Search

Your search keyword '"S. DiDonato"' showing total 99 results

Search Constraints

Start Over You searched for: Author "S. DiDonato" Remove constraint Author: "S. DiDonato"
99 results on '"S. DiDonato"'

Search Results

1. Biological abnormalities of peripheral A2A receptors in a large representation of polyglutamine disorders and Huntington's disease stages

2. Eleventh meeting of The European Neurological Society21–25 April, 2001, Paris, France

4. Massive Star-Forming Host Galaxies of Quasars on Sloan Digital Sky Survey Stripe 82

5. Fourth meeting of the European Neurological Society 25–29 June 1994 Barcelona, Spain

6. Concordance of Clinical Forms of Epilepsy in Families with Several Affected Members

8. Increasing complexity of the karyotype in 50 human gliomas. Progressive evolution and de novo occurrence of cytogenetic alterations

9. Contributors

10. A new stable-isotope dilution method for measurement of orotic acid utilizing solvent-extracted urine

12. Muscle oxphos enzymes and mtDNA lesions in parkinson's disease patients

13. Myopathies due to enzyme deficiencies

14. Systemic carnitine deficiency with peripheral nerve involvement morphological and biochemical study

16. Creation of a Novel Virtual Reality Simulation to Increase Nursing Skills in Management of Workplace Violence.

17. Exploring Medical Student Experiences of Trauma in the Emergency Department: Opportunities for Trauma-informed Medical Education.

18. Maternal Perspective of Inpatient Methadone Initiation: Opportunities to Increase Retention in Treatment.

19. Racial/Ethnic Disparities in Mental Healthcare in Youth With Incarcerated Parents.

20. Youth Trauma Histories are Associated with Under-diagnosis and Under-treatment of Co-occurring Youth Psychiatric Symptoms.

21. Implementation and Outcomes of the Trauma Ambassadors Program: A Case Study of Trauma-Informed Youth Leadership Development.

22. A Qualitative Exploration of the Use of Service Dogs in Veterans with Post Traumatic Stress Disorder and Traumatic Brain Injury.

23. Be(e)coming pollinators: Beekeeping and perceptions of environmentalism in Massachusetts.

24. Predictors of Clinician-Reported Self-Efficacy in Treating Trauma-Exposed Youth.

25. Caught off guard by covid-19: Now what?

26. Change Across Time in Cancer-Related Traumatic Stress Symptoms of Siblings of Children with Cancer: A Preliminary Investigation.

27. The strength of green ties: Massachusetts cranberry grower social networks and effects on climate change attitudes and action.

28. Psychosocial Assessment as a Standard of Care in Pediatric Cancer.

29. Family psychosocial risk screening guided by the Pediatric Psychosocial Preventative Health Model (PPPHM) using the Psychosocial Assessment Tool (PAT).

30. Double image. Adding PET/MR systems into the imaging unit mix.

32. Cholesterol defect is marked across multiple rodent models of Huntington's disease and is manifest in astrocytes.

33. The gene coding for PGC-1alpha modifies age at onset in Huntington's Disease.

34. Early symptoms in spinocerebellar ataxia type 1, 2, 3, and 6.

35. Frataxin gene point mutations in Italian Friedreich ataxia patients.

36. Genetic analysis of candidate genes modifying the age-at-onset in Huntington's disease.

37. The S18Y polymorphism in the UCHL1 gene is a genetic modifier in Huntington's disease.

38. Pathways to motor incoordination: the inherited ataxias.

39. Limited efficacy of the HSV-TK/GCV system for gene therapy of malignant gliomas and perspectives for the combined transduction of the interleukin-4 gene.

40. Underestimation of ovarian pathology: a review.

41. Errors in Huntington disease diagnostic test caused by trinucleotide deletion in the IT15 gene.

42. Deletion mapping of gliomas suggest the presence of two small regions for candidate tumor-suppressor genes in a 17-cM interval on chromosome 10q.

43. Nuclear DNA origin of cytochrome c oxidase deficiency in Leigh's syndrome: genetic evidence based on patient's-derived rho degrees transformants.

44. Early-onset encephalomyopathy associated with tissue-specific mitochondrial DNA depletion: a morphological, biochemical and molecular-genetic study.

45. Sequence analysis of mitochondrial DNA in a new maternally inherited encephalomyopathy.

46. Absence of mutations and identification of two polymorphisms in the SSCP and sequence analysis of p21CKI gene in malignant gliomas.

47. The gene (NFE2L1) for human NRF-1, an activator involved in nuclear-mitochondrial interactions, maps to 7q32.

48. Redefinition of the coding sequence of the MXI1 gene and identification of a polymorphic repeat in the 3' non-coding region that allows the detection of loss of heterozygosity of chromosome 10q25 in glioblastomas.

49. Genotype to phenotype correlations in mitochondrial encephalomyopathies associated with the A3243G mutation of mitochondrial DNA.

50. Can we avoid AVED?

Catalog

Books, media, physical & digital resources