Idioma: Inglés
Publicado por University of Georgia Press, 2010
ISBN 10: 0820328936 ISBN 13: 9780820328935
Librería: Greenway, Chattanooga, TN, Estados Unidos de America
EUR 39,81
Cantidad disponible: 1 disponibles
Añadir al carritohardcover. Condición: Very good condition. very clean,fast ship.
Librería: GreatBookPrices, Columbia, MD, Estados Unidos de America
EUR 13,45
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Añadir al carritoCondición: As New. Unread book in perfect condition.
Librería: GreatBookPrices, Columbia, MD, Estados Unidos de America
EUR 13,91
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Añadir al carritoCondición: New.
Idioma: Inglés
Publicado por Cambridge University Press, 2025
ISBN 10: 1009530372 ISBN 13: 9781009530378
Librería: California Books, Miami, FL, Estados Unidos de America
EUR 25,37
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Añadir al carritoCondición: New.
Idioma: Inglés
Publicado por Cambridge University Press, GB, 2025
ISBN 10: 1009530372 ISBN 13: 9781009530378
Librería: Rarewaves.com USA, London, LONDO, Reino Unido
EUR 30,43
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Añadir al carritoPaperback. Condición: New. SCN2A encodes a voltage-gated sodium channel (designated NaV1.2) vital for generating neuronal action potentials. Pathogenic SCN2A variants are associated with a diverse array of neurodevelopmental disorders featuring neonatal or infantile onset epilepsy, developmental delay, autism, intellectual disability and movement disorders. SCN2A is a high confidence risk gene for autism spectrum disorder and a commonly discovered cause of neonatal onset epilepsy. This remarkable clinical heterogeneity is mirrored by extensive allelic heterogeneity and complex genotype-phenotype relationships partially explained by divergent functional consequences of pathogenic variants. Emerging therapeutic strategies targeted to specific patterns of NaV1.2 dysfunction offer hope to improving the lives of individuals affected by SCN2A-related disorders. This Element provides a review of the clinical features, genetic basis, pathophysiology, pharmacology and treatment of these genetic conditions authored by leading experts in the field and accompanied by perspectives shared by affected families. This title is also available as Open Access on Cambridge Core.
Librería: GreatBookPricesUK, Woodford Green, Reino Unido
EUR 14,15
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Añadir al carritoCondición: New.
Librería: GreatBookPricesUK, Woodford Green, Reino Unido
EUR 16,80
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Añadir al carritoCondición: As New. Unread book in perfect condition.
Idioma: Inglés
Publicado por Cambridge University Press, 2025
ISBN 10: 1009530372 ISBN 13: 9781009530378
Librería: Ria Christie Collections, Uxbridge, Reino Unido
EUR 24,80
Cantidad disponible: 1 disponibles
Añadir al carritoCondición: New. In.
Idioma: Inglés
Publicado por Cambridge University Press -, 2025
ISBN 10: 1009530372 ISBN 13: 9781009530378
Librería: Chiron Media, Wallingford, Reino Unido
EUR 21,81
Cantidad disponible: 3 disponibles
Añadir al carritopaperback. Condición: New.
Idioma: Inglés
Publicado por Cambridge University Press, 2025
ISBN 10: 1009530372 ISBN 13: 9781009530378
Librería: Books Puddle, New York, NY, Estados Unidos de America
EUR 38,27
Cantidad disponible: 4 disponibles
Añadir al carritoCondición: New.
Idioma: Inglés
Publicado por Cambridge University Press, 2025
ISBN 10: 100953033X ISBN 13: 9781009530330
Librería: Revaluation Books, Exeter, Reino Unido
EUR 70,98
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Añadir al carritoHardcover. Condición: Brand New. 75 pages. 6.00x0.25x9.00 inches. In Stock. This item is printed on demand.
Idioma: Inglés
Publicado por Cambridge University Press, GB, 2025
ISBN 10: 1009530372 ISBN 13: 9781009530378
Librería: Rarewaves.com UK, London, Reino Unido
EUR 27,77
Cantidad disponible: Más de 20 disponibles
Añadir al carritoPaperback. Condición: New. SCN2A encodes a voltage-gated sodium channel (designated NaV1.2) vital for generating neuronal action potentials. Pathogenic SCN2A variants are associated with a diverse array of neurodevelopmental disorders featuring neonatal or infantile onset epilepsy, developmental delay, autism, intellectual disability and movement disorders. SCN2A is a high confidence risk gene for autism spectrum disorder and a commonly discovered cause of neonatal onset epilepsy. This remarkable clinical heterogeneity is mirrored by extensive allelic heterogeneity and complex genotype-phenotype relationships partially explained by divergent functional consequences of pathogenic variants. Emerging therapeutic strategies targeted to specific patterns of NaV1.2 dysfunction offer hope to improving the lives of individuals affected by SCN2A-related disorders. This Element provides a review of the clinical features, genetic basis, pathophysiology, pharmacology and treatment of these genetic conditions authored by leading experts in the field and accompanied by perspectives shared by affected families. This title is also available as Open Access on Cambridge Core.
Idioma: Inglés
Publicado por Cambridge University Press, 2025
ISBN 10: 1009530372 ISBN 13: 9781009530378
Librería: Revaluation Books, Exeter, Reino Unido
EUR 20,71
Cantidad disponible: 1 disponibles
Añadir al carritoPaperback. Condición: Brand New. 75 pages. 6.00x0.20x9.00 inches. In Stock. This item is printed on demand.
Idioma: Inglés
Publicado por Cambridge University Press, 2025
ISBN 10: 1009530372 ISBN 13: 9781009530378
Librería: Majestic Books, Hounslow, Reino Unido
EUR 36,13
Cantidad disponible: 4 disponibles
Añadir al carritoCondición: New. Print on Demand.
Idioma: Inglés
Publicado por Cambridge University Press, 2025
ISBN 10: 1009530372 ISBN 13: 9781009530378
Librería: Biblios, Frankfurt am main, HESSE, Alemania
EUR 37,76
Cantidad disponible: 4 disponibles
Añadir al carritoCondición: New. PRINT ON DEMAND.
Año de publicación: 2024
Librería: Gyan Books Pvt. Ltd., Delhi, India
EUR 30,21
Cantidad disponible: Más de 20 disponibles
Añadir al carritoLeather Bound. Condición: New. Language: English. Presenting an Exquisite Leather-Bound Edition, expertly crafted with Original Natural Leather that gracefully adorns the spine and corners. The allure continues with Golden Leaf Printing that adds a touch of elegance, while Hand Embossing on the rounded spine lends an artistic flair. This masterpiece has been meticulously reprinted in 2024, utilizing the invaluable guidance of the original edition published many years ago in 1915. The contents of this book are presented in classic black and white. Its durability is ensured through a meticulous sewing binding technique, enhancing its longevity. Imprinted on top-tier quality paper. A team of professionals has expertly processed each page, delicately preserving its content without alteration. Due to the vintage nature of these books, every page has been manually restored for legibility. However, in certain instances, occasional blurriness, missing segments, or faint black spots might persist. We sincerely hope for your understanding of the challenges we faced with these books. Recognizing their significance for readers seeking insight into our historical treasure, we've diligently restored and reissued them. Our intention is to offer this valuable resource once again. We eagerly await your feedback, hoping that you'll find it appealing and will generously share your thoughts and recommendations. Lang: - English, Pages: : - 264, Print on Demand. If it is a multi-volume set, then it is only a single volume. We are specialised in Customisation of books, if you wish to opt different color leather binding, you may contact us. This service is chargeable. Product Disclaimer: Kindly be informed that, owing to the inherent nature of leather as a natural material, minor discolorations or textural variations may be perceptible. Explore the FOLIO EDITION (12x19 Inches): Available Upon Request. 264.
Idioma: Inglés
Publicado por Cambridge University Press, 2025
ISBN 10: 1009530372 ISBN 13: 9781009530378
Librería: Books From California, Simi Valley, CA, Estados Unidos de America
EUR 11,83
Cantidad disponible: 4 disponibles
Añadir al carritopaperback. Condición: Very Good. Cover and edges may have some wear.