149 results on '"Venturini, Giulia"'
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2. In vivo analysis of onset and progression of retinal degeneration in the Nr2e3rd7/rd7 mouse model of enhanced S-cone sensitivity syndrome
3. Author Correction: In vivo analysis of onset and progression of retinal degeneration in the Nr2e3rd7/rd7 mouse model of enhanced S-cone sensitivity syndrome
4. Molecular Mechanisms Underlying Vascular Liver Diseases: Focus on Thrombosis
5. Testing web-based solutions for improving reading tasks in dyslexic and neuro-typical users
6. Endoscopic ultrasound direct portal pressure measurement in patients with porto-sinusoidal vascular disorder and clinically significant portal hypertension: a comparison with hepatic venous pressure gradient measurement
7. Emulating clinical pressure waveforms in cell culture using an Arduino-controlled millifluidic 3D-printed platform for 96-well plates
8. Tuning Nursing Educational in an Italian academic context
9. In vivo analysis of onset and progression of retinal degeneration in the Nr2e3 rd7/rd7 mouse model of enhanced S-cone sensitivity syndrome
10. Emulating clinical pressure waveforms in cell culture using an Arduino-controlled 3D-printed platform for 96-well plates
11. The GQ Hype List.
12. Whole genome sequencing in patients with retinitis pigmentosa reveals pathogenic DNA structural changes and NEK2 as a new disease gene
13. Effect of a wound healing protocol on patients with stage III and IV pressure ulcers: a preliminary observational study
14. High-Throughput Hydrostatic Pressure Waveform Control
15. Molecular profile in body fluids in subjects enrolled in a randomised trial for lung cancer screening: Perspectives of integrated strategies for early diagnosis
16. Differential Dimerization of Variants Linked to Enhanced S-Cone Sensitivity Syndrome (ESCS) Located in the NR2E3 Ligand-Binding Domain
17. Epidemiological aspects of urinary incontinence in a female population of an Italian region
18. Dominant PRPF31 Mutations Are Hypostatic to a Recessive CNOT3 Polymorphism in Retinitis Pigmentosa: A Novel Phenomenon of “Linked Trans-Acting Epistasis”
19. IDENTIFYING GIFTED STUDENTS IN ITALY: RELIABILITY AND VALIDITY OF THE ITALIAN VERSION OF THE GATES-2.
20. THU-302 - Endoscopic ultrasound direct portal pressure measurement in patients with porto-sinusoidal vascular disorder and clinically significant portal hypertension: a comparison with hepatic venous pressure gradient measurement
21. PLEKHG5 deficiency leads to an intermediate form of autosomal-recessive Charcot–Marie–Tooth disease
22. Quantitative analysis of carbonic anhydrase IX mRNA in human non-small cell lung cancer
23. Quality of Life for Caregivers of Persons With Alzheimerʼs Disease Living in Sardinia, Italy
24. Positive and negative impact in caring for older people living in Sardinia, Italy: J10-84
25. Preliminary results from the reliability and validity of the stroke impact scale in Italy: F51-83
26. In vivo analysis of onset and progression of retinal degeneration in the Nr2e3rd7/rd7 mouse model of enhanced S-cone sensitivity syndrome.
27. Vessel health and preservation: An integrative review
28. An integrated system for Peripherally Inserted Central Catheter tip confirmation in oncology and haematology patients.
29. L’autovalutazione delle competenze cliniche infermieristiche in Area Critica
30. PLEKHG5 deficiency leads to an intermediate form of autosomal-recessive Charcot-Marie-Tooth disease
31. Testing web-based solutions for improving reading tasks in students with dyslexia
32. Vessel health and preservation: An integrative review.
33. Transcriptional regulation of PRPF31 gene expression by MSR1 repeat elements causes incomplete penetrance in retinitis pigmentosa
34. Transcriptional regulation of PRPF31 gene expression by MSR1 repeat elements causes incomplete penetrance in retinitis pigmentosa
35. Dominant PRPF31 Mutations Are Hypostatic to a Recessive CNOT3 Polymorphism in Retinitis Pigmentosa: A Novel Phenomenon of 'Linked Trans-Acting Epistasis'
36. Transcriptional regulation of PRPF31 gene expression by MSR1 repeat elements causes incomplete penetrance in retinitis pigmentosa
37. Homozygosity mapping reveals novel and known mutations in Pakistani families with inherited retinal dystrophies
38. Two specific mutations are prevalent causes of recessive retinitis pigmentosa in North American patients of Jewish ancestry
39. Novel Approach Identifies SNPs in SLC2A10 and KCNK9 with Evidence for Parent-of-Origin Effect on Body Mass Index
40. Molecular Genetics of FAM161A in North American Patients with Early-Onset Retinitis Pigmentosa
41. DominantPRPF31Mutations Are Hypostatic to a RecessiveCNOT3Polymorphism in Retinitis Pigmentosa: A Novel Phenomenon of “LinkedTrans-Acting Epistasis”
42. Documentare la gestione del wound-care: quali ripercussioni sugli outcome assistenziali.
43. CNOT3 Is a Modifier of PRPF31 Mutations in Retinitis Pigmentosa with Incomplete Penetrance
44. Clinicopathologic and Molecular Analysis of a Choroidal Pigmented Schwannoma in the Context of a PTEN Hamartoma Tumor Syndrome
45. The Experience of Quality of Life for Caregivers of People With Alzheimer’s Disease Living in Sardinia, Italy
46. Differential Dimerization of Variants Linked to Enhanced S-Cone Sensitivity Syndrome (ESCS) Located in the NR2E3 Ligand-Binding Domain.
47. Novel Approach Identifies SNPs in SLC2A10 and KCNK9 with Evidence for Parent-of-Origin Effect on Body Mass Index.
48. Molecular Genetics of FAM161A in North American Patients with Early-Onset Retinitis Pigmentosa.
49. The self-evaluation of clinical nursing competence in Critical Area.
50. L'autovalutazione delle competenze cliniche infermieristiche in Area Critica.
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