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Human Hypothalamus


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Table of Contents

Part I. Nuclei of the human hypothalamus: cytoarchitecture, chemoarchitecture, functional neuroanatomy, topographic neuropathology. 1. Introduction. 1.1 Anatomical borders of the hypothalamus. 1.2 Strategic research and structure-function relationships. 1.3 The autopsy and brain banking. 1.4 Confounding factors. 1.5 Parameters of neuronal metabolic activity in postmortem tissue. 1.6 Fetal hypothalamic development and adult markers of the human hypothalamic nuclei. 2. Nucleus basalis of Meynert (NBM) and diagonal band of Broca (DBB). 2.1 Anatomy. 2.2 Chemoarchitecture. 2.3 Alzheimer's disease. 2.4 Neuronal loss vs. atrophy. 2.5 Neurotrophin receptors in the NBM. 2.6 Other disorders affecting the NBM and DBB. 3. Islands of Calleja, insulae terminalis. 4. Suprachiasmatic nucleus (SCN) and pineal gland. 4.1 Circadian, seasonal, monthly and circaseptan rhythms in the SCN. 4.2 SCN development, birth and circadian rhythms. 4.3 Circadian and circannual rhythms in aging and Alzheimer's disease. 4.4 The SCN in relation to sex, reproduction and sexual orientation. 4.5 Melatonin and its receptors. 5. Sexually dimorphic nucleus of the preoptic area (SDN-POA) = intermediate nucleus = interstitial nucleus of the anterior hypothalamus (INAH-1) = preoptic nucleus. 5.1 Nomenclature and homology to the rat SDN-POA. 5.2 Development, sexual differentiation, aging and Alzheimer's disease. 6. Other sexual dimorphisms. 6.1. Interstitial nucleus of the anterior hypothalamus (INAH)-2 and -3. 6.2 Anterior commissure, the interthalamic adhesion, corpora mamillaria and the third ventricle. 6.3 Sex hormone receptor distribution. 7. Bed nucleus of the stria terminalis (BST) and the septum. 7.1 The BST. 7.2 Reversed sex differences in the BST in transsexuals. 7.3 The septum verum. 8. Supraoptic and paraventricular nucleus (SON, PVN). 8.1 The fetal SON, PVN in birth and development. 8.2 Colocalization of tyrosine-hydroxylase (TH) with oxytocin and vasopressin. 8.3 The SON and PVN in aging and Alzheimer's disease. 8.4 (a) Vasopressin secretion in various disorders: (b) Vasopressin administration in various disorders. 8.5 Corticotropin-releasing hormone (CRH) neurons in the PVN. 8.6 Thyrotropin-releasing hormone (TRH) neurons in the PVN. 8.7 Other neuroactive compounds in the SON, PVN and periventricular nucleus. 9. Ventromedial nucleus (VMN; nucleus of Cajal). 10. Dorsomedial nucleus (DMN). 11. Infundibular nucleus (arcuate nucleus), subventricular nucleus and median eminence. 12. Lateral tuberal nucleus (NTL). 12.1 Chemoarchitecture and function. 12.2 The NTL in neurodegenerative diseases. 13. Tuberomamillary complex. 13.1 Anatomy. 13.2 Neurodegenerative diseases and schizophrenia. 13.3 Posterior hypothalamic area. 14. Lateral hypothalamic area (LHA) and intermediate hypothalamic area (IHA). 15. Subthalamic nucleus and zona incerta. 15.1 Subthalamic nucleus. 15.2 Zona incerta. 16. Corpora mamillaria. References.

Promotional Information

This volume is part of the Handbook of Clinical Neurology series, the world's most comprehensive source of information in neurology. Now in its third generation, the series has an unparalleled reputation for providing the latest foundational research, diagnosis, and treatment protocols essential for both basic neuroscience research and clinical neurology.

About the Author

Dick Swaab (1944) earned his medical and doctoral degrees at the University of Amsterdam, where he became involved in brain research during his third year of medical school. He was Director of the Netherlands Institute for Brain Research from 1978 to 2005. Since 1979 he is Professor of Neurobiology at the Medical Faculty, University of Amsterdam. In 1985, Dr. Swaab founded the Netherlands Brain Bank (NBB) to serve as a source of clinically and neuropathologically well-documented research tissue. Since its founding, the Brain Bank has provided samples from more than 4,000 autopsies to 500 research groups in 25 countries. He was director of the NBB until 2005. He is Leader Research team Neuropsychiatric Disorders, Neth. Inst for Neuroscience, an institute of the Royal Netherlands Academy of Arts and Sciences (KNAW). Swaab is also appointed for 2011-2017 Chao Kuang Piu Chair of Zhejiang University, Hangzhou, P.R. China. His major research interests focus on, sexual differentiation of the human brain in relation to gender identity and sexual orientation, aging of the brain, Alzheimer's disease, the neurobiological basis of depression, suicide and eating disorders. He has published over 540 papers in SCI journals, authored more than 200 chapters in books, and edited more than 60 books. Swaab mentored 84 PhD students from which 16 are now full professor. He is "Companion in the Order of the Dutch Lion", bestowed by her Royal Majesty Queen Beatrix of the Netherlands. In 2008 Swaab obtained the Academy medal for his role in national and international neuroscience. Dick Swaab is author of the 2 volume monograph The Human Hypothalamus that appeared in the Handbook of Clinical Neurology series, Elsevier, Amsterdam (1000 pp) and the Dutch best seller We are our Brains (450.000 copies sold), that is translated in 14 languages. A children's version of the book (You are your brains) has also appeared in Dutch in 2013 and Russian (2014). Swaab's H-factor is 76.


'To many neuropathologists, the human hypothalamus may be nothing more than a few ml of neuroendocrine tissue that is all too often ignored or excluded from standard neuropathological examinations or brain maps. With the advent of the first two volumes of the third series of the "Handbook of Clinical neurology", Dick Swaab changes that perception permanently by compiling and reviewing simply everything there is to know about this structure in a 1,000-page monograph............If one book can change the traditional clinical perception of the hypothalamus as an evolutionary ancient, endocrine structure of little importance, this monograph will.' - Journal of Neuropathology and Experimental Neurology

'It is unusally rich in historical detail, and the illustrations are of exeptionally good quality' - Journal of Neuroendocrinology

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