366 results on '"Cordelli, Duccio Maria"'
Search Results
52. sj-pdf-1-cep-10.1177_03331024231164361 - Supplemental material for Children under 6 years with acute headache in Pediatric Emergency Departments. A 2-year retrospective exploratory multicenter Italian study
53. Early Immunotherapy and Longer Corticosteroid Treatment Are Associated With Lower Risk of Relapsing Disease Course in Pediatric MOGAD
54. Pediatric Moyamoya Disease and Syndrome in Italy: A Multicenter Cohort
55. Pediatric Headache in Primary Care and Emergency Departments: Consensus with RAND/UCLA Method
56. Psychopathological Impact in Patients with History of Rheumatic Fever with or without Sydenham’s Chorea: A Multicenter Prospective Study
57. KETASER01 protocol: What went right and what went wrong
58. Etiology, characteristics and outcome of seizures after pediatric hematopoietic stem cell transplantation
59. Pediatric Moyamoya Disease and Syndrome in Italy: A Multicenter Cohort
60. The PURPLE N study: objective and perceived nutritional status in children and adolescents with cerebral palsy
61. Cognitive, Behavioral, and Sensory Profile of Pallister–Killian Syndrome: A Prospective Study of 22 Individuals
62. Expanding Phenotype of Poirier–Bienvenu Syndrome: New Evidence from an Italian Multicentrical Cohort of Patients
63. Sleep in Children With Pallister Killian Syndrome: A Prospective Clinical and Videopolysomnographic Study
64. Epilepsy features in ARID1B-related Coffin-Siris syndrome
65. Expanding the Neurological Phenotype of Ring Chromosome 10 Syndrome: A Case Report and Review of the Literature
66. Early vagus nerve stimulator implantation as a main predictor of positive outcome in pediatric patients with epileptic encephalopathy
67. Additional file 2 of Sleep disorders reveal distress among children and adolescents during the Covid-19 first wave: results of a large web-based Italian survey
68. Additional file 1 of Sleep disorders reveal distress among children and adolescents during the Covid-19 first wave: results of a large web-based Italian survey
69. Conventional magnetic resonance imaging and diffusion tensor imaging studies in children with novel GPR56 mutations: further delineation of a cobblestone-like phenotype
70. Neurological Phenotype of Mowat-Wilson Syndrome
71. Relationship between Sensory Alterations and Repetitive Behaviours in Children with Autism Spectrum Disorders: A Parents’ Questionnaire Based Study
72. Inflammatory disease of the central nervous system induced by anti-GD2 monoclonal antibody in a patient with high risk neuroblastoma
73. A mutation in PAK3 with a dual molecular effect deregulates the RAS/MAPK pathway and drives an X-linked syndromic phenotype
74. Prospective study on long-term treatment with oxcarbazepine in pediatric epilepsy
75. Early onset absence epilepsy with onset in the first year of life: A multicenter cohort study
76. Additional file 1 of Mowat-Wilson syndrome: growth charts
77. Additional file 1 of Targeted re-sequencing for early diagnosis of genetic causes of childhood epilepsy: the Italian experience from the ‘beyond epilepsy’ project
78. Autism Spectrum Disorder and Anorexia Nervosa. Is There a Link? An Italian Experience
79. Early Implantation as a Main Predictor of Response to Vagus Nerve Stimulation in Childhood-Onset Refractory Epilepsy
80. Cyclic Vomiting Syndrome in Children
81. Computed Tomography in Acute Severe Central Nervous System Complications in Children Treated for Cancer: Still a Useful Diagnostic Tool in the Emergency Setting
82. Epilepsy in Mowat–Wilson syndrome: Delineation of the electroclinical phenotype
83. Status epilepticus as a main manifestation of posterior reversible encephalopathy syndrome after pediatric hematopoietic stem cell transplantation
84. Bathing epilepsy: report of two Caucasian cases
85. Myoclonic epilepsy with photosensitivity in infants with Pallister-Killian Syndrome
86. Characteristics of Acute Nystagmus in the Pediatric Emergency Department
87. Mowat-Wilson Syndrome: Growth Charts
88. Post-ictal circulating levels of allopregnanolone in children with partial or generalized seizures
89. Diagnostic Targeted Resequencing in 349 Patients with Drug-Resistant Pediatric Epilepsies Identifies Causative Mutations in 30 Different Genes
90. Results From an Italian Expanded Access Program on Cannabidiol Treatment in Highly Refractory Dravet Syndrome and Lennox–Gastaut Syndrome.
91. Early Implantation as a Main Predictor of Response to Vagus Nerve Stimulation in Childhood-Onset Refractory Epilepsy.
92. Sleep in Mowat-Wilson Syndrome: a clinical and video-polysomnographic study
93. A novel mutation in SPART gene causes a severe neurodevelopmental delay due to mitochondrial dysfunction with complex I impairments and altered pyruvate metabolism
94. AB1066 DEFICIENCY OF ADENOSINE DEAMINASE 2: THE IMPORTANCE OF A DIAGNOSIS BEFORE IRREVERSIBLE DAMAGE
95. Acute ataxia in paediatric emergency departments: a multicentre Italian study
96. In Troyer syndrome Spartin loss induces Complex I impairments and alters pyruvate metabolism
97. Computed Tomography in Acute Severe Central Nervous System Complications in Children Treated for Cancer: Still a Useful Diagnostic Tool in the Emergency Setting.
98. Quadriceps muscle strength in Duchenne muscular dystrophy and effect of corticosteroid treatment.
99. Bi-allelic mutations in TRAPPC2L result in a neurodevelopmental disorder and have an impact on RAB11 in fibroblasts
100. Pediatric epilepsies misdiagnosed as gastrointestinal disorders
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