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Phenylketonuria (PKU), an autosomal recessive inherited metabolic disorder, is caused by a mutation in the phenylalanine hydroxylase (PAH) gene on the 12th chromosome. Defective PAH activity ultimately leads to increased...
Purpose This study is to use a simple algorithm based on patient’s age to reduce the overall biological detriment associated with PET/CT.
Materials and Methods A total of 421 consecutive patients...
BACKGROUND: To systematically review the literature for methods to localize the genial tubercle as a means for performing an advancement of the genioglossus muscle.
METHODS: PubMed, Google Scholar, CRISP, EMBASE, CINAHL,...