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Quoted phrase not found in phrase index: "Developmental and epileptic encephalopathy, 11"
Page 1
Global prevalence of developmental disabilities in children and adolescents: A systematic umbrella review.
Olusanya BO, Smythe T, Ogbo FA, Nair MKC, Scher M, Davis AC. Olusanya BO, et al. Front Public Health. 2023 Feb 16;11:1122009. doi: 10.3389/fpubh.2023.1122009. eCollection 2023. Front Public Health. 2023. PMID: 36891340 Free PMC article.
RESULTS: Based on our inclusion criteria, 10 systematic reviews reporting prevalence estimates for attention-deficit/hyperactivity disorder, autism spectrum disorder, cerebral palsy, developmental intellectual disability, epilepsy, hearing loss, vision loss and d …
RESULTS: Based on our inclusion criteria, 10 systematic reviews reporting prevalence estimates for attention-deficit/hyperactivity disorder, …
Comparative safety of antiepileptic drugs for neurological development in children exposed during pregnancy and breast feeding: a systematic review and network meta-analysis.
Veroniki AA, Rios P, Cogo E, Straus SE, Finkelstein Y, Kealey R, Reynen E, Soobiah C, Thavorn K, Hutton B, Hemmelgarn BR, Yazdi F, D'Souza J, MacDonald H, Tricco AC. Veroniki AA, et al. BMJ Open. 2017 Jul 20;7(7):e017248. doi: 10.1136/bmjopen-2017-017248. BMJ Open. 2017. PMID: 28729328 Free PMC article. Review.
PRIMARY AND SECONDARY OUTCOME MEASURES: Cognitive developmental delay and autism/dyspraxia were primary outcomes. Attention-deficit hyperactivity disorder, language delay, neonatal seizures, psychomotor developmental delay and social impairment were secondary outcom …
PRIMARY AND SECONDARY OUTCOME MEASURES: Cognitive developmental delay and autism/dyspraxia were primary outcomes. Attention-deficit h …
Dyke-Davidoff-Masson Syndrome: Main clinical and radiological findings- systematic literature review.
Rondão MBA, Hsu BRRHS, Centeno RS, de Aguiar PHP. Rondão MBA, et al. Seizure. 2023 Aug;110:58-68. doi: 10.1016/j.seizure.2023.04.020. Epub 2023 Jun 3. Seizure. 2023. PMID: 37327751 Review.
RESULTS: The mean age of the patients was 19.44 (0-83 years), and the majority were male (55.32%). The most common types of epileptic seizures were generalised tonic-clonic seizures (31 cases), focal impaired awareness seizures (20 cases), focal motor seizures (13 cases), …
RESULTS: The mean age of the patients was 19.44 (0-83 years), and the majority were male (55.32%). The most common types of epileptic …
Peri-Insular Hemispherotomy: A Systematic Review and Institutional Experience.
Yates CF, Malone S, Riney K, Shah U, Wood MJ. Yates CF, et al. Pediatr Neurosurg. 2023;58(1):18-28. doi: 10.1159/000529098. Epub 2023 Jan 13. Pediatr Neurosurg. 2023. PMID: 36693334 Free PMC article.
Hydrocephalus was most common in the youngest patient cohorts. Developmental pathology was present in 114 (40.8%) patients, who had fewer Engel 1 outcomes compared to those with acquired pathology (69.1% vs. 83.7%, p = 0.0167). The local series included 13 patients, 11 …
Hydrocephalus was most common in the youngest patient cohorts. Developmental pathology was present in 114 (40.8%) patients, who had f …
Epilepsy in LAMA2-related muscular dystrophy: A systematic review of the literature.
Salvati A, Bonaventura E, Sesso G, Pasquariello R, Sicca F. Salvati A, et al. Seizure. 2021 Oct;91:425-436. doi: 10.1016/j.seizure.2021.07.020. Epub 2021 Jul 21. Seizure. 2021. PMID: 34325301 Free article. Review.
To date, there is no systematic characterization of epilepsy in LAMA2-RD, and its impact on neurodevelopment and on the clinical course remains poorly established. ...This systematic review helps to show that epilepsy in LAMA2-RD may be more than an ancillary manife …
To date, there is no systematic characterization of epilepsy in LAMA2-RD, and its impact on neurodevelopment and on the clinical cour …
Clinical presentation, natural history, and outcomes for infantile intracranial cavernous malformations: case series and systematic review of the literature.
Goyal A, Fernandes-Torres J, Flemming KD, Williams LN, Daniels DJ. Goyal A, et al. Childs Nerv Syst. 2023 Jun;39(6):1545-1554. doi: 10.1007/s00381-023-05903-6. Epub 2023 Mar 14. Childs Nerv Syst. 2023. PMID: 36917267 Review.
Most cavernomas (64%, 23/36) were supratentorial, while 30% (n = 11) were located in brainstem and 5.5% (n = 2) in the cerebellum. ...Surgical resection may be associated with high rates of epilepsy cure and provide improvement in neurological function in a select n …
Most cavernomas (64%, 23/36) were supratentorial, while 30% (n = 11) were located in brainstem and 5.5% (n = 2) in the cerebellum. .. …
Molecular Diagnostic Yield of Exome Sequencing and Chromosomal Microarray in Cerebral Palsy: A Systematic Review and Meta-analysis.
Srivastava S, Lewis SA, Cohen JS, Zhang B, Aravamuthan BR, Chopra M, Sahin M, Kruer MC, Poduri A. Srivastava S, et al. JAMA Neurol. 2022 Dec 1;79(12):1287-1295. doi: 10.1001/jamaneurol.2022.3549. JAMA Neurol. 2022. PMID: 36279113 Free PMC article.
RESULTS: In the meta-analysis of ES yield in CP, the overall diagnostic yield of ES among the cohorts (15 study cohorts comprising 2419 individuals from 11 articles) was 23% (95% CI, 15%-34%). The diagnostic yield across cryptogenic CP cohorts was 35% (95% CI, 27%-45%), co …
RESULTS: In the meta-analysis of ES yield in CP, the overall diagnostic yield of ES among the cohorts (15 study cohorts comprising 2419 indi …
Efficacy and tolerability of fenfluramine in patients with Dravet syndrome: A systematic review and meta-analysis.
Sharawat IK, Panda PK, Kasinathan A, Panda P, Dawman L, Joshi K. Sharawat IK, et al. Seizure. 2021 Feb;85:119-126. doi: 10.1016/j.seizure.2020.12.016. Epub 2021 Jan 11. Seizure. 2021. PMID: 33461030 Free article.
BACKGROUND: Dravet syndrome (DS) is an infantile-onset developmental and epileptic encephalopathy syndrome with limited treatment options. ...A greater proportion of patients in the fenfluramine arm achieved >25 %, >50 %, >75 % and 100 % seizure redu …
BACKGROUND: Dravet syndrome (DS) is an infantile-onset developmental and epileptic encephalopathy syndrome with limited …
The co-occurrence of epilepsy and autism: A systematic review.
Lukmanji S, Manji SA, Kadhim S, Sauro KM, Wirrell EC, Kwon CS, Jetté N. Lukmanji S, et al. Epilepsy Behav. 2019 Sep;98(Pt A):238-248. doi: 10.1016/j.yebeh.2019.07.037. Epub 2019 Aug 6. Epilepsy Behav. 2019. PMID: 31398688
OBJECTIVE: We aimed to review the literature to determine the incidence and prevalence of autism in epilepsy and epilepsy in autism, conditions that are often comorbid. ...When excluding studies that investigated patients with syndromic epilepsy or develop …
OBJECTIVE: We aimed to review the literature to determine the incidence and prevalence of autism in epilepsy and epilepsy in a …
Characteristics of Developmental and Epileptic Encephalopathy Associated with PACS2 p.Glu209Lys Pathogenic Variant-Our Experience and Systematic Review of the Literature.
Stoian A, Bajko Z, Bălașa R, Andone S, Stoian M, Ormenișan I, Muntean C, Bănescu C. Stoian A, et al. Biomolecules. 2024 Feb 23;14(3):270. doi: 10.3390/biom14030270. Biomolecules. 2024. PMID: 38540691 Free PMC article. Review.
BACKGROUND: Developmental and epileptic encephalopathies (DEE) encompass a group of rare diseases with hereditary and genetic causes as well as acquired causes such as brain injuries or metabolic abnormalities. ...Facial dysmorphism and other or …
BACKGROUND: Developmental and epileptic encephalopathies (DEE) encompass a group of rare diseases with hereditar …
21 results