Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Arie Fisher"'
Publikováno v:
Frontiers in Neurology, Vol 8 (2017)
A 56-year-old woman with various neurological signs which developed over a 1-year period was admitted for evaluation. MRI showed a markedly abnormal signal in the cervical spine. Despite treatment with IV steroids, she developed a progressive myelopa
Externí odkaz:
https://doaj.org/article/e87cb2fc480f4a90b3b327aa83016062
Autism spectrum disorder (ASD) is a common neurodevelopmental condition. The American Academy of Paediatrics and American Academy of Neurology do not recommend routine brain magnetic resonance imaging (MRI) in the assessment of ASD. The need for a br
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::27b0bcedb6f35d78af56958b2baa81df
https://doi.org/10.21203/rs.3.rs-2294626/v1
https://doi.org/10.21203/rs.3.rs-2294626/v1
Publikováno v:
Journal of American Association for Pediatric Ophthalmology and Strabismus. 25:250-252
Acute cerebellitis is a rare condition with a highly heterogenous clinical course, ranging from self-limiting mild symptoms to a fulminant presentation. Symptoms include headache, vomiting, fever, ataxia, dysarthria, intention tremor, meningism, seiz
Publikováno v:
Multiple Sclerosis Journal. 25:295-299
Background and objectives: Epileptic seizures frequently occur in people with multiple sclerosis (MS) and are thought to represent a manifestation of cortical pathology. However, at present, seizures are not considered to be a typical clinical presen
Publikováno v:
Abstracts.
Background Despite advances in prevention strategies the diagnosis of neonatal sepsis and clinical decision making remains challenging. Empirical antibiotic treatment is given to neonates when sepsis is suspected. However, clinical and laboratory sig
Publikováno v:
Abstracts.
Background Classical Phenylketonuria (PKU) is an autosomal recessively inherited disorder in phenylalanine metabolism caused by profound deficiency of the enzyme phenylalanine hydroxylase (PAH). Newborn screening for PKU was introduced in Ireland in
Publikováno v:
Abstracts.
A 16 month old toddler presented with global developmental delay, truncal hypotonia and microcephaly. Her background history was significant for bilateral developmental dysplasia of the hip, recurrent upper respiratory tract infections, conductive he