A
Aatif M. Husain
Researcher at Duke University
Publications - 148
Citations - 4454
Aatif M. Husain is an academic researcher from Duke University. The author has contributed to research in topics: Epilepsy & Medicine. The author has an hindex of 32, co-authored 124 publications receiving 3639 citations. Previous affiliations of Aatif M. Husain include United States Department of Veterans Affairs & Durham University.
Papers
More filters
Journal ArticleDOI
Consensus statement on continuous EEG in critically ill adults and children, part I: indications.
Susan T. Herman,Nicholas S. Abend,Thomas P. Bleck,Kevin E. Chapman,Frank W. Drislane,Ronald G. Emerson,Elizabeth E. Gerard,Cecil D. Hahn,Aatif M. Husain,Aatif M. Husain,Peter W. Kaplan,Suzette M. LaRoche,Marc R. Nuwer,Mark Quigg,James J. Riviello,Sarah E. Schmitt,Liberty A. Simmons,Tammy Tsuchida,Lawrence J. Hirsch +18 more
TL;DR: CCEEG has an important role in detection of secondary injuries such as seizures and ischemia in critically ill adults and children with altered mental status.
Journal ArticleDOI
American Clinical Neurophysiology Society's Standardized Critical Care EEG Terminology: 2021 Version.
Lawrence J. Hirsch,Michael W.K. Fong,Markus Leitinger,Suzette M. LaRoche,Sándor Beniczky,Nicholas S. Abend,Jong Woo Lee,Courtney J. Wusthoff,Cecil D. Hahn,M. Brandon Westover,Elizabeth E. Gerard,Susan T. Herman,Hiba A. Haider,Gamaleldin Osman,Andres Rodriguez-Ruiz,Carolina B. Maciel,Emily J. Gilmore,Andres Fernandez,Eric Rosenthal,Jan Claassen,Aatif M. Husain,Ji Yeoun Yoo,Elson L. So,Peter W. Kaplan,Marc R. Nuwer,Michel J.A.M. van Putten,Raoul Sutter,Frank W. Drislane,Eugen Trinka,Nicolas Gaspard +29 more
TL;DR: In the early 2000s, a subcommittee of the American Clinical Neurophysiology Society (ACNS) set out to standardize terminology of periodic and rhythmic EEG patterns in the critically ill to aid in future research involving such patterns as mentioned in this paper.
Book
Handbook of EEG Interpretation
TL;DR: This handbook is a highly useful tool for residents, fellows, clinicians, and neurophysiology technologists looking for quick and reliable EEG information, regardless of specialty or level of training.
Journal ArticleDOI
Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes.
Erin L. Heinzen,Rodney A. Radtke,Thomas J. Urban,Gianpiero L. Cavalleri,Chantal Depondt,Anna C. Need,Nicole M. Walley,Paola Nicoletti,Dongliang Ge,Claudia B. Catarino,John S. Duncan,Dalia Kasperaviciūte,Sarah K. Tate,Luis O. Caboclo,Josemir W. Sander,Lisa M. S. Clayton,Kristen N. Linney,Kevin V. Shianna,Curtis Gumbs,Jason Smith,Kenneth D. Cronin,Jessica M. Maia,Colin P. Doherty,Massimo Pandolfo,David Leppert,David Leppert,Lefkos T. Middleton,Rachel A. Gibson,Marvin Johnson,Marvin Johnson,Paul M. Matthews,Paul M. Matthews,David A. Hosford,Reetta Kälviäinen,Kai Eriksson,Anne-Mari Kantanen,Thomas Dorn,Jörg Hansen,Günter Krämer,Bernhard J. Steinhoff,Heinz Gregor Wieser,Dominik Zumsteg,Marcos Ortega,Nicholas W. Wood,Julie Huxley-Jones,Mohamad A. Mikati,William Gallentine,Aatif M. Husain,Patrick G. Buckley,Raymond L. Stallings,Mihai V. Podgoreanu,Norman Delanty,Sanjay M. Sisodiya,David Goldstein +53 more
TL;DR: Genome-wide screens to identify copy number variation in patients with a diverse spectrum of epilepsy syndromes and in neurologically-normal controls implicate 16p13.11 and possibly other large deletions as risk factors for a wide range of epilepsy disorders, and they appear to point toward haploinsufficiency as a contributor to the pathogenicity of deletions.
Predispose to a Diverse Spectrum of Sporadic Epilepsy Syndromes
Erin L. Heinzen,Rodney A. Radtke,Thomas J. Urban,Gianpiero L. Cavalleri,Chantal Depondt,Anna C. Need,Nicole M. Walley,Paola Nicoletti,Dongliang Ge,Claudia B. Catarino,John S. Duncan,Sarah K. Tate,Luís Otávio Sales Ferreira Caboclo,Josemir W. Sander,Kristen N. Linney,Kevin V. Shianna,Curtis Gumbs,Jason Smith,Kenneth D. Cronin,Jessica M. Maia,Colin P. Doherty,Massimo Pandolfo,David Leppert,Lefkos T. Middleton,Rachel A. Gibson,Marvin Johnson,Paul M. Matthews,Bernhard J. Steinhoff,Nicholas W. Wood,Mohamad A. Mikati,William Gallentine,Aatif M. Husain,Patrick G. Buckley,Raymond L. Stallings,Mihai V. Podgoreanu,Norman Delanty,Sanjay M. Sisodiya,David Goldstein +37 more
TL;DR: In this paper, the role of 16p13.11 deletions, as well as other structural variation, in epilepsy disorders, was evaluated using genome-wide screens to identify copy number variation in 3812 patients with a diverse spectrum of epilepsy syndromes and in 1299 neurologically normal controls.