Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Tony M. McGrath"'
Publikováno v:
Child Neurology Open. 10:2329048X2311610
We describe an atypical presentation of a girl with aromatic L-amino acid decarboxylase (AADC) deficiency identified via a genetic testing program for children with epilepsy. At 21 months of age, she presented with poor head control, diffuse hypotoni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::867ce68fb4c377a010b0749895fbe4f5
https://doi.org/10.1177/2329048x231161027
https://doi.org/10.1177/2329048x231161027
Publikováno v:
Pediatric Neurology. 48:227-231
Although pyridoxine-dependent seizures have been reported for decades, pyridoxamine phosphate oxidase deficiency has only been recently described. Pyridoxamine phosphate oxidase (PNPO) is one of a series of enzymes involved in converting pyridoxine t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfd8835d5c2a28781a597e0c4ec71948
https://doi.org/10.1016/j.pediatrneurol.2012.11.006
https://doi.org/10.1016/j.pediatrneurol.2012.11.006
Publikováno v:
Journal of Child Neurology. 26:1260-1264
Children with sickle cell anemia are at risk for brain injury. Physicians obtain brain magnetic resonance imaging (MRI) for clinical indications to determine if a patient has developed a brain injury. Controversy exists whether all children with sick
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6c77d5093229f0ea13c995b8a6efd4e
https://doi.org/10.1177/0883073811405054
https://doi.org/10.1177/0883073811405054
Autor:
Tony M. McGrath, Leon S. Dure
Publikováno v:
Current Treatment Options in Neurology. 5:275-278
Paroxysmal dyskinesias are rare movement disorders. The onset of paroxysmal dyskinesias in childhood are typically idiopathic (sporadic or familial), whereas those in adulthood are usually secondary to an identifiable cause. Paroxysmal dyskinesias ar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc59afdf21d1c3d699a1a777cb42b85f
https://doi.org/10.1007/s11940-003-0032-x
https://doi.org/10.1007/s11940-003-0032-x
Autor:
W. Jerry Oakes, Camille Broome, Curtis J. Rozzelle, Leon S. Dure, Tony M. McGrath, Chevis N. Shannon
Publikováno v:
The Chiari Malformations ISBN: 9781461463689
This chapter describes the experiences of a multidisciplinary clinic specializing in the diagnosis and management of Chiari 1 malformations (C1M). Data were collected regarding reasons for referral and outcomes and indicate that approximately half of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0cdafe5261361a2f21e437dce763ff3e
https://doi.org/10.1007/978-1-4614-6369-6_31
https://doi.org/10.1007/978-1-4614-6369-6_31
Publikováno v:
Headache. 51(7)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f8b50194d60e45b61d9d59157dec207e
https://pubmed.ncbi.nlm.nih.gov/21649657
https://pubmed.ncbi.nlm.nih.gov/21649657
Publikováno v:
Pediatric neurology. 45(4)
Monosomy 1p36 is a clinically recognizable syndrome that is considered to be the most common terminal deletion syndrome. It has characteristic clinical features that include craniofacial dysmorphism, congenital anomalies, hearing deficits, developmen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ce220098cf7005df5dbe333982501ae
https://pubmed.ncbi.nlm.nih.gov/21907895
https://pubmed.ncbi.nlm.nih.gov/21907895
Publikováno v:
Headache: The Journal of Head and Face Pain. 51:1167-1168
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::573e8bf41a6dbc358b3504812ccaf893
https://doi.org/10.1111/j.1526-4610.2011.01933.x
https://doi.org/10.1111/j.1526-4610.2011.01933.x
Autor:
Tony M. McGrath, Ismail A. Khatri
Publikováno v:
Journal of Child Neurology. 17:792-792
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b943ea88ed4bbb55fd37dd9e4df5d22e
https://doi.org/10.1177/08830738020170101904
https://doi.org/10.1177/08830738020170101904