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15 results

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Quoted phrase not found in phrase index: "frontal tuber"
Page 1
Infantile spasms in tuberous sclerosis complex.
Curatolo P, Seri S, Verdecchia M, Bombardieri R. Curatolo P, et al. Brain Dev. 2001 Nov;23(7):502-7. doi: 10.1016/s0387-7604(01)00300-x. Brain Dev. 2001. PMID: 11701245 Review.
The high incidence of infantile spasms (IS) and hypsarrhythmia in tuberous sclerosis complex (TSC) has long been emphasized but it is now clear that infants with TSC show clinical and EEG differences from those with classical West syndrome. ...The presence of IS due to TSC …
The high incidence of infantile spasms (IS) and hypsarrhythmia in tuberous sclerosis complex (TSC) has long been emphasized but it is …
Behavioral aspects of pediatric epilepsy syndromes.
Besag FM. Besag FM. Epilepsy Behav. 2004 Feb;5 Suppl 1:S3-13. doi: 10.1016/j.yebeh.2003.11.002. Epilepsy Behav. 2004. PMID: 14725841 Review.
The work on this syndrome in children with tuberous sclerosis has demonstrated an association between temporal lobe tubers and autism. ...Juvenile myoclonic epilepsy has been associated with very variable behavioral traits, sometimes with immature personality featur …
The work on this syndrome in children with tuberous sclerosis has demonstrated an association between temporal lobe tubers and …
Behavioral and cognitive aspects of tuberous sclerosis complex.
Prather P, de Vries PJ. Prather P, et al. J Child Neurol. 2004 Sep;19(9):666-74. doi: 10.1177/08830738040190090601. J Child Neurol. 2004. PMID: 15563012 Review.
Approximately half of individuals diagnosed with tuberous sclerosis complex present with global intellectual impairment and developmental psychopathologies. ...The evolving neurocognitive literature suggests that frontal brain systems might be most consistently disr …
Approximately half of individuals diagnosed with tuberous sclerosis complex present with global intellectual impairment and developme …
Hypothalamic Hamartomas: A comprehensive review of literature - Part 2: Medical and surgical management update.
Alomari SO, El Houshiemy MN, Bsat S, Moussalem CK, Allouh M, Omeis IA. Alomari SO, et al. Clin Neurol Neurosurg. 2020 Aug;195:106074. doi: 10.1016/j.clineuro.2020.106074. Epub 2020 Jul 7. Clin Neurol Neurosurg. 2020. PMID: 32663735 Review.
They arise from the floor of the third ventricle, tuber cinereum, or mammillary bodies. Estimated incidence ranges from 1 in 50,000 to 1 in 1,000,000. ...
They arise from the floor of the third ventricle, tuber cinereum, or mammillary bodies. Estimated incidence ranges from 1 in 50,000 t …
Attention-deficit hyperactivity disorder (ADHD) and tuberous sclerosis complex.
D'Agati E, Moavero R, Cerminara C, Curatolo P. D'Agati E, et al. J Child Neurol. 2009 Oct;24(10):1282-7. doi: 10.1177/0883073809341272. J Child Neurol. 2009. PMID: 19805824 Review.
The neurobiological basis of attention-deficit hyperactivity disorder (ADHD) in tuberous sclerosis complex is still largely unknown. Cortical tubers may disrupt several brain networks that control different types of attention. Frontal lobe dysfunction due to …
The neurobiological basis of attention-deficit hyperactivity disorder (ADHD) in tuberous sclerosis complex is still largely unknown. …
Genetic malformations of the cerebral cortex and epilepsy.
Guerrini R. Guerrini R. Epilepsia. 2005;46 Suppl 1:32-7. doi: 10.1111/j.0013-9580.2005.461010.x. Epilepsia. 2005. PMID: 15816977 Review.
About 65% of patients have severe epilepsy, often Lennox-Gastaut syndrome. Recessive bilateral frontal polymicrogyria has been linked to chromosome 16q12.2-21....
About 65% of patients have severe epilepsy, often Lennox-Gastaut syndrome. Recessive bilateral frontal polymicrogyria has been linked …
Neonatal subependymal giant cell astrocytoma.
Medhkour A, Traul D, Husain M. Medhkour A, et al. Pediatr Neurosurg. 2002 May;36(5):271-4. doi: 10.1159/000058432. Pediatr Neurosurg. 2002. PMID: 12053047 Review.
Subependymal giant cell astrocytoma (SEGCA) is a benign, slow-growing glial tumor that manifests with signs and symptoms of obstructive hydrocephalus most often in adolescent patients with tuberous sclerosis complex (TSC). Neonatal highly aggressive SEGCA is very rare. We …
Subependymal giant cell astrocytoma (SEGCA) is a benign, slow-growing glial tumor that manifests with signs and symptoms of obstructive hydr …
MRI and CT features of cerebellar degeneration.
Huang YP, Tuason MY, Wu T, Plaitakis A. Huang YP, et al. J Formos Med Assoc. 1993 Jun;92(6):494-508. J Formos Med Assoc. 1993. PMID: 8106035 Review.
Cerebellar atrophy is more marked in the hemispheres than in the vermis, while the brain stem shows little change. The frontal and parietal sulci are usually slightly prominent. In cerebello-olivary atrophy (also called cortical cerebellar degeneration), there is atrophy o …
Cerebellar atrophy is more marked in the hemispheres than in the vermis, while the brain stem shows little change. The frontal and pa …
Tuberous Sclerosis, Type II Diabetes Mellitus and the PI3K/AKT/mTOR Signaling Pathways-Case Report and Literature Review.
Jurca CM, Kozma K, Petchesi CD, Zaha DC, Magyar I, Munteanu M, Faur L, Jurca A, Bembea D, Severin E, Jurca AD. Jurca CM, et al. Genes (Basel). 2023 Feb 8;14(2):433. doi: 10.3390/genes14020433. Genes (Basel). 2023. PMID: 36833359 Free PMC article. Review.
Tuberous sclerosis complex (TSC) is a rare autosomal dominant neurocutaneous syndrome. It is manifested mainly in cutaneous lesions, epilepsy and the emergence of hamartomas in several tissues and organs. ...Brain MRI displayed a distinctive TS aspect with five bilateral h …
Tuberous sclerosis complex (TSC) is a rare autosomal dominant neurocutaneous syndrome. It is manifested mainly in cutaneous lesions, …
Malignant tumors in tuberous sclerosis complex: a case report and review of the literature.
Liu C, Lele SM, Goodenberger MH, Reiser GM, Christiansen AJ, Padussis JC. Liu C, et al. BMC Med Genomics. 2024 May 27;17(1):144. doi: 10.1186/s12920-024-01913-8. BMC Med Genomics. 2024. PMID: 38802873 Free PMC article. Review.
BACKGROUND: Tuberous sclerosis complex (TSC) is a rare, autosomal dominant genetic disease that arises from TSC1 or TSC2 genetic mutations. ...Later, a brain MRI revealed two small cortical tubers, one in each frontal lobe, that were asymptomatic; the patient …
BACKGROUND: Tuberous sclerosis complex (TSC) is a rare, autosomal dominant genetic disease that arises from TSC1 or TSC2 genetic muta …
15 results