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1. Distinct neurodevelopmental and epileptic phenotypes associated with gain- and loss-of-function GABRB2 variantsResearch in context

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3. Modelling the impact of protein-kinase R allelic variant on HIV biomarkers trajectories by means of latent class mixed models

4. Genotype–phenotype correlations and disease mechanisms in PEX13-related Zellweger spectrum disorders

5. Risk of HIV viral rebound in HIV infected patients on direct acting antivirals (DAAs) treatment for HCV.

6. Risk for non-AIDS-defining and AIDS-defining cancer of early versus delayed initiation of antiretroviral therapy

7. Genotype-phenotype correlations and expansion of the molecular spectrum of AP4M1-related hereditary spastic paraplegia

8. Increase in the Level of Proinflammatory Cytokine HMGB1 in Nasal Fluids of Patients With Rhinitis and its Sequestration by Glycyrrhizin Induces Eosinophil Cell Death

9. Inhibition of G-protein signalling in cardiac dysfunction of intellectual developmental disorder with cardiac arrhythmia (IDDCA) syndrome

10. HIV-1 recombinant forms in immigrants regularly residing in Milan, northern Italy

11. A Moderation Analysis of Perfectionism, Cultural Sensitivity, and Counselors-In-Training Attitudes Toward Non-Dominant Sexual Identities

12. Tay-Sachs Disease: Two Novel Rare HEXA Mutations from Pakistan and Morocco

13. Allelic and phenotypic heterogeneity in Junctophillin-3 related neurodevelopmental and movement disorders

14. De novo mutation in SLC25A22 gene: expansion of the clinical and electroencephalographic phenotype

15. Clinical features and comorbidity pattern of HCV infected migrants compared to native patients in care in Italy: A real-life evaluation of the PITER cohort

16. Genetic Anomalies of the Respiratory Tract

17. Cannabinoid receptor 2-63 RR variant is independently associated with severe necroinflammation in HIV/HCV coinfected patients.

18. De Novo and Bi-allelic Pathogenic Variants in NARS1 Cause Neurodevelopmental Delay Due to Toxic Gain-of-Function and Partial Loss-of-Function Effects

19. Biallelic MFSD2A variants associated with congenital microcephaly, developmental delay, and recognizable neuroimaging features

20. Temporal-parietal-occipital epilepsy in GEFS+ associated with SCN1A mutation

21. A paradigmatic autistic phenotype associated with loss of PCDH11Y and NLGN4Y genes

22. Bi-allelic variants in OGDHL cause a neurodevelopmental spectrum disease featuring epilepsy, hearing loss, visual impairment, and ataxia

23. Human Immunodeficiency Virus Continuum of Care in 11 European Union Countries at the End of 2016 Overall and by Key Population: Have We Made Progress?

24. Virological response and retention in care according to time of starting ART in Italy: data from the Icona Foundation Study cohort

25. High rates of sustained virological response despite premature discontinuation of directly acting antivirals in HCV-infected patients treated in a real-life setting

26. Bi-allelic variants in SPATA5L1 lead to intellectual disability, spastic-dystonic cerebral palsy, epilepsy, and hearing loss

27. Distinct gene-set burden patterns underlie common generalized and focal epilepsies

28. Is physician assessment of alcohol consumption useful in predicting risk of severe liver disease among people with HIV and HIV/HCV co-infection?

29. Broad neurodevelopmental features and cortical anomalies associated with a novel de novo KMT2A variant in Wiedemann-Steiner syndrome

30. Electroclinical features and outcome of ANKRD11-related KBG syndrome: A novel report and literature review

31. HMGB1: A pleiotropic activity

32. Identification of common genetic markers of paroxysmal neurological disorders using a network analysis approach

33. Cisgender Professional Counselors’ Experiences with Trans* Clients

34. Clinical and Laboratory Features of 184 Italian Pediatric Patients Affected with Selective IgA Deficiency (SIgAD): a Longitudinal Single-Center Study

35. Neuromuscular and Neuroendocrinological Features Associated With ZC4H2-Related Arthrogryposis Multiplex Congenita in a Sicilian Family: A Case Report

36. An Open Retrospective Study of a Standardized Cannabidiol Based-Oil in Treatment-Resistant Epilepsy

37. Erratum to: Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia

39. Impact of PNPLA3 variants on liver histology of 168 patients with HIV infection and chronic hepatitis C

40. Genotype-Phenotype Correlations in Neurofibromatosis Type 1: A Single-Center Cohort Study

41. Homozygous SCN1B variants causing early infantile epileptic encephalopathy 52 affect voltage-gated sodium channel function

42. Biallelic Variants in KIF17 Associated with Microphthalmia and Coloboma Spectrum

43. Mitochondrial DNA analysis from exome sequencing data improves diagnostic yield in neurological diseases

44. Incidence and risk factors for liver enzyme elevation among naive HIV-1-infected patients receiving ART in the ICONA cohort

45. Effectiveness of dolutegravir-based regimens as either first-line or switch antiretroviral therapy: data from the Icona cohort

46. Economic Consequences of Investing in Anti-HCV Antiviral Treatment from the Italian NHS Perspective: A Real-World-Based Analysis of PITER Data

47. Evolution of major non-HIV-related comorbidities in HIV-infected patients in the Italian Cohort of Individuals, Naïve for Antiretrovirals (ICONA) Foundation Study cohort in the period 2004-2014

48. Impact of social determinants on antiretroviral therapy access and outcomes entering the era of universal treatment for people living with HIV in Italy

49. First-line antiretroviral therapy with efavirenz plus tenofovir disiproxil fumarate/emtricitabine or rilpivirine plus tenofovir disiproxil fumarate/emtricitabine: a durability comparison

50. Benign familial infantile epilepsy associated with KCNQ3 mutation: a rare occurrence or an underestimated event?