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2. Dissecting the multifaceted contribution of the mitochondrial genome to autism spectrum disorder

3. Maternally inherited genetic variants of CADPS2 are present in Autism Spectrum Disorders and Intellectual Disability patients

4. Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders.

5. Cassidy and Allanson's Management of Genetic Syndromes

7. Seizures in trisomy 18: Prevalence, description, and treatment

8. The delineation of the <scp>Wolf‐Hirschhorn</scp> syndrome over six decades: Illustration of the ongoing advances in phenotype analysis and cytogenomic technology

10. DELETION 4p

11. Perinatal distress in 1p36 deletion syndrome can mimic hypoxic ischemic encephalopathy

12. Risk of hepatic neoplasms in Wolf-Hirschhorn syndrome (4p-): Four new cases and review of the literature

13. Natural history study of adults with <scp>Wolf–Hirschhorn</scp> syndrome 1: Case series of personally observed 35 individuals

14. Natural history study of adults with Wolf-Hirschhorn syndrome 2: Patient-reported outcomes study

15. Correlating Neuroimaging and CNVs Data: 7 Years of Cytogenomic Microarray Analysis on Patients Affected by Neurodevelopmental Disorders

16. Episignatures Stratifying Helsmoortel-Van Der Aa Syndrome Show Modest Correlation with Phenotype

17. Episignatures stratifying ADNP syndrome show modest correlation with phenotype

18. An integrated analysis of rare CNV and exome variation in Autism Spectrum Disorder using the Infinium PsychArray

19. A survey of antiepileptic drug responses identifies drugs with potential efficacy for seizure control in Wolf–Hirschhorn syndrome

20. Cassidy and Allanson's Management of Genetic Syndromes

21. Delineation of MidXq28-duplication syndrome distal to MECP2 and proximal to RAB39B genes

22. Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia

23. Lack of replication of previous autism spectrum disorder GWAS hits in European populations

24. De Novo Variants in the F-Box Protein FBXO11 in 20 Individuals with a Variable Neurodevelopmental Disorder

25. Common and rare variants of microRNA genes in autism spectrum disorders

26. Analysis ofCHRNA7rare variants in autism spectrum disorder susceptibility

27. Five children with deletions of 1p34.3 encompassing AGO1 and AGO3

28. Nine patients with Xp22.31 microduplication, cognitive deficits, seizures, and talipes anomalies

29. Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders

30. 6p25 Interstitial deletion in two dizygotic twins with gyral pattern anomaly and speech and language disorder

31. Spectrum of epilepsy and electroencephalogram patterns in idic (15) syndrome

32. Developmental Trajectories in Syndromes With Intellectual Disability, With a Focus on Wolf-Hirschhorn and Its Cognitive–Behavioral Profile

33. Contribution of common and rare variants of the PTCHD1 gene to autism spectrum disorders and intellectual disability

34. Chromosomal microarray testing identifies a 4p terminal region associated with seizures in Wolf-Hirschhorn syndrome

35. The behavioral phenotype of the idic(15) syndrome

36. Cognitive-behavioral features of Wolf-Hirschhorn syndrome and other subtelomeric microdeletions

37. FG syndrome, an X-linked multiple congenital anomaly syndrome: The clinical phenotype and an algorithm for diagnostic testing

38. Further characterization of the new microdeletion syndrome of 16p11.2-p12.2

39. Spectrum of epilepsy and electroencephalogram patterns in Wolf-Hirschhorn syndrome: experience with 87 patients

40. Update on the clinical features and natural history of Wolf-Hirschhorn (4p-) syndrome: Experience with 87 patients and recommendations for routine health supervision

41. Cognitive-behavioral features of children with Wolf-Hirschhorn syndrome: Preliminary report of 12 cases

42. Analysis of X chromosome inactivation in autism spectrum disorders

43. Spectrum of epilepsy in terminal 1p36 deletion syndrome

44. Comprehensive analysis of Wolf–Hirschhorn syndrome using array CGH indicates a high prevalence of translocations

45. The Italian XLMR bank: a clinical and molecular database

46. MECP2 deletions and genotype–phenotype correlation in Rett syndrome

47. Wolf-Hirschhorn syndrome: A review and update

48. Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways

49. Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder

50. The yield of subtelomeric FISH analysis in the evaluation of autistic spectrum disorders

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