daniel weinberger (38 Ergebnisse)

Hardcover. Zustand: Very Good. No Jacket. May have limited writing in cover pages. Pages are unmarked. ~ ThriftBooks: Read More, Spend Less.

Hardcover. Zustand: Very Good. No Jacket. Former library book; May have limited writing in cover pages. Pages are unmarked. ~ ThriftBooks: Read More, Spend Less.

Zustand: Very Good. 1st Edition. Former library copy. Pages intact with possible writing/highlighting. Binding strong with minor wear. Dust jackets/supplements may not be included. Includes library markings. Stock photo provided. Product includes identifying sticker. Better World Books: Buy Books. Do Good.

Hardback. Zustand: Very Good. The book has been read, but is in excellent condition. Pages are intact and not marred by notes or highlighting. The spine remains undamaged.

Hardcover. Zustand: Very Good. The Genetics of Cognitive Neuroscience (Issues in Clinical and Cognitive Neuropsychology) This book is in very good condition and will be shipped within 24 hours of ordering. The cover may have some limited signs of wear but the pages are clean, intact and the spine remains undamaged. This book has clearly been well maintained and looked after thus far. Money back guarantee if you are not satisfied. See all our books here, order more than 1 book and get discounted shipping.

Hardcover. Zustand: Very Good. This book is in very good condition and will be shipped within 24 hours of ordering. The cover may have some limited signs of wear but the pages are clean, intact and the spine remains undamaged. This book has clearly been well maintained and looked after thus far. Money back guarantee if you are not satisfied. See all our books here, order more than 1 book and get discounted shipping.

Zustand: Muy bueno. : Esta obra es una referencia esencial y exhaustiva sobre la esquizofrenia, una de las enfermedades mentales más complejas y comunes que afectan a la humanidad. Editada por los renombrados psiquiatras Steven R. Hirsch y Daniel R. Weinberger, la segunda edición ofrece una visión actualizada que abarca desde los aspectos descriptivos y las causas de la enfermedad hasta los tratamientos físicos, psicológicos y sociales más recientes.El libro reúne contribuciones de expertos de Estados Unidos, Reino Unido y Europa, filtrando la vasta cantidad de investigación actual para ofrecer información de relevancia clínica. Incluye secciones sobre modelos orgánicos, estudios genéticos y estructurales, así como un capítulo novedoso que presenta la perspectiva del paciente, convirtiéndose en una herramienta indispensable tanto para psiquiatras en formación como para profesionales en ejercicio. EAN: 9780632063888 Tipo: Libros Categoría: Salud y Bienestar|Ciencias Título: Schizophrenia Autor: Steven R. Hirsch| Daniel R. Weinberger Editorial: Wiley-Blackwell Idioma: en Páginas: 768 Formato: tapa dura.

Zustand: Very Good. Pages intact with possible writing/highlighting. Binding strong with minor wear. Dust jackets/supplements may not be included. Stock photo provided. Product includes identifying sticker. Better World Books: Buy Books. Do Good.

Hardcover. Zustand: Good. Some bumping to the board edges and a previous owner's name on a label inside. Orders received by 3pm Sent from the UK that weekday in recyclable card packaging.

Hardcover. Zustand: New. No Jacket. 1st Edition. Cornell University Press, 1975. First edition. Hardbound. New, issued without dust jacket. Still in shrink wrap! A perfect unread copy. 1180 pages. Size: 6 1/2" x 9 1/2". [F5600].

Hardcover. Zustand: As New. 1st Edition.

Hardcover. Zustand: Good. No Jacket. Missing dust jacket; Pages can have notes/highlighting. Spine may show signs of wear. ~ ThriftBooks: Read More, Spend Less.

Zustand: Fair. This is an ex-library book and may have the usual library/used-book markings inside.This book has hardback covers. In fair condition, suitable as a study copy. No dust jacket. Please note the Image in this listing is a stock photo and may not match the covers of the actual item,850grams, ISBN:9781841842295.

Hardcover. Zustand: Fair. 3. Condition: Redelijk. Binding: Hardcover. Edition: 3. Year: 2011. Language: Engels. Description: Strak boek met sporen kaft. Schutblad vol geschreven verder schoon. Binnenwerk zeer goed. Enkele gebruik-/opslagsporen.

Zustand: New. This is a Brand-new US Edition. This Item may be shipped from US or any other country as we have multiple locations worldwide.

Zustand: New. This is a Brand-new US Edition. This Item may be shipped from US or any other country as we have multiple locations worldwide.

Zustand: New. pp. 400 114 Illus.

Zustand: Good. 4to., 130 pp., Very Good, Paper Wraps with sun-fading, staining, rubbing, & edge wear on covers; staining on edges of text block; shelf wear. Final Galley Proofs.

Zustand: New. This is a Brand-new US Edition. This Item may be shipped from US or any other country as we have multiple locations worldwide.

Zustand: New. In.

Gebunden. Zustand: New.

hardcover. Zustand: Very Good.

Hardcover. Zustand: Brand New. 1st edition. 170 pages. 10.12x6.89x0.59 inches. In Stock.

Hardback, 330x238mm, 144p, throughout colour illustrations, English/ Dutch (NL) edition . ISBN 9789085866947. Dit boek is gerealiseerd naar aanleiding van de installatie Daniel's Vision in het MAS voor de afdeling Leven en Dood. Over Goden en Mensen 0 g.

Zustand: New. In.

Zustand: New. In.

Taschenbuch. Zustand: Neu. N-Acetylaspartate | A Unique Neuronal Molecule in the Central Nervous System | John Moffett (u. a.) | Taschenbuch | xvii | Englisch | 2014 | Springer | EAN 9781489988881 | Verantwortliche Person für die EU: Springer Verlag GmbH, Tiergartenstr. 17, 69121 Heidelberg, juergen[dot]hartmann[at]springer[dot]com | Anbieter: preigu.

Zustand: New. In.

Buch. Zustand: Neu. Druck auf Anfrage Neuware - Printed after ordering - N-acetylaspartate, or NAA, is the acetylated form of the amino acid aspartate, and it is present exclusively in the nervous system. Indeed, NAA is one of the most highly concentrated chemicals found in the brain of humans and animals, and yet the functions served by this brain-specific metabolite remain elusive, and controversial. Despite the uncertainties surrounding the functions of NAA in the development and operation of the nervous system, this molecule has attracted the attention of researchers and clinicians for two distinct reasons. First, the acetyl proton on NAA gives off a very prominent signal in water-suppressed, proton magnetic resonance spectroscopy (MRS), which permits clinicians to monitor levels of NAA in the brains of patients in a non-invasive manner. Because NAA is found primarily in neurons, and because the levels in the brain have been found to change rapidly after injury, or slowly during neurodegenerative diseases, MRS has become a preferred method of analyzing nerve cell dysfunction and death without surgical intervention. The second reason that NAA has attracted attention in recent years is that a congenital genetic disorder of NAA metabolism has been found to be the cause of the neurodegenerative disorder known as Canavan's disease. Canavan's disease is an inherited leukodystrophy that involves myelination pathologies of cortical white matter, leading to death within 10 years of birth. The genetic mutation results in a defective enzyme that de-acetylates NAA in the brain, resulting in a significant rise in NAA levels in the brain and urine. This enzyme, known as aspartoacylase (ASPA), appears to be involved in the process of myelination, such that a defective enzyme results in a disruption of the myelination of nerve fibers during development. The purpose of this symposium is to bring together investigators from around the world who are interested in the study of NAA, and the roles it plays in neuronaldevelopment and functioning. It is hoped that bringing researchers and clinicians together in such a forum will facilitate rapid progress in this emerging field, and will help lead to discoveries that can alleviate the suffering caused by a deadly, inheritable infantile disease.

Taschenbuch. Zustand: Neu. Druck auf Anfrage Neuware - Printed after ordering - N-acetylaspartate, or NAA, is the acetylated form of the amino acid aspartate, and it is present exclusively in the nervous system. Indeed, NAA is one of the most highly concentrated chemicals found in the brain of humans and animals, and yet the functions served by this brain-specific metabolite remain elusive, and controversial. Despite the uncertainties surrounding the functions of NAA in the development and operation of the nervous system, this molecule has attracted the attention of researchers and clinicians for two distinct reasons. First, the acetyl proton on NAA gives off a very prominent signal in water-suppressed, proton magnetic resonance spectroscopy (MRS), which permits clinicians to monitor levels of NAA in the brains of patients in a non-invasive manner. Because NAA is found primarily in neurons, and because the levels in the brain have been found to change rapidly after injury, or slowly during neurodegenerative diseases, MRS has become a preferred method of analyzing nerve cell dysfunction and death without surgical intervention. The second reason that NAA has attracted attention in recent years is that a congenital genetic disorder of NAA metabolism has been found to be the cause of the neurodegenerative disorder known as Canavan's disease. Canavan's disease is an inherited leukodystrophy that involves myelination pathologies of cortical white matter, leading to death within 10 years of birth. The genetic mutation results in a defective enzyme that de-acetylates NAA in the brain, resulting in a significant rise in NAA levels in the brain and urine. This enzyme, known as aspartoacylase (ASPA), appears to be involved in the process of myelination, such that a defective enzyme results in a disruption of the myelination of nerve fibers during development. The purpose of this symposium is to bring together investigators from around the world who are interested in the study of NAA, and the roles it plays in neuronaldevelopment and functioning. It is hoped that bringing researchers and clinicians together in such a forum will facilitate rapid progress in this emerging field, and will help lead to discoveries that can alleviate the suffering caused by a deadly, inheritable infantile disease.