Stephan heather (22 risultati)

paperback. Condizione: Very Good. Connecting readers with great books since 1972! Used books may not include companion materials, and may have some shelf wear or limited writing. We ship orders daily and Customer Service is our top priority.

paperback. Condizione: Good.

paperback. Condizione: Good. Most items will be dispatched the same or the next working day. A copy that has been read but remains in clean condition. All of the pages are intact and the cover is intact and the spine may show signs of wear. The book may have minor markings which are not specifically mentioned.…

Paperback. Condizione: 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.

Paperback. Condizione: Good. Stephen is a little kid with big dreams of playing football. The odds are against him when he is tested and faced with challenges. This is a story of a boy who worked hard to defy the odds and become a leader. Heyworth, Heather (illustratore).

paperback. Condizione: Very Good. Cover and edges may have some wear.

Condizione: New.

Paperback. Condizione: 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.…

Condizione: As New. Unread book in perfect condition.

Condizione: New.

Condizione: As New. Unread book in perfect condition.

Soft cover. Condizione: Near Fine. Bructo, Phil; Cassada, Jackie; Dansky, Richard: Hatshorn, Jennifer; Hatch, Robert; Herman, Stephan; Howard, Chris; Lemke, Ian; McCoy, Angel; Mick, Neil; Rea, Nicky PLAYERS GUIDE FOR CHANGELING: THE DREAMING Clarkston, CA: White Wolf Publishing, Inc. 1996 NF 190pp. 4to. Cover does show some shelf wear with light wear and bumping along the edges. There is a small tear at the top of the spine on the front cover. Text is clean and colours are bright. Binding has loosened inside the front cover but remains strong throughout the book. Overall book is in near fine condition and has lasted very well. *This book is oversized and may require extra shipping charges.*. Beel, Stuart P.; Diterlizzi, Tony; Fields, Lee; Fooden, Dave; Jackson, Mark; LeBlanc, Brian; Kudelka, Andrew; McKinney, Heather; Rex, Adam; Timbrook, Joshua Gabriel; Tucker, Drew (illustratore). …

paperback. Condizione: As New.

Condizione: New. In English.

Paperback. Condizione: Brand New. 425 pages. 9.00x6.00x1.00 inches. In Stock.

Condizione: New.

Hardcover. Condizione: Used - Very Good. Condizione sovraccoperta: No jacket, as issued. First Edition. Limited edition of 100 copies; Brown fabric over boards with gilt stamped text on spine and cover. Minor scuffing to covers, corners square, book block clean, square and tight.

Paperback. Condizione: 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.…

Condizione: New.

Condizione: New.

Condizione: New. Print on Demand.

Condizione: New. PRINT ON DEMAND.