Volume 11 - Tables of Contents

Number 4, December 1995

Reviews & Comments

• Adrenal Insufficiency and Bronchopulmonary Dysplasia in Low Birth Weight Infants  
• Effects of Differences in Dietary Fat on Growth, Energy and Nutrient Intake From Infancy to 8 Years of Age  
• Evidence for Partial Growth Hormone Insensitivity Among Patients With Idiopathic Short Stature
• Predictive Factors in the Determination of Final Height in Boys With Constitutional Delay of Growth and Puberty  
• Reduced Growth Hormone Secretion With Maintained Periodicity Following Cranial Irradiation in Children With Acute Lymphoblastic Leukaemia Longitudinal Data on Growth and Final Height in Diabetic Children  
• Role of Steroidogenic Acute Regulatory Protein in Adrenal and Gonadal Steroidogenesis  
• Zinc Deficiency in a Breast Fed Premature Infant  
• Zinc Supplementation and Growth of Infants Born Small for Gestational Age  

Number 3, September 1995

Feature Article

THE NEUROENDOCRINOLOGY OF PUBERTY
Jean-Pierre Bourguignon, MD, PhD

Reviews & Comments

• A Cluster of Sulfatase Genes on Xp22.3: Mutations in Chondrodysplasia Punctata (CDPX) and Implications for Warfarin Embryopathy  
• A Constitutively Active Mutant PTH-PTHrP Receptor in Jansen-Type Metaphyseal Chondrodysplasia  
• Chronic Metabolic Acidosis Decreases Albumin Synthesis and Induces Negative Nitrogen Balance in Humans  
• Endocrinology of the Carbohydrate-Deficient Glycoprotein Syndrome Type 1 From Birth Through Adolescence  
• Genetic Heterogeneity in Multiple Epiphyseal Dysplasia  
• Metabolic Modulation of the Growth Hormone-Releasing Activity of Hexarelin in Man  
• Pelvic Ultrasonography: Early Differentiation Between Isolated Premature Thelarche and Central Precocious Puberty  
• Recommendations for Standardized Human Pedigree Nomenclature  
• Telomeres and Telomerase: Cancer, Immortality, and Mental Retardation
• Thanatophoric Dysplasia (Types I and II) Caused by Distinct Mutations in Fibroblast Growth Factor Receptor 3  
• Trisomy 18, Molecular Studies, Parental Origin and Cell Division in the Extra Chromosome 18 Material  

Number 2, June 1995

Feature Article

Magnetic Resonance Imaging in Pituitary Disease
Raphaël Rappaport, MD

Reviews & Comments

• Body Composition and Spontaneous GH Secretion in Normal Short Stature Children  
• Catch-up Growth, Persisting Short Stature, and Adult Height of Children Born Small for Gestational Age
• Cognitive Abilities Associated With the Silver-Russell Syndrome  
• Deconvolution Analysis of Spontaneous Nocturnal Growth Hormone Secretion in Prepubertal Children With Preterminal Chronic Renal Failure and With End-Stage Renal Disease
• Delayed Adolescent Growth in Homozygous Sickle Cell Disease  
• Detection of Subtelomeric Chromosomal Rearrangements in Idiopathic Mental Retardation  
• Estrogen Levels in Childhood Determined by an Ultrasensitive Recombinant Cell Bioassay  
• Family History of Alzheimer's Disease May Increase Risk of Birth of Children With Down Syndrome  
• Gene Therapy for Cystic Fibrosis  
• Gene Therapy for Familial Hypercholesterolemia  
• Growth of Short Normal Children in Puberty Treated for 3 Years With Growth Hormone (GH) Alone or in Association With Gonadotropin-Releasing Hormone Agonist (GnRHa)  
• Identical Mutations in the FGFR2 Gene Cause Both Pfeiffer and Crouzon Syndrome Phenotypes  
• Is the Etiology of Insulin-Dependent Diabetes Mellitus Related to Superantigen Involvement?  
• Molecular Basis of Mammalian Sexual Determination: Activation of Mullerian Inhibiting Substance Gene Expression by SRY  
• Mouse Obese Gene and Its Human Homologue  
• Neurofibromatosis Type 1 Due to Germ-Line Mosaicism in a Clinically Normal Father  
• Normal Final Height After Treatment for Acute Lymphoblastic Leukemia Without Irradiation  

Number 1, March 1995

Feature Article

OSTEOCHONDRODYSPLASIAS WITH MILD CLINICAL MANIFESTATIONS: A GUIDE FOR ENDOCRINOLOGISTS AND OTHERS
Richard M. Pauli, MD, PhD

Reviews & Comments

• Catch-up Growth After Glucocorticoid Excess: A Mechanism Intrinsic to the Growth Plate  
• Estrogen Resistance Caused by a Mutation in the Estrogen-Receptor Gene in a Man  
• Growth Hormone Releasing Activity by Intranasal Administration of a Synthetic Hexapeptide (Hexarelin)  
• Growth of Short Normal Children in Puberty Treated for 3 Years With Growth Hormone Alone or in Association With Gonadotropin-Releasing Hormone Agonist  
• Longitudinal Analysis of Somatic Development in Pediatric Patients\ With IDDM, Part 1: Genetic Influences on Height and Weight  
• Long-Term GH Therapy in GHD and Non-GHD Boys: Effect on Bone Age and Pubertal Maturation  
• Part 2: Final Height Attainment in Girls and Boys With Insulin-Dependent Diabetes Mellitus  
• Predicting Adult Stature Without Using Skeletal Age: The Khamis-Roche Method  
• Preliminary Localization of a Gene for Autosomal Dominant Hypoparathyroidism to Chromosome 3q13  
• Prenatal Treatment of Congenital Adrenal Hyperplasia: A Review  
• Sex, SOX, and the Skeleton  
• Susceptibility Gene Loci for Insulin-Dependent Diabetes Mellitus (IDDM): A Review  
• The Genes for Crouzon Craniofacial Dysostosis and Pfeiffer Syndrome Are Fibroblast Growth Factor Receptor Genes
• The Small Nuclear Ribonucleoprotein-Associated Polypeptide N (SNRPN) Gene in Prader-Willi and Angelman Syndromes

Last Updated: 6/12/2009

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