Idiopathic nephrotic syndrome newly affects 1–3 per 100,000 children per year.
Approximately 85% of cases show complete remission of proteinuria following …

Congenital nephrotic syndrome (CNS) is a heterogeneous group of disorders characterized
by nephrotic-range proteinuria, hypoalbuminaemia and oedema, which manifest in utero or …

Coenzyme Q10 (CoQ10) has a number of vital functions in all cells, both mitochondrial and
extra-mitochondrial. In addition to its key role in mitochondrial oxidative phosphorylation …

Abstract Primary Coenzyme Q (CoQ) deficiencies are clinically heterogeneous conditions
and lack clear genotype-phenotype correlations, complicating diagnosis and prognostic …

Coenzyme Q10 (CoQ10), which plays a key role in the electron transport chain by providing
an adequate, efficient supply of energy, has another relevant function as an antioxidant …

Primary Coenzyme Q10 (CoQ10) deficiency is an ultra-rare disorder caused by defects in
genes involved in CoQ10 biosynthesis leading to multidrug-resistant nephrotic syndrome as …

Mitochondrial cytopathies include a heterogeneous group of diseases that are characterized
by impaired oxidative phosphorylation, leading to multi organ involvement and progressive …

Congenital nephrotic syndrome (CNS) is a heterogeneous group of disorders presenting
with massive proteinuria within the first 3 months of life almost inevitably leading to end …

Abstract Coenzyme Q10/COQ10, an essential cofactor in the electron‐transport chain is
involved in ATP production. Primary COQ10 deficiency is clinically and genetically a …

Steroid-resistant nephrotic syndrome (SRNS) is a genetically heterogeneous kidney disease
that is the second most frequent cause of kidney failure in the first 2 decades of life. Despite …