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Correction to: Diagnosis and treatment of Chiari Malformation and syringomyelia in adults: International Consensus Document.
- Published in:
- 2022
- By:
- Publication type:
- Correction Notice
Diagnosis and treatment of Chiari malformation and syringomyelia in adults: international consensus document.
- Published in:
- Neurological Sciences, 2022, v. 43, n. 2, p. 1327, doi. 10.1007/s10072-021-05347-3
- By:
- Publication type:
- Article
Diagnosis and treatment of Chiari malformation type 1 in children: the International Consensus Document.
- Published in:
- Neurological Sciences, 2022, v. 43, n. 2, p. 1311, doi. 10.1007/s10072-021-05317-9
- By:
- Publication type:
- Article
The management of Chiari malformation type 1 and syringomyelia in children: a review of the literature.
- Published in:
- Neurological Sciences, 2021, v. 42, n. 12, p. 4965, doi. 10.1007/s10072-021-05565-9
- By:
- Publication type:
- Article
GEN-O-MA project: an Italian network studying clinical course and pathogenic pathways of moyamoya disease-study protocol and preliminary results.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Neuroradiological diagnosis of Chiari malformations.
- Published in:
- Neurological Sciences, 2011, v. 32, p. 283, doi. 10.1007/s10072-011-0695-0
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- Publication type:
- Article
Treatment for Chiari 1 malformation (CIM): analysis of a pediatric surgical series.
- Published in:
- 2011
- By:
- Publication type:
- Journal Article
The neurophysiological balance in Chiari type 1 malformation (CM1), tethered cord and related syndromes.
- Published in:
- Neurological Sciences, 2011, v. 32, p. 311, doi. 10.1007/s10072-011-0692-3
- By:
- Publication type:
- Article
Neurological pictures in Paediatric Chiari I malformation.
- Published in:
- Neurological Sciences, 2011, v. 32, p. 295, doi. 10.1007/s10072-011-0744-8
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- Publication type:
- Article
Can Chiari malformation negatively affect higher mental functioning in developmental age?
- Published in:
- Neurological Sciences, 2011, v. 32, p. 307, doi. 10.1007/s10072-011-0779-x
- By:
- Publication type:
- Article
Treatment for Chiari 1 malformation (CIM): analysis of a pediatric surgical series.
- Published in:
- Neurological Sciences, 2011, v. 32, p. 321, doi. 10.1007/s10072-011-0731-0
- By:
- Publication type:
- Article
Language abilities and gestural communication in a girl with bilateral perisylvian syndrome: a clinical and rehabilitative follow-up.
- Published in:
- Neurological Sciences, 2010, v. 31, n. 4, p. 471, doi. 10.1007/s10072-010-0309-2
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- Publication type:
- Article
The Key Search Subtest of the Behavioural Assessment of the Dysexecutive Syndrome in Children (BADS-C) Instrument Reveals Impaired Planning Without External Constraints in Children With Neurofibromatosis Type 1.
- Published in:
- Journal of Child Neurology, 2017, v. 32, n. 4, p. 387, doi. 10.1177/0883073816683322
- By:
- Publication type:
- Article
Electroencephalographic (EEG) Photoparoxysmal Responses Under 5 Years of Age.
- Published in:
- Journal of Child Neurology, 2015, v. 30, n. 13, p. 1824, doi. 10.1177/0883073815583687
- By:
- Publication type:
- Article
Increase of Circulating Endothelial Progenitor Cells and Released Angiogenic Factors in Children with Moyamoya Arteriopathy.
- Published in:
- International Journal of Molecular Sciences, 2023, v. 24, n. 2, p. 1233, doi. 10.3390/ijms24021233
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- Publication type:
- Article
The Lipid Asset Is Unbalanced in Peripheral Nerve Sheath Tumors.
- Published in:
- International Journal of Molecular Sciences, 2022, v. 23, n. 1, p. 61, doi. 10.3390/ijms23010061
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- Publication type:
- Article
Plasma Lipid Profiling Contributes to Untangle the Complexity of Moyamoya Arteriopathy.
- Published in:
- International Journal of Molecular Sciences, 2021, v. 22, n. 24, p. 13410, doi. 10.3390/ijms222413410
- By:
- Publication type:
- Article
Vascular Remodeling in Moyamoya Angiopathy: From Peripheral Blood Mononuclear Cells to Endothelial Cells.
- Published in:
- International Journal of Molecular Sciences, 2020, v. 21, n. 16, p. 5763, doi. 10.3390/ijms21165763
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- Publication type:
- Article
Genetic/epigenetic effects in NF1 microdeletion syndrome: beyond the haploinsufficiency, looking at the contribution of not deleted genes.
- Published in:
- Human Genetics, 2024, v. 143, n. 6, p. 775, doi. 10.1007/s00439-024-02683-0
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- Publication type:
- Article
The noncoding RNA AK127244 in 2p16.3 locus: A new susceptibility region for neuropsychiatric disorders.
- Published in:
- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2018, v. 177, n. 6, p. 557, doi. 10.1002/ajmg.b.32649
- By:
- Publication type:
- Article
Chiari I malformation in defined genetic syndromes in children: are there common pathways?
- Published in:
- Child's Nervous System, 2019, v. 35, n. 10, p. 1727, doi. 10.1007/s00381-019-04319-5
- By:
- Publication type:
- Article
Chiari 1 malformation and untreated sagittal synostosis: a new subset of complex Chiari?
- Published in:
- Child's Nervous System, 2019, v. 35, n. 10, p. 1741, doi. 10.1007/s00381-019-04283-0
- By:
- Publication type:
- Article
Unique combination of myxopapillary ependymoma and conus lipoma with subcutaneous extension in an 11-month-old child.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
Novel mutations in SLC16A2 associated with a less severe phenotype of MCT8 deficiency.
- Published in:
- Metabolic Brain Disease, 2019, v. 34, n. 6, p. 1565, doi. 10.1007/s11011-019-00464-7
- By:
- Publication type:
- Article
Surgical Management of Chiari 1.5 in Children: A Truly Different Disease?
- Published in:
- Journal of Clinical Medicine, 2024, v. 13, n. 6, p. 1708, doi. 10.3390/jcm13061708
- By:
- Publication type:
- Article
Visuoperceptual Impairment in Children with NF1: From Early Visual Processing to Procedural Strategies.
- Published in:
- Behavioural Neurology, 2019, p. 1, doi. 10.1155/2019/7146168
- By:
- Publication type:
- Article
A Translational Approach to Spinal Neurofibromatosis: Clinical and Molecular Insights from a Wide Italian Cohort.
- Published in:
- Cancers, 2023, v. 15, n. 1, p. 59, doi. 10.3390/cancers15010059
- By:
- Publication type:
- Article
Risk of Optic Pathway Glioma in Neurofibromatosis Type 1: No Evidence of Genotype–Phenotype Correlations in a Large Independent Cohort.
- Published in:
- Cancers, 2019, v. 11, n. 12, p. 1838, doi. 10.3390/cancers11121838
- By:
- Publication type:
- Article
Brain Tumors in NF1 Children: Influence on Neurocognitive and Behavioral Outcome.
- Published in:
- Cancers, 2019, v. 11, n. 11, p. 1772, doi. 10.3390/cancers11111772
- By:
- Publication type:
- Article
CGH Findings in Children with Complex and Essential Autistic Spectrum Disorder.
- Published in:
- Journal of Autism & Developmental Disorders, 2023, v. 53, n. 2, p. 615, doi. 10.1007/s10803-020-04833-5
- By:
- Publication type:
- Article
Response to 'characteristics of 2p15-p16.1 microdeletion syndrome: review and description of two additional patients'.
- Published in:
- Congenital Anomalies, 2015, v. 55, n. 4, p. 191, doi. 10.1111/cga.12119
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- Publication type:
- Article
Case report: SLC6A1 mutations presenting with isolated absence seizures: description of 2 novel cases.
- Published in:
- Frontiers in Neuroscience, 2023, p. 1, doi. 10.3389/fnins.2023.1219244
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- Publication type:
- Article
The TAND checklist: a useful screening tool in children with tuberous sclerosis and neurofibromatosis type 1.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Sepiapterin reductase deficiency: A Treatable Mimic of Cerebral Palsy.
- Published in:
- Annals of Neurology, 2012, v. 71, n. 4, p. 520, doi. 10.1002/ana.22685
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- Publication type:
- Article
126 novel mutations in Italian patients with neurofibromatosis type 1.
- Published in:
- Molecular Genetics & Genomic Medicine, 2015, v. 3, n. 6, p. 513, doi. 10.1002/mgg3.161
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- Publication type:
- Article
Clinical and Molecular Spectrum of Myotonia and Periodic Paralyses Associated With Mutations in SCN4A in a Large Cohort of Italian Patients.
- Published in:
- Frontiers in Neurology, 2020, v. 11, p. 1, doi. 10.3389/fneur.2020.00646
- By:
- Publication type:
- Article
Fluorescein-guided resection of plexiform neurofibromas: how I do it.
- Published in:
- Acta Neurochirurgica, 2019, v. 161, n. 10, p. 2141, doi. 10.1007/s00701-019-04038-5
- By:
- Publication type:
- Article
Cognitive and Behavioral Outcome of Pediatric Low-Grade Central Nervous System Tumors Treated Only with Surgery: A Single Center Experience.
- Published in:
- Diagnostics (2075-4418), 2023, v. 13, n. 9, p. 1568, doi. 10.3390/diagnostics13091568
- By:
- Publication type:
- Article
Verbal and Gestural Communication in Children With Bilateral Perisylvian Polymicrogyria.
- Published in:
- Journal of Child Neurology, 2007, v. 22, n. 9, p. 1090, doi. 10.1177/0883073807306247
- By:
- Publication type:
- Article
Neuropsychological Effects of Frontal Lobe Epilepsy in Children.
- Published in:
- Journal of Child Neurology, 2002, v. 17, n. 9, p. 661, doi. 10.1177/088307380201700902
- By:
- Publication type:
- Article
A novel CLN8 mutation in late-infantile-onset neuronal ceroid lipofuscinosis (LINCL) reveals aspects of CLN8 neurobiological function.
- Published in:
- Human Mutation, 2009, v. 30, n. 7, p. 1104, doi. 10.1002/humu.21012
- By:
- Publication type:
- Article
Simultaneous Detection of NF1, SPRED1, LZTR1, and NF2 Gene Mutations by Targeted NGS in an Italian Cohort of Suspected NF1 Patients.
- Published in:
- Genes, 2020, v. 11, n. 6, p. 671, doi. 10.3390/genes11060671
- By:
- Publication type:
- Article
Non-Coding RNA and Tumor Development in Neurofibromatosis Type 1: ANRIL Rs2151280 Is Associated with Optic Glioma Development and a Mild Phenotype in Neurofibromatosis Type 1 Patients.
- Published in:
- Genes, 2019, v. 10, n. 11, p. 892, doi. 10.3390/genes10110892
- By:
- Publication type:
- Article
A PDE10A de novo mutation causes childhood-onset chorea with diurnal fluctuations.
- Published in:
- 2017
- By:
- Publication type:
- Case Study