Researchers at the Hunter Nelson Sturge-Weber Center, Kennedy Krieger Institute, Baltimore, reviewed the records of 100 consecutive children and adults with confirmed Sturge-Weber syndrome (SWS) to determine the nature and prognosis of associated seizures
OBJECTIVE:Almost two-thirds of patients with Sturge-Weber syndrome (SWS) have epilepsy, and half of ...
Sturge–Weber syndrome (SWS) is a rare congenital disorder belongs to a group of disorders collecti...
Background: Patients with Sturge-Weber syndrome type 1 (SWS1) have a port-wine birthmark (PWB) as cu...
The aim of this studs was to examine the haemodynamic response to seizures in three infants with Stu...
The Struge-Weber syndrome is the third most common neurodermal disease after neurofibromatosis and t...
Regional cerebral blood flow during seizure activity, measured by transcranial Doppler sonography, a...
Sturge-Weber syndrome (SWS) is a neurogenetic disease with an incidence of 1 in 20.000-50.000 live b...
BACKGROUND: We summarize the history of individuals with Sturge-Weber syndrome (SWS) to inform clini...
The paper addresses the relatively rare inherited neurodermal disorder – Sturge-Weber syndrome that ...
Investigators from the University of Montreal studied potential predictors of epilepsy in young pati...
Sturge-Weber syndrome is characterized by the presence of a port-wine nevus, epilepsy, stroke-like e...
Infants with a high-risk distribution of port-wine stains are commonly screened for Sturge-Weber syn...
Sturge-Weber syndrome (SWS) is a rare disorder that occurs sporadically with a frequency of 1:50,000...
Background: Epilepsy in typical Sturge-Weber syndrome (SWS) is common, and many questions remain reg...
OBJECTIVE: To determine whether the extent and degree of glucose hypometabolism defined by PET corre...
OBJECTIVE:Almost two-thirds of patients with Sturge-Weber syndrome (SWS) have epilepsy, and half of ...
Sturge–Weber syndrome (SWS) is a rare congenital disorder belongs to a group of disorders collecti...
Background: Patients with Sturge-Weber syndrome type 1 (SWS1) have a port-wine birthmark (PWB) as cu...
The aim of this studs was to examine the haemodynamic response to seizures in three infants with Stu...
The Struge-Weber syndrome is the third most common neurodermal disease after neurofibromatosis and t...
Regional cerebral blood flow during seizure activity, measured by transcranial Doppler sonography, a...
Sturge-Weber syndrome (SWS) is a neurogenetic disease with an incidence of 1 in 20.000-50.000 live b...
BACKGROUND: We summarize the history of individuals with Sturge-Weber syndrome (SWS) to inform clini...
The paper addresses the relatively rare inherited neurodermal disorder – Sturge-Weber syndrome that ...
Investigators from the University of Montreal studied potential predictors of epilepsy in young pati...
Sturge-Weber syndrome is characterized by the presence of a port-wine nevus, epilepsy, stroke-like e...
Infants with a high-risk distribution of port-wine stains are commonly screened for Sturge-Weber syn...
Sturge-Weber syndrome (SWS) is a rare disorder that occurs sporadically with a frequency of 1:50,000...
Background: Epilepsy in typical Sturge-Weber syndrome (SWS) is common, and many questions remain reg...
OBJECTIVE: To determine whether the extent and degree of glucose hypometabolism defined by PET corre...
OBJECTIVE:Almost two-thirds of patients with Sturge-Weber syndrome (SWS) have epilepsy, and half of ...
Sturge–Weber syndrome (SWS) is a rare congenital disorder belongs to a group of disorders collecti...
Background: Patients with Sturge-Weber syndrome type 1 (SWS1) have a port-wine birthmark (PWB) as cu...