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pro vyhledávání: '"Danielle Nolan"'
Autor:
Danielle Nolan, Daniel Arndt
Publikováno v:
Symptom-Based Approach to Pediatric Neurology ISBN: 9783031104930
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::834824ad90a61fa65cf0408dd1018e5c
https://doi.org/10.1007/978-3-031-10494-7_16
https://doi.org/10.1007/978-3-031-10494-7_16
Publikováno v:
Journal of Child Neurology. 34:94-98
Background: Levetiracetam is prescribed for a broad spectrum of seizure types but does not have a specific indication for absence epilepsy. We hypothesized that levetiracetam is commonly prescribed for children with absence epilepsies and evaluated t
Autor:
Danielle, Nolan, John, Fink
Publikováno v:
Handbook of clinical neurology. 148
Discovery of nearly 200 genes implicated in epilepsy and insights into the molecular and cellular pathways involved are transforming our knowledge of the causes, classifications, diagnosis, and in some cases, treatments for individuals with chronic s
Autor:
Danielle Nolan, John K. Fink
Discovery of nearly 200 genes implicated in epilepsy and insights into the molecular and cellular pathways involved are transforming our knowledge of the causes, classifications, diagnosis, and in some cases, treatments for individuals with chronic s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::89e374c3858148dd0f07930450b64297
https://doi.org/10.1016/b978-0-444-64076-5.00030-2
https://doi.org/10.1016/b978-0-444-64076-5.00030-2
Autor:
Yu Kawai, Danielle Nolan, Michael W. Quasney, Andrea G. DeMonbrun, Bram Dolcourt, Nasuh Malas, Rebecca S. Chambers
Publikováno v:
Pediatrics. 139
A 14-year-old previously healthy female was transferred from a local emergency department after being found unresponsive at home. Parental questioning revealed she had fever and pharyngitis 2 weeks before presentation. Past mental health history was
Autor:
Martha D. Carlson, Danielle Nolan
Publikováno v:
Journal of child neurology. 31(7)
Genetic heterogeneity in neurologic disorders has been an obstacle to phenotype-based diagnostic testing. The authors hypothesized that information compiled via whole exome sequencing will improve clinical diagnosis and management of pediatric neurol