Results 31 to 40 of about 118,175 (273)

Novel Actin and Cofilin Aggregations in Juvenile-Onset Dystonia

open access: yesPediatric Neurology Briefs, 2002
The brains of identical twins with juvenile-onset dystonia were examined at Emory University, Atlanta, Georgia.
J Gordon Millichap
doaj   +1 more source

Phenotypic Diversity and Outcomes in Pediatric NMDA Receptor Encephalitis: A 15‐Year Retrospective Study from the Largest Children's Hospital in the United States

open access: yesAdvanced Science, EarlyView.
ABSTRACT Anti‐NMDAR encephalitis (NMDARE) is an autoantibody‐mediated disorder characterized by seizures, movement disorders, neurocognitive deficits, and psychosis, but the complete phenotypic heterogeneity, and outcomes are incompletely understood in children.
Alexander J. Sandweiss   +9 more
wiley   +1 more source

Review of The Bluestocking Archive, Emory Women Writers Resource Project, and Women’s Travel Writing, 1780-1840: A Bio-Bibliographical Database

open access: yesABO : Interactive Journal for Women in the Arts 1640-1830, 2016
Review of The Bluestocking Archive, Emory Women Writers Resource Project, and Women's Travel Writing 1780-1840.
Megan Peiser
doaj   +1 more source

Wrinkle‐Adaptive Kirigami Wearables With Anisotropic Deformability for Sleep EEG Monitoring

open access: yesAdvanced Science, EarlyView.
This article introduces a wrinkle‐adaptive, kirigami‐structured wearable EEG patch that personalizes electrode‐skin conformity to stabilize the interface and enable wireless, high‐quality sleep monitoring. ABSTRACT Wearable electroencephalography (EEG) devices offer a promising solution for continuous brain monitoring outside laboratory settings ...
Jungmin Kim   +5 more
wiley   +1 more source

In Memoriam: JQ Johnson

open access: yesJournal of Librarianship and Scholarly Communication, 2012
I first met JQ Johnson in person at the Frye Leadership Institute, held at Emory University in the summer of 2008. Frye, at that point, was an intensive two week experience that brought together 47 librarians and information and educational technology ...
Deborah Barreau
doaj   +2 more sources

Authorship in Africana Studies

open access: yesSouthern Spaces, 2015
Joan Anim-Addo, Arturo Lindsay, Robert F. Reid-Pharr, and Martha Southgate discuss authority and authorship in Africana Studies at the 2014 Callaloo Conference. For a print version of some conference materials, see Callaloo 38, no. 3 (Summer 2015).
Joan Anim-Addo   +3 more
doaj   +1 more source

A Population‐Based Assessment of Cancer Risk in Children With VACTERL

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Cancer risk in children with VACTERL, a nonrandom co‐occurrence of ≥ 3 defects (vertebral, anal, cardiac, tracheoesophogeal fistula, renal, and limb), remains unclear. We evaluated this association in a population‐based study. We analyzed data from the Genetic Overlap Between Anomalies and Cancer in Kids (GOBACK) Study, a US registry linkage ...
Ji Yun Tark   +15 more
wiley   +1 more source

Integrating Authentic Research Into the Emory-Tibet Science Initiative

open access: yesFrontiers in Communication, 2022
We are at a historic point in which scientists and Tibetan monastics are working together to investigate ancient questions of mind and matter, and to serve the best interests of humanity.
Robin Nusslock   +4 more
doaj   +1 more source

Rationale of New Grading System: Central Compartment Atopic Disease

open access: yesInternational Forum of Allergy &Rhinology, EarlyView.
ABSTRACT Background Central compartment atopic disease (CCAD) has recently been recognized as a distinct phenotype within the spectrum of type 2–dominant chronic rhinosinusitis (CRS). Although international guidelines highlight polypoid changes in the central nasal cavity, standardized diagnostic and classification criteria are still lacking.
Ramón Moreno‐Luna   +11 more
wiley   +1 more source

Individualized Atrophy‐Based Prediction of Dementia Progression in Familial Frontotemporal Lobar Degeneration With Bayesian Linear Mixed‐Effects Modeling

open access: yesAnnals of Neurology, EarlyView.
Objective Age of symptom onset is highly variable in familial frontotemporal lobar degeneration (f‐FTLD). Accurate prediction of onset would inform clinical management and trial enrollment. Prior studies indicate that individualized maps of brain atrophy can predict conversion to dementia in f‐FTLD.
Shubir Dutt   +82 more
wiley   +1 more source

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