The results of an Italian collaborative study on Tuberous Sclerosis Complex (TSC) are reported. 252 patients with TSC are the object of this study: 192 cases evaluated in 36 Italian Paediatric Institutions and 60 cases observed at the Paediatric Institute of the University of Siena. The numerosity of our series is not sufficient to evaluate the incidence and prevalence of the disease in Italy. However the collaborative study allowed us to obtain reliable information about the type and frequency of the clinical and instrumental findings observed in TSC. In particular our data indicated that the CNS was very frequently involved. Neuroimaging techniques (brain CT and MRI) indicated the presence of cerebral abnormalities in 96 per cent of the c...
Aim: In the study we reassessed the clinical features of 22 patients diagnosed with tuberous scle-ro...
Tuberous sclerosis complex (TSC) is an autosomal dominant disorder characterized by the development ...
Background: Tuberous sclerosis complex (TSC) is a rare autosomal dominant genetic disorder. Many gap...
The results of an Italian collaborative study on Tuberous Sclerosis Complex (TSC) are reported. 252 ...
Tuberous sclerosis complex (TSC) is a genetic disorder characterized by multiple hamartomas in sever...
<p>The purpose of establishing and maintaining a tuberous sclerosis registry is to collect data on t...
Aim: This study was planned with the aim of retrospectively reviewing the clinical and laboratory fi...
© 2018, Springer Science+Business Media, LLC, part of Springer Nature. The article is a contribution...
Objective: To present the baseline data of the international TuberOus SClerosis registry to increase...
The results of a collaborative Italian study on Neurofibromatosis type 1 (NF1) among the Pediatric I...
Tuberous sclerosis complex (TSC) is an autosomal dominant disorder with multi-system involvement and...
© 2017, Sociedad Chilena de Pediatria. All rights reserved. Introduction: Tuberous sclerosis complex...
Tuberous sclerosis complex (TSC) is an autosomal dominant genetic neurocutaneous disorder, with hete...
Aim: We aimed to study tuberous sclerosis-associated neuropsychiatric disorders (TAND) in children a...
Objective Tuberous sclerosis complex is an autosomal dominant neurocutaneous disease that presents w...
Aim: In the study we reassessed the clinical features of 22 patients diagnosed with tuberous scle-ro...
Tuberous sclerosis complex (TSC) is an autosomal dominant disorder characterized by the development ...
Background: Tuberous sclerosis complex (TSC) is a rare autosomal dominant genetic disorder. Many gap...
The results of an Italian collaborative study on Tuberous Sclerosis Complex (TSC) are reported. 252 ...
Tuberous sclerosis complex (TSC) is a genetic disorder characterized by multiple hamartomas in sever...
<p>The purpose of establishing and maintaining a tuberous sclerosis registry is to collect data on t...
Aim: This study was planned with the aim of retrospectively reviewing the clinical and laboratory fi...
© 2018, Springer Science+Business Media, LLC, part of Springer Nature. The article is a contribution...
Objective: To present the baseline data of the international TuberOus SClerosis registry to increase...
The results of a collaborative Italian study on Neurofibromatosis type 1 (NF1) among the Pediatric I...
Tuberous sclerosis complex (TSC) is an autosomal dominant disorder with multi-system involvement and...
© 2017, Sociedad Chilena de Pediatria. All rights reserved. Introduction: Tuberous sclerosis complex...
Tuberous sclerosis complex (TSC) is an autosomal dominant genetic neurocutaneous disorder, with hete...
Aim: We aimed to study tuberous sclerosis-associated neuropsychiatric disorders (TAND) in children a...
Objective Tuberous sclerosis complex is an autosomal dominant neurocutaneous disease that presents w...
Aim: In the study we reassessed the clinical features of 22 patients diagnosed with tuberous scle-ro...
Tuberous sclerosis complex (TSC) is an autosomal dominant disorder characterized by the development ...
Background: Tuberous sclerosis complex (TSC) is a rare autosomal dominant genetic disorder. Many gap...