

A nonsense PAX6 mutation in a family with congenital aniridia
por: Han, Kyoung Hee, et al.
Publicado: (2016)

Kidney Transplantation in Patients with Atypical Hemolytic Uremic Syndrome due to Complement Factor H Deficiency: Impact of Liver Transplantation
por: Kim, Sejin, et al.
Publicado: (2017)

Post-Transplant Lymphoproliferative Diseases in Pediatric Kidney Allograft Recipients with Epstein-Barr Virus Viremia
por: Hyun, Hyesun, et al.
Publicado: (2019)

Acute kidney injury associated with Yersinia pseudotuberculosis infection: Forgotten but not gone
por: Kim, Ye Kyung, et al.
Publicado: (2019)

Erratum: Post-Transplant Lymphoproliferative Diseases in Pediatric Kidney Allograft Recipients with Epstein-Barr Virus Viremia
por: Hyun, Hyesun, et al.
Publicado: (2020)

Higher Incidence of BK Virus Nephropathy in Pediatric Kidney Allograft Recipients with Alport Syndrome
por: Cho, Young Hoon, et al.
Publicado: (2019)

Anemia and Iron Deficiency in Children with Chronic Kidney Disease (CKD): Data from the Know-Ped CKD Study
por: Lee, Keum Hwa, et al.
Publicado: (2019)

Outcomes of chronic dialysis in Korean children with respect to survival rates and causes of death
por: Chang, Hye Jin, et al.
Publicado: (2014)

Left-ventricular diastolic dysfunction in Korean children with chronic kidney disease: data from the KNOW-Ped CKD study
por: Kim, Jeong Yeon, et al.
Publicado: (2020)

Renal Syndromic Hearing Loss Is Common in Childhood-onset Chronic Kidney Disease
por: Kim, Ji Hyun, et al.
Publicado: (2020)

Genotype and Phenotype Analyses in Pediatric Patients with HNF1B Mutations
por: Lim, Seon Hee, et al.
Publicado: (2020)

Intellectual Functioning of Pediatric Patients with Chronic Kidney Disease: Results from the KNOW-Ped CKD
por: Kang, Na Ri, et al.
Publicado: (2021)

Acute kidney injury in childhood-onset nephrotic syndrome: Incidence and risk factors in hospitalized patients
por: Kim, Mi Young, et al.
Publicado: (2018)

Validity and reliability of the Korean version of the pediatric quality of life ESRD module
por: Park, Ki-Soo, et al.
Publicado: (2012)

Nephrotic syndrome: what's new, what's hot?
por: Kang, Hee Gyung, et al.
Publicado: (2015)

Targeted Exome Sequencing Provided Comprehensive Genetic Diagnosis of Congenital Anomalies of the Kidney and Urinary Tract
por: Ahn, Yo Han, et al.
Publicado: (2020)

A case of pseudohypoaldosteronism type 1 with a mutation in the mineralocorticoid receptor gene
por: Lee, Se Eun, et al.
Publicado: (2011)

A Premature Baby with Severe Oligohydramnios and Hypotension: a Case Report of Renal Tubular Dysgenesis
por: Min, Jeesu, et al.
Publicado: (2020)

A familial case of Blau syndrome caused by a novel NOD2 genetic mutation
por: Kim, Woojoong, et al.
Publicado: (2016)

Renal transplantation in a patient with Bartter syndrome and glomerulosclerosis
por: Lee, Se Eun, et al.
Publicado: (2011)

Posttransplantation lymphoproliferative disorder after pediatric solid organ transplantation: experiences of 20 years in a single center
por: Jeong, Hyung Joo, et al.
Publicado: (2017)

Measurement of Fluid Status Using Bioimpedance Methods in Korean Pediatric Patients on Hemodialysis
por: Yang, Eun Mi, et al.
Publicado: (2017)

A case of Bartter syndrome type I with atypical presentations
por: Lee, Eun Hye, et al.
Publicado: (2010)

Efficacy and safety of rituximab in childhood-onset, difficult-to-treat nephrotic syndrome: A multicenter open-label trial in Korea
por: Ahn, Yo Han, et al.
Publicado: (2018)

Mineral bone disorder in children with chronic kidney disease: Data from the KNOW-Ped CKD (Korean cohort study for outcome in patients with pediatric chronic kidney disease) study
por: Jung, Jiwon, et al.
Publicado: (2023)

Corrigendum: Mineral bone disorder in children with chronic kidney disease: data from the KNOW-Ped CKD (Korean cohort study for outcome in patients with pediatric chronic kidney disease) study
por: Jung, Jiwon, et al.
Publicado: (2023)

Markers of disease and steroid responsiveness in paediatric idiopathic nephrotic syndrome: Whole-transcriptome sequencing of peripheral blood mononuclear cells
por: Kang, Hee Gyung, et al.
Publicado: (2017)

KNOW-Ped CKD (KoreaN cohort study for outcomes in patients with pediatric CKD): Design and methods
por: Kang, Hee Gyung, et al.
Publicado: (2016)

Genotype and Phenotype Analysis in Pediatric Patients with Cystinuria
por: Kim, Ji Hyun, et al.
Publicado: (2017)

Two Novel Mutations in the Aquaporin 2 Gene in a Girl with Congenital Nephrogenic Diabetes Insipidus
por: Cheong, Hae Il, et al.
Publicado: (2005)

Long-term repeated rituximab treatment for childhood steroid-dependent nephrotic syndrome
por: Kim, Ji Hyun, et al.
Publicado: (2017)

Factors affecting serum concentration of vancomycin in critically ill oliguric pediatric patients receiving continuous venovenous hemodiafiltration
por: Lee, Bongjin, et al.
Publicado: (2018)

Loss of podocalyxin causes a novel syndromic type of congenital nephrotic syndrome
por: Kang, Hee Gyung, et al.
Publicado: (2017)

Outcome of Antimicrobial Therapy of Pediatric Urinary Tract Infections Caused by Extended-Spectrum β-Lactamase-Producing Enterobacteriaceae
por: Lee, Bongjin, et al.
Publicado: (2013)

A Pediatric Case of a D-Penicillamine Induced ANCA-associated Vasculitis Manifesting a Pulmonary-Renal Syndrome
por: Kang, Sena, et al.
Publicado: (2019)

A novel mutation of CLCNKB in a Korean patient of mixed phenotype of Bartter-Gitelman syndrome
por: Cho, Hee-Won, et al.
Publicado: (2016)

Reninoma: a rare cause of curable hypertension
por: Kim, Ji Hye, et al.
Publicado: (2019)

Cannot write session to /tmp/vufind_sessions/sess_74a16eudectjjqd75ahosf55hm