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Step-by-Step Problem Solving, Grade 4
Book 1 of 4: Step-by-Step Problem SolvingLanguage: English
Published by Frank Schaffer Publications, 2012
ISBN 10: 1609964799 ISBN 13: 9781609964795
Seller: WorldofBooks, Goring-By-Sea, WS, United Kingdom
Seller rating 5 out of 5 stars
Paperback. Condition: 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.
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SCN2A-Related Disorders (Elements in Genetics in Epilepsy)
Language: English
Published by Cambridge University Press, 2025
ISBN 10: 1009530372 ISBN 13: 9781009530378
Seller: Books From California, Simi Valley, CA, U.S.A.
Seller rating 4 out of 5 stars
paperback. Condition: Very Good. Cover and edges may have some wear.
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Scn2a-related Disorders
Language: English
Published by Cambridge University Press, 2025
ISBN 10: 1009530372 ISBN 13: 9781009530378
Condition: New.
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SCN2A-Related Disorders (Elements in Genetics in Epilepsy)
Language: English
Published by Cambridge University Press, 2025
ISBN 10: 1009530372 ISBN 13: 9781009530378
Condition: New.
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Scn2a-related Disorders
Language: English
Published by Cambridge University Press, 2025
ISBN 10: 1009530372 ISBN 13: 9781009530378
Condition: As New. Unread book in perfect condition.
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SCN2A-Related Disorders
Language: English
Published by Cambridge University Press, GB, 2025
ISBN 10: 1009530372 ISBN 13: 9781009530378
Seller: Rarewaves.com USA, London, LONDO, United Kingdom
Seller rating 5 out of 5 stars
Paperback. Condition: 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.
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SCN2A-Related Disorders (Elements in Genetics in Epilepsy)
Language: English
Published by Cambridge University Press, 2025
ISBN 10: 1009530372 ISBN 13: 9781009530378
Condition: New.
-
SCN2A-Related Disorders (Elements in Genetics in Epilepsy)
Language: English
Published by Cambridge University Press, 2025
ISBN 10: 1009530372 ISBN 13: 9781009530378
Condition: New.
-
SCN2A-Related Disorders (Elements in Genetics in Epilepsy)
Language: English
Published by Cambridge University Press, 2025
ISBN 10: 1009530372 ISBN 13: 9781009530378
Condition: New.
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SCN2A-Related Disorders (Elements in Genetics in Epilepsy)
Language: English
Published by Cambridge University Press -, 2025
ISBN 10: 1009530372 ISBN 13: 9781009530378
paperback. Condition: New.
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SCN2A-Related Disorders (Elements in Genetics in Epilepsy)
Language: English
Published by Cambridge University Press, 2025
ISBN 10: 1009530372 ISBN 13: 9781009530378
Seller: Ria Christie Collections, Uxbridge, United Kingdom
Seller rating 5 out of 5 stars
£ 21.20
£ 11.98 shipping
Ships from United Kingdom to U.S.A.Quantity: Over 20 available
Add to basketCondition: New. In.
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Scn2a-related Disorders
Language: English
Published by Cambridge University Press, 2025
ISBN 10: 1009530372 ISBN 13: 9781009530378
Seller: GreatBookPricesUK, Woodford Green, United Kingdom
Seller rating 5 out of 5 stars
Condition: New.
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Scn2a-related Disorders
Language: English
Published by Cambridge University Press, 2025
ISBN 10: 1009530372 ISBN 13: 9781009530378
Seller: GreatBookPricesUK, Woodford Green, United Kingdom
Seller rating 5 out of 5 stars
Condition: As New. Unread book in perfect condition.
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Players Guide For Changeling: The Dreaming
Language: English
Published by White Wolf Publishing, Inc., Clarkston, CA, 1996
ISBN 10: 156504701X ISBN 13: 9781565047013
Seller: George Strange's Bookmart, Brandon, MB, Canada
Seller rating 5 out of 5 stars
Soft cover. Condition: Near Fine. Beel, Stuart P.; Diterlizzi, Tony; Fields, Lee; Fooden, Dave; Jackson, Mark; LeBlanc, Brian; Kudelka, Andrew; McKinney, Heather; Rex, Adam; Timbrook, Joshua Gabriel; Tucker, Drew (illustrator). 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.*.
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SCN2A-Related Disorders (Elements in Genetics in Epilepsy)
Language: English
Published by Cambridge University Press, 2025
ISBN 10: 100953033X ISBN 13: 9781009530330
Seller: Ria Christie Collections, Uxbridge, United Kingdom
Seller rating 5 out of 5 stars
£ 59.63
£ 11.98 shipping
Ships from United Kingdom to U.S.A.Quantity: Over 20 available
Add to basketCondition: New. In.
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Big Rock Candy Mountain
Published by P B T Publishing House/Thomas House Publications, 1992
First Edition
Hardcover. Condition: Used - Very Good. 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.
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Paperback. Condition: Brand New. 425 pages. 9.00x6.00x1.00 inches. In Stock.
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SCN2A-Related Disorders
Language: English
Published by Cambridge University Press, GB, 2025
ISBN 10: 1009530372 ISBN 13: 9781009530378
Paperback. Condition: 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.
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SCN2A-Related Disorders
Language: English
Published by Cambridge University Press, 2025
ISBN 10: 1009530372 ISBN 13: 9781009530378
Paperback. Condition: Brand New. 75 pages. 6.00x0.20x9.00 inches. In Stock. This item is printed on demand.
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SCN2A-Related Disorders
Language: English
Published by Cambridge University Press, 2025
ISBN 10: 100953033X ISBN 13: 9781009530330
Hardcover. Condition: Brand New. 75 pages. 6.00x0.25x9.00 inches. In Stock. This item is printed on demand.
