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Truswell AS

T., Viswanatha, G

Perturbation of serum carnitine levels in human adults by chronic renal disease and dialysis therapy

Although almost every definition of Peyronies disease refers to it as a wound healing disorder, we found only a few cases where that was the cause of the diagnosis

Trials should also incorporate sex-specific analyses, age related stratification, and clinically relevant comorbidities such as gastrointestinal dysfunction and sleep problems, all of which can modulate treatment efficacy

Rare mutations in the SLC22A5 gene can cause a genetic condition called primary carnitine deficiency, which is usually discovered in infancy because it affects brain function, muscle function, and blood glucose levels