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Serum IGF-I and IGFBP-3 Reference Values from a Chemiluminescent Assay in Normal Children and Adolescents of Hispanic and Italian Origin: Presence of Sexual Dimorphism in IGF-I Values
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E.A. Chaler,
Published/Copyright:
December 1, 2009
Published Online: 2009-12
©2011 by Walter de Gruyter GmbH & Co.
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Articles in the same Issue
- TABLE OF CONTENTS
- The Cost of Non-Compliance in Congenital Adrenal Hyperplasia
- Giant Macroorchidism in Congenital Adrenal Hyperplasia
- Serum Osteoprotegrin (OPG) and Receptor Activator of Nuclear Factor κΒ (RANKL) in Healthy Children and Adolescents
- Relationships Between Osteoprotegerin (OPG), Receptor Activator of Nuclear Factor κΒ Ligand (RANKL), and Growth Hormone (GH) Secretory Status in Short Children
- Neonatal Screening for Biotidinidase Deficiency: Results of a 1-year Pilot Study in Four Cities in Central Anatolia
- Alterations of Carbohydrate and Lipoprotein Metabolism in Childhood Obesity - Impact of Insulin Resistance and Acanthosis Nigricans
- Serum IGF-I and IGFBP-3 Reference Values from a Chemiluminescent Assay in Normal Children and Adolescents of Hispanic and Italian Origin: Presence of Sexual Dimorphism in IGF-I Values
- Serum Insulin-like Growth Factor-I and Insulin-like Growth Factor Binding Protein-3 Levels in Children with Zinc Deficiency and the Effect of Zinc Supplementation on these Parameters
- Maternal and Neonatal Urinary Iodine Excretion and Neonatal TSH in Relation to Use of Antiseptic During Caesarean Section in an Iodine Sufficient Area
- Benefit of Early Commencement of Growth Hormone Therapy in Children with Prader-Willi Syndrome
- Enzyme Replacement Therapy in an Infant with Pompe's Disease with Severe Cardiomyopathy
- Treatment of Familial Male-limited Precocious Puberty (Testotoxicosis) with Anastrozole and Bicalutamide in a Boy with a Novel Mutation in the Luteinizing Hormone Receptor
- Mutational Analysis of the Androgen Receptor Gene in Two Indian Families with Partial Androgen Insensitivity Syndrome
- Hypoketotic Hypoglycemia with Myolysis and Hypoparathyroidism: An Unusual Association in Medium Chain Acyl-CoA Desydrogenase Deficiency (MCADD)
- High Dose Calcitriol in Osteopetrorickets
- Pediatric Glipizide Ingestion, Onset of Hypoglycemia, and Octreotide
- INDEX
- CALENDAR
Articles in the same Issue
- TABLE OF CONTENTS
- The Cost of Non-Compliance in Congenital Adrenal Hyperplasia
- Giant Macroorchidism in Congenital Adrenal Hyperplasia
- Serum Osteoprotegrin (OPG) and Receptor Activator of Nuclear Factor κΒ (RANKL) in Healthy Children and Adolescents
- Relationships Between Osteoprotegerin (OPG), Receptor Activator of Nuclear Factor κΒ Ligand (RANKL), and Growth Hormone (GH) Secretory Status in Short Children
- Neonatal Screening for Biotidinidase Deficiency: Results of a 1-year Pilot Study in Four Cities in Central Anatolia
- Alterations of Carbohydrate and Lipoprotein Metabolism in Childhood Obesity - Impact of Insulin Resistance and Acanthosis Nigricans
- Serum IGF-I and IGFBP-3 Reference Values from a Chemiluminescent Assay in Normal Children and Adolescents of Hispanic and Italian Origin: Presence of Sexual Dimorphism in IGF-I Values
- Serum Insulin-like Growth Factor-I and Insulin-like Growth Factor Binding Protein-3 Levels in Children with Zinc Deficiency and the Effect of Zinc Supplementation on these Parameters
- Maternal and Neonatal Urinary Iodine Excretion and Neonatal TSH in Relation to Use of Antiseptic During Caesarean Section in an Iodine Sufficient Area
- Benefit of Early Commencement of Growth Hormone Therapy in Children with Prader-Willi Syndrome
- Enzyme Replacement Therapy in an Infant with Pompe's Disease with Severe Cardiomyopathy
- Treatment of Familial Male-limited Precocious Puberty (Testotoxicosis) with Anastrozole and Bicalutamide in a Boy with a Novel Mutation in the Luteinizing Hormone Receptor
- Mutational Analysis of the Androgen Receptor Gene in Two Indian Families with Partial Androgen Insensitivity Syndrome
- Hypoketotic Hypoglycemia with Myolysis and Hypoparathyroidism: An Unusual Association in Medium Chain Acyl-CoA Desydrogenase Deficiency (MCADD)
- High Dose Calcitriol in Osteopetrorickets
- Pediatric Glipizide Ingestion, Onset of Hypoglycemia, and Octreotide
- INDEX
- CALENDAR