Results 11 to 20 of about 5,403,298 (185)
Tuberous Sclerosis Complex: A Roadmap for Future Research
Pediatric Neurology Briefs, 2016 Investigators from the NINDS and the Tuberous Sclerosis Alliance sponsored a workshop in March 2015, which joined basic scientists and clinicians with expertise in various aspects of Tuberous Sclerosis Complex (TSC), in order to assess the current state ...
Anna Jeong
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Tuberous Sclerosis Complex : A Case Report
Saintika Medika, 2019 Tuberous Sclerosis Complex (TSC) is an autosomal dominant inherited neurocutaneous disorder. Tuberous Sclerosis Complex is caused by mutations in tumor suppressor gene (TSC), both TSC1 and TSC2.
Rofiq, Aunur +2 more
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Tuberous Sclerosis Complex: Early Diagnosis in Infants [PDF]
Pediatric Neurology Briefs, 2018 Investigators from the Tuberous Sclerosis Complex (TSC) Autism Center of Excellence Research conducted two concurrent prospective longitudinal studies to analyze the timing and pattern of clinical presenting symptoms of TSC in infants to facilitate ...
Stephen Lewis Nelson, Brittani M Wild
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Tuberous Sclerosis Complex and Arachnoid Cysts [PDF]
Pediatric Neurology Briefs, 2014 Investigators at the Massachusetts General Hospital, Boston, MA, and Universitat Autonoma de Barcelona, Spain, assessed the prevalence and characteristics of arachnoid cysts in a cohort of 220 patients with tuberous sclerosis complex (TSC)
John J Millichap, J Gordon Millichap
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Reversed Halo Sign in Tuberous Sclerosis Complex
Case Reports in Radiology, 2013 We describe a reversed halo sign in a teenage girl with tuberous sclerosis complex (TSC). Lung manifestations of TSC include lung cysts corresponding to lymphangioleiomyomatosis and small nodules indicating multifocal micronodular pneumocyte hyperplasia (
Akihiko Shiraishi +5 more
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Autism and Epilepsy in Tuberous Sclerosis Complex
Pediatric Neurology Briefs, 2001 The relationship between autism and epilepsy and functional brain abnormalities in children with tuberous sclerosis complex (TSC) were examined at the Children’s Hospital of Michigan, Wayne State University ...
J Gordon Millichap
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Epilepsy and preventive antiepileptic treatment in tuberous sclerosis complex. Literature review
Neurologijos seminarai, 2023 Tuberous sclerosis complex (TSC) is a rare genetic disorder characterized by the presence of benign tumors in many organs. The pathogenic mutation is found in either the TSC1 or TSC2 tumor suppressor genes. The presence of cortical or subcortical tubers
I. Kasiulevičiūtė
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Perfect match: mTOR inhibitors and tuberous sclerosis complex
Orphanet Journal of Rare Diseases, 2022 Highlights Hyperactivation of mammalian target of rapamycin (mTOR) is essential in the pathogenesis of tuberous sclerosis complex (TSC) and can serve as a therapeutic target. mTOR inhibitors have shown considerable success in multiple clinical trials for
Cong Luo +8 more
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All tubers are not created equal: Cerebellar tubers in a pediatric patient with tuberous sclerosis
Radiology Case Reports, 2021 Tuberous sclerosis complex (TSC) is a rare autosomal dominant disease characterized by multiple tumors throughout the body. Supratentorial hamartomas (or tubers), are a very common CNS feature of TSC. Cerebellar tubers are much less common in TSC.
Sanjeeva Weerasinghe, BS +1 more
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The Neurodevelopmental Pathogenesis of Tuberous Sclerosis Complex (TSC). [PDF]
Front Neuroanat, 2020 Tuberous sclerosis complex (TSC) is a model disorder for understanding brain development because the genes that cause TSC are known, many downstream molecular pathways have been identified, and the resulting perturbations of cellular events are ...
Feliciano DM.
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