Explore Books on
phenylketonuria

Flowers for Algernon

By Daniel Keyes

Phenylketonuria

By Frank Lewis Lyman

Protect from PKU

By Florence Scott

Phenylketonuria detection in the newborn infant as a routine hospital procedure

By Robert Guthrie

Genetic screening

By National Research Council (U.S.). Committee for the Study of Inborn Errors of Metabolism.

Phenylketonuria

By Willard R. Centerwall

Low protein cookery for phenylketonuria

By Virginia E. Schuett

National survey of treatment programs for PKU and selected other inherited metabolic diseases

By Virginia E. Schuett

Phenylketonuria and allied metabolic diseases

By Kenneth F. Swaiman

PKU and the schools

By Robert Arthur Henderson

Vitamin B-6 status, energy and protein intakes, and amino acids in the diets and plasma of school-aged patients with Phenylketonuria

By Annie Prince

Dietary phenylalanine and brain function

By Richard J. Wurtman

Prefrontal cortex cognitive deficits in children treated early and continuously for PKU

By Adele Diamond

The influence of diet-induced hyperphenylalaninemia on molecular neurochemistry and learning behavior in the rat

By James L. Mottin

Practical developments in inherited metabolic diseases

By G. M. Addison

Treatment programs for PKU in the United States

By Harry A. Waisman Center on Mental Retardation and Human Development.

Low-protein cuisine

By Cathy Lorimer

Newborn screening for genetic-metabolic diseases

By Neil A. Holtzman

The child with phenylketonuria

By J. B. Holton

PKU in California

By Cunningham, George

Proceedings

By International Conference on Inborn Errors of Metabolism Dubrovnik, Yugoslavia 1966.

Sztuczna fenyloketonuria u szczurów

By Krystyna Bełżecka

Recommended guidelines for PKU programs for the newborn

By United States. Maternal and Child Health Service.

State laws pertaining to phenylketonuria as of November 1970

By United States. Maternal and Child Health Service.