All Stories

  1. The Evolution of the Role of Imaging in the Diagnosis of Craniosynostosis: A Narrative Review
  2. Vitamin B12 Deficiency and West Syndrome: An Uncommon but Preventable Cause of Neurological Disorder. Report on Three Cases, One of Them with Late Onset during Vitamin B12 Treatment
  3. Dynamic and Static Splinting for Treatment of Developmental Dysplasia of the Hip: A Systematic Review
  4. Secondary Scoliosis as a Complication of Acute Transverse Myelitis in a Child
  5. Poland Syndrome with Atypical Malformations Associated to a de novo 1.5 Mb Xp22.31 Duplication
  6. Chromosome 15q BP3 to BP5 deletion is a likely locus for speech delay and language impairment: Report on a four‐member family and an unrelated boy
  7. Advanced olfactory neuroblastoma in a teenager: a clinical case and short review of literature
  8. Epileptic Seizures in Non-syndromic Megalencephaly (MEG): A Case Series in our Department
  9. Cerebral Palsy in Children: Evaluation of Clinical Outcomes
  10. PRRT2 gene variant in a child with dysmorphic features, congenital microcephaly, and severe epileptic seizures: genotype-phenotype correlation?
  11. Haemophilic arthropathy: A narrative review on the use of intra‐articular drugs for arthritis
  12. Acute Motor Axonal Neuropathy in a 5-Month-Old Child
  13. Focal Neuropathy Mimicking Focal Dystonia in a Child: Diagnostic and Rehabilitative Tools
  14. Cerebral White Matter Lesions and Dysmorphisms: Signs Suggestive of 6p25 Deletion Syndrome—Literature Review
  15. Optic Neuropathy, Secondary to Ethmoiditis, and Onodi Cell Inflammation during Childhood: A Case Report and Review of the Literature
  16. Short-Term Neurodevelopmental Outcome in Term Neonates Treated with Phenobarbital versus Levetiracetam: A Single-Center Experience
  17. Molecular Mechanism Involved in the Pathogenesis of Early-Onset Epileptic Encephalopathy
  18. Grisel Syndrome in Pediatric Age: A Single-Center Italian Experience and Review of the Literature
  19. Epilepsy in Children: From Diagnosis to Treatment with Focus on Emergency
  20. Arterial ischemic stroke (AIS) in childhood: clinical report from a single control center
  21. Serum concentrations of perfluorinated compounds among children living in Sicily (Italy)
  22. Epilepsy in Children: From Diagnosis to Treatment
  23. Expression of the OAS Gene Family Is Highly Modulated in Subjects Affected by Juvenile Dermatomyositis, Resembling an Immune Response to a dsRNA Virus Infection
  24. Grisel’s syndrome caused by Mycoplasma pneumoniae infection: a case report and review of the literature
  25. Ptosis in childhood
  26. A Probable Topiramate-induced Limbs Paraesthesia and Rigid Fingers Flexion
  27. Chromosome 2p15-p16.1 microduplication in a boy with congenital anomalies: Is it a distinctive syndrome?
  28. Benign and severe early-life seizures: a round in the first year of life
  29. Acute hyperkinetic movement disorders in Italian paediatric emergency departments
  30. Pyridoxine Add-On Treatment for the Control of Behavioral Adverse Effects Induced by Levetiracetam in Children: A Case-Control Prospective Study
  31. Electroclinical findings and long-term outcomes in epileptic patients with inv dup (15)
  32. Microcephaly/Trigonocephaly, Intellectual Disability, Autism Spectrum Disorder, and Atypical Dysmorphic Features in a Boy with Xp22.31 Duplication
  33. Electroclinical pattern and epilepsy evolution in an infant with Miller–Dieker syndrome
  34. Clinical spectrum of woolly hair: indications for cerebral involvement
  35. Cervical neurenteric cyst and Klippel-Feil syndrome: An abrupt onset of myelopathic signs in a young patient
  36. Biological Drugs in Guillain-Barré Syndrome: An Update
  37. A New Patient with Potocki–Lupski Syndrome: A Literature Review
  38. Resuming the obsolete term “small head”: when microcephaly occurs without cognitive impairment
  39. Erratum: Single-Epileptic Spasms with or without Hypsarrhythmia: A Study of 16 Patients
  40. A clinical review on megalencephaly
  41. Single-Epileptic Spasms with or without Hypsarrhythmia: A Study of 16 Patients
  42. Pediatric status epilepticus: improved management with new drug therapies?
  43. Randomized Comparison of Helmet CPAP Versus High-Flow Nasal Cannula Oxygen in Pediatric Respiratory Distress
  44. Epilepsy
  45. Clinical Course of N-Methyl-D-Aspartate Receptor Encephalitis and the Effectiveness of Cyclophosphamide Treatment
  46. Therapeutic approaches to pediatric pseudotumor cerebri: New insights from literature data
  47. Ataxia in children: early recognition and clinical evaluation
  48. Inherited human IRAK-1 deficiency selectively impairs TLR signaling in fibroblasts
  49. Pediatric autoimmune encephalitis
  50. Levetiracetam in neonatal seizures as first-line treatment: A prospective study
  51. Hyperprolinemia Type IA
  52. The Gut–brain axis: A new pathogenic view of neurologic symptoms – Description of a pediatric case
  53. The Role of Dendritic Cells in Central Nervous System Autoimmunity: Focusing on Multiple Sclerosis and Emerging Therapeutics Targeting Dendritic Cells
  54. Array-CGH in pediatric neurology: A prospective observational study
  55. Congenital muscular dystrophy: from muscle to brain
  56. Aripiprazole for the treatment of irritability and aggression in children and adolescents affected by autism spectrum disorders
  57. A girl with a 14.7 Mb 3q26.32–q28 duplication
  58. Child Abuse Syndrome (CAS): A Newly Recognized Distinct Entity
  59. A neurocutaneous phenotype with paired hypo- and hyperpigmented macules, microcephaly and stunted growth as prominent features
  60. Prognostic Challenges of SCN1A Genetic Mutations: Report on Two Children with Mild Features
  61. A mild phenotype associated with a de novo microdeletion 10q23.1-q23.2: a new patient with a novel feature
  62. Total Hemi-overgrowth in Pigmentary Mosaicism of the (Hypomelanosis of) Ito Type
  63. Acetaminophen administration in pediatric age: an observational prospective cross-sectional study
  64. Holoprosencephaly and Recurrent Episodes of Severe Neurogenic Hypernatremia
  65. Nervous system involvement in clinical peripheral inflammation: A description of three pediatric cases
  66. Seizures Are Not a Prevalent Feature of Wyburn-Mason Syndrome
  67. Nevus Sebaceous and Its Association With Neurologic Involvement
  68. Refractory absence seizures: An Italian multicenter retrospective study
  69. Natalizumab in multiple sclerosis: discontinuation, progressive multifocal leukoencephalopathy and possible use in children
  70. Clinical dissection of childhood occipital epilepsy of Gastaut and prognostic implication
  71. The usefulness of immunotherapy in pediatric neurodegenerative disorders: A systematic review of literature data
  72. Congenital generalized hypertrichosis: the skin as a clue to complex malformation syndromes
  73. Epilepsy and innate immune system: A possible immunogenic predisposition and related therapeutic implications
  74. Peripheral neuropathy in a child with Mycoplasma pneumoniae infections
  75. Propranolol: Effectiveness and Failure in Infantile Cutaneous Hemangiomas
  76. Legumes steam allergy in childhood: Update of the reported cases
  77. Incidence of Mediterranean Spotted Fever in Sicilian children: a clinical-epidemiological observational retrospective study from 1987 to 2010
  78. Hypomelanosis of Ito: a round on the frequency and type of epileptic complications
  79. A Selective Mutism Arising from First Language Attrition, Successfully Treated with Paroxetine-CBT Combination Treatment
  80. Asthma and hypoxia
  81. Sodium metabisulphite allergy with multiple food and drug hypersensitivities in a five-year-old child: A case report and literature review
  82. The natural history of spinal neurofibromatosis: a critical review of clinical and genetic features
  83. Epileptic seizures as a manifestation of cow’s milk allergy: a studied relationship and description of our pediatric experience
  84. Hydranencephaly: cerebral spinal fluid instead of cerebral mantles
  85. Infantile spasms syndrome, West syndrome and related phenotypes: What we know in 2013
  86. Three Cases of Palatal Tics and Gilles De La Tourette Syndrome
  87. Unilateral Eye Blinking Arising From the Ictal Ipsilateral Occipital Area
  88. Clinical guidelines in pediatric headache: evaluation of quality using the AGREE II instrument
  89. Down syndrome and arterial ischemic stroke in childhood: A potential immunologic link with selective IgG4 subclass deficiency
  90. Usefulness of video-EEG in the paediatric emergency department
  91. Wide spectrum of congenital anomalies including choanal atresia, malformed extremities, and brain and spinal malformations in a girl with a de novo 5.6-Mb deletion of 13q12.11-13q12.13
  92. Corrigendum to “Lacosamide in pediatric and adult patients: Comparison of efficacy and safety” [Seizure 22 (2013) 210–216]
  93. Targeting inflammation as a therapeutic strategy for drug-resistant epilepsies
  94. Corrigendum to “Reflex myoclonic epilepsy in infancy: A multicenter clinical study” [Epilepsy Res. 103 (2013) 237–244]
  95. Klippel-Trenaunay syndromein a boy with concomitant ipsilateral overgrowth and undergrowth
  96. Rapid Spontaneous Resolution of Fibromatosis Colli in a 3-Week-Old Girl
  97. A new clinical feature associated with familial early-onset of dystonic-guttural tics: An unusual diagnosis of PANDAS
  98. Valproate in adolescents with photosensitive epilepsy with generalized tonic–clonic seizures only
  99. Polysomnographic evaluation of non-invasive ventilation in children with neuromuscular disease
  100. The immunomodulatory effect of probiotics beyond atopy: an update
  101. Electroclinical Features and Long-Term Outcome of Cryptogenic Epilepsy in Children with Down Syndrome
  102. Gelastic seizures due to hypothalamic hamartoma: Rapid resolution after endoscopic tumor disconnection
  103. Noninvasive ventilation in pediatric emergency care: a literature review and description of our experience
  104. Noninvasive ventilation for acute respiratory distress in children with central nervous system disorders
  105. Clinical dissection of early onset absence epilepsy in children and prognostic implications
  106. Spinal Neurofibromatosis with Central Nervous System Involvement in a Set of Twin Girls and a Boy: Further Expansion of the Phenotype
  107. Reflex myoclonic epilepsy in infancy: a critical review
  108. Sublingual immunotherapy in preschool children: an update
  109. Lacosamide in pediatric and adult patients: Comparison of efficacy and safety
  110. Natural history of neurofibromatosis type 2 with onset before the age of 1 year
  111. Reflex myoclonic epilepsy in infancy: A multicenter clinical study
  112. Congenital familial myasthenic syndromes: disease and course in an affected dizygotic twin pair
  113. West Syndrome Treatment: New Roads for an Old Syndrome
  114. Cutaneous and Leptomeningeal Hemangiomas With Impressive Benign Evolution
  115. The Immunomodulatory Effect of Probiotics Beyond Atopy: An Update
  116. Hemihydranencephaly: living with half brain dysfunction
  117. Congenital myasthenic syndromes: Clinical and molecular report on 7 Sicilian patients
  118. Acute Glomerulonephritis in a Child withChlamydia pneumoniaeInfection: A Case Report
  119. Vitamin D3 an ever green molecule
  120. Non-Epileptik Psikojen Nöbetler: Klinik Pratikte Çözülmesi Zor Tanısal Bir Problem
  121. Interstitial 16p13.3 microduplication: Case report and critical review of genotype–phenotype correlation
  122. Apneic crises: A clue for MECP2 testing in severe neonatal hypotonia-respiratory failure
  123. Spine and brain malformations in a patient obligate carrier of MTHFR with autism and mental retardation
  124. Autonomic Dysfunction Manifesting With Asymmetric Face Flushing and Paroxysmal Nonconvulsive Episodes
  125. Primary Headaches in Children: Clinical Findings and the Association with other Conditions
  126. Nevus vascularis mixtus (cutaneous vascular twin nevi) associated with intracranial vascular malformation of the Dyke–Davidoff–Masson type in two patients
  127. Diagnosis and management of catamenial seizures: a review
  128. Ohtahara syndrome with emphasis on recent genetic discovery
  129. Congenital talipes equinovarus: an epidemiological study in Sicily
  130. Acquired Peripheral Neuropathy: A Report on 20 Children
  131. An 11-Year Follow-up Study of Neonatal-Onset, Bath-Induced Alternating Hemiplegia of Childhood in Twins
  132. Microcephaly associated with Legg-Calvè-Perthes disease in two siblings
  133. Hepatic echinococcosis: Clinical and therapeutic aspects
  134. The role of micronutrients in the diet of HIV-1-infected individuals
  135. Primary headache: Role of investigations in a cohort of young children and adolescents
  136. Generalised epilepsy with febrile seizures plus (GEFS+): molecular analysis in a restricted area
  137. Long-term outcome of epilepsy in Kabuki syndrome
  138. Hopkins’ syndrome
  139. P16.10 Update on childhood-onset spinal muscular atrophy: a retrospective study of 75 cases
  140. Erratum to “Recurrent Hopkin's syndrome: A case report and review of the literature” [J Neurol Sci 297 (2010) 89–91]
  141. Long-term neurological outcome of a sextuplet pregnancy
  142. Acute Disseminated Encephalomyelitis: A Long-Term Prospective Study and Meta-Analysis
  143. Dysembryoplastic Neuroepithelial Tumors: A Prospective Clinicopathologic and Outcome Study of 13 Children
  144. Recurrent Hopkin's syndrome: A case report and review of the literature
  145. Neurological Manifestations in Individuals with Pure Cutaneous or Syndromic (Ruggieri-Happle Syndrome) Phenotypes with “Cutis Tricolor”: A Study of 14 Cases
  146. First case of dizygous twins with X-linked α-thalassemia/mental retardation syndrome showing wide clinical variability
  147. The neurology of coeliac disease in childhood: what is the evidence? A systematic review and meta-analysis
  148. A boy born with multiple lesions of atrophoderma
  149. Neonatal onset of bath-induced alternating hemiplegia of childhood
  150. Neonatal Autoimmune Hypothyroidism: A Patient Report
  151. Lissencephalic syndromes brain and beyond
  152. The aristaless Arx gene one gene for many interneuronopathies
  153. Recurrent obstructive hydrocephalus in a 4-month-old infant
  154. Microcephaly, sensorineural deafness and Currarino triad with duplication–deletion of distal 7q
  155. Headache in Pediatric Patients With Celiac Disease and Its Prevalence as a Diagnostic Clue
  156. A Syndrome with Coarse Face, Mental Retardation and Unusual Stereotyped Movements
  157. Ganglioneuroblastoma-associated Vitamin D Deficiency Rickets
  158. Incidence and causes of neonatal hyperbilirubinemia in a center of Catania
  159. Symptomatic hypocalcemia in an epileptic child treated with valproic acid plus lamotrigine: a case report
  160. Voluntary selective big toe dorsal flection: pseudo-Babinski phenomenon?
  161. Two siblings with a homozygous MTHFR C677T (G80A-RFC1) mutation and stroke
  162. Infantile spasms in the setting of Sturge–Weber syndrome
  163. Headache in paediatric patients with celiac disease and its prevalence as a diagnostic clue
  164. Neurofibromatosis type 1 and infantile spasms
  165. Reply
  166. Pseudohypoparathyroidism Ia With Evans Syndrome
  167. Congenital Lymphedema-lymphangiectasia Associated With Scrotal Angiokeratoma (Fordyce Type) and Hearing Impairment
  168. Low Prevalence of Neurologic and Psychiatric Manifestations in Children with Gluten Sensitivity
  169. Neonatal onset of hot water reflex seizures in monozygotic twins subsequently manifesting episodes of alternating hemiplegia
  170. Otologic findings in children with gastroesophageal reflux
  171. Polyneuritis Cranialis: Full Recovery after Intravenous Immunoglobulins
  172. Rotavirus and Celiac Disease
  173. Protective effects of the sigma agonist Pre-084 in the rat retina
  174. Anton-Babinski syndrome in a child with early-stage adrenoleukodystrophy
  175. Callosal anomalies with interhemispheric cyst: Expanding the phenotype
  176. Chronic Yersinia Enterocolitis Infection Presenting as Intestinal Obstruction
  177. Increased Antistreptococcal Antibody Titers and Anti—Basal Ganglia Antibodies in Patients With Tourette Syndrome: Controlled Cross-Sectional Study
  178. Topical Review: Autoimmune Neuropsychiatric Disorders Associated With Streptococcal Infection: Sydenham Chorea, PANDAS, and PANDAS Variants
  179. Blink reflex abnormalities in children with Tourette syndrome
  180. Septo-Optic Dysplasia Complex: A Heterogeneous Malformation Syndrome
  181. Clinical Heterogeneity in Familial Congenital Ptosis: Analysis of Fourteen Cases in One Family Over Five Generations
  182. STROKE IN TWO CHILDREN WITH MYCOPLASMA PNEUMONIAE INFECTION A CAUSAL OR CASUAL RELATIONSHIP?
  183. Callosal anomalies with interhemispheric cyst: Expanding the phenotype
  184. A Complex Brain Malformation Syndrome with Rhombencephalosynapsis, Preaxial Hexadactyly plus Facial and Skull Anomalies
  185. Congenital Insensitivity to Pain with Anhidrosis (NTRK1 Mutation) and Early Onset Renal Disease: Clinical Report on Three Sibs with a 25-Year Follow-Up in One of Them
  186. Liver transplantation in a child with celiac disease
  187. CNS findings in three cases of septo-optic dysplasia, including one with semilobar holoprosencephaly
  188. Fetal Cells in Maternal Blood: A Six-Fold Increase in Women who have Undergone Amniocentesis and Carry a Fetus with Down Syndrome: A Multicenter Study
  189. Ophthalmological manifestations in segmental neurofibromatosis type 1
  190. Epilepsy is not a Prominent Feature of Primary Autism
  191. Peripheral Neuropathy as First Sign of Ulcerative Colitis in a Child
  192. Anti-brain antibodies in PANDAS versus uncomplicated streptococcal infection
  193. Autoimmune Hepatitis Associated with Celiac Disease in Childhood: Report of Two Cases
  194. Worldwide distribution and broader clinical spectrum of muscle-eye-brain disease
  195. Reply to Dr Hahn
  196. Congenital muscular dystrophy with adducted thumbs, ptosis, external ophthalmoplegia, mental retardation and cerebellar hypoplasia: a novel form of CMD
  197. Lobar Holoprosencephaly
  198. White matter changes mimicking a leukodystrophy in a patient with Mucopolysaccharidosis: characterization by MRI
  199. Clinical heterogeneity in eyelid myoclonia, with absences, and epilepsy
  200. Holoprosencephaly (Lobar Form) Associated With Bilateral Vocal Cord Palsy
  201. Long-Term Survival in a Child With Arthrogryposis Multiplex Congenita and Spinal Muscular Atrophy
  202. Neuropsychological assessment in children with absence epilepsy
  203. A Genomewide Screen for Autism Susceptibility Loci
  204. Fetal Nucleated Red Blood Cell Counts in Peripheral Blood of Mothers Bearing Down Syndrome Fetus
  205. Neuropsychological assessment in children with absence epilepsy
  206. Lack of progression of brain atrophy in Aicardi-Goutières syndrome
  207. Hemihydranencephaly: Case Report and Literature Review
  208. Hemihydranencephaly: Case Report and Literature Review
  209. Noninvasive prenatal diagnosis of chromosomal aneuploidies by isolation and analysis of fetal cells from maternal blood
  210. Arthrogryposis Multiplex Congenita and Pituitary Ectopia. A Case Report
  211. Tuberous breast deformity in an adolescent girl with Hurler-Scheie syndrome
  212. Diabetes insipidus in neurobrucellosis
  213. Diffuse Polymicrogyria Associated With Congenital Hydrocephalus, Craniosynostosis, Severe Mental Retardation, and Minor Facial and Genital Anomalies
  214. Colobomatous microphthalmia, microcephaly with cerebellar hypoplasia: Association or new syndrome?
  215. Colobomatous microphthalmia, microcephaly with cerebellar hypoplasia: Association or new syndrome?
  216. Temporal Triangular Alopecia in Association With Mental Retardation and Epilepsy in a Mother and Daughter
  217. Recurrent peripheral neuropathy in a girl with celiac disease
  218. Extraordinary intrathecal bone reaction in β-thalassaemia intermedia
  219. Marin-Amat Syndrome: Case Report and Review of the Literature
  220. Vein of Galen Malformation and Infantile Spasms