• <em>HNRNPU</em>-Related Neurodevelopmental Disorder
• <em>SCN8A</em> mutation in a child presenting with seizures and developmental delays
• A generalized multistage approach to oral and nasal intubation in infants with Pierre Robin sequence: A retrospective review
• A patient with early myoclonic encephalopathy (EME) with a de novo KCNQ2 mutation
• A Rare Case of Neonatal Hypomagnesemia with Secondary Hypocalcemia Caused by a Novel Homozygous TRPM6 Gene Variant
• A survey around the Italian pediatric units on current clinical practice for Sleep Disordered Breathing (SDB)
• Adverse Events in Young and Preterm Infants Receiving Topical Timolol for Infantile Hemangioma
• Airway abnormalities and pulmonary complications in long-term treated late-onset Pompe disease: Diagnostic and interventional by flexible bronchoscopy
• Alexander Disease
• An episode of acute encephalopathy with biphasic seizures and late reduced diffusion followed by hemiplegia and intractable epilepsy observed in a patient with a novel frameshift mutation in HNRNPU
• An intronic variant in BRAT1 creates a cryptic splice site, causing epileptic encephalopathy without prominent rigidity
• An Unusual Case of Neonatal High-Output Heart Failure: Infantile Hepatic Hemangioma
• Apparent life-threatening event in infancy
• Arnold-Chiari type 1 malformation in Potocki-Lupski syndrome
• Balloon dilation and rapid maxillary expansion: a novel combination treatment for congenital nasal pyriform aperture stenosis in an infant
• BRAT1 mutations are associated with infantile epileptic encephalopathy, mitochondrial dysfunction, and survival into childhood
• Brimonidine Toxicity Secondary to Topical Use for an Ulcerated Hemangioma
• Bronchopulmonary Dysplasia
• Caffeine disrupts ataxia telangiectasia mutated gene-related pathways and exacerbates acetaminophen toxicity in human fetal immortalized hepatocytes
• Carbonic Anhydrase II Deficiency: A Rare Case of Severe Obstructive Sleep Apnea
• Case report: Fatal infantile hypertonic myofibrillar myopathy with compound heterozygous mutations in the <em>CRYAB</em> gene
• Case report: Fatal infantile hypertonic myofibrillar myopathy with compound heterozygous mutations in the CRYAB gene
• Central Apneas Due to the CLIFAHDD Syndrome Successfully Treated with Pyridostigmine
• Clinical semiology of temporal lobe seizures in preschool children: contribution of invasive recording to anatomical classification
• Control of the cardiovascular and respiratory systems during sleep
• Corrigendum: Improving CPAP adherence in adults with obstructive sleep apnea syndrome: A scoping review of motivational interventions
• Corrigendum: Study protocol of a randomized controlled trial of motivational interviewing-based intervention to improve adherence to continuous positive airway pressure in patients with obstructive sleep apnea syndrome: The MotivAir study
• Decrease in blood pressure during continuous positive airway pressure treatment for obstructive sleep apnoea: still searching for predictive factors
• Detection and treatment of respiratory disorders in obese children: Obstructive sleep apnea syndrome and obesity hypoventilation syndrome
• Determinants of Sleepiness at Wheel and Missing Accidents in Patients With Obstructive Sleep Apnea
• EEG and clinical characteristics of neonatal parechovirus encephalitis
• Epileptic Encephalopathy Due to <em>BRAT1</em> Pathogenic Variants
• Expanding the neurodevelopmental phenotype of PURA syndrome
• Expanding the phenotype of congenital central hypoventilation syndrome impacts management decisions
• Extending the KCNQ2 encephalopathy spectrum: clinical and neuroimaging findings in 17 patients
• Factors Influencing Neonatal Gut Microbiome and Health with a Focus on Necrotizing Enterocolitis
• Feasibility of parent-attended ambulatory polysomnography in children with suspected obstructive sleep apnea
• Gas exchange parameters for the prediction of obstructive sleep apnea in infants
• Gastroesophageal Reflux Disease in a One-Week-Old Infant Presenting With Cyanosis and Respiratory Distress
• Gender Affects Long-Term Neurological Outcome of Neonates
• Genotype-phenotype correlations in hyperekplexia: apnoeas, learning difficulties and speech delay
• Giant pattern VEPs in children
• HTRA2 Defect: A Recognizable Inborn Error of Metabolism with 3-Methylglutaconic Aciduria as Discriminating Feature Characterized by Neonatal Movement Disorder and Epilepsy-Report of 11 Patients
• Hyperferritinemia in neonatal and infantile human parechovirus-3 infection in comparison with other infectious diseases
• Hyperventilation and seizures in an adolescent female
• Identification of a novel GRIN2D variant in a neonate with intractable epileptic encephalopathy-a case report
• Impact of prone positioning in infants with Pierre Robin sequence: a polysomnography study
• Improving CPAP Adherence in Adults With Obstructive Sleep Apnea Syndrome: A Scoping Review of Motivational Interventions
• Infantile Apparent Life-Threatening Events, an Educational Review
• Infantile hypophosphatasia combined with vitamin B6-responsive seizures and reticular formation lesions on magnetic resonance imaging: A case report
• Intractable apnoeic seizures in a child with a deletion typically associated with Williams syndrome
• Joubert Syndrome: A Rare Radiological Case
• KCNQ2 mutation in an infant with encephalopathy of infancy with migrating focal seizures
• KIF5A mutations cause an infantile onset phenotype including severe myoclonus with evidence of mitochondrial dysfunction
• Knockout of sodium pump α3 subunit gene (Atp1a3^-/-) results in perinatal seizure and defective respiratory rhythm generation
• Lack of mitochondrial complex I assembly factor NDUFAF2 results in a distinctive infantile-onset brainstem neurodegenerative disease with early lethality
• Lethal neonatal rigidity and multifocal seizure syndrome--report of another family with a BRAT1 mutation
• Long survival in Leigh syndrome: new cases and review of literature
• Longitudinal polysomnographic findings in infantile Pompe disease
• Lung ultrasound supports clinical evaluation of feeding competence development in preterm neonates
• m.8993T&gt;G-Associated Leigh Syndrome with Hypocitrullinemia on Newborn Screening
• Manual therapy for the pediatric population: a systematic review
• Migraine and Sleep in Children: A Bidirectional Relationship
• Mild obstructive sleep apnea increases hypertension risk, challenging traditional severity classification
• Multiorgan involvement and management in children with Down syndrome
• Multiple Sulfatase Deficiency
• NALCN Dysfunction as a Cause of Disordered Respiratory Rhythm With Central Apnea
• Neonatal SCN2A encephalopathy: A peculiar recognizable electroclinical sequence
• Neurocognitive evaluation of children with down syndrome and obstructive sleep apnea syndrome
• Nonketotic Hyperglycinemia in Tunisia. Report upon a Series of 69 Patients
• Novel mutations in <em>SLC6A5</em> with benign course in hyperekplexia
• Obstructive Sleep Apnea Syndrome (OSAS), metabolic syndrome and mental health in small enterprise workers. feasibility of an Action for Health
• Obstructive sleep apnea syndrome and public health: the Italian way
• OSA and Work-Related Injuries: Searching for Evidence
• Overnight Video-Polysomnographic Studies in Children with Intractable Epileptic Encephalopathies
• Perioperative apnea in infants with hypertrophic pyloric stenosis: A systematic review
• Pharmacological Treatment of Severe Breathing Abnormalities in a Case of <em>HNRNPU</em> Epileptic Encephalopathy
• Phenotypic and genetic spectrum of SCN8A-related disorders, treatment options, and outcomes
• Polysomnographic findings in infantile Pompe disease
• Postoperative apnea after pyloromyotomy for infantile hypertrophic pyloric stenosis
• Prolonged Video-EEG and Heart Rate Variability can Elucidate Autonomic Dysregulation in Infantile Apneic Seizures
• Pulse transit time as a diagnostic test for OSA in children with Down syndrome
• Rapid and safe response to low-dose carbamazepine in neonatal epilepsy
• Refractory Epilepsy in a Toddler With PPP2R1A Gene Mutation and Congenital Hydrocephalus
• Respiratory dysfunction in a mouse model of spinocerebellar ataxia type 7
• Respiratory involvement and sleep-related disorders in CMT1A: case report and review of the literature
• Respiratory problems owing to severe metabolic alkalosis in infants presenting with hypertrophic pyloric stenosis
• Risk of Occupational Accidents in Workers with Obstructive Sleep Apnea: Systematic Review and Meta-analysis
• Schaaf-Yang syndrome overview: Report of 78 individuals
• Seizures in trisomy 18: Prevalence, description, and treatment
• Severe encephalopathy associated with SARS-CoV-2 Omicron BA.1 variant infection in a neonate
• Sleep Apnea, Sleepiness, and Driving Risk
• Sleep problems in Rett syndrome animal models: A systematic review
• Spinal muscular atrophy with respiratory distress syndrome (SMARD1): Case report and review of literature
• Study protocol of a randomized controlled trial of motivational interviewing-based intervention to improve adherence to continuous positive airway pressure in patients with obstructive sleep apnea syndrome: The MotivAir study
• The "Italian way" to counteract obstructive sleep apnoea syndrome in children
• The gain of function SCN1A disorder spectrum: novel epilepsy phenotypes and therapeutic implications
• The role of sleep laboratory polygraphy in the evaluation of obstructive sleep apnea syndrome in Robin infants
• Unattended home sleep studies for the diagnosis of obstructive sleep apnea in a population of French children
• Weird Laughing in Hyperekplexia: A new phenotype associated with a novel mutation in the GLRA1 gene?