53 results on '"del Giudice Emanuele"'
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2. Nephrogenic Diabetes Insipidus in Childhood: Assessment of Volume Status and Appropriate Fluid Replenishment
3. Nephrogenic Diabetes Insipidus in Childhood: Assessment of Volume Status and Appropriate Fluid Replenishment
4. The rs72613567: TA Variant in the Hydroxysteroid 17-beta Dehydrogenase 13 Gene Reduces Liver Damage in Obese Children
5. Micturition Syncope in Childhood: How to Recognize and Manage It
6. The Role of Inflammation on Vitamin D Levels in a Cohort of Pediatric Patients With Inflammatory Bowel Disease
7. The Membrane-bound O-Acyltransferase7 rs641738 Variant in Pediatric Nonalcoholic Fatty Liver Disease
8. Outcomes of a Cohort of Prenatally Diagnosed and Early Enrolled Patients with Congenital Solitary Functioning Kidney
9. Bisphenol A is associated with insulin resistance and modulates adiponectin and resistin gene expression in obese children
10. Novel association between the nonsynonymous A803G polymorphism of the N‐acetyltransferase 2 gene and impaired glucose homeostasis in obese children and adolescents
11. A girl with incomplete Prader–Willi syndrome and negative MS-PCR, found to have mosaic maternal UPD-15 at SNP array
12. Bioavailable Vitamin D in Obese Children: The Role of Insulin Resistance
13. A case of Rubinstein-Taybi syndrome associated with growth hormone deficiency in childhood
14. TM6SF2 E167K variant is associated with severe steatosis in chronic hepatitis C, regardless of PNPLA3 polymorphism
15. Reply
16. Cardiac Autonomic Regulation in Response to a Mixed Meal Is Impaired in Obese Children and Adolescents: The Role Played by Insulin Resistance
17. Brain magnetic resonance in the routine management of Rubinstein-Taybi syndrome (RTS) can prevent life-threatening events and neurological deficits
18. Association Between a Polymorphism in Cannabinoid Receptor 2 and Severe Necroinflammation in Patients With Chronic Hepatitis C
19. Familial trisomy 6p in mother and daughter
20. Predicting Metabolic Syndrome in Obese Children and Adolescents: Look, Measure and Ask
21. Early Left Ventricular Abnormalities in Children with Heterozygous Familial Hypercholesterolemia
22. The Cannabinoid Receptor type 2 Q63R variant increases the risk of celiac disease: Implication for a novel molecular biomarker and future therapeutic intervention
23. Association of the cannabinoid receptor 2 (CB2) Gln63Arg polymorphism with indices of liver damage in obese children: An alternative way to highlight the CB2 hepatoprotective properties
24. Anthropometric Indices Are Not Satisfactory Predictors of Metabolic Comorbidities in Obese Children and Adolescents
25. Effects of a Mixed Meal on Hemodynamics and Autonomic Control of the Heart in Patients with Type 1 Diabetes
26. Hepcidin in Obese Children as a Potential Mediator of the Association between Obesity and Iron Deficiency
27. Effect of the rs997509 Polymorphism on the Association between Ectonucleotide Pyrophosphatase Phosphodiesterase 1 and Metabolic Syndrome and Impaired Glucose Tolerance in Childhood Obesity
28. Atrial Myocardial Deformation Properties in Obese Nonhypertensive Children
29. Association Analysis Indicates That a Variant GATA-Binding Site in the PIK3CB Promoter Is a Cis-Acting Expression Quantitative Trait Locus for This Gene and Attenuates Insulin Resistance in Obese Children
30. A Single-Nucleotide Polymorphism in the p110β Gene Promoter Is Associated with Partial Protection from Insulin Resistance in Severely Obese Adolescents
31. Pontine hyperperfusion in sporadic hyperekplexia
32. Effect of the melanocortin-3 receptor C17A and G241A variants on weight loss in childhood obesity1–3
33. Insulin Gene Variable Number of Tandem Repeats (INS VNTR) Genotype and Metabolic Syndrome in Childhood Obesity
34. Abnormal myocardial deformation properties in obese, non-hypertensive children: an ambulatory blood pressure monitoring, standard echocardiographic, and strain rate imaging study
35. Growth acceleration in prepubertal obese children: Role of hyperinsulinaemia
36. The Leu34Phe ProCART Mutation Leads to Cocaine- and Amphetamine-Regulated Transcript (CART) Deficiency: A Possible Cause for Obesity in Humans
37. No Evidence for Association Between Dyslexia and DYX1C1 Functional Variants in a Group of Children and Adolescents From Southern Italy
38. An Insertional Polymorphism of the Proopiomelanocortin Gene Is Associated with Fasting Insulin Levels in Childhood Obesity
39. WEIGHT LOSS IN OBESE CHILDREN WITH THE POMC R236G VARIANT
40. CART Peptides: Modulators of Mesolimbic Dopamine, Feeding, and Stress
41. Mutational screening of the pyy3-36 and his receptor in childhood obesity
42. MC3R GENE VARIANT AFFECTS BOBY FAT LOSS DURING A WEIGHT REDUCTION PROGRAM FOR CHILDHOOD OBESITY
43. 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
44. Clinical and molecular evaluation of non-dominant hereditary spherocytosis
45. Gilbert's syndrome accounts for the phenotypic variability of congenital dyserythropoietic anemia type II (CDA-II)
46. EVALUATION OF LEPTIN PROTEIN LEVELS IN PATIENTS WITH COOLEY'S ANAEMIA
47. Bilirubin levels in the acute hemolytic crisis of G6PD deficiency are related to Gilbert's syndrome
48. Frequent de novo monoallelic expression of beta-spectrin gene (SPTB) in children with hereditary spherocytosis and isolated spectrin deficiency
49. High frequency of de novo mutations in ankyrin gene (ANK1) in children with hereditary spherocytosis
50. Novel band 3 variants (bands 3 Foggia, Napoli I and Napoli II) associated with hereditary spherocytosis and band 3 deficiency: status of the D38A polymorphism within the EPB3 locus
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