126 results on '"Budisteanu, M."'
Search Results
2. Abundant pleiotropy across neuroimaging modalities identified through a multivariate genome-wide association study
3. Floating-Harbor syndrome: Presentation of the first Romanian patient with a SRCAP mutation and review of the literature
4. Abundant pleiotropy across neuroimaging modalities identified through a multivariate genome-wide association study
5. Menke-Hennekam syndrome 1: A Case Report
6. Genomic imbalances of chromosome 15 in patients with autistic features and global developmental delay
7. Determinants of satisfaction with the detection process of autism in Europe:results from the ASDEU study
8. Intervention services for autistic adults:an ASDEU study of autistic adults, carers, and professionals’ experiences
9. P.0343 Early detection, diagnosis and intervention services for children with autism spectrum disorder across europe according to the gross domestic product
10. Chromosome Y Isodicentrics in two Cases with Ambiguous genitalia and Features of Turner Syndrome
11. Multidisciplinary approach in children with autism spectrum disorder
12. The psychiatric phenotype of 15q11.2-q13.3 duplications
13. Behavior problems associated with brain heterotopia
14. Correction to: Early Detection, Diagnosis and Intervention Services for Young Children with Autism Spectrum Disorder in the European Union (ASDEU): Family and Professional Perspectives (Journal of Autism and Developmental Disorders, (2020), 50, 9, (3380-3394), 10.1007/s10803-019-04253-0)
15. Early detection, diagnosis and intervention services for young children with autism spectrum disorder in the European Union (ASDEU):family and professional perspectives
16. Autistic adult diagnosis, co-occurring conditions and interventions: good practices, services gaps, areas for improvement
17. Biophysical Psychiatry-How Computational Neuroscience Can Help to Understand the Complex Mechanisms of Mental Disorders
18. FLOATING-HARBOR SYNDROME: PRESENTATION OF THE FIRST ROMANIAN PATIENT WITH A SRCAP MUTATION AND REVIEW OF THE LITERATURE
19. ASD prevalence study across Europe: developing a school-based screening approach in the ASDEU project
20. The impact of Moyamoya syndrome in a patient with neurofibromatosis type I
21. P140 Clinical caracterization of a new case with chromosome 3 terminal microdeletion, involving chl1 gene
22. Use of early intervention for young children with autism spectrum disorder across Europe
23. Use of early intervention for young children with autism spectrum disorder across Europe
24. P138 – 3000: Neonatal brachial plexus palsy – Romanian single centre experience over 6 years
25. PP11.11 – 2673: Phelan-McDermid syndrome in two siblings with complex phenotype
26. Floating-Harbor syndrome: Presentation of the first Romanian patient with a SRCAPmutation and review of the literature
27. P290 – 1926 Nine years experience in SMA – the basis for Romanian National Registry
28. PP8.5 – 2096 Genetic intellectual disability; the Romanian experience based on clinical, cytogenetic and array-CGH techniques
29. P174 – 2114 Intracerebral calcifications in children with progressive neurological clinical picture: diagnostic difficulties through clinical cases
30. P236 – 1972 Angelman syndrome – an update of our clinical experience
31. P291 – 2006 Preliminary data of National Romanian Registry of DMD patients
32. P40 – 1882 What is the predominant feature of epilepsy in Down syndrome?
33. O92 – 2108 The classification of epilepsies using the ILAE revised terminology and concepts for organization of seizures and epilepsies and ICD-10 – challenges in clinical practice
34. P-764 - (MICRO)deletion/(MICRO)duplication syndromes in children with mental retardation
35. P-765 - Management of children with angelman syndrome
36. P08.1 Investigation of genetic causes of mental retardation in Romanian children
37. Xq28 duplication in a boy with mental retardation, hyperkinesia and dysmorphic features - a case report
38. Investigation of mental retardation etiology in romanian children using clinical, cytogenetic and array-CGH diagnostic techniques
39. P341 Behaviour phenotypes in children with chromosomal diseases
40. Early-onset multiple sclerosis: clinical and evolutive features
41. Cerebral venous thrombosis in child the role of the early intervention
42. NMP015 Special features of acute motor deficit in childhood: exemplification through clinical cases
43. NMP04 Diagnosis of spinal muscular atrophies in Romania
44. P02-302 - Investigation of mental retardation etiology in romanian children using clinical, cytogenetic and array-CGH diagnostic techniques
45. P02-208 - Xq28 duplication in a boy with mental retardation, hyperkinesia and dysmorphic features - a case report
46. P140 Clinical caracterization of a new case with chromosome 3 terminal microdeletion, involving chl1 gene
47. Use of early intervention for young children with autism spectrum disorder across Europe
48. Review of structural neuroimaging and genetic findings in autism spectrum disorder - a clinical perspective.
49. A rare cause of epileptic encephalopathy: case report of a novel patient with PEHO-like phenotype and CCDC88A gene pathogenic variants.
50. Non-Suicidal Self-Injury (NSSI) Patterns in Adolescents from a Romanian Child Psychiatry Inpatient Clinic.
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