Results 41 to 50 of about 48,998 (266)

Nutritional Follow-Up in Indigenous Children Under Five Years in Colombia

open access: yesChildren
Background/Objectives: Indigenous children in La Guajira, Colombia, live in a context of structural vulnerability that may compromise growth and nutritional status.
Pedro Barrera-López   +3 more
doaj   +1 more source

Functional gastrointestinal disorders in infants: to treat, observe or correct?

open access: yesZdorovʹe Rebenka, 2020
The article discusses the functional disorders of the gastrointestinal tract in infants. The prevalence of functional gastrointestinal disorders is extremely high in all age groups, but in young children, functional diseases are actually a normal variant:
O.Yu. Belousova, L.V. Kazaryan
doaj   +1 more source

Genotype–Phenotype Correlations of Monoallelic PFIC Variants in Pediatric Liver Disease: A Multicenter Retrospective Cohort Study

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Progressive familial intrahepatic cholestasis (PFIC) is classically caused by biallelic pathogenic variants, yet monoallelic variants of uncertain significance (VUS) in PFIC‐associated genes are increasingly identified in children with cholestasis, creating diagnostic uncertainty.
Brett J. Hoskins   +9 more
wiley   +1 more source

Nutrición y desarrollo psicomotor durante el primer semestre de vida Nutrition and psichomotor development during the first six months of life

open access: yesSalud Pública de México, 1998
Objetivo. Estudiar el desarrollo psicomotor de niños pequeños de una comunidad rural pobre y mal alimentada y relacionarlo con la alimentación y nutrición tanto de su madre como de ellos mismos. Material y métodos.
ADOLFO CHÁVEZ   +4 more
doaj  

The use of choline supplementation in premature newborns: a systematic review

open access: yesRevista Paulista de Pediatria
Objective: To identify the routes and doses of choline supplementation required to meet the metabolic demands of preterm infants. Data Source: The information was searched in three databases: US National Library of Medicine National Institute of ...
Ligia Modelli Rodrigues   +2 more
doaj   +1 more source

Nutritional Deficiencies in Children of the First 3 Years of Life, According to a Multicenter Study in Ukraine

open access: yesZdorovʹe Rebenka, 2013
Taking into account the fact that in Ukraine today there is not enough researches that summarize the data on the nutritional status of young children, the prevalence of eating disorders and lack of basic macro- and micronutrients in children, the ...
S.L. Nyankovsky   +8 more
doaj   +1 more source

COX14 Variants Are Associated With Mitochondrial Complex IV Deficiency Nuclear Type 10 (MC4DN10)

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT COX14 encodes a transmembrane protein essential for cytochrome c oxidase (COX) complex assembly. A homozygous missense variant in COX14 was reported in three siblings from a single consanguineous family with severe, fatal infantile mitochondrial complex IV deficiency nuclear type 10 (MC4DN10; MIM# 619053).
Elias K. Awad   +7 more
wiley   +1 more source

La desnutrición infantil en el medio rural mexicano Children malnutrition in rural Mexico

open access: yesSalud Pública de México, 1998
Objetivo. Conocer la situación nutricional de la población infantil del medio rural mexicano, comparándola con la situación previa y localizando las zonas más afectadas. Material y métodos. La muestra estuvo conformada por 38 232 familias, pertenecientes
ABELARDO AVILA-CURIEL   +4 more
doaj  

Nutritional Deficiencies in Children of the First 3 Years of Life, According to a Multicenter Study in Ukraine

open access: yesZdorovʹe Rebenka, 2015
Taking into account the fact that in Ukraine today there is not enough researches that summarize the data on the nutritional status of young children, the prevalence of eating disorders and lack of basic macro- and micronutrients in children, the ...
S.L. Nyankovsky   +8 more
doaj   +1 more source

The EXPLAIN Study: Exploring Arthrogryposis Multiplex Congenita in Adults in Norway — A Description of Demographic, Medical, and Neurological Findings

open access: yesAmerican Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Arthrogryposis Multiplex Congenita (AMC) encompasses several hundred conditions with diverse genetic, pathophysiological, and clinical origins. The overarching EXPLAIN study explores underlying causes and implications of AMC and represents the largest clinical cohort of adults with AMC reported to date.
My Vuong Hermansen   +5 more
wiley   +1 more source

Home - About - Disclaimer - Privacy