Clinical Pediatric Endocrinology, Fifth Edition by Fima Lifshitz

By Fima Lifshitz

This re-creation of the benchmark textual content on scientific pediatric endocrinology nonetheless is still on the leading edge of global medical opinion. moreover, the fashion, which has been the hallmark of the e-book for the final two decades, has been maintained for this 5th Edition.

New positive aspects of this 5th variation include:


  • Special new chapters conceal the fetal origins of grownup illness and the
    endocrine results and administration of serious illness
  • Now opens with a easy technology part summarizing the mechanisms of hormone motion, genomics, proteomics and the appliance of molecular biology to medical practice
  • Two new co-editors were brought - Peter Clayton and Rosalind Brown
  • Every bankruptcy has been updated

Content:
Chapter 1 ideas of Hormone motion (pages 1–17): Melissa Westwood
Chapter 2 Genetics, Genomics, Proteomics, and Bioinformatics (pages 18–44): Peter Kopp
Chapter three Measuring Hormones, Molecular checks, and Their medical software (pages 45–66): Jan M. Wit and Marcel Karperien
Chapter four Congenital issues of the Hypothalamic?Pituitary Axis (pages 67–89): Ameeta Mehta and Mehul T. Dattani
Chapter five basic and Disordered progress (pages 90–112): Leena Patel and Peter E. Clayton
Chapter 6 Genetic Syndromes and Dysmorphology (pages 113–123): Jennifer Batch
Chapter 7 obtained Abnormalities of the Hypothalamic?Pituitary Axis resulting in development Impairment (pages 124–152): Dennis J. Brenner and Edward O. Reiter
Chapter eight improvement of the Reproductive platforms (pages 153–170): John C. Achermann
Chapter nine Ambiguous Genitalia (pages 171–182): Ieuan A. Hughes
Chapter 10 general and irregular Puberty (pages 183–210): Mehul T. Dattani and Peter C. Hindmarsh
Chapter eleven Gynecology (pages 211–217): Sarah M. Creighton
Chapter 12 The Thyroid and its issues (pages 218–253): Rosalind S. Brown and Stephen Huang
Chapter thirteen The Parathyroid and problems of Calcium Metabolism (pages 254–279): Jeremy Allgrove
Chapter 14 problems of Bone Metabolism (pages 280–292): Ingrid A. Holm
Chapter 15 The Adrenal Cortex and its problems (pages 293–351): Walter L. Miller
Chapter sixteen Polyglandular Syndromes (pages 352–366): Catherine J. Owen, Tim D. Cheetham and Simon H.S. Pearce
Chapter 17 problems of Water stability (pages 367–395): Rebecca P. eco-friendly, Joseph A. Majzoub and Louis J. Muglia
Chapter 18 Endocrine Programming and the Fetal and Early?Life Origins of grownup sickness (pages 396–409): Caroline H.D. Fall
Chapter 19 Weight legislation and Monogenic weight problems (pages 410–418): I. Sadaf Farooqi
Chapter 20 Metabolic effects of weight problems and Their administration (pages 419–435): Michael Freemark
Chapter 21 Diabetes Mellitus (pages 436–473): Andrew W. Norris and Joseph I. Wolfsdorf
Chapter 22 Hypoglycemia (pages 474–491): Khalid Hussain and Mark J. Dunne
Chapter 23 Endocrine outcomes of Systemic illness: severe sickness (pages 492–504): Greet Van Den Berghe
Chapter 24 outcomes of Radiotherapy, Chemotherapy, and Bone Marrow Transplant (pages 505–522): Helena A. Davies
Chapter 25 assessments and basic Values in Pediatric Endocrinology (pages 523–564): Lesley J. Tetlow and Peter E. Clayton

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Extra info for Clinical Pediatric Endocrinology, Fifth Edition

Sample text

Microarrays are being used clinically for mutational analysis of several human disease genes, for the identification of viral sequence variations, and for largescale analyses of transcripts. These techniques provide the foundation to expand from a focus on single genes to analyses at the scale of the genome. A variety of mass spectrometrybased techniques is emerging for high-throughput applications, such as sequencing, genotyping, and analyses of proteins and proteomes. Cloning of DNA Cloning refers to the isolation of a DNA fragment that can be propagated indefinitely.

Examples of mutations. The coding strand is shown with the encoded amino acid sequence in the one-letter code and the three-letter code. 2). The GH gene is a member of a large gene cluster that includes a growth hormone variant gene as well as several structurally related chorionic somatomammotrophin genes and pseudogenes, which are highly homologous but functionally inactive relatives of a normal gene. Because such gene clusters contain multiple homologous DNA sequences arranged along the same chromosome, they are particularly prone to undergo recombination and, consequently, gene duplication or deletion.

This generates extension products of variable length. The four dideoxynucleotides can be distinguished by using different fluorophores, and the sequence can be deciphered after gel or capillary electrophoresis. The computer generates a chromatogram for easy visualization of the sequence. Upper right: Digestion of DNA with restriction endonucleases. Restriction enzymes recognize specific sequences, usually palindromes of 4–6 bp. Cleavage of DNA with a particular enzyme digests the DNA into a characteristic collection of fragments.

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