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Licensed Unlicensed Requires Authentication Published by De Gruyter March 1, 2010

Melatonin and Elimination of Kynurenines in Children with Down's Syndrome

  • J. Uberos, , J. Romero, , A. Molina-Carballo, and A. Muñoz-Hoyos,
From the journal Journal of Pediatric Endocrinology and Metabolism
https://doi.org/10.1515/JPEM.2010.23.3.277
Published Online: 2010-03

©2011 by Walter de Gruyter GmbH & Co.

From the journal
Journal of Pediatric Endocrinology and Metabolism
Journal of Pediatric Endocrinology and Metabolism
Volume 23 Issue 3
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TABLE OF CONTENTS
Intrauterine Growth Restriction Still a Riddle
Abnormal Urinary Steroid Profiles in Hypertensive Obese Children
Intrauterine Growth Restriction as a Potential Risk Factor for Disease Onset in Adulthood
Growth Hormone Deficiency: Transition from Adolescence to Adulthood. Highlights from a Latin-American Serono Symposia International Foundation Conference
Central Diabetes Insipidus in Association with Neonatal Brain Abscess
Abnormal Urinary Steroid Profiles in Four Hypertensive Obese Children
Umbilical Waist-to-Height Ratio and Trunk Fat Mass Index (DXA) as Markers of Central Adiposity and Insulin Resistance in Argentinean Children with a Family History of Metabolic Syndrome
Childhood-Onset Narcolepsy, Obesity and Puberty in Four Consecutive Children: A Close Temporal Link
Does Childhood Overweight, Parental Perception of Overweight, or Family History of Diabetes Mellitus Increase Parental Perception of Type 2 Diabetes Risk for their Child?
Varying Presentation of Type 1 Polyglandular Failure in India
Melatonin and Elimination of Kynurenines in Children with Down's Syndrome
A Study of Three Polymorphic Sites of the ADA Gene in Children with Type 1 Diabetes Mellitus
p53 Codon 72 Polymorphism and Type 1 Diabetes Mellitus
Bacteraemia Complicating Rotavirus Gastroenteritis Klebsiella pneumoniae Bacteraemia Complicating Rotavirus Gastroenteritis in Two Infants with Glucocorticoid Deficiency
Addison's Disease and Severe Encephalopathy in an Infant with HIV Infection
Progressive Osseous Heteroplasia Caused by a Novel Nonsense Mutation in the GNAS1 Gene
Mauriac Syndrome - A Modern Reality
Mutation of the MIF Type II Receptor in Two Brothers
CALENDAR
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