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22 results on '"Di Donato S"'

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1. A validated prognostic classifier for V600EBRAF-mutated metastatic colorectal cancer: the ‘BRAF BeCool’ study

2. Suicidal ideation in a European Huntington's disease population

3. Are all people with diabetes and cardiovascular risk factors or microvascular complications at very high risk? Findings from the Risk and Prevention Study

4. Normal and mutant HTT interact to affect clinical severity and progression in Huntington disease

5. N-3 fatty acids in patients with multiple cardiovascular risk factors

6. β-Defensin Genomic Copy Number Does Not Influence the Age of Onset in Huntington's Disease

7. Incidence of Friedreich ataxia in Italy estimated from consanguineous marriages

8. A 1.5-Mb deletion in 17p11.2-p12 is frequently observed in Italian families with hereditary neuropathy with liability to pressure palsies

9. Upfront FOLFOXIRI plus bevacizumab and reintroduction after progression versus mFOLFOX6 plus bevacizumab followed by FOLFIRI plus bevacizumab in the treatment of patients with metastatic colorectal cancer (TRIBE2): a multicentre, open-label, phase 3, randomised, controlled trial

10. Italian survey on cetuximab-based therapy of elderly patients with metastatic colorectal cancer

11. Assessment of Ramucirumab plus paclitaxel as switch maintenance versus continuation of first-line chemotherapy in patients with advanced HER-2 negative gastric or gastroesophageal junction cancers: The ARMANI phase III trial

12. Spinocerebellar ataxia type 28: A novel autosomal dominant cerebellar ataxia characterized by slow progression and ophthalmoparesis

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

14. Relative Frequencies of CAG Expansions in Spinocerebellar Ataxia and Dentatorubropallidoluysian Atrophy in 116 Italian Families

15. Plasma 24S-hydroxycholesterol correlation with markers of Huntington disease progression

16. The influence of gender on phenotype and disease progression in patients with Huntington's disease

17. Friedreich's Ataxia: Autosomal Recessive Disease Caused by an Intronic GAA Triplet Repeat Expansion

18. Brain-derived neurotrophic factor in patients with Huntington's disease

19. Spinocerebellar ataxia types 1, 2, 3, and 6: disease severity and nonataxia symptoms

20. Plasma 24S-hydroxycholesterol and caudate MRI in pre-manifest and early Huntingtons disease

21. SCA28, a novel form of autosomal dominant cerebellar ataxia on chromosome 18p11.22-q11.2

22. Multisystem triglyceride storage disease is due to a specific defect in the degradation of endocellularly synthesized triglycerides

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