484 results on '"Fazzi E"'
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2. POS1299 LONG-TERM NEURODEVELOPMENTAL OUTCOME OF CHILDREN BORN TO SYSTEMIC SCLEROSIS WOMEN: PEDIATRIC NEUROPSYCHIATRIC ASSESSMENT THROUGH A SET OF VALIDATED TOOLS
3. Post-partum Women's Anxiety and Parenting Stress: Home-Visiting Protective Effect During the COVID-19 Pandemic
4. AB0661 NEUROPSYCHOLOGICAL OUTCOME OF CHILDREN BORN TO WOMEN WITH SYSTEMIC SCLEROSIS ASSESSED THROUGH A SELF-ADMINISTERED MULTIDISCIPLINARY QUESTIONNAIRE: RESULTS FROM A MONOCENTRIC COHORT
5. Leber's Congenital Amaurosis: Is There an Autistic Component?
6. Neurodevelopmental Disorder in Children Affected by Ocular Albinism Type 1
7. Repetitive and Stereotyped Behaviors in Neurodevelopmental Disorders: More than a Movement Disorder
8. A Novel X-linked Mutation of CACNA1F Gene in Two Male Siblings Presenting Nystagmus
9. Visual Function Classification System for children with cerebral palsy: development and validation
10. Relationship between visual acuity, visual evoked patterned potentials done at different spatial frequencies and fundus findings in more than 100 Cerebral Visual Impairment affected subjects
11. SEISMIC VULNERABILITY ASSESSMENT OF THE TRIUMPHAL ARCH OF CARACALLA IN VOLUBILIS (MOROCCO): PAST EVENTS AND PROVISIONS FOR THE FUTURE
12. AB0423 NEUROPSYCHIATRIC OUTCOME OF CHILDREN BORN TO WOMEN WITH SYSTEMIC LUPUS ERYTHEMATOSUS (SLE) WOMEN AND EXPOSED IN UTERO TO AZATHIOPRINE: A CASE-CONTROL STUDY.
13. Aicardi–Goutières syndrome
14. Clinical and molecular characteristics of 1qter microdeletion syndrome: delineating a critical region for corpus callosum agenesis/hypogenesis
15. Visual function and motor skills in children with spastic diplegia
16. Recovery of visual functions after early acquired occipital damage
17. Waiting times for diagnosis of attention-deficit hyperactivity disorder in children and adolescents referred to Italian ADHD centers must be reduced
18. Cryptic deletions are a common finding in “balanced” reciprocal and complex chromosome rearrangements: a study of 59 patients
19. Pharmacological Treatment of Anorexia Nervosa: A Retrospective Study in Preadolescents and Adolescents
20. Leberʼs congenital amaurosis: is there an autistic component?
21. Nephronophthisis type 1 deletion syndrome with neurological symptoms: Prevalence and significance of the association
22. Rates of neonatal death and cerebral palsy associated with fetal growth restriction among very low birthweight infants. A temporal analysis
23. NPHP1 gene deletion is a rare cause of Joubert syndrome related disorders
24. Correlation between clinical and ultrasound findings in preterm infants with cystic periventricular leukomalacia
25. Family-centred care for children and young people with cerebral palsy: results from an Italian multicenter observational study
26. La percezione della qualità delle cure erogate nei servizi di riabilitazione italiani per bambini con paralisi cerebrale: risultati di uno studio osservazionale multicentrico
27. Cerebral cavernous angiomas: an atypical case in infancy
28. Primary and Secondary Stereotypies in Children: A Pilot Standardized Protocol and Video Analysis
29. Proposal of a New Diagnostic Score for Aicardi–Goutières Syndrome
30. Social Cognition in Children Autism Spectrum Disorders: An Eye Tracking Study
31. Environmental Adaptation and Early Visual Training to Promote Neurodevelopment in Infants with Visual Impairment: A Pilot Study
32. Partial Seizures in the First Year of Life: Treatment with Vigabatrin.
33. iPSC-DERIVED NEURAL STEM CELLS CULTURED ON ENGINEERED SUBSTRATES AS AN IN VITRO MODEL FOR AICARDI-GOUTIÈRES SYNDROME
34. Developmental Delay, Tremors, and EEG Abnormalities: A Case of KCTD7 Gene Mutation
35. Variable Phenotype Expression of a Maternally Inherited 16P13.11 Deletion in Twin Brothers with Epilepsy
36. Incontinentia Pigmenti in a Newborn Male with Klinefelter Syndrome: Clinical, Electroencephalographic, and Neuroimaging Findings
37. Differenze tra il profilo neurovisivo dei neonati a termine e dei neonati prematuri valutati attraverso un nuovo strumento clinico: NAVEG (Neonatal Assessment Visual European Grid)
38. Studio del profilo neurovisivo in neonati a termine e in nati prematuri: NAVEG (Neonatal Assessment Visual European Grid), un nuovo strumento clinico
39. Patient-reported outcomes measure for children born preterm: validation of the SOLE VLBWI Questionnaire, a new quality of life self-assessment tool
40. Oculomotor control in children with cerebral palsy
41. Recommendations for the rehabilitation of children with cerebral palsy
42. Long-term neurodevelopmental outcome of children born to prospectively followed pregnancies of women with systemic lupus erythematosus and/or antiphospholipid syndrome
43. Neurodevelopmental profile in Angelman syndrome: more than low intelligence quotient
44. Neuropsychological profiles in children with spastic diplegia with particoular attention to visuo-cognitive abilities
45. Higher visual abilitiesd learning difficulties in children with cerebral palsy
46. Visual impairment in cerebral palsy
47. Il profilo cognitivo e le difficoltà di apprendimento nelle forme spastiche bilaterali con disordini visuo-percettivi
48. Shock cardiogeno al’esordio di sclerosi multipla in maschio di 13 anni
49. Utilità dello screening genetico in Sclerosi Tuberosa paucisintomatica
50. Gli UBOs sono sempre asintomatici?
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