44 results on '"Castaldo G"'
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2. Atrial fibrillation: Epigenetic aspects and role of sodium-glucose cotransporter 2 inhibitors
3. 623 Preliminary assessment of nasal and colon-derived primary cells theratyping for a personalized medicine approach in people with cystic fibrosis carrying ultra-rare genotypes
4. Common carp exposed to binary mixtures of Cd(II) and Zn(II): A study on metal bioaccumulation and ion-homeostasis
5. Physiological performance of common carp (Cyprinus carpio, L., 1758) exposed to a sublethal copper/zinc/cadmium mixture
6. Antagonistic bioaccumulation of waterborne Cu(II) and Cd(II) in common carp (Cyprinus carpio) and effects on ion-homeostasis and defensive mechanisms
7. AGGRESSIVE WEIGHT LOSS PROGRAM WITH A KETOGENIC INDUCTION PHASE FOR THE TREATMENT OF CHRONIC PLAQUE PSORIASIS
8. Investigating the effects of a sub-lethal metal mixture of Cu, Zn and Cd on bioaccumulation and ionoregulation in common carp, Cyprinus carpio
9. SUN-PO143: Aggressive Weight Loss Program with a Ketogenic Induction Phase for the Treatment of Chronic Plaque Psoriasis
10. Limited oxidative stress in common carp (Cyprinus carpio, L., 1758) exposed to a sublethal tertiary (Cu, Cd and Zn) metal mixture
11. WS10.6 Intra-individual biological variation in sweat chloride concentrations
12. SUN-P213: An Observational Study of Sequential Protein-Sparing, Very Low-Calorie Ketogenic Diet (OLOPROTEIC® DIET) and Hypocaloric Mediterranean-Like Diet for the Treatment of Obesity
13. Aglucidic Enteral Nutritional Therapy “AENT”: Impact on psoriasis and fibromyalgia, insulin-sensitive diseases
14. Prediction of acute pancreatitis risk based on PIP score in children with cystic fibrosis
15. WS21.7 Identification and characterization of two novel mutations in conserved sequences tags (CSTs) of CFTR gene
16. 10 The role of complex alleles in patients with cystic fibrosis and L997F
17. WS21.3 Clinical variability in patients with cystic fibrosis and D1152H mutation
18. Aberrant F8 gene intron 1 inversion with concomitant duplication and deletion in a severe hemophilia A patient from Southern Italy
19. CO27 EPIGENETIC EFFECTS OF BUTYRATE IN CHILDREN WITH CONGENITAL CHLORIDE DIARRHEA: AN IN-VIVO AND IN-VITRO STUDY
20. 663 poster REDUCTION OF RECTAL, SIGMOID AND BLADDER SIDE EFFECTS IN CERVICAL CANCER PATIENTS TREATED WITH 3D HDR BRACHYTHERAPY
21. MODIFIED DOSE FRACTIONATION BY BIOLOGICAL EQUIVALENT DOSE VOLUME HISTOGRAM IN IMRT OF NON SMALL CELL LUNG CANCER
22. 97P A NEW 3D CONFORMATIONAL SOLUTION RADIOTHERAPY OF MALIGNANT PLEURAL MESOTHELIOMA
23. HOW TO COMBINE RADIATION AND MONOCLONAL ANTIBODY THERAPIES IN HEAD AND NECK CANCER?
24. 82P RADIOBIOLOGICAL ANALYSIS OF MODIFIED FRACTIONATIONS IN IMRT OF NON SMALL CELL LUNG CANCER
25. PA57 ACUTE RECURRENT PANCREATITIS AND GENETIC RISK FACTORS: A CASE REPORT
26. PA55 GENOTYPE PREDICTS THE RESPONSE TO THERAPY IN CHILDREN WITH CONGENITAL CHLORIDE DIARRHEA
27. An MBL2 haplotype and ABCB4 variants modulate the risk of liver disease in cystic fibrosis patients: A multicentre study
28. CO5 UTILITY OF MULTIDISCIPLINARY APPROACH TO SHWACHMAN-DIAMOND SYNDROME IN CHILDREN
29. Early pregnancy loss in celiac women: The role of genetic markers of thrombophilia
30. PP7 EFFICACY OF BUTYRATE THERAPY IN CONGENITAL CHLORIDE DIARRHEA: PRELIMINARY RESULTS OF A RANDOMIZED, DOUBLE-BLIND, CROSS-OVER, MULTICENTER STUDY
31. MODULATED DOSE FRACTIONATIONS OF COMBINED SIB IMRT/MONOCLONAL ANTIBODY TREATMENT IN HEAD AND NECK CANCER
32. 110 poster: Differences in the Rectal Dose Distribution Between Intra and Post Planning in Prostate Brachiterapy With 125I
33. “Classic” and “new” genetic prothrombotic risk factors in children with portal vein thrombosis
34. Epidemiology and a novel procedure for large scale analysis of CFTR rearrangements in classic and atypical CF patients: A multicentric Italian study
35. ATYPCAL CYSTIC FIBROSIS (ACF): AN EXPERIENCE OF A CYSTIC FIBROSIS CENTER
36. MOLECULAR ANALYSIS OF GENES ENCODING CFTR INTERACTORS OF SLC26 FAMILY IN CF PATIENTS: PRELIMINARY RESULTS
37. DIRECT SEQUENCING OF CSTs IN CYSTIC FIBROSIS PATIENTS BEARING UNDEFINITE GENOTYPE
38. Innate immunity and paediatric onset inflammatory bowel diseases: A human beta defensins genotype investigation
39. A case of Buerger's disease associated with MTHFR CT mutation homozygosity: a possible therapeutic support
40. Atrial fibrillation: Epigenetic aspects and role of sodium-glucose cotransporter 2 inhibitors
41. Ossiculoplasty in incudostapedial joint defects: audiologic outcomes of three type of partial ossicular prostheses in retrospective clinical study 1995‐2015
42. DNA methylation state of BDNF gene is not altered in prefrontal cortex and striatum of schizophrenia subjects
43. Mannose-binding lectin genetic analysis: possible protective role of the HYPA haplotype in the development of recurrent urinary tract infections in men
44. DIRECT SEQUENCING OF CSTs IN CYSTIC FIBROSIS PATIENTS BEARING UNDEFINITE GENOTYPE
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