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WORKSHOP ISLAND 3 ALGEBRAIC ASPECTS OF INTEGRABILITY.
- Published in:
- Glasgow Mathematical Journal, 2009, v. 51, n. A, p. 1, doi. 10.1017/S0017089508004734
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- Publication type:
- Article
WORKSHOP ISLAND 3 ALGEBRAIC ASPECTS OF INTEGRABILITY.
- Published in:
- Glasgow Mathematical Journal, 2009, v. 51, n. A, p. 1, doi. 10.1017/S0017089508004734
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- Publication type:
- Article
Clinical spectrum and genotype-phenotype associations of KCNA2-related encephalopathies.
- Published in:
- 2017
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- Publication type:
- journal article
Epileptic activity is a surrogate for an underlying etiology and stopping the activity has a limited impact on developmental outcome.
- Published in:
- Epilepsia (Series 4), 2015, v. 56, n. 10, p. 1477, doi. 10.1111/epi.13105
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- Publication type:
- Article
Towards the identification of a genetic basis for Landau- Kleffner syndrome.
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- Epilepsia (Series 4), 2014, v. 55, n. 6, p. 858, doi. 10.1111/epi.12645
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- Publication type:
- Article
Reduction of seizure frequency after epilepsy surgery in a patient with STXBP1 encephalopathy and clinical description of six novel mutation carriers.
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- Epilepsia (Series 4), 2013, v. 54, n. 5, p. e74, doi. 10.1111/epi.12124
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- Publication type:
- Article
Benzodiazepines in the acute management of seizures with autonomic manifestations: Anticipate complications!
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- Epilepsia (Series 4), 2011, v. 52, n. 10, p. e156, doi. 10.1111/j.1528-1167.2011.03201.x
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- Publication type:
- Article
Status epilepticus in fragile X syndrome.
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- Epilepsia (Series 4), 2010, v. 51, n. 12, p. 2470, doi. 10.1111/j.1528-1167.2010.02761.x
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- Publication type:
- Article
A case of SUDEP in a patient with Dravet syndrome with SCN1A mutation.
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- Epilepsia (Series 4), 2010, v. 51, n. 9, p. 1915, doi. 10.1111/j.1528-1167.2010.02691.x
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- Publication type:
- Article
Cryptogenic Late-Onset Epileptic Spasms or Late Infantile Epileptogenic Encephalopathy?
- Published in:
- 2007
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- Publication type:
- Letter
Ketogenic diet treatment in diffuse intrinsic pontine glioma in children: Retrospective analysis of feasibility, safety, and survival data.
- Published in:
- Cancer Reports, 2021, v. 4, n. 5, p. 1, doi. 10.1002/cnr2.1383
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- Publication type:
- Article
Partial Rhombencephalosynapsis and Chiari Type II Malformation in a Child: a True Association Supported by DTI Tractography.
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- Cerebellum, 2012, v. 11, n. 1, p. 227, doi. 10.1007/s12311-011-0300-3
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- Publication type:
- Article
Childhood-Onset Movement Disorders Can Mask a Primary Immunodeficiency: 6 Cases of Classical Ataxia-Telangiectasia and Variant Forms.
- Published in:
- 2022
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- Publication type:
- Case Study
Riboflavin in cyclic vomiting syndrome: efficacy in three children.
- Published in:
- 2016
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- Publication type:
- journal article
Diagnostic potential of IL6 and other blood-based inflammatory biomarkers in mild traumatic brain injury among children.
- Published in:
- Frontiers in Neurology, 2024, p. 1, doi. 10.3389/fneur.2024.1432217
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- Publication type:
- Article
SCN8A heterozygous variants are associated with anoxic‐epileptic seizures.
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- American Journal of Medical Genetics. Part A, 2020, v. 182, n. 5, p. 1209, doi. 10.1002/ajmg.a.61513
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- Publication type:
- Article
SERPINI1 pathogenic variants: An emerging cause of childhood-onset progressive myoclonic epilepsy.
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- American Journal of Medical Genetics. Part A, 2017, v. 173, n. 9, p. 2456, doi. 10.1002/ajmg.a.38317
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- Publication type:
- Article
A Review of Targeted Therapies for Monogenic Epilepsy Syndromes.
- Published in:
- Frontiers in Neurology, 2022, v. 13, p. 1, doi. 10.3389/fneur.2022.829116
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- Publication type:
- Article
Epilepsy: Old Syndromes, New Genes.
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- Current Neurology & Neuroscience Reports, 2014, v. 14, n. 6, p. 1, doi. 10.1007/s11910-014-0447-7
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- Publication type:
- Article
Neurodevelopmental problems of unaccompanied refugee and migrant children: a new challenge for pediatric neurologists.
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- 2019
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- Publication type:
- Letter
Focal cortical malformations in children with early infantile epilepsy and PCDH19 mutations: case report.
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- 2018
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- Publication type:
- Case Study
Head stereotypies in STXBP1 encephalopathy.
- Published in:
- Developmental Medicine & Child Neurology, 2013, v. 55, n. 8, p. 769, doi. 10.1111/dmcn.12197
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- Publication type:
- Article
Severe childhood encephalopathy with dyskinesia and prolonged cognitive disturbances: evidence for anti- N-methyl-d-aspartate receptor encephalitis.
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- Developmental Medicine & Child Neurology, 2010, v. 52, n. 5, p. e78, doi. 10.1111/j.1469-8749.2009.03542.x
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- Publication type:
- Article
Quantum Cohomology via Vicious and Osculating Walkers.
- Published in:
- Letters in Mathematical Physics, 2014, v. 104, n. 7, p. 771, doi. 10.1007/s11005-014-0685-2
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- Publication type:
- Article
Highly Enantioselective Rhodium-Catalyzed Hydrogenation of 2-(2-Methoxy-2-oxoethyl)acrylic Acid - A Convenient Access of Enantiomerically Pure Isoprenoid Building Blocks.
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- European Journal of Organic Chemistry, 2003, v. 2003, n. 17, p. 3453, doi. 10.1002/ejoc.200300222
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- Publication type:
- Article
Feasibility, tolerability and efficacy of the ketogenic diet in children with drug‐resistant epilepsy in Vietnam.
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- Epilepsia Open, 2023, v. 8, n. 4, p. 1484, doi. 10.1002/epi4.12825
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- Publication type:
- Article
Letter on: 3D figure of epilepsy syndromes.
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- Epilepsia Open, 2023, v. 8, n. 3, p. 1202, doi. 10.1002/epi4.12762
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- Publication type:
- Article
The phenotypic spectrum of X‐linked, infantile onset ALG13‐related developmental and epileptic encephalopathy.
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- Epilepsia (Series 4), 2021, v. 62, n. 2, p. 325, doi. 10.1111/epi.16761
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- Publication type:
- Article
Epileptic networks are strongly connected with and without the effects of interictal discharges.
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- Epilepsia (Series 4), 2016, v. 57, n. 7, p. 1086, doi. 10.1111/epi.13400
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- Publication type:
- Article
ZMYND11 variants are a novel cause of centrotemporal and generalised epilepsies with neurodevelopmental disorder.
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- Clinical Genetics, 2021, v. 100, n. 4, p. 412, doi. 10.1111/cge.14023
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- Publication type:
- Article
Paroxysmal events in glucose transporter type 1 deficiency syndrome: Early identification of their true nature is important.
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- Developmental Medicine & Child Neurology, 2024, v. 66, n. 11, p. 1403, doi. 10.1111/dmcn.16000
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- Publication type:
- Article
Pyridoxine or pyridoxal‐5‐phosphate treatment for seizures in glycosylphosphatidylinositol deficiency: A cohort study.
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- Developmental Medicine & Child Neurology, 2022, v. 64, n. 6, p. 789, doi. 10.1111/dmcn.15142
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- Publication type:
- Article
Drug-Level Monitoring on Admission for Presurgical Epilepsy Evaluation.
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- European Neurology, 2017, v. 78, n. 1/2, p. 105, doi. 10.1159/000479003
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- Publication type:
- Article
Postoperative EEG in Hemimegalencephaly.
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- European Neurology, 2012, v. 68, n. 6, p. 358, doi. 10.1159/000342239
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- Publication type:
- Article
Comment on: Ketogenic diet treatment in recurrent diffuse intrinsic pontine glioma in children: A safety and feasibility study.
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- Pediatric Blood & Cancer, 2019, v. 66, n. 7, p. N.PAG, doi. 10.1002/pbc.27664
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- Publication type:
- Article
Comment on: Ketogenic diet treatment in recurrent diffuse intrinsic pontine glioma in children: A safety and feasibility study.
- Published in:
- 2019
- By:
- Publication type:
- Letter
Cylindric Hecke Characters and Gromov–Witten Invariants via the Asymmetric Six-Vertex Model.
- Published in:
- Communications in Mathematical Physics, 2021, v. 381, n. 2, p. 591, doi. 10.1007/s00220-020-03906-x
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- Publication type:
- Article
Cylindric Versions of Specialised Macdonald Functions and a Deformed Verlinde Algebra.
- Published in:
- Communications in Mathematical Physics, 2013, v. 318, n. 1, p. 173, doi. 10.1007/s00220-012-1630-9
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- Publication type:
- Article
Desaturation During Cry in the Neonatal Period.
- Published in:
- Global Pediatric Health, 2018, v. 5, p. 1, doi. 10.1177/2333794X18764515
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- Publication type:
- Article
Clinical Cases and the Molecular Profiling of a Novel Childhood Encephalopathy-Causing GNAO1 Mutation P170R.
- Published in:
- Cells (2073-4409), 2023, v. 12, n. 20, p. 2469, doi. 10.3390/cells12202469
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- Publication type:
- Article
Dravet Syndrome (Severe Myoclonic Epilepsy in Infancy): A Retrospective Study of 16 Patients.
- Published in:
- Journal of Child Neurology, 2007, v. 22, n. 2, p. 185, doi. 10.1177/0883073807300294
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- Publication type:
- Article
Seizures and Epilepsies due to Channelopathies and Neurotransmitter Receptor Dysfunction: A Parallel between Genetic and Immune Aspects.
- Published in:
- Molecular Syndromology, 2016, v. 7, n. 4, p. 197, doi. 10.1159/000447707
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- Publication type:
- Article
Characterization of glycosylphosphatidylinositol biosynthesis defects by clinical features, flow cytometry, and automated image analysis.
- Published in:
- Genome Medicine, 2018, v. 10, p. 1, doi. 10.1186/s13073-017-0510-5
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- Publication type:
- Article