Results 31 to 40 of about 529,955 (177)
Behavioral deficits in a rat model of maternal PKU [PDF]
Phenylketonuria was experimentally induced in one group of pregnant rats by supplementing their diets with α-methylphenylalanine and phenylalanine on Days 10-21 of gestation. Control groups were either pair fed or ad-lib fed. Offspring of the drug-treated mothers were deficient on several measures of swimming development, active avoidance acquisition ...
Ann T. Hanulak, Elaine M. Hull
openaire +1 more source
Exploring Communication Patterns in the Discussion of Maternal PKU Syndrome Between Parents and Daughters [PDF]
Maternal PKU syndrome is the collection of features and birth defects that arise from uncontrolled phenylalanine levels in a pregnant woman with phenylalanine hydroxylase (PAH) deficiency, previously known as phenylketonuria (PKU).
Andrews, Hannah Beth
core +1 more source
Introduction Iron deficiency is the most prevalent micronutrient deficiency in pregnancy globally responsible for nearly 120 000 maternal deaths per year and a fifth of maternal mortality. Over 46% of pregnant women in Africa and 62% of pregnant women in
Haron Njiru +3 more
doaj +1 more source
Phenylketonuria is an inborn error of phenylalanine metabolism caused by a phenylalanine hydroxylase deficiency. To prevent the occurrence of neurological symptoms and maternal complications resulting from phenylketonuria, patients must adhere to a ...
Yoichi Wada +5 more
doaj +1 more source
Respect PKU staff, our frontliners [PDF]
Facing of the outbreak of the Covid-19 that has been declared a pandemic by the World Health Organization (WHO), the Center for Health (PKU), Universiti Malaysia Pahang (UMP) is always on alert to fight the spread of the outbreak in both university ...
UMP, PNC
core +1 more source
Selected Abstracts of the 19th International Workshop on Neonatology and Pediatrics; Cagliari (Italy); October 18th-21st, 2023 FROM WOMB TO AGING, FROM MEDICAL HISTORY TO ARTIFICIAL INTELLIGENCE The Workshop has been organized with the patronage of
--- Various Authors
doaj +1 more source
JDong-pku/South-Altyn-Orogen v.1.0
<p><a href="https://github.com/JDong-pku/South-Altyn-Orogen/files/4006736/Supporting.Information.S1.docx">Supporting Information S1.docx</a></p ...
JDong-pku
core +1 more source
Congenital Heart Disease in Maternal Phenylketonuria: Report from the Maternal PKU Collaborative Study [PDF]
The frequency and types of congenital heart disease in offspring from pregnancies in women with hyperphenylalaninemia were examined in the international prospective Maternal Phenylketonuria Collaborative Study. Relationships of congenital heart disease in offspring to the basal blood phenylalanine level in the mother, metabolic control through diet ...
H L, Levy +10 more
openaire +2 more sources
Importância do diagnóstico e tratamento da fenilcetonúria Diagnoses and treatment of phenylketonuria
A fenilcetonúria (PKU) é o mais comum dos erros congênitos do metabolismo de aminoácidos. Resulta da deficiência da fenilalanina hidroxilase, enzima que catalisa a conversão de fenilalanina em tirosina.
Nádia VM de Mira +1 more
doaj +1 more source
Effect of Family Income, Education, Occupation, and Birth Weight on Child Growth at Aisyiyah III Kindergarten, in Kadipiro, Indonesia [PDF]
Background: Children under five years old are the future generation. Stages of child development during the golden period require stimulation to increase the potential of healthy children.
Murti, Bhisma +2 more
core +1 more source

