Search

Your search keyword '"Giudice E"' showing total 132 results

Search Constraints

Start Over You searched for: Author "Giudice E" Remove constraint Author: "Giudice E" Topic humans Remove constraint Topic: humans
132 results on '"Giudice E"'

Search Results

1. Diagnostic issues faced by a rare disease healthcare network during Covid-19 outbreak: data from the Campania Rare Disease Registry

2. Development and implementation of the AIDA International Registry for patients with Behçet's disease

3. Impact of COVID-19 on the imaging diagnosis of cardiac disease in Europe

4. Intermittent macrothrombocytopenia in a novel patient with Takenouchi-Kosaki syndrome and review of literature

5. Impaired fasting glucose and impaired glucose tolerance in children and adolescents with overweight/obesity

6. Impact of age on the selection of nuclear cardiology stress protocols: The INCAPS (IAEA nuclear cardiology protocols) study

7. Nuclear cardiology practices and radiation exposure in Africa: results from the IAEA Nuclear Cardiology Protocols Study (INCAPS)

8. No effect of MTP polymorphisms on PNPLA3 in HCV-correlated steatosis

9. White blood cell count may identify abnormal cardiometabolic phenotype and preclinical organ damage in overweight/obese children

10. Nuclear cardiology practice in Asia: Analysis of radiation exposure and best practice for myocardial perfusion imaging ― results from the IAEA nuclear cardiology protocols cross-sectional study (INCAPS)

11. Nuclear Cardiology Practices and Radiation Exposure in the Oceania Region: results From the IAEA Nuclear Cardiology Protocols Study (INCAPS)

12. Exon-disrupting deletions ofNRXN1in idiopathic generalized epilepsy

13. Comparison of non-HDL-cholesterol versus triglycerides-to-HDL-cholesterol ratio in relation to cardiometabolic risk factors and preclinical organ damage in overweight/obese children: the CARITALY study

14. Health consequences of obesity in children and adolescents

15. Estimating the Reduction in the Radiation Burden From Nuclear Cardiology Through Use of Stress-Only Imaging in the United States and Worldwide

16. Gender Differences in Radiation Dose from Nuclear Cardiology Studies Across the World Findings from the INCAPS Registry

17. Comparison of Radiation Doses and Best-Practice Use for Myocardial Perfusion Imaging in US and Non-US Laboratories: Findings From the IAEA (International Atomic Energy Agency) Nuclear Cardiology Protocols Study

18. Opportunities for improvement on current nuclear cardiology practices and radiation exposure in Latin America: Findings from the 65-country IAEA Nuclear Cardiology Protocols cross-sectional Study (INCAPS)

19. Current worldwide nuclear cardiology practices and radiation exposure: results from the 65 country IAEA Nuclear Cardiology Protocols Cross-Sectional Study (INCAPS)

20. No evidence for association between dyslexia and DYX1C1 functional variants in a group of children and adolescents from Southern Italy

21. Phenotypic spectrum and prevalence of INPP5E mutations in Joubert Syndrome and related disorders

22. Dandy-Walker malformation and Wisconsin syndrome: novel cases add further insight into the genotype-phenotype correlations of 3q23q25 deletions

23. Clinical and molecular evaluation of non-dominant hereditary spherocytosis

24. Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1,2q22.3 and 17q21.32

25. FREQUENCY OF GILBERT'S SYNDROME ASSOCIATED WITH UGTA1 (TA)(7) POLYMORPHISM IN SOUTHERN ITALY

26. Pontine Tegmental Cap Dysplasia: developmental and cognitive outcome in three adolescent patients

27. Suppression of CDA II expression in a homozygote

28. MKS3/TMEM67 mutations are a major cause of COACH Syndrome, a Joubert Syndrome related disorder with liver involvement

29. Decision making at the bedside: diagnosis of hereditary spherocytosis in a transfused infant

30. Hereditary spherocytosis: from clinical to molecular defects

31. L-Carnitine in the treatment of mild or moderate hepatic encephalopathy

32. CNS involvement in OFD1 syndrome: a clinical, molecular, and neuroimaging study

33. Mild Elliptocytosis Associated With the Alpha-34 Arg-]trp Mutation In Spectrin Genova (alpha(i/74))

34. Molecular heterogeneity of hereditary elliptocytosis in Italy

35. Atypical aspects of hypertensive encephalopathy in childhood

36. Spectrin Anastasia (alpha I/78): a new spectrin variant (alpha 45 Arg-->Thr) with moderate elliptocytogenic potential

37. Clinical and biochemical study of thalassemia intermedia in Campania (southern Italy)

38. Smith Lemli-Opitz syndrome: A contribution to the delineation of a cognitive/behavioral phenotype

39. Mutational Screening of the CART Gene in Obese Children: Identifying a Mutation (Leu34Phe) Associated with Reduced Resting Energy Expenditure and Cosegregating with Obesity Phenotype in a Large Family

40. Increased membrane protein phosphorylation and anion transport activity in chorea-acanthocytosis

41. Epilepsy in inherited metabolic disorders: A pediatric series

42. Hereditary spherocytosis (HS) due to loss of anion exchange transporter

43. Unexplained Bilateral Occipital Calcification and Reduced Vision

44. Recommendations on Complementary Feeding as a Tool for Prevention of Non-Communicable Diseases (NCDs)—Paper Co-Drafted by the SIPPS, FIMP, SIDOHaD, and SINUPE Joint Working Group

45. Phenotypes of prediabetes and metabolic risk in Caucasian youths with overweight or obesity

46. Molecular screening of PROKR2 gene in girls with idiopathic central precocious puberty

47. Preclinical signs of liver and cardiac damage in youth with metabolically healthy obese phenotype

48. A new index to simplify the screening of hypertension in overweight or obese youth

49. MKRN3 circulating levels in Prader–Willi syndrome: a pilot study

50. A new formula to improve the screening of impaired glucose tolerance in youths with overweight or obesity

Catalog

Books, media, physical & digital resources