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Licensed Unlicensed Requires Authentication Published by De Gruyter July 1, 2002

Obesity and Lipid Profiles in Children and Adolescents

  • O. Friedland, , D. Nemet, , N. Gorodnitsky, , B. Wolach, and A. Eliakim,
From the journal Journal of Pediatric Endocrinology and Metabolism
https://doi.org/10.1515/JPEM.2002.15.7.1011
Published Online: 2002-07

©2011 by Walter de Gruyter GmbH & Co.

From the journal
Journal of Pediatric Endocrinology and Metabolism
Journal of Pediatric Endocrinology and Metabolism
Volume 15 Issue 7
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TABLE OF CONTENTS
Bruno Weber's 70th Birthday
Amative Orientation: The Hormonal Hypothesis Examined
When Should We Measure Growth Hormone Binding Protein?
Serum Leptin and Leptin Binding Activity in Children and Adolescents with Hypothalamic Dysfunction
Linear Growth in Children with Congenital Hypothyroidism Detected by Neonatal Screening and Treated Early: A Longitudinal Study
Systematic Ultrasound Screening as a Significant Tool for Early Detection of Thyroid Carcinoma in Belarus
Decreased Cortisol Secretion in Nonclassical 21-Hydroxylase Deficiency Before and During Glucocorticoid Therapy
ABCC8 (SUR1) and KCNJ11 (KIR6.2) Mutations in Persistent Hyperinsulinemic Hypoglycemia of Infancy and Evaluation of Different Therapeutic Measures
Clinical Predictors of Mucormycosis in Children with Type 1 Diabetes Mellitus
Continuous Subcutaneous Insulin Infusion in the Treatment of Children and Adolescents with Type I Diabetes Mellitus
Obesity and Lipid Profiles in Children and Adolescents
Adolescent Rickets in Saudi Arabia: A Rich and Sunny Country
Iodine and Selenium Deficiency in School-children in an Endemic Goiter Area in Turkey
No Seasonality of Birth in Children with Type 1 Diabetes Mellitus in Ankara, Turkey
Growth Retardation in Children with IgA Deficiency
Intronic Mutation in the Growth Hormone Receptor Gene in a Peruvian Girl with Laron Syndrome
Novel Mutation Involving the Translation Initiation Codon of the Growth Hormone Receptor Gene (GHR) in a Patient with Laron Syndrome
Molecular Analysis of Frasier Syndrome: Mutation in the WT1 Gene in a Girl with Gonadal Dysgenesis and Nephronophthisis
Growth and Ovarian Function in Girls with 48,XXXX Karyotype - Patient Report and Review of the Literature
FORUM & CORRESPONDENCE. BOOK REVIEWS. CALENDAR
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