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Quoted phrase not found in phrase index: "Complex cortical dysplasia with other brain malformations 5"
Page 1
Meningiomas in lymphangioleiomyomatosis.
Moss J, DeCastro R, Patronas NJ, Taveira-DaSilva A. Moss J, et al. JAMA. 2001 Oct 17;286(15):1879-81. doi: 10.1001/jama.286.15.1879. JAMA. 2001. PMID: 11597290
Since 30% to 40% of patients with tuberous sclerosis complex (TSC) have LAM, we routinely screen patients with LAM for brain lesions found in TSC. ...PATIENTS: Two hundred fifty women with sporadic LAM who were referred for screening by magnetic resonance imaging (M …
Since 30% to 40% of patients with tuberous sclerosis complex (TSC) have LAM, we routinely screen patients with LAM for brain l …
Pathophysiology of neurodevelopmental mTOR pathway-associated epileptic conditions: Current status of biomedical research.
Gruber V, Scholl T, Samueli S, Gröppel G, Mühlebner A, Hainfellner JA, Feucht M. Gruber V, et al. Clin Neuropathol. 2019 Sep/Oct;38(5):210-224. doi: 10.5414/NP301214. Clin Neuropathol. 2019. PMID: 31347492 Review.
In this review, special focus is put on the prototypes of "mTORpathies": tuberous sclerosis complex (TSC) and focal cortical dysplasia (FCD) type IIb. We review recent research data on mTORpathies, with emphasis on cortical tubers and FCD-like lesions …
In this review, special focus is put on the prototypes of "mTORpathies": tuberous sclerosis complex (TSC) and focal cortical …
Epilepsy in neurofibromatosis type 1.
Pecoraro A, Arehart E, Gallentine W, Radtke R, Smith E, Pizoli C, Kansagra S, Abdelnour E, McLendon R, Mikati MA. Pecoraro A, et al. Epilepsy Behav. 2017 Aug;73:137-141. doi: 10.1016/j.yebeh.2017.05.011. Epub 2017 Jul 18. Epilepsy Behav. 2017. PMID: 28633092
Three of the six patients with MTS underwent temporal lobectomy with subsequent control of their seizures with confirmation of MTS on pathology in 3/3 and presence of coexisting focal cortical dysplasia (FCD) in 2/3. We also have observed three additional pat …
Three of the six patients with MTS underwent temporal lobectomy with subsequent control of their seizures with confirmation of MTS on pathol …
Rhinencephalon changes in tuberous sclerosis complex.
Manara R, Brotto D, Bugin S, Pelizza MF, Sartori S, Nosadini M, Azzolini S, Iaconetta G, Parazzini C, Murgia A, Peron A, Canevini P, Labriola F, Vignoli A, Toldo I. Manara R, et al. Neuroradiology. 2018 Aug;60(8):813-820. doi: 10.1007/s00234-018-2045-x. Epub 2018 Jun 17. Neuroradiology. 2018. PMID: 29909560
PURPOSE: Despite complex olfactory bulb embryogenesis, its development abnormalities in tuberous sclerosis complex (TSC) have been poorly investigated. ...Cortical tuber number was visually assessed and a neurological severity score was o …
PURPOSE: Despite complex olfactory bulb embryogenesis, its development abnormalities in tuberous sclerosis complex …
Tuberous sclerosis complex: genetics to pathogenesis.
Narayanan V. Narayanan V. Pediatr Neurol. 2003 Nov;29(5):404-9. doi: 10.1016/j.pediatrneurol.2003.09.002. Pediatr Neurol. 2003. PMID: 14684235 Review.
Desiree-Magloire Bourneville first reported tuberous sclerosis complex as "tuberous sclerosis of the cerebral convolutions" in 1880. This disorder is characterized by multiple hamartomas in several organs, particularly the brain. Commonly recognized clinical feature …
Desiree-Magloire Bourneville first reported tuberous sclerosis complex as "tuberous sclerosis of the cerebral convolutions" in 1880. …
alpha-[11C]-methyl-L-tryptophan PET for tracer localization of epileptogenic brain regions: clinical studies.
Kumar A, Asano E, Chugani HT. Kumar A, et al. Biomark Med. 2011 Oct;5(5):577-84. doi: 10.2217/bmm.11.68. Biomark Med. 2011. PMID: 22003906 Free PMC article. Review.
In nontuberous sclerosis complex patients with cortical dysplasia, increased AMT uptake is usually associated with cortical dysplasia type IIB and a very good surgical outcome. ...The neuropathological similarities between tubers and type IIB …
In nontuberous sclerosis complex patients with cortical dysplasia, increased AMT uptake is usually associated with c …
Vigabatrin-associated brain magnetic resonance imaging abnormalities and clinical symptoms in infants with tuberous sclerosis complex.
Stevering C, Lequin M, Szczepaniak K, Sadowski K, Ishrat S, De Luca A, Leemans A, Otte W, Kwiatkowski DJ, Curatolo P, Weschke B, Riney K, Feucht M, Krsek P, Nabbout R, Jansen A, Wojdan K, Sijko K, Glowacka-Walas J, Borkowska J, Domanska-Pakiela D, Moavero R, Hertzberg C, Hulshof H, Scholl T, Petrák B, Maminak M, Aronica E, De Ridder J, Lagae L, Jozwiak S, Kotulska K, Braun K, Jansen F. Stevering C, et al. Epilepsia. 2025 Feb;66(2):356-368. doi: 10.1111/epi.18190. Epub 2024 Dec 6. Epilepsia. 2025. PMID: 39641935 Free PMC article.
OBJECTIVE: Previous retrospective studies have reported vigabatrin-associated brain abnormalities on magnetic resonance imaging (VABAM), although clinical impact is unknown. ...RESULTS: Prevalence of VABAM in VGB-treated TSC patients was 35.5%. VABAM-like …
OBJECTIVE: Previous retrospective studies have reported vigabatrin-associated brain abnormalities on magnetic resonance imagin …
SOD1 mediates lysosome-to-mitochondria communication and its dysregulation by amyloid-β oligomers.
Norambuena A, Sun X, Wallrabe H, Cao R, Sun N, Pardo E, Shivange N, Wang DB, Post LA, Ferris HA, Hu S, Periasamy A, Bloom GS. Norambuena A, et al. Neurobiol Dis. 2022 Jul;169:105737. doi: 10.1016/j.nbd.2022.105737. Epub 2022 Apr 20. Neurobiol Dis. 2022. PMID: 35452786 Free PMC article.
Mechanistically, tau, another key factor in AD pathogenesis and other tauopathies, reduced the lysosomal content of the tuberous sclerosis complex (TSC), thereby increasing NiMA and suppressing SOD1 activity and mtDNA synthesis. AbetaOs inhibited these actions. Dysregulati …
Mechanistically, tau, another key factor in AD pathogenesis and other tauopathies, reduced the lysosomal content of the tuberous sclerosis …
The cerebral cortex malformation in thanatophoric dysplasia: neuropathology and pathogenesis.
Hevner RF. Hevner RF. Acta Neuropathol. 2005 Sep;110(3):208-21. doi: 10.1007/s00401-005-1059-8. Acta Neuropathol. 2005. PMID: 16133544 Review.
Thanatophoric dysplasia (TD) is a relatively common, fatal form of chondrodysplastic dwarfism in which the cerebral cortex displays a unique and complex malformation. ...The cortical malformation is interpreted with regard to developmental mecha …
Thanatophoric dysplasia (TD) is a relatively common, fatal form of chondrodysplastic dwarfism in which the cerebral cortex displays a …
Tuberous sclerosis complex in adulthood: focus on epilepsy prognosis.
Licchetta L, Bruschi G, Stipa C, Belotti LMB, Ferri L, Mostacci B, Vignatelli L, Minardi R, Di Vito L, Muccioli L, Boni A, Tinuper P, Bisulli F. Licchetta L, et al. Epilepsy Behav. 2024 Apr;153:109688. doi: 10.1016/j.yebeh.2024.109688. Epub 2024 Feb 29. Epilepsy Behav. 2024. PMID: 38428171
At logistic regression univariate analysis, ID (OR 7.9, 95 % CI 1.8--34.7), multiple seizure types lifelong (OR 13.2, 95 % CI 2.6- 67.2), spasms/tonic seizures at presentation (OR 6.5, 95 % CI 1.2--35.2), a higher seizure frequency at onset (OR 5.4, 95 % CI 1.2--24. …
At logistic regression univariate analysis, ID (OR 7.9, 95 % CI 1.8--34.7), multiple seizure types lifelong (OR 13.2, 95 % CI 2.6- 67.2), sp …
30 results