Skip Navigation
Skip to contents
Results by Year

View Wide

Filter

ARTICLE TYPE

PUBLICATION DATE

3 results
Display

Protein substitutions as new-generation pharmanutrition approach to managing phenylketonuria

Keskin FN, Şahin TÖ, Capasso R, Ağagündüz D

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Algorithm for Reducing Overall Biological Detriment Caused by PET/ CT: an Age‑Based Study

Spadafora M, Sannino P, Mansi L, Mainolfi C, Capasso R, Giorgio E, Fiordoro S, Imbimbo S, Masone F, Evangelista L

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Genial tubercle position and genioglossus advancement in obstructive sleep apnea (OSA) treatment: a systematic review

Chang ET, Kwon YD, Jung J, Capasso R, Riley R, Liu SC, Camacho M

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,...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close

Go to Top

Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr