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pro vyhledávání: '"John T. MacDonald"'
Publikováno v:
Frontiers in Behavioral Neuroscience, Vol 12 (2018)
We explored associations between EEG pathophysiology and emotional/behavioral (E/B) problems of children with two types of epilepsy using standard parent questionnaires and two new indicators: tantrums recorded by parents at home and brief, emotion-e
Externí odkaz:
https://doaj.org/article/ac850f781a6d41ecaf91018ef087be71
Publikováno v:
Frontiers in Behavioral Neuroscience
Frontiers in Behavioral Neuroscience, Vol 12 (2018)
Frontiers in Behavioral Neuroscience, Vol 12 (2018)
We explored associations between EEG pathophysiology and emotional/behavioral (E/B) problems of children with two types of epilepsy using standard parent questionnaires and two new indicators: tantrums recorded by parents at home and brief, emotion-e
Autor:
Laura A. Foster, David Nascene, Gerald V. Raymond, John T. MacDonald, Thomas R. Henry, Brian P. Moran, Peter I. Karachunski, Maria R. Johnson
Publikováno v:
Pediatric neurology. 66
Background Genetic alterations are significant causes of epilepsy syndromes; especially early-onset epileptic encephalopathies and voltage-gated sodium channelopathies are among the best described. Mutations in the SCN2A subunit of voltage-gated sodi
Publikováno v:
Journal of Pediatric Ophthalmology & Strabismus. 49:184-188
Purpose: To evaluate whether visual impairment in albinism contributes significantly to the acquisition of normal reading skills. Methods: The authors administered standardized reading tests to 41 children and 18 adults with albinism. The Young Child
Autor:
Beth R. Kutzbach, John T. MacDonald, Kathy M. Hogue, Ann M. Holleschau, Kimberly Merrill, C. Gail Summers, Sara J. Downes
Publikováno v:
Journal of American Association for Pediatric Ophthalmology and Strabismus. 13:191-195
Introduction Human albinism is a genetic condition associated with visual impairment that affects many aspects of daily life. Office measurements of visual acuity do not necessarily reflect daily visual function and health status. This study used the
Autor:
C. Gail Summers, John T. MacDonald, Ann M. Holleschau, Beth R. Kutzbach, Kimberly Merrill, Katherine M. Hogue, Sara J. Downes
Publikováno v:
Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus. 15(1)
Introduction The MNREAD reading acuity (RA) charts use continuous-text reading to measure (1) RA, ie, the smallest size of print that the patient can resolve; (2) maximum reading speed (MRS); and (3) critical print size (CPS), ie, the smallest print
Publikováno v:
Journal of child neurology. 22(12)
Attention-deficit/hyperactivity disorder (ADHD) is a common diagnosis in children and adults. Human albinism is an uncommon genetic condition associated with visual impairment that may affect behavior. To determine if there is a relationship between
Publikováno v:
Ophthalmology. 115(10)
Objectives To evaluate neurologic development in children with albinism. Design Observational cohort series. Participants and/or Controls Seventy-eight children with albinism, ages 4 to 18 years. Methods Parents completed a developmental questionnair
Autor:
John T. MacDonald
Publikováno v:
Journal of child neurology. 21(6)
Autor:
John T. MacDonald
Publikováno v:
Pediatric Neurology. 36:175-176
A healthy 5-year-old male reported a clicking sound in both ears. Neurologic examination was normal except for an audible clicking noise that could be heard when within 10 cm of either ear and bilateral rapid rhythmic movements of the soft palate. Al