Zobrazeno 1 - 10
of 12
pro vyhledávání: '"S. E. Aylett"'
Publikováno v:
The British Journal of Dermatology
Summary Background The spectrum of central nervous system (CNS) abnormalities described in association with congenital melanocytic naevi (CMN) includes congenital, acquired, melanotic and nonmelanotic pathology. Historically, symptomatic CNS abnormal
Publikováno v:
The British journal of dermatology. 171(4)
Facial port-wine stains (PWSs) are usually isolated findings; however, when associated with cerebral and ocular vascular malformations they form part of the classical triad of Sturge-Weber syndrome (SWS).To evaluate the associations between the pheno
Publikováno v:
Developmental Medicine & Child Neurology. 41:480-485
Autor:
Brian G. R. Neville, Fenella J. Kirkham, J. H. Cross, Stewart Boyd, Wui K. Chong, S. E. Aylett
Publikováno v:
Developmental Medicine & Child Neurology. 41:480-485
The aim of this study was to examine the haemodynamic response to seizures in three infants with Sturge-Weber syndrome by measuring regional cerebral blood flow using transcranial Doppler sonography and 99mTc HMPAO SPECT. Time-locked video/digital EE
Publikováno v:
Developmental Medicine & Child Neurology. 49:697-699
Sturge-Weber syndrome (SWS) is a sporadic disorder characterized by naevus (port wine stain), a pial angioma, and glaucoma. The angioma comprises abnormal tortuous vessels on the leptomeninges with underlying brain gliosis, calcification, and atrophy
Publikováno v:
European Child & Adolescent Psychiatry. 5:222-225
A girl aged 9 years with Rasmussen's encephalitis previously treated by left temporal lobectomy suddenly developed prolonged attacks of extremely rapid respirations associated with poverty of body movements and greatly reduced facial movements with l
Publikováno v:
European archives of paediatric dentistry : official journal of the European Academy of Paediatric Dentistry. 10(1)
AIM: To investigate the oral health of children with intractable epilepsy attending the UK National Centre for Young People with Epilepsy. STUDY DESIGN AND METHODS: 39 children and adolescents with intractable epilepsy at a residential school, the UK
Publikováno v:
Seizure. 14(5)
Summary Purpose: To provide information on the incidence, types and circumstances of injuries sustained in a group of young people with epilepsy using protective helmets. Methods: Thirty-three residential students (21 M, 12 F, age range 5–21, mean
Publikováno v:
Developmental medicine and child neurology. 41(7)
The aim of this study was to examine the haemodynamic response to seizures in three infants with Sturge-Weber syndrome by measuring regional cerebral blood flow using transcranial Doppler sonography and 99mTc HMPAO SPECT. Time-locked video/digital EE
Publikováno v:
Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery. 14(3)
A 14-year-old boy presented acutely with occipital headache, nausea and vomiting. MRI showed obstructive hydrocephalus and marked bilateral cerebellar swelling with increased signal on T2-weighted imaging. Following treatment with oral corticosteroid