Development and validation of machine-learning models of diet management for hyperphenylalaninemia: a multicenter retrospective study-Reference-Cited by-同舟云学术

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Development and validation of machine-learning models of diet management for hyperphenylalaninemia: a multicenter retrospective study

Published:2024-09-11 Issue:1 Volume:22 Page:
ISSN:1741-7015
Container-title:BMC Medicine
language:en
Short-container-title:BMC Med

Author:

Su Yajie,Wang Yaqiong,He Jinfeng,Wang Huijun,A Xian,Jiang Haili,Lu Wei,Zhou Wenhao,Li Long

Funder

Science and Technology Introduction Innovation Project of People's Hospital in Xinjiang Uygur Autonomous Region

National Natural Science Foundation of China

Natural Science Foundation of Xinjiang Uygur Autonomous Region

Publisher

Springer Science and Business Media LLC

Link

https://link.springer.com/content/pdf/10.1186/s12916-024-03602-w.pdf

Reference37 articles.

1. Rajabi F, Rohr F, Wessel A, Martell L, Dobrowolski SF, Guldberg P, et al. Phenylalanine hydroxylase genotype-phenotype associations in the United States: a single center study. Mol Genet Metab. 2019;128(4):415–21.

2. Hillert A, Anikster Y, Belanger-Quintana A, Burlina A, Burton BK, Carducci C, et al. The Genetic Landscape and Epidemiology of Phenylketonuria. Am J Hum Genet. 2020;107(2):234–50.

3. Camp KM, Parisi MA, Acosta PB, Berry GT, Bilder DA, Blau N, et al. Phenylketonuria Scientific Review Conference: state of the science and future research needs. Mol Genet Metab. 2014;112(2):87–122.

4. van Spronsen FJ, van Rijn M, Dorgelo B, Hoeksma M, Bosch AM, Mulder MF, et al. Phenylalanine tolerance can already reliably be assessed at the age of 2 years in patients with PKU. J Inherit Metab Dis. 2009;32(1):27–31.

5. Darling PB, Dunn M, Gilani GS, Ball RO, Pencharz PB. Phenylalanine kinetics differ between formula-fed and human milk-fed preterm infants. J Nutr. 2004;134(10):2540–5.

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