COQ8B nephropathy: Early detection and optimal treatment

Genetic spectrum of renal disease for 1001 Chinese children based on a multicenter registration system

(2019) Jia Rao et al.   CLINICAL GENETICS

Follow-up results of patients with ADCK4 mutations and the efficacy of CoQ10 treatment

(2017) Mustafa Atmaca et al.   PEDIATRIC NEPHROLOGY

Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics

(2016) Sarah S. Kalia et al.   GENETICS IN MEDICINE

Exploring the genetic basis of early-onset chronic kidney disease

(2016) Asaf Vivante et al.   Nature Reviews Nephrology

ADCK4-Associated Glomerulopathy Causes Adolescence-Onset FSGS

(2015) E. Korkmaz et al.   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

Update: Ambulatory Blood Pressure Monitoring in Children and Adolescents

(2014) Joseph T. Flynn et al.   HYPERTENSION

Oscillometric 24-h ambulatory blood pressure reference values in Hong Kong Chinese children and adolescents

(2014) Gabriel W.K. Yip et al.   JOURNAL OF HYPERTENSION

Evaluation and Management of Chronic Kidney Disease: Synopsis of the Kidney Disease: Improving Global Outcomes 2012 Clinical Practice Guideline

(2013) Paul E. Stevens   ANNALS OF INTERNAL MEDICINE

ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ10 biosynthesis disruption

(2013) Shazia Ashraf et al.   JOURNAL OF CLINICAL INVESTIGATION

Should mean arterial pressure be included in the definition of ambulatory hypertension in children?

(2013) Terezie Šuláková et al.   PEDIATRIC NEPHROLOGY

COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness

(2011) Saskia F. Heeringa et al.   JOURNAL OF CLINICAL INVESTIGATION

Screening for NPHS2 Mutations May Help Predict FSGS Recurrence after Transplantation

(2011) T. C. Jungraithmayr et al.   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY