04.26.2004

ENDOCRINE DISEASES

• Andrologic-Complete Urology and Andrology InfoBase
• Hypogonadism hypogonadotropic - DermIS Atlas
• Precocious Puberty Home Page
• Primary Hyperparathryoidism-Fact Sheet
• Precocious Puberty - facts sheets-Nat.Ins.Child Health & Hum.Dev
• PolyCystic Ovary Syndrome-Jewish Hospital
• Human Biological Database Interchange (Diabetes)
• Hypoglycaemia - fact sheet (Lecture)
• Intersex - fact sheet (Lecture)
• Normal Puberty And Pubertal Disorders - fact sheet (Lecture)
• Pituitary Gigantism-Images in Clinical Medicine
• Precocious Puberty in Boys-editorials (NEJM 1999)
• The Child With Ambiguous Genitalia - article 1999 (Medscape)
• Pseudohypoparathyroidism- Wheeless
• Dominantly inherited hyperinsulinism caused by a mutation in the sulfonylurea receptor type 1-article 2000

General Aspects

• The Ray Williams Institute of Paediatric Endocrinology Sydney, Australia
• Pediatrics Endocrine Lectures
• RWI Endocrine Testing Procedures Table of Contents
• Insulin-like growth factors-WWW
• Human Growth Foundation
• Child Growth Foundation-HomePage
• GENE CATALOG OF HUMAN GENES OF INTEREST IN ENDOCRINOLOGY AND REPRODUCTION

Acromegaly

• Acromegaly - NIDDK
• Acromegaly - MedNets

Adrenal Disease

• Adrenal Disease-Virtual Hospital
• Adrenal Disease - Family Practice Handbook
• Congenital Adrenal Hyperplasia
• Congenital adrenal hyperplasia - Pediatric Encyclopedia
• Congenital Adrenal Hyperplasia - fact sheet (Lecture)

Androgen Insensitivity Syndrome

• Androgen Insensitivity Syndrome-review by L Pinsky,MA Trifiro-GeneClinics1999
• A Novel Explanation for Resistance to Androgens-editorial 2000

Diabetes Mellitus

• Cellular mechanisms of insulin resistance-article 2000
• Signaling pathways in insulin action-art.by Pessin and Saltiel 2000
• The molecular and physiological basis of insulin resistance-art. by Saltiel 2000
• Birth weight and non-insulin dependent diabetes-art.by McCance et al. 2000
• Should we screen for gestational diabetes-art.by Soares et al. 1997
• Diabetes-a time for excitement and concern-edit. by Orchard 1998
• (Russian)-Новая классификация, диагностика сахарного диабета-статья
• the first positional cloning of a gene for type 2 diabetes-comments 2000
• A calpain-10 gene polymorphism is associated with reduced muscle mRNA levels and insulin resistance-article 2000
• New gene implicated in type 2 diabetes-news 10.07.00
• Diabetes - Human Biological Database Interchange
• Diabetes Mellitus - Handbook (Australia)
• Genetics of Diabetes - Human Biological Database Interchange
• Childhood Diabetes Mellitus - fact sheet (Lecture)
• C282Y mutation and type 2 diabetes-letter 2000
• Role of C282Y mutation in haemochromatosis gene in development of type 2 diabetes-article 2000

Obesity

• Melanocortin-4 receptor mutations are a frequent and heterogeneous cause of morbid obesity- art. by Vaisse et al. 2000
• Dominant and recessive inheritance of morbid obesity associated with melanocortin 4 receptor deficiency-art. byFarooqi et al.2000

Pseudohypoparathyroidism

• imprinting defect in pseudohypoparathyroidism type IB-article2000

Short Stature

• Welcome to LPA Online - Little People of America
• The Growth Hormone Deficiency
• Pediatrics-Short Stature-Virtual Hospital
• Pediatrics-Short Stature - Handbook online
• Child Growth Foundation-HomePage
• Growth Hormone Deficiency-minireview
• Growth Delay, Constitutional - NORD
• Growth Hormone Deficiency - NORD
• Growth And Disorders Of Growth - fact sheet (Lecture)
• Human Growth Foundation - WWW Home Page
• Little People of America-HomePage
• Short Stature Foundation - NORD (info)

Thyroid Disease

• Thyroid Foundation of Canada Home Page
• Thyroid Disease - Human Biological Database Interchange
• Thyroid Diseases - MEDLINEplus
• Thyroid Disorders in Children
• The Thyroid Foundation of America Home
• Hypothyroidism-Virtual Hospital
• Hypothyroidism - Univ Iowa Family Practice Handbook
• Hyperthyroidism & Thyrotoxicosis-minireview
• Congenital Hypothyroidism - fact sheet (Lecture)
• Congenital Hypothyoidism-minireview
• Genetics of Thyroid Disease-Human Biological Database Interchange
• Human Biological Database Interchange (Thyroid Diseases)
• Screening for Congenital Hypothyroidism-review