Volume 22 - Tables of Contents

Number 4, December 2006 - Download pdf of entire issue

Featured Article

MOLECULAR PATHOGENESIS OF ACHONDROPLASIA
William A. Horton, MD
Director, Research Center
Shriners Hospital for Children
Oregon Health & Science University
Portland, Oregon

From The Editor’s Desk

Reviews & Comments

• Highlights of the Endocrine Society’s 88th Annual Meeting, Boston MA, June 24-28, 2006
• Aromatase Inhibitor Effect on Near-final Height of Boys with Constitutional Delay of Puberty
• Genetic Medicine: Dream, Reality or Something in Between?
• Catch-down of SGA and AGA Infants Born to Short-statured Parents
• Interleukin Deficiency Leads To Hyperphagia, Obesity, and Insulin Resistance
• Insulin and Sulfonylureas in Diabetic Patients with Kir6.2 Mutations
• Acidosis and Protein Kinase: A Novel Mechanism of Growth Failure

E-Reviews & Comments

• Highlights of the European Society for Paediatric Endocrinology 45th Annual Meeting, Rotterdam, Netherlands, June 30th-July 3rd, 2006
• A Third Signaling Pathway for the Type 1 IGF Receptor
• Androgen Levels as a Risk Factor for Metabolic Syndrome in Adolescent Girls with Polycystic Ovary Syndrome
• Are Adolescent Boys with Klinefelter Syndrome Androgen Deficient?
• Autistic-like Traits Associated with Elevated Prenatal Androgens
• Consensus Statement on Management of Intersex Disorders
• Critical Genes in Down Syndrome
• Inhaled Corticosteroids in Asthma
• Recurrence of Craniopharyngiomas
• Retinoid Signaling Determines Germ Cell Fate in Mice
• The Re-emerging Burden of Rickets
• Transitioning Children with Chronic Diseases to Adult Care

Number 3, September 2006 - Download pdf of entire issue

Featured Article

THE SOTOS SYNDROME - NSD1 HAPLOINSUFFICIENCY: CEREBRAL GIGANTISM UPDATE
ALLEN W. ROOT, MD
FRANK B. DIAMOND, JR., MD
Departments of Pediatrics and Biochemistry and Molecular Biology
University of South Florida College of Medicine, Tampa, FL
All Children’s Hospital, St. Petersburg, FL

From The Editor’s Desk

Reviews & Comments

• Autoimmune Growth Hormone Deficiency: Whittling Away at Some of the Idiopathics
• Final Height in Girls with Precocious Puberty Treated with GnRHa and Oxandrolone
• Germline KRAS, BRAF, and MAPK Mutations in Noonan and Cardio-Facio-Cutaneous-Syndrome
• Idiopathic Short Stature: Psychosocial Development and GH Treatment
• IGF-I During High-dose Growth Hormone Treatment of Children Born SGA
• Impaired Cognitive Function in Congential Adrenal Hyperplasia
• Imprinting, Transcription Factories, and Igf2 Regulation
• Treatment for Marfan Syndrome

E-Reviews & Comments

• Birth Length and Weight in Congenital Adrenal Hyperplasia
• Brain Function Regulation by SRY
• Brain Structure and Cognitive Deficits in Klinefelter’s Syndrome
• Congenital Contractures and Embryonic Myosin
• Diagnostic Imaging Modalities in Congenital Hypothyroidism
• Farnesylation in Experimental Progeria
• Growth Hormone Receptor, Calorie Restriction and Longevity in Mice
• Hippocampal Growth Hormone: Modulation by Estrogen and Stress
• Quality of Life and Mental Health in Adolescents Seeking Bariatric Surgery
• Sex Assignment: Attitudes and Practices of Pediatric Urologists

Number 2, June 2006 - Download pdf of entire issue

Feature Article

GROWTH HORMONE AND MORTALITY IN PRADER-WILLI SYNDROME
Phillip D.K. Lee, MD, FAAP, FACE

Reviews & Comments

• Defective Enzyme Degradation in Johanson-Blizzard Syndrome
• Endocrinological and Auxological Abnormalities in Children with Optic Nerve Hypoplasia: A Prospective Study
• Ghrelin Receptor Mutation: A Novel Pathogenic Mechanism of Growth Failure
• Growth Hormone Receptor Exon-3 and Response to Growth Hormone Treatment
• Growth Hormone Resistance in Noonan Syndrome: From Cause to Clinical Outcome
• IGF-I and IQ in Middle Childhood
• Obestatin Opposes Ghrelin’s Effects on Food Intake
• Signal Transduction and Cardio-Facial Syndromes

E-Reviews & Comments

• Fetal Thyroid Gland Monitoring in Graves Disease during Pregnancy
• Effects of GH Replacement in Adult GH Deficiency on Patient-Reported Outcomes and Cognitive Function: A Meta-Analysis
• Growth Hormone Treatment in Children with Rheumatic Disease, Corticosteroid Induced Growth Retardation, and Osteopenia
• Loss of Fibroblast Growth Factor Signaling Causes LADD Syndrome
• Neurodevelopmental Outcomes in Congenital Hypothyroidism
• Sclerosteosis/Sclerostin and Bone Mineral Density
• Steroids, Insulin and Ecdysome in Cell Growth
• Truth-telling and Turner Syndrome: The Importance of Diagnostic Disclosure

From the Editor’s Desk

Number 1, March 2006 - Download pdf of entire issue

Feature Article

GROWTH AND MINERALS: ZINC
Masayuki Kaji, MD and Yoshikazu Nishi, MD

Reviews & Comments

• Summary Highlights: ESPE and LWPES Joint Meeting
• Measured versus Reported Parental Height
• Apnea in Prader-Willi Syndrome Patients on Growth Hormone Therapy
• Suppression of Aging
• Motivations for GH/GnRHa Treatment and Psychosocial Functioning
• Efficacy of Growth Hormone During Transition from Adolescence to Adulthood in Patients with Growth Hormone Deficiency
• Pituitary GH-secretory Cells
• Genomic Alterations in Human Embryonic Stem Cells

E-Reviews & Comments

• Cardiovascular Effects in rhGH Treated GH Deficient Adults
• Children’s Vitilization by Testosterone Gel
• Defective Matrix Turnover Causes SEMD-Missouri
• Joint Mobility and Type 1 Diabetes Complications
• Nomenclature for Intersex
• RMRP is an Essential Cell Growth Regulator
• Silver-Russell Syndrome Epimutations
• X-Chromosome Inactivation and Autoimmune Thyroid Disease

From the Editor’s Desk

Last Updated: 6/12/2009

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