175 results on '"Barozzi S"'
Search Results
2. Early prelingual auditory development in Italian infants and toddlers analysed through the Italian version of the Infant-Toddler Meaningful Auditory Integration Scale (IT-MAIS)
3. Dynamic Posturography
4. Audiovestibular disorders as autoimmune reaction in patients with melanoma
5. Inherited thrombocytopenia caused by ANKRD26 mutations misdiagnosed and treated as myelodysplastic syndrome: report on two cases
6. Bio-inspired approaches to design smart fabrics
7. Diagnosis and Treatment of Equilibrium Disorders in Whiplash Injuries: Posture and Stance Disorders
8. R705H mutation of MYH9 is associated with MYH9-related disease and not only with non-syndromic deafness DFNA17
9. Understanding biological dynamics: following cells and molecules to track functions and mechanisms
10. Photoactivation of pa-GFP in 3D: optical tools for spatial confinement
11. Positive response to nickel and azathioprine treatment
12. Spatial control of pa-GFP photoactivation in living cells
13. MR Imaging in Menière Disease: Is the Contact between the Vestibular Endolymphatic Space and the Oval Window a Reliable Biomarker?
14. MR imaging of endolymphatic hydrops in Ménière’s disease: not all that glitters is gold
15. PA-GFP 3D localized photo-activation and tracking in living cells
16. A Comparison of Nature and Technical Sounds for Tinnitus Therapy
17. Magnetic domain wall tweezers: a new tool for mechanobiology studies on individual target cells
18. Early prelingual auditory development in Italian infants and toddlers analysed through the Italian version of the Infant-Toddler Meaningful Auditory Integration Scale (IT-MAIS).
19. Neurotological disorders, allergy to metals, and dental amalgam fillings
20. Spatial control of pa-GFP photoactivation in living cells
21. Il compenso
22. Caratteristiche biologiche responsabili di pressione selettiva in batteri psicrotrofi patogeni e deterioranti isolati da carni macinate - Atti della XIV Conferenza Nazionale OXOID La Sicurezza Microbiologica nella produzione di alimenti per il 21° secolo 1, 115-120, 2005
23. R705H mutation ofMYH9is associated withMYH9-related disease and not only with non-syndromic deafness DFNA17
24. Inherited thrombocytopenia caused by ANKRD26mutations misdiagnosed and treated as myelodysplastic syndrome: report on two cases
25. Bilateral Sudden Sensorineural Hearing Loss and Chronic Venous Cerebrospinal Insufficiency: A Case Report
26. Understanding biological dynamics: following cells and molecules to track functions and mechanisms
27. Audiological and vestibular findings in the Kabuki syndrome
28. Improvement of left visuo-spatial hemineglect by left-sided transcutaneous electrical stimulation
29. 3D localized photoactivation of pa-GFP in living cells using two-photon interactions.
30. Bilateral sudden sensorineural hearing loss and chronic venous cerebrospinal insufficiency: a case report.
31. NOVEL PERSPECTIVES IN GENOTYPE-PHENOTYPE CORRELATIONS IN MYH9-RELATED DISEASE: NO LONGER JUST A MATTER OF HEAD OR TAIL
32. Clinical and pathogenetic characterization of ETV6-related thrombocytopenia (ETV6-RT), an inherited thrombocytopenia (IT) predisposing to childhood acute lymphoblastic leukemia (ALL)
33. ETV6-RELATED THROMBOCYTOPENIA (ETV6-RT): CLINICAL AND PATHOGENETIC CHARACTERIZATION OF AN INHERITED THROMBOCYTOPENIA (IT) PREDISPOSING TO CHILDHOOD ACUTE LYMPHOBLASTIC LEUKEMIA (ALL)
34. Clinical and pathogenetic features of ETV6 related thrombocytopenia with predisposition to acute lymphoblastic leukemia
35. Saccule and tinnitus: Is a possible connection?
36. Petri net-based real time simulation of industrial plants.
37. SARS-CoV-2 infection induces DNA damage, through CHK1 degradation and impaired 53BP1 recruitment, and cellular senescence
38. Mutations in the 5' UTR of ANKRD26, the ankirin repeat domain 26 gene, cause an autosomal-dominant form of inherited thrombocytopenia, THC2
39. Pathogenetic and clinical study of a patient with thrombocytopenia due to the p.E527K gain-of-function variant of SRC
40. ATR is essential for preservation of cell mechanics and nuclear integrity during interstitial migration
41. Inherited thrombocytopenia caused by ANKRD26 mutations misdiagnosed and treated as myelodysplastic syndrome: report on two cases
42. Capitolo I (Le fattispecie incriminatrici configurabili sul posto di lavoro: un quadro di sintesi); Capitolo 5 (La rilevanza penale del 'patrimonio' nella gestione del rapporto di lavoro); Appendice di approfondimento (A. La 'parte generale' del diritto penale: un quadro di sintesi; B. Il diritto penale 'post-moderno', tra principio di stretta legalità e discrezionalità giurisprudenziale)
43. Understanding biological dynamics: following cells and molecules to track functions and mechanisms
44. Prevalence and Voice Characteristics of Laryngeal Pathology in an Italian Voice Therapy-seeking Population
45. R705H mutation of MYH9 is associated with MYH9-related disease and not only with non-syndromic deafness DFNA17
46. Platelet diameters in inherited thrombocytopenias: analysis of 376 patients with all known disorders
47. MYH9-related disease: Five novel mutations expanding the spectrum of causative mutations and confirming genotype/phenotype correlations
48. MYH9-related Disorders: Report on a Patient of Greek Origin Presenting With Macroscopic Hematuria and Presenile Cataract, Caused by an R1165C Mutation
49. Mutations responsible for MYH9-related thrombocytopenia impair SDF-1-driven migration of megakaryoblastic cells
50. Bacteria-induced gap junctions in tumors favor antigen cross-presentation and antitumor immunity
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