E
E. S. Roach
Researcher at Ohio State University
Publications - 42
Citations - 2461
E. S. Roach is an academic researcher from Ohio State University. The author has contributed to research in topics: Tuberous sclerosis & Magnetic resonance imaging. The author has an hindex of 17, co-authored 42 publications receiving 2387 citations. Previous affiliations of E. S. Roach include Wake Forest University & University of Texas Southwestern Medical Center.
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Tuberous Sclerosis Complex Consensus Conference: Revised Clinical Diagnostic Criteria
TL;DR: The clinical diagnostic criteria for tuberous sclerosis complex were simplified and revised to reflect both new clinical information and an improved understanding of the disorder derived from molecular genetic studies, which requires two or more distinct types of lesions.
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Tuberous Sclerosis Consensus Conference: Recommendations for Diagnostic Evaluation
TL;DR: Recommendations were made for diagnostic evaluation at the time of diagnosis, when testing helps both to establish the diagnosis and to identify potential complications, and suggestions for the use of diagnostic tests to identify family members who have tuberous sclerosis complex.
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Report of the Diagnostic Criteria Committee of the National Tuberous Sclerosis Association
TL;DR: The committee intends these criteria to be adaptable, susceptible to modification as data are collected by empiricism, and to make some assumptions about the specificity of lesions, assumptions which will need to be tested during the next decade.
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Cerebral Venous Sinus Thrombosis in Children : A Multicenter Cohort From the United States
TL;DR: It is concluded that cerebral venous thrombosis predominantly affects children younger than age 6 months and Mortality is high (25%) in neonatal cerebral venOUS thromBosis.
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A locus for paroxysmal kinesigenic dyskinesia maps to human chromosome 16.
TL;DR: A paroxysmal kinesigenic dyskinesia (PKD) locus lies within an 18 cM interval on 16p 11.2-q11.2, between D16S3100 and D 16S771, which could be caused by different mutations in the same gene or two distinct genes may lie within this region.