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 titl
ABBOTT, MEGAN (UNIVERSITY OF COLORADO SCHOOL OF MEDICINE),BENDER, KEVIN J. (UNIVERSITY OF CALIFORNIA, SAN FRANCISCO),BRUNKLAUS, ANDREAS (ROYAL HOSPITAL FOR CHILDREN AND UNIVERSITY OF GLASGOW),DEMAREST, SCOTT (UNIVERSITY OF COLORADO SCHOOL OF MEDICINE),EGAN, SHAWN (FAMILIESCN2A FOUNDATION),HAVILAND, ISABEL (BOSTON CHILDREN’S HOSPITAL AND HARVARD MEDICAL SCHOOL),KEARNEY, JENNIFER A. (NORTHWESTERN UNIVERSITY FEINBERG SCHOOL OF MEDICINE),SCHUST MYERS, LEAH (FAMILIESCN2A FOUNDATION),OLSON, HEATHER E. (BOSTON CHILDREN'S HOSPITAL AND HARVARD MEDICAL SCHOOL)
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 titl
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9781009530378Mladinska knjiga ID
9781009530378Leto izida
2025Datum izida
02.01.2025Število strani
96Status dobavljivosti
7-10 delovnih dniZbirka
Elements in Genetics in EpilepsyZaložnik
Cambridge University PressAvtor
Abbott, Megan (University of Colorado School of Medicine),Bender, Kevin J. (University of California, San Francisco),Brunklaus, Andreas (Royal Hospital for Children and University of Glasgow),Demarest, Scott (University of Colorado School of Medicine),Egan, Shawn (FamilieSCN2A Foundation),Haviland, Isabel (Boston Children’s Hospital and Harvard Medical School),Kearney, Jennifer A. (Northwestern University Feinberg School of Medicine),Schust Myers, Leah (FamilieSCN2A Foundation),Olson, Heather E. (Boston Children's Hospital and Harvard Medical School)Urednik
GEORGE, JR., ALFRED L. (NORTHWESTERN UNIVERSITY FEINBERG SCHOOL OF MEDICINE)Dimenzije
228 x 152 x 8BIC
MJNOpis
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.Pogosto kupljeno skupaj
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