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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 (Elements in Genetics in Epilepsy)
Language: English
Published by Cambridge University Press, 2025
ISBN 10: 1009530372 ISBN 13: 9781009530378
Condition: New.
-
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
US$ 31.73
Free Shipping
Ships from United Kingdom to U.S.A.Quantity: Over 20 available
Add to basketPaperback. 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 CUP, 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
Seller: Ria Christie Collections, Uxbridge, United Kingdom
Seller rating 5 out of 5 stars
US$ 29.85
US$ 16.10 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 (Elements in Genetics in Epilepsy)
Language: English
Published by Cambridge University Press -, 2025
ISBN 10: 1009530372 ISBN 13: 9781009530378
US$ 25.56
US$ 20.82 shipping
Ships from United Kingdom to U.S.A.Quantity: 3 available
Add to basketpaperback. Condition: New.
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Hardcover. Condition: VG. 1st Edition. 259pp, black cloth with gilt title at spine, light general wear, bookplate at front pastedown, minor toning at pastedowns, in lightly worn and soiled dust jacket, with minor, shallow chipping at spine ends and the ends of the folds, now housed in protective Brodart. A novel from the Kentucky author. From the dust jacket, "Agatha -- is she the gentle, kind, warm-hearted person she purports to be? Or is she a voracious, deceitful opportunist who uses the three men in her life to achieve her own selfish ends?" Includes an obituary notice from the author's passing in 2013 at the age of 99. Very scarce, with Worldcat locating but three copies.
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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
US$ 83.89
US$ 16.10 shipping
Ships from United Kingdom to U.S.A.Quantity: Over 20 available
Add to basketCondition: New. In.
-
SCN2A - Related Disorders (Elements in Genetics in Epilepsy)
Language: English
Published by Cambridge University Press, 2025
ISBN 10: 100953033X ISBN 13: 9781009530330
Seller: Kennys Bookshop and Art Galleries Ltd., Galway, GY, Ireland
Seller rating 5 out of 5 stars
Condition: New.
-
SCN2A-Related Disorders
Language: English
Published by Cambridge University Press, GB, 2025
ISBN 10: 1009530372 ISBN 13: 9781009530378
US$ 29.55
US$ 87.36 shipping
Ships from United Kingdom to U.S.A.Quantity: Over 20 available
Add to basketPaperback. 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.
-
SCN2A-Related Disorders (Elements in Genetics in Epilepsy)
Language: English
Published by Cambridge University Press, 2025
ISBN 10: 100953033X ISBN 13: 9781009530330
Condition: New.
-
SCN2A - Related Disorders (Elements in Genetics in Epilepsy)
Language: English
Published by Cambridge University Press, 2025
ISBN 10: 100953033X ISBN 13: 9781009530330
Condition: New.
-
Hardcover. Condition: Very Good +. fILTER (signed and numbered) edited and conceived by Jennifer Foster. A hand made, hardcover magazine. Poetry by Foster, G.C. Waldrep, Joshua Beckman, Arlana Kelly, John Olson, Linden Ontjes, Christine Deavel, Rebecca Hoogs, Monica Fambrough, Christine Hume, Susan Parr, Melanie Noel, Tyler Gaston, Isabel Ducharme. Art work by Elizabeth Bisegna Gaston, Elsa Thiemann, Jennifer Zwick, Elizabeth Jameson. Unpaginated, hardcover, tipped-in artworks in color and black and white. 7 1/4" x 7 1/4". Number 147 in an edition of 200. Signed by Jennifer Foster. Some rubbing to the cover otherwise very good + condition.
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SCN2A-Related Disorders
Language: English
Published by Cambridge University Press, 2025
ISBN 10: 1009530372 ISBN 13: 9781009530378
US$ 24.27
US$ 13.44 shipping
Ships from United Kingdom to U.S.A.Quantity: 1 available
Add to basketPaperback. 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
US$ 83.20
US$ 13.44 shipping
Ships from United Kingdom to U.S.A.Quantity: 1 available
Add to basketHardcover. Condition: Brand New. 75 pages. 6.00x0.25x9.00 inches. In Stock. This item is printed on demand.
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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
US$ 116.24
US$ 8.74 shipping
Ships from United Kingdom to U.S.A.Quantity: 4 available
Add to basketCondition: New. Print on Demand.
-
SCN2A-Related Disorders (Elements in Genetics in Epilepsy)
Language: English
Published by Cambridge University Press, 2025
ISBN 10: 100953033X ISBN 13: 9781009530330
Condition: New. PRINT ON DEMAND.
