Change language
English Deutsch
Change currency
€ EUR £ GBP $ USD
Licensed Unlicensed Requires Authentication Published by De Gruyter February 1, 2004

Clinical, Biochemical and Molecular Investigations of Three Taiwanese Children with Laron Syndrome

  • C. Yang, , J.Y.-R. Chen, , C.-C. Lai, , H.-C. Lin, , G.-C. Yeh, and H.-H. Hsu,
From the journal Journal of Pediatric Endocrinology and Metabolism
https://doi.org/10.1515/JPEM.2004.17.2.165
Published Online: 2004-02

©2011 by Walter de Gruyter GmbH & Co.

From the journal
Journal of Pediatric Endocrinology and Metabolism
Journal of Pediatric Endocrinology and Metabolism
Volume 17 Issue 2
Submit manuscript

Journal and Issue

Articles in the same Issue

TABLE OF CONTENTS
A Perspective on the Approach to the Intersex Child Born with Genital Ambiguity
Should Serum IGF-I Concentrations be Monitored Routinely During Growth Hormone Therapy?
Absence of Y Chromosome Microdeletions in Patients with Cryptorchidism and Hypospadias
Congenital Gonadotropin Deficiency in Boys: Management During Childhood
Nonclassic 21-Hydroxylase Deficiency in Croatia
Clinical, Biochemical and Molecular Investigations of Three Taiwanese Children with Laron Syndrome
HLA Alleles and Type 1 Diabetes Mellitus in Low Disease Incidence Populations of Southern Europe: A Comparison of Greeks and Albanians
Type 2 Diabetes Mellitus in Children - An Increasing Health Problem in Mexico
Soy Protein Formulas in Children: No Hormonal Effects in Long-term Feeding
Left Ventricular Systolic and Diastolic Functions in Children Living in a Moderate-Severe Iodine Deficiency Area
Severe Transient Neonatal Hyperinsulinism Associated with Hyperlactataemia in Non-asphyxiated Infants
Signal Transducer and Activator of Transcription-1 (STAT1), but Not STAT5b, Regulates IGF-I Receptor Gene Expression in an Osteosarcoma Cell Line
Body Mass Index and Hypothalamic Morphology on MRI in Children with Congenital Midline Cerebral Abnormalities
Continuous Subcutaneous Insulin Infusion Pump Treatment in Children with Type 1 Diabetes Mellitus
Management of Central Diabetes Insipidus with Oral Desmopressin in a Premature Neonate
Congenital Hypothyroidism Caused by a Unique Thyroid Peroxidase Allele Containing Two Mutations, C1708T and C2737T
Cortisol and Estradiol Secretion by a Benign Virilizing Adrenocortical Tumor in a Prepubertal Girl
Growth Hormone Deficiency Associated with Methylmalonic Acidemia
BOOK REVIEWS. CALENDAR
Downloaded on 4.12.2023 from https://www.degruyter.com/document/doi/10.1515/JPEM.2004.17.2.165/html
Scroll to top button