Thyroid Gland Development and Function
As is the case in all fields of medicine, developmental endocrinology is now being studied at the molecular level. In this volume world-class researchers review the advances of the past decade in the study of normal and abnormal organogenesis of the thyroid gland and of the ontogeny of its function. They describe human thyroid development and its defects with the help of genetic studies in mouse models. Genetic defects of thyroid hormone synthesis are covered and their clinical relevance debated. The important field of thyroid cancer in the context of spontaneous occurrence and as part of familial neoplasia syndromes is described in detail. Finally, the important problem of environmental iodine deficiency which has emerged as a global public health concern is addressed.
For the first time, a decade of work is presented in a concise and highly readable form. Offering valuable insight both for senior clinicians and graduate students, this publication will be of central interest to basic scientists involved in developmental biology as well as to pediatricians and endocrinologists dealing with patients with congenital disorders of thyroid function.
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Table of Contents
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1 - 14: Murine Models for the Study of Thyroid Gland DevelopmentByMario De Felice;Mario De FeliceaDipartimento di Biologia e Patologia Molecolare e Cellulare,Università Federico II, Napoli, eb IRGS, Biogem s.c.a r.l., Ariano Irpino (AV), ItaliaSearch for other works by this author on:Roberto Di LauroRoberto Di LauroaDipartimento di Biologia e Patologia Molecolare e Cellulare,Università Federico II, Napoli, eb IRGS, Biogem s.c.a r.l., Ariano Irpino (AV), ItaliaSearch for other works by this author on:
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15 - 28: Familial Forms of Thyroid DysgenesisByMireille Castanet;Mireille CastanetaPaediatric Endocrinology Unit and INSERM U845, Hôpital Necker-Enfants Malades andSearch for other works by this author on:Michel Polak;Michel PolakaPaediatric Endocrinology Unit and INSERM U845, Hôpital Necker-Enfants Malades andSearch for other works by this author on:Juliane LégerJuliane Légerb Paediatric Endocrinology Unit, Hôpital Robert Debré, Paris, FranceSearch for other works by this author on:
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29 - 42: Possible Non-Mendelian Mechanisms of Thyroid DysgenesisByJohnny Deladoëy;Johnny DeladoëyaEndocrinology Service and Research Center, Department of Pediatrics, Sainte-Justine Hospital, University of Montreal, Montreal, Que., Canada;Search for other works by this author on:Gilbert Vassart;Gilbert Vassartb Genetics Service, Erasme Hospital and Institute of Interdisciplinary Research (IRIBHM), Free University of Brussels (U.L.B.), Brussels, BelgiumSearch for other works by this author on:Guy Van VlietGuy Van VlietaEndocrinology Service and Research Center, Department of Pediatrics, Sainte-Justine Hospital, University of Montreal, Montreal, Que., Canada;Search for other works by this author on:
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43 - 61: Thyroid Imaging in ChildrenByCatherine Garel;Catherine GarelaDepartments of Paediatric Imaging andSearch for other works by this author on:Juliane LégerJuliane Légerb Paediatric Endocrinology, Hôpital Robert Debré, Assistance Publique-Hôpitaux de Paris, Paris, FranceSearch for other works by this author on:
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62 - 85: Clinical and Biological Consequences of Iodine Deficiency during PregnancyByDaniel GlinoerDaniel GlinoerDivision of Endocrinology, Department of Internal Medicine, Thyroid Investigation Clinic, University Hospital Saint Pierre, Brussels, BelgiumSearch for other works by this author on:
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86 - 98: Ontogenesis of Thyroid Function and Interactions with Maternal FunctionByM.J. Obregon;M.J. ObregonInstituto de Investigaciones Biomedicas, Centro mixto ‘Alberto Sols’ (CSIC-UAM),Madrid, SpainSearch for other works by this author on:R.M. Calvo;R.M. CalvoInstituto de Investigaciones Biomedicas, Centro mixto ‘Alberto Sols’ (CSIC-UAM),Madrid, SpainSearch for other works by this author on:F. Escobar del Rey;F. Escobar del ReyInstituto de Investigaciones Biomedicas, Centro mixto ‘Alberto Sols’ (CSIC-UAM),Madrid, SpainSearch for other works by this author on:G. Morreale de EscobarG. Morreale de EscobarInstituto de Investigaciones Biomedicas, Centro mixto ‘Alberto Sols’ (CSIC-UAM),Madrid, SpainSearch for other works by this author on:
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99 - 117: New Phenotypes in Thyroid Dyshormonogenesis: Hypothyroidism due to DUOX2 MutationsByJosé C. Moreno;José C. MorenoDepartment of Internal Medicine, Erasmus Medical Center, Erasmus University,Rotterdam, The NetherlandsSearch for other works by this author on:Theo J. VisserTheo J. VisserDepartment of Internal Medicine, Erasmus Medical Center, Erasmus University,Rotterdam, The NetherlandsSearch for other works by this author on:
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118 - 126: Thyroid Hormone Transporter DefectsByAnnette GrütersAnnette GrütersInstitute for Experimental Pediatric Endocrinology, Charité Children’s Hospital,Humboldt and Free University, Berlin, GermanySearch for other works by this author on:
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127 - 139: Novel Biological and Clinical Aspects of Thyroid Hormone MetabolismByAlexandra M. Dumitrescu;Alexandra M. DumitrescuaDepartments of Medicine andSearch for other works by this author on:Samuel RefetoffSamuel RefetoffaDepartments of Medicine andb Pediatrics andc Committee on Genetics, University of Chicago, Chicago, Ill., USASearch for other works by this author on:
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140 - 172: Papillary and Follicular Thyroid Cancers in ChildrenByVasyl Vasko;Vasyl VaskoaDepartment of Pediatrics, Uniformed Services University of the Health Sciences, Bethesda, Md.,Search for other works by this author on:Andrew J. Bauer;Andrew J. BaueraDepartment of Pediatrics, Uniformed Services University of the Health Sciences, Bethesda, Md.,b Department of Pediatrics, Walter Reed Army Medical Center, Washington, D.C.,Search for other works by this author on:R. Michael Tuttle;R. Michael Tuttlec Department of Endocrinology, Memorial Sloan Kettering Cancer Center, New York, N.Y., andSearch for other works by this author on:Gary L. FrancisGary L. Francisd Department of Pediatrics, Medical College of Virginia, Virginia Commonwealth University, Richmond, Va., USASearch for other works by this author on:
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173 - 187: Hereditary Medullary Thyroid Carcinoma: How Molecular Genetics Made Multiple Endocrine Neoplasia Type 2 a Paediatric DiseaseByGabor Szinnai;Gabor SzinnaiaPaediatric Endocrinology and INSERM U845 andc Paediatric Endocrinology, University Children’s Hospital Basel, Basel, SwitzerlandSearch for other works by this author on:Sabine Sarnacki;Sabine Sarnackib Paediatric Surgery, Hôpital Necker-Enfants Malades, Paris, France;Search for other works by this author on:Michel PolakMichel PolakaPaediatric Endocrinology and INSERM U845 andSearch for other works by this author on: