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Pediatric Headache in Primary Care and Emergency Departments: Consensus with RAND/UCLA Method.
- Published in:
- Life (2075-1729), 2022, v. 12, n. 2, p. N.PAG, doi. 10.3390/life12020142
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- Publication type:
- Article
Quadriceps muscle strength in Duchenne muscular dystrophy and effect of corticosteroid treatment.
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- Acta Myologica, 2020, v. 39, n. 4, p. 200, doi. 10.36185/2532-1900-023
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- Publication type:
- Article
Mowat-Wilson syndrome: growth charts.
- Published in:
- 2020
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- Publication type:
- journal article
Post-Traumatic Headache in Children after Minor Head Trauma: Incidence, Phenotypes, and Risk Factors.
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- Children, 2023, v. 10, n. 3, p. 534, doi. 10.3390/children10030534
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- Publication type:
- Article
Autozygosity-driven genetic diagnosis in consanguineous families from Italy and the Greater Middle East.
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- Human Genetics, 2020, v. 139, n. 11, p. 1429, doi. 10.1007/s00439-020-02187-7
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- Publication type:
- Article
Cannabidiol in the acute phase of febrile infection‐related epilepsy syndrome (FIRES).
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- Epilepsia Open, 2023, v. 8, n. 2, p. 685, doi. 10.1002/epi4.12740
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- Publication type:
- Article
KETASER01 protocol: What went right and what went wrong.
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- Epilepsia Open, 2022, v. 7, n. 3, p. 532, doi. 10.1002/epi4.12627
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- Publication type:
- Article
Clinical and psychopathological profiles of children with somatic symptom disorders in a pediatric emergency unit: an observational study before and during the SARS-CoV-2 pandemic.
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- European Journal of Pediatrics, 2023, v. 182, n. 4, p. 1731, doi. 10.1007/s00431-023-04850-3
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- Publication type:
- Article
Cyclic Vomiting Syndrome in Children.
- Published in:
- Frontiers in Neurology, 2020, v. 11, p. N.PAG, doi. 10.3389/fneur.2020.583425
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- Publication type:
- Article
Anti-Inflammatory and Immunomodulatory Effect of High-Dose Immunoglobulins in Children: From Approved Indications to Off-Label Use.
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- Cells (2073-4409), 2023, v. 12, n. 19, p. 2417, doi. 10.3390/cells12192417
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- Publication type:
- Article
Relationship between Sensory Alterations and Repetitive Behaviours in Children with Autism Spectrum Disorders: A Parents' Questionnaire Based Study.
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- Brain Sciences (2076-3425), 2021, v. 11, n. 4, p. 484, doi. 10.3390/brainsci11040484
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- Publication type:
- Article
Sleep in Children With Pallister Killian Syndrome: A Prospective Clinical and Videopolysomnographic Study.
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- Frontiers in Neurology, 2021, v. 12, p. 1, doi. 10.3389/fneur.2021.796828
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- Publication type:
- Article
Results From an Italian Expanded Access Program on Cannabidiol Treatment in Highly Refractory Dravet Syndrome and Lennox–Gastaut Syndrome.
- Published in:
- Frontiers in Neurology, 2021, v. 11, p. 1, doi. 10.3389/fneur.2021.673135
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- Publication type:
- Article
Symmetric polymicrogyria and pachygyria associated with TUBB2B gene mutations.
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- European Journal of Human Genetics, 2012, v. 20, n. 9, p. 995, doi. 10.1038/ejhg.2012.21
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- Publication type:
- Article
Down Syndrome: how to communicate the diagnosis.
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- Italian Journal of Pediatrics, 2023, v. 49, n. 1, p. 1, doi. 10.1186/s13052-023-01419-6
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- Publication type:
- Article
Sleep disorders reveal distress among children and adolescents during the Covid-19 first wave: results of a large web-based Italian survey.
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- Italian Journal of Pediatrics, 2021, v. 47, n. 1, p. 1, doi. 10.1186/s13052-021-01083-8
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- Publication type:
- Article
Autism spectrum disorder and anorexia nervosa: an Italian prospective study.
- Published in:
- Italian Journal of Pediatrics, 2021, v. 47, n. 1, p. 1, doi. 10.1186/s13052-021-01006-7
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- Publication type:
- Article
Aromatic L-Amino-Acid Decarboxylase Deficiency Screening by Analysis of 3-O-Methyldopa in Dried Blood Spots: Results of a Multicentric Study in Neurodevelopmental Disorders.
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- Genes, 2023, v. 14, n. 9, p. 1828, doi. 10.3390/genes14091828
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- Publication type:
- Article
Status Epilepticus in Chromosomal Disorders Associated with Epilepsy: A Systematic Review.
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- Genes, 2023, v. 14, n. 2, p. 299, doi. 10.3390/genes14020299
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- Publication type:
- Article
Cognitive, Behavioral, and Sensory Profile of Pallister–Killian Syndrome: A Prospective Study of 22 Individuals.
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- Genes, 2022, v. 13, n. 2, p. 356, doi. 10.3390/genes13020356
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- Publication type:
- Article
Expanding the Neurological Phenotype of Ring Chromosome 10 Syndrome: A Case Report and Review of the Literature.
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- Genes, 2021, v. 12, n. 10, p. 1513, doi. 10.3390/genes12101513
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- Publication type:
- Article
Neurological Phenotype of Mowat-Wilson Syndrome.
- Published in:
- Genes, 2021, v. 12, n. 7, p. 982, doi. 10.3390/genes12070982
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- Publication type:
- Article
Correction: Olfactory bulb anomalies in KBG syndrome mouse model and patients.
- Published in:
- 2024
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- Publication type:
- Correction Notice
Correction: Olfactory bulb anomalies in KBG syndrome mouse model and patients.
- Published in:
- 2024
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- Publication type:
- Correction Notice
Olfactory bulb anomalies in KBG syndrome mouse model and patients.
- Published in:
- BMC Medicine, 2024, v. 22, n. 1, p. 1, doi. 10.1186/s12916-024-03363-6
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- Publication type:
- Article
Olfactory bulb anomalies in KBG syndrome mouse model and patients.
- Published in:
- BMC Medicine, 2024, v. 22, n. 1, p. 1, doi. 10.1186/s12916-024-03363-6
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- Publication type:
- Article
Prospective study on long-term treatment with oxcarbazepine in pediatric epilepsy.
- Published in:
- Journal of Neurology, 2009, v. 256, n. 9, p. 1527, doi. 10.1007/s00415-009-5157-8
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- Publication type:
- Article
Identification of Potential Clusters of Signs and Symptoms to Prioritize Patients’ Eligibility for AADCd Screening by 3-OMD Testing: An Italian Delphi Consensus.
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- Behavioural Neurology, 2024, v. 2024, p. 1, doi. 10.1155/2024/1023861
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- Publication type:
- Article
Relapse risk factors in anti-N-methyl-D-aspartate receptor encephalitis.
- Published in:
- 2019
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- Publication type:
- journal article
Efficacy and Safety of Pulse Intravenous Methylprednisolone in Pediatric Epileptic Encephalopathies: Timing and Networks Consideration.
- Published in:
- Journal of Clinical Medicine, 2024, v. 13, n. 9, p. 2497, doi. 10.3390/jcm13092497
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- Publication type:
- Article
A mutation in PAK3 with a dual molecular effect deregulates the RAS/MAPK pathway and drives an X-linked syndromic phenotype.
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- Human Molecular Genetics, 2014, v. 23, n. 13, p. 3607, doi. 10.1093/hmg/ddu070
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- Publication type:
- Article
Inflammatory disease of the central nervous system induced by anti-GD2 monoclonal antibody in a patient with high risk neuroblastoma.
- Published in:
- 2014
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- Publication type:
- case study
Inflammatory disease of the central nervous system induced by anti-G<sub>D2</sub> monoclonal antibody in a patient with high risk neuroblastoma.
- Published in:
- Pediatric Blood & Cancer, 2014, v. 61, n. 8, p. 1521, doi. 10.1002/pbc.24982
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- Publication type:
- Article
Status epilepticus as a main manifestation of posterior reversible encephalopathy syndrome after pediatric hematopoietic stem cell transplantation.
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- Pediatric Blood & Cancer, 2012, v. 58, n. 5, p. 785, doi. 10.1002/pbc.23344
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- Publication type:
- Article
Early Implantation as a Main Predictor of Response to Vagus Nerve Stimulation in Childhood-Onset Refractory Epilepsy.
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- Journal of Child Neurology, 2021, v. 36, n. 5, p. 365, doi. 10.1177/0883073820974855
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- Publication type:
- Article
Computed Tomography in Acute Severe Central Nervous System Complications in Children Treated for Cancer: Still a Useful Diagnostic Tool in the Emergency Setting.
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- Journal of Child Neurology, 2021, v. 36, n. 3, p. 169, doi. 10.1177/0883073820962354
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- Publication type:
- Article
Early onset absence epilepsy with onset in the first year of life: A multicenter cohort study.
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- Epilepsia (Series 4), 2013, v. 54, p. 66, doi. 10.1111/epi.12311
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- Publication type:
- Article
CDKL5 deficiency-related neurodevelopmental disorders: a multi-center cohort study in Italy.
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- Journal of Neurology, 2024, v. 271, n. 8, p. 5368, doi. 10.1007/s00415-024-12421-1
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- Publication type:
- Article
Diverse faces of GNAO1: mild forms in epilepsy and autism.
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- Journal of Neurology, 2024, v. 271, n. 7, p. 3777, doi. 10.1007/s00415-024-12418-w
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- Publication type:
- Article
Children under 6 years with acute headache in Pediatric Emergency Departments. A 2-year retrospective exploratory multicenter Italian study.
- Published in:
- Cephalalgia, 2023, v. 43, n. 6, p. 1, doi. 10.1177/03331024231164361
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- Publication type:
- Article
Cytogenetic and molecular characterization of a recombinant X chromosome in a family with a severe neurologic phenotype and macular degeneration.
- Published in:
- Molecular Cytogenetics (17558166), 2015, v. 8, n. 1, p. 1, doi. 10.1186/s13039-015-0164-1
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- Publication type:
- Article
Epilepsy in Mowat-Wilson syndrome: Delineation of the electroclinical phenotype.
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- American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 2, p. 273, doi. 10.1002/ajmg.a.35717
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- Publication type:
- Article
A novel mutation in SPART gene causes a severe neurodevelopmental delay due to mitochondrial dysfunction with complex I impairments and altered pyruvate metabolism.
- Published in:
- FASEB Journal, 2019, v. 33, n. 10, p. 1, doi. 10.1096/fj.201802722R
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- Publication type:
- Article
Targeted re-sequencing for early diagnosis of genetic causes of childhood epilepsy: the Italian experience from the 'beyond epilepsy' project.
- Published in:
- Italian Journal of Pediatrics, 2020, v. 46, n. 1, p. 1, doi. 10.1186/s13052-020-00860-1
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- Publication type:
- Article
The Role of the Noradrenergic System in Eating Disorders: A Systematic Review.
- Published in:
- International Journal of Molecular Sciences, 2021, v. 22, n. 20, p. 11086, doi. 10.3390/ijms222011086
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- Publication type:
- Article