Zobrazeno 1 - 10
of 322
pro vyhledávání: '"E S, Roach"'
Autor:
Cynthia L. Coulter, Richard W. Leech
Publikováno v:
Journal of Child Neurology. 5:262-263
Autor:
Coulter, Cynthia L., Leech, Richard W.
Publikováno v:
Journal of Child Neurology; July 1990, Vol. 5 Issue: 3 p262-263, 2p
Autor:
Chung, Clara W. T.1,2,3 (AUTHOR) c.w.chung@unsw.edu.au, Bournazos, Adam M.4,5,6 (AUTHOR), Chan, Lok Chi Denise2,3 (AUTHOR), Sarkozy, Vanessa2,3 (AUTHOR), Lawson, John2 (AUTHOR), Kennedy, Sean E.2,3 (AUTHOR), Cooper, Sandra T.4,5,6 (AUTHOR), Kirk, Edwin P.1,3,7 (AUTHOR), Mowat, David1,2,3 (AUTHOR)
Publikováno v:
Molecular Genetics & Genomic Medicine. Oct2024, Vol. 12 Issue 10, p1-10. 10p.
Autor:
E. S. Roach, Balbir Singh
Publikováno v:
Pediatrics in Review. 19:132-136
1. Balbir V. Singh, MD* 2. E. S. Roach, MD* 1. 2. *Division of Pediatric Neurology, Department of Neurology, The University of Texas Southwestern Medical Center, Dallas, TX. Headache is an age-old problem that affects both children and adults; it is
Publikováno v:
Journal of Child Neurology. 23:26-31
This study presents a large multicenter cohort of children with cerebral venous thrombosis from 5 centers in the United States and analyzes their clinical findings and risk factors. Seventy patients were included in the study (25 neonates, 35%). The
Autor:
Michael S. Cartwright, E. Boltshauser, R. W. Baloh, Andrea Klein, E S Roach, H Mamsa, J. C. Jen
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 78:523-526
Background: Familial hemiplegic migraine (FHM) is an unusual migraine syndrome characterised by recurrent transient attacks of unilateral weakness or paralysis as part of the migraine aura. Genetically and clinically heterogeneous, FHM1 is caused by
Autor:
A. M. Marini, E. S. Roach, D. F. Hanley, Mitchell F. Brin, Douglas S. Goodin, Dale J. Lange, ML Goldstein, John H. Ferguson, M. R. Nuwer, S. van den Noort, P. Altrocchi, P. B. Goelick, R. S. Goldman
Publikováno v:
Archives of Clinical Neuropsychology. 16:255-269
Autor:
E. S. Roach, Steven Sparagana
Publikováno v:
Current Opinion in Neurology. 13:115-119
Tuberous sclerosis complex is an autosomal dominant disorder that causes significant complications in multiple organ systems. Both basic science and clinical research on tuberous sclerosis complex have flourished in recent years, improving our unders
Publikováno v:
Journal of Child Neurology. 14:401-407
At the recent Tuberous Sclerosis Consensus Conference, a subcommittee proposed recommendations to guide the rational use of diagnostic studies in patients with tuberous sclerosis complex. Recommendations were made for diagnostic evaluation at the tim
Publikováno v:
Journal of Child Neurology. 13:624-628
At the recent tuberous sclerosis complex consensus conference, the clinical diagnostic criteria for tuberous sclerosis complex were simplified and revised to reflect both new clinical information about tuberous sclerosis complex and an improved under