Results 271 to 280 of about 48,194 (317)

Evaluation of Body Composition and Biochemical Parameters in Adult Phenylketonuria. [PDF]

Nutrients
Balci MC, Karaca M, Gunes D, Korbeyli HK, Selamioglu A, Gokcay G.   +5 more
europepmc   +1 more source

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PKU-I2IQA: An Image-to-Image Quality Assessment Database for AI Generated Images

arXiv.org, 2023
As image generation technology advances, AI-based image generation has been applied in various fields and Artificial Intelligence Generated Content (AIGC) has garnered widespread attention.
Jiquan Yuan, Xinyan Cao, Changjin Li, Fanyi Yang, Jinlong Lin, Xixin Cao   +5 more
semanticscholar   +1 more source

You shall not (by)pass!: practical, secure, and fast PKU-based sandboxing

European Conference on Computer Systems, 2022
Memory Protection Keys for Userspace (PKU) is a recent hardware feature that allows programs to assign virtual memory pages to protection domains, and to change domain access permissions using inexpensive, unprivileged instructions.
Alexios Voulimeneas, Jonas Vinck, Ruben Mechelinck, Stijn Volckaert   +3 more
semanticscholar   +1 more source

PKU: niet altijd ‘PKU’

Tijdschrift voor Kindergeneeskunde, 2010
Neonatale screening beoogt ernstige behandelbare aandoeningen bij de pasgeborene op te sporen. Een positieve screening voor fenylketonurie (PKU) betekent niet per definitie dat het gaat om hyperfenylalaninemie ten gevolge van klassieke PKU.
Croonen, E.A., Jonckheere, A.I., Morava, E.   +2 more
openaire   +4 more sources

Molecular genetics of PKU

Journal of Inherited Metabolic Disease, 1986
AbstractThis review summarizes the isolation of rat phenylalanine hydroxylase mRNA and its use in the synthesis of its cDNA. As rat cDNA cross‐hybridized with human phenylalanine hydroxylase mRNA, the rat cDNA probe was used to screen a human liver cDNA library.
Savio L. C. Woo, Flemming Güttler
openaire   +3 more sources

Maternal PKU syndrome in an exceptional family with unexpected PKU

Journal of Inherited Metabolic Disease, 1986
AbstractMild maternal phenylketonuria needs treatment during pregnancy.
E. E. E. Meuleman, J. B. C. de Klerk, H. J. Dijkhuis, Sybe K. Wadman   +3 more
openaire   +3 more sources

Discontinuing the PKU Diet

Pediatrics, 1986
In response to the article by Seashore et al, "Loss of Intellectual Function in Children With Phenylketonuria After Relaxation of Dietary Phenylalanine Restriction" (Pediatrics 1985;75:266-232): we have had a similar experience at the PKU Outpatient Clinic at the Bancroft School in Haddonfield, NJ.
Gabor Barabas, Wendy S. Matthews
openaire   +3 more sources

PKU-SafeRLHF: A Safety Alignment Preference Dataset for Llama Family Models

arXiv.org
In this work, we introduce the PKU-SafeRLHF dataset, designed to promote research on safety alignment in large language models (LLMs). As a sibling project to SafeRLHF and BeaverTails, we separate annotations of helpfulness and harmlessness for question ...
Jiaming Ji, Donghai Hong, Borong Zhang, Boyuan Chen, Josef Dai, Boren Zheng, Tianyi Qiu, Boxun Li, Yaodong Yang   +8 more
semanticscholar   +1 more source

Breastfeeding the Infant with PKU

Journal of Human Lactation, 1997
Breastfeeding is possible with children who have phenylketonuria. Based on the decisions made by the breastfeeding mother and the infant's physician, there are multiple methods of management which can be utilized to provide breast milk for the infant with PKU.
Laura L. Duncan, Sonyia B. Elder
openaire   +3 more sources