Stuart Handwerger, MD and a distinguished panel of clinicians and experts review the most significant recent developments in molecular and cellular biology, powerful advances that have produced new diagnostic methods and improved treatments for many pediatric endocrine diseases. Topics range from the growth hormone/prolactin/placental lactogen gene family and their regulation of growth, to steroid hormones, sexual development, and mineral corticoid action. Additional chapters examine the pathophysiology of insulin-dependent diabetes mellitus, the molecular genetics of thyroid cancer, the molecular basis of hypophosphatemic rickets, and inherited diabetes insipidus. Molecular and Cellular Pediatric Endocrinology offers today's clinicians and researchers not only the latest findings on endocrine diseases in their pediatric manifestations, but also highly practical insights into today's cutting-edge diagnostics, treatment strategies, and powerful new therapeutics.

"Pescovitz and Eugster, both affiliated with the Section for Pediatric Endocrinology/Diabetology at Indiana University School of Medicine, provide essential information on the mechanisms, diagnosis, and management of pediatric endocrine disorders. Aspects of human development and physiology are combined with information on etiology, diagnosis, and treatment. Within each of the traditional endocrine systems, contemporary molecular genetics and developmental endocrinology are presented, followed by material on specific clinical disorders and therapeutic strategies. Interspersed throughout the book are chapters devoted to emerging issues such as childhood obesity, short stature, and treatment of children with disorders of sexual differentiation. B&w photos and diagnostic images are included. Annotation : 2004 Book News, Inc., Portland, OR (booknews.com)"--[source inconnue].

Celebrating more than twenty years as the single best source in the field, this Fifth Edition has now expanded into two cornerstone volumes with 53 fully inclusive chapters and 73 renowned contributors that comprehensively address every topic and trend relevant to the identification, diagnosis, and management of endocrine and endocrine-related diso

Completely updated, the new edition of this easy-to-reference text examines the physiological, biochemical, and genetic aspects of pediatric endocrine disorders. Leaders in the field discuss the hottest topics-including genetics, diabetes and obesity-impacting today’s endocrine practice, keeping you up to date. A user-friendly organization speeds you to the information you need, and conceptual illustrations and photographs depict the latest advances with consistency and clarity. It’s the guidance you need to provide effective, state-of-the-art care for your pediatric and neonatal patients. Examines the physiological, biochemical, and genetic aspects of endocrine disorders all in one convenient reference. Incorporates the importance of molecular biology as it relates to developmental and pediatric endocrinology. Offers expanded coverage of genetics, diabetes and obesity-topics of increasing concern in pediatric endocrinology today. Presents the work of many new contributors for fresh perspectives on the current state of pediatric endocrinology. Provides new tables of normal values and growth charts for monitoring your patients’ progress. Concepts, Endocrine Disorders of the Newborn, Endocrine Disorders of Childhood and Adolescence, and Laboratory Tests and Imaging-making the material easy to navigate.

Celebrating more than twenty years as the single best source in the field, this Fifth Edition has now expanded into two cornerstone volumes with 53 fully inclusive chapters and 73 renowned contributors that comprehensively address every topic and trend relevant to the identification, diagnosis, and management of endocrine and endocrin

This first edition of Principles and Practice of Pediatric Endocrinology brings together 30 authors from 4 countries to present an update on the molecular basis of endocrine disorders in infants, children and adolescents as well as the diagnosis and treatment of these conditions. It is intended for the use of practitioners, fellows and clinical and “bench-top” researchers in this field, and presents advances in each of 12 areas of the normal and abnormal endocrine state. The work is a tribute to all those past and present whose research and clinical efforts resulted in the rapidly increasing accumulation of knowledge in this field, and includes comprehensive, practical clinical presentations in the form of an Atlas following each chapter after the comprehensive introductory chapter by Drs. Root and Rogol. This publication owes a great debt to Lawson Wilkins, a Baltimore pediatrician who first formally established the separate discipline of pediatric endocrinology, to Edwards Park, Fuller Albright, Bob Blizzard, Claude Migeon, Harold and Helen Harrison, James Tanner and to so many others: giants upon whose shoulders pediatric endocrinologists stand. Disorders of growth and pubertal development are the cornerstones of pediatrics as they are present in many children with chronic illness as well as in children whose growth and pubertal development are influenced by genetics and family history. These may have identifiable causes in pituitary, thyroid, adrenal or gonadal function, and examples are well represented in this book. Obesity and diabetes (types I and 2) are, likewise, diseases of childhood that are becoming increasingly and significantly prevalent and are included in this work. Disorders of calcium/phosphorus (especially the often forgotten but not gone Vitamin D deficiency rickets) and water metabolism are presented, and errors of sexual differentiation (an increasingly controversial issue) are highlighted. It is the hope of the editors that this work will assist the practitioner and researcher in this field in his or her efforts to diagnose, treat and establish the etiology of endocrine disorders in infants, children and adolescents.

It is an authentic privilege to have the opportunity to assemble and edit a new volume on "Prolactin," the first in several decades to be devoted to this fascinating hormone in all its aspects. The obvious clinical rationale for understanding prolactin (PRL) is the frequent occurrence of prolactinomas, the most common type of pituitary tumor. Fortunately, medical management of prolactinomas can be based on our under standing of the physiology of hypothalamic control of the lactotroph. Armed with this knowledge, therapies for proiactinomas are highly successful and well tolerated. Be cause of the historical and practical importance of knowledge regarding the hypothala mus-Iactotroph axis, the first chapters of this volume are dedicated to reviewing the physiology, development, and cell biology of lactotroph regulation. Chapters focusing on prolactinomas and related clinical issues follow these. PRL is the primary hormone that is responsible for "parental care" in many verte brate species. This reproductive strategy is not unique to mammals, but it has devel oped through evolution to be the central distinguishing feature of the mammalian life cycle. Among the mammals, mice have become the most effective research species in recent years. This can be traced to the development of a wide range of methods for manipulating mouse genetics, and thereby influencing development, physiology and behavior. Mice also provide a profound illustration of the physiological challenges faced in maternity. Female mice undergo a post-partum estrous, and often are both pregnant and lactating simultaneously.