Age as a main determinant of renal functional damage in urinary tract infection

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Spectrum of movement disorders and neurotransmitter abnormalities in paediatric POLG disease.

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Reversible infantile respiratory chain deficiency is a unique, genetically heterogenous mitochondrial disease.

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Information for genetic management of mtDNA disease: sampling pathogenic mtDNA mutants in the human germline and in placenta.

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Secondary skeletal surveys yield significant additional injuries: a retrospective review.

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Age as a main determinant of renal functional damage in urinary tract infection

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Correction to: Spectrum of movement disorders and neurotransmitter abnormalities in paediatric POLG disease.

Spectrum of movement disorders and neurotransmitter abnormalities in paediatric POLG disease.

Reversible infantile respiratory chain deficiency is a unique, genetically heterogenous mitochondrial disease.

The clinical, histochemical, and molecular spectrum of PEO1 (Twinkle)-linked adPEO.

The effect of diet on the expression of lipase genes in the midgut of the lightbrown apple moth (Epiphyas postvittana Walker; Tortricidae).

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Paediatric familial hypercholesterolaemia in Australia: a real-world registry study.

Quality and concordance of international paediatric sepsis guidelines: a cross-sectional appraisal from the SENTINEL International study.

Clinically significant night-to-night variability in overnight oximetry screening for obstructive sleep apnoea in children with Down syndrome: a retrospective review of screening data.

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Texture and nutrient content of commercial baby foods supplied in spouted pouches, compared to other packaging.

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