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A Feature Extraction Method for P2P Botnet Detection Using Graphic Symmetry Concept.
- Published in:
- Symmetry (20738994), 2019, v. 11, n. 3, p. 326, doi. 10.3390/sym11030326
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- Article
Frequency-Octupling Millimeter-Wave Optical Vector Signal Generation via an I/Q Modulator-Based Sagnac Loop.
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- Symmetry (20738994), 2019, v. 11, n. 1, p. 84, doi. 10.3390/sym11010084
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- Article
Hypomyelinating disorders in China: The clinical and genetic heterogeneity in 119 patients.
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- PLoS ONE, 2018, v. 13, n. 2, p. 1, doi. 10.1371/journal.pone.0188869
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- Article
An Automatic Welding Robot for the Roof of Spiral Steel Silo.
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- Processes, 2023, v. 11, n. 11, p. 3049, doi. 10.3390/pr11113049
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- Publication type:
- Article
Genotype-phenotype correlation of deletions and duplications of 4p: case reports and literature review.
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- Frontiers in Genetics, 2023, p. 1, doi. 10.3389/fgene.2023.1174314
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- Article
Analysis of SCN1A mutation and parental origin in patients with Dravet syndrome.
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- Journal of Human Genetics, 2010, v. 55, n. 7, p. 421, doi. 10.1038/jhg.2010.39
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- Article
A Novel Wireless Sensor Network Evolution Model Based on Energy-Efficiency.
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- International Journal of Online Engineering, 2017, v. 13, n. 3, p. 4, doi. 10.3991/ijoe.v13i03.6855
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- Article
Adaptive Neuro-Fuzzy Inference System for Classification of Background EEG Signals from ESES Patients and Controls.
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- Scientific World Journal, 2014, p. 1, doi. 10.1155/2014/140863
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- Publication type:
- Article
Identification of Novel ARSA Mutations in Chinese Patients with Metachromatic Leukodystrophy.
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- International Journal of Genomics, 2018, p. 1, doi. 10.1155/2018/2361068
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- Publication type:
- Article
Wheat root exudates suppress faba bean Fusarium wilt disease.
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- Food & Energy Security, 2024, v. 13, n. 3, p. 1, doi. 10.1002/fes3.550
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- Article
P2P Botnet Detection Based on Nodes Correlation by the Mahalanobis Distance.
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- Information (2078-2489), 2019, v. 10, n. 5, p. 160, doi. 10.3390/info10050160
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- Article
Intercropping with wheat suppressed Fusarium wilt in faba bean and modulated the composition of root exudates.
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- Plant & Soil, 2020, v. 448, n. 1/2, p. 153, doi. 10.1007/s11104-019-04413-2
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- Article
Instance Segmentation Method Based on Improved Mask R-CNN for the Stacked Electronic Components.
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- Electronics (2079-9292), 2020, v. 9, n. 6, p. 886, doi. 10.3390/electronics9060886
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- Publication type:
- Article
Case Report: A Case of Epileptic Disorder Associated With a Novel CNTN2 Frameshift Variant in Homozygosity due to Maternal Uniparental Disomy.
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- Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.743833
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- Article
Case Report: Causative De novo Variants of KCNT2 for Developmental and Epileptic Encephalopathy.
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- Frontiers in Genetics, 2021, v. 11, p. 1, doi. 10.3389/fgene.2021.649556
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- Publication type:
- Article
Genetic Etiologies in Developmental and/or Epileptic Encephalopathy With Electrical Status Epilepticus During Sleep: Cohort Study.
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- Frontiers in Genetics, 2021, v. 11, p. N.PAG, doi. 10.3389/fgene.2021.607965
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- Article
Analysis of the Phenotypic Variability as Well as Impact of Early Diagnosis and Treatment in Six Affected Families With ALDH7A1 Deficiency.
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- Frontiers in Genetics, 2021, v. 11, p. N.PAG, doi. 10.3389/fgene.2021.644447
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- Publication type:
- Article
Complex Mosaicism of Two Distinct Mutations in a Female Patient With KCNA2 -Related Encephalopathy: A Case Report.
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- Frontiers in Genetics, 2020, v. 11, p. N.PAG, doi. 10.3389/fgene.2020.00911
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- Publication type:
- Article
De novo variants in AGO1 recapitulate a heterogeneous neurodevelopmental disorder phenotype.
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- Clinical Genetics, 2022, v. 101, n. 4, p. 459, doi. 10.1111/cge.14114
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- Article
A prediction model integrating synchronization biomarkers and clinical features to identify responders to vagus nerve stimulation among pediatric patients with drug‐resistant epilepsy.
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- CNS Neuroscience & Therapeutics, 2022, v. 28, n. 11, p. 1838, doi. 10.1111/cns.13923
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- Article
Mathematical Methods for Sensitive Information Mining Method of News Communication Platform Based on Big Data IOT Analysis.
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- Mathematical Problems in Engineering, 2022, p. 1, doi. 10.1155/2022/1606183
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- Article
Clinical features and underlying etiology of children with Lennox–Gastaut syndrome.
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- Journal of Neurology, 2024, v. 271, n. 8, p. 5392, doi. 10.1007/s00415-024-12465-3
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- Publication type:
- Article
GABRB3-related epilepsy: novel variants, clinical features and therapeutic implications.
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- Journal of Neurology, 2022, v. 269, n. 5, p. 2649, doi. 10.1007/s00415-021-10834-w
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- Publication type:
- Article
Long-term outcomes of epilepsy surgery in tuberous sclerosis complex.
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- Journal of Neurology, 2017, v. 264, n. 6, p. 1146, doi. 10.1007/s00415-017-8507-y
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- Article
Germline de novo variants in CSNK2B in Chinese patients with epilepsy.
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- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-53484-9
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- Publication type:
- Article
Simultaneous quantification of alpha-aminoadipic semialdehyde, piperideine-6-carboxylate, pipecolic acid and alpha-aminoadipic acid in pyridoxine-dependent epilepsy.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-47882-2
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- Publication type:
- Article
PCDH19-related epilepsy in mosaic males: The phenotypic implication of genotype and variant allele frequency.
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- Frontiers in Neurology, 2022, v. 13, p. 01, doi. 10.3389/fneur.2022.1041509
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- Article
Genetic and phenotypic spectrum of Chinese patients with epilepsy and photosensitivity.
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- Frontiers in Neurology, 2022, v. 16, p. 01, doi. 10.3389/fneur.2022.907228
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- Article
Startle-Induced Epileptic Spasms: A Clinical and Video-EEG Study.
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- Frontiers in Neurology, 2022, v. 13, p. 1, doi. 10.3389/fneur.2022.878504
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- Publication type:
- Article
The Clinical Features and Long-Term Follow-Up of Vitamin B6-Responsive Infantile Spasms in a Chinese Cohort.
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- Frontiers in Neurology, 2022, v. 13, p. 1, doi. 10.3389/fneur.2022.895978
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- Article
Clinical Diagnosis, Treatment, and <i>ALDH7A1</i> Mutations in Pyridoxine-Dependent Epilepsy in Three Chinese Infants.
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- PLoS ONE, 2014, v. 9, n. 3, p. 1, doi. 10.1371/journal.pone.0092803
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- Publication type:
- Article
The genotype and phenotype of CACNA1A variants related developmental and epileptic encephalopathy.
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- Journal of Epilepsy (2096-0247), 2022, v. 8, n. 5, p. 407, doi. 10.7507/2096-0247.202204012
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- Publication type:
- Article
Identification of an Identical de Novo SCAMP5 Missense Variant in Four Unrelated Patients With Seizures and Severe Neurodevelopmental Delay.
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- Frontiers in Pharmacology, 2020, v. 11, p. N.PAG, doi. 10.3389/fphar.2020.599191
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- Article
A Rare Presentation Characterized by Epileptic Spasms in ALDH7A1 , Pyridox(am)ine-5′-Phosphate Oxidase, and PLPBP Deficiency.
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- Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.804461
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- Article
RESEARCH ON MULTI-AGENT SYSTEMS IN A SMART SMALL GRID FOR RESOURCE APPORTIONMENT AND PLANNING.
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- Scalable Computing: Practice & Experience, 2021, v. 22, n. 2, p. 203, doi. 10.12694/scpe.v22i2.1895
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- Article
Virtual Network Embedding Based on Topology Potential.
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- Entropy, 2018, v. 20, n. 12, p. 941, doi. 10.3390/e20120941
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- Article
Phenotypes and PRRT2 mutations in Chinese families with benign familial infantile epilepsy and infantile convulsions with paroxysmal choreoathetosis.
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- BMC Neurology, 2013, v. 13, n. 1, p. 1, doi. 10.1186/1471-2377-13-209
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- Article
Phenotypes and PRRT2 mutations in Chinese families with benign familial infantile epilepsy and infantile convulsions with paroxysmal choreoathetosis.
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- 2013
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- Publication type:
- journal article
Aesthetic reconstruction of thumb or finger partial defect with trimmed toe-flap transfer.
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- Microsurgery, 2007, v. 27, n. 2, p. 74, doi. 10.1002/micr.20310
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- Article
The relationship between the characteristics of burst suppression pattern and different etiologies in epilepsy.
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- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-95040-4
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- Article
Thermal Wave Scattering and Temperature Concentration around the Opening in Platinum–Rhodium Leaky Plates.
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- Metals (2075-4701), 2020, v. 10, n. 7, p. 946, doi. 10.3390/met10070946
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- Publication type:
- Article
Tongue Biting Event in Patients with Sleep-Related Facial Mandibular Myoclonus: A Case Series Study.
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- Nature & Science of Sleep, 2024, v. 16, p. 207, doi. 10.2147/NSS.S433628
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- Publication type:
- Article
Epileptic seizure detection by combining robust-principal component analysis and least square-support vector machine.
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- International Journal of Imaging Systems & Technology, 2017, v. 27, n. 4, p. 368, doi. 10.1002/ima.22240
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- Publication type:
- Article
POLR3-related leukodystrophy caused by biallelic POLR3A and 1C pathogenic variants: a single-center experience.
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- Frontiers in Neurology, 2024, p. 1, doi. 10.3389/fneur.2024.1355484
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- Article
A long journey to treat epilepsy with the gut microbiota.
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- Frontiers in Cellular Neuroscience, 2024, p. 1, doi. 10.3389/fncel.2024.1386205
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- Article
SCN2A -Related Epilepsy: The Phenotypic Spectrum, Treatment and Prognosis.
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- Frontiers in Molecular Neuroscience, 2022, v. 15, p. 1, doi. 10.3389/fnmol.2022.809951
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- Article
Phenotypic Spectrum and Prognosis of Epilepsy Patients With GABRG2 Variants.
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- Frontiers in Molecular Neuroscience, 2022, v. 15, p. 1, doi. 10.3389/fnmol.2022.809163
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- Article
Identification of novel ATP7A mutations and prenatal diagnosis in Chinese patients with Menkes disease.
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- Metabolic Brain Disease, 2017, v. 32, n. 4, p. 1123, doi. 10.1007/s11011-017-9985-4
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- Publication type:
- Article
Novel phenotypes of pyridox(am)ine-5'-phosphate oxidase deficiency and high prevalence of c.445_448del mutation in Chinese patients.
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- Metabolic Brain Disease, 2017, v. 32, n. 4, p. 1081, doi. 10.1007/s11011-017-9995-2
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- Article
Phenotype of heterozygous variants of dehydrodolichol diphosphate synthase.
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- Developmental Medicine & Child Neurology, 2022, v. 64, n. 1, p. 125, doi. 10.1111/dmcn.14976
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- Article