1,061 results on '"Miraglia del Giudice, Emanuele"'
Search Results
152. Predicting Metabolic Syndrome in Obese Children and Adolescents: Look, Measure and Ask
153. Acute Kidney Injury and Renal Tubular Damage in Children With Type 1 Diabetes Mellitus Onset
154. Early Renal Ultrasound in Congenital Solitary Kidney May Help to Select Patients at Lower Risk of Associated Vesicoureteral Reflux
155. Dehydrated patient without clinically evident cause: A case report
156. Congenital diabetes mellitus
157. Micturition Syncope in Childhood
158. Prevalence of and factors associated to chronic kidney disease and hypertension in a cohort of children with juvenile idiopathic arthritis
159. Nonalcoholic Fatty Liver Disease and Estimated Insulin Resistance in Obese Youth: A Mendelian Randomization Analysis
160. Influence of genetic variants in FADS2 and ELOVL2 genes on BMI and PUFAs homeostasis in children and adolescents with obesity
161. Addome acuto come presentazione di imene imperforato con idrometrocolpo nel neonato
162. How to interpret symptoms, signs and investigations of dehydration in children with gastroenteritis
163. A Particular Form of “Urolithiasis” in a Toddler
164. Genetic Evaluation of Patients With Delayed Puberty and Congenital Hypogonadotropic Hypogonadism: Is it Worthy of Consideration?
165. Pretreatment Endocrine Disorders Due to Optic Pathway Gliomas in Pediatric Neurofibromatosis Type 1: Multicenter Study
166. The rs72613567:TA Variant in the Hydroxysteroid 17-beta Dehydrogenase 13 Gene Reduces Liver Damage in Obese Children
167. Effects of a Mixed Meal on Hemodynamics and Autonomic Control of the Heart in Patients with Type 1 Diabetes
168. The N-terminal 11 amino acids of human erythrocyte band 3 are critical for aldolase binding and protein phosphorylation: implications for band 3 function
169. Effect of the rs997509 Polymorphism on the Association between Ectonucleotide Pyrophosphatase Phosphodiesterase 1 and Metabolic Syndrome and Impaired Glucose Tolerance in Childhood Obesity
170. 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
171. A Single-Nucleotide Polymorphism in the p110β Gene Promoter Is Associated with Partial Protection from Insulin Resistance in Severely Obese Adolescents
172. Effect of the melanocortin-3 receptor C17A and G241A variants on weight loss in childhood obesity1–3
173. Insulin Gene Variable Number of Tandem Repeats (INS VNTR) Genotype and Metabolic Syndrome in Childhood Obesity
174. WEIGHT LOSS IN OBESE CHILDREN WITH THE POMC R236G VARIANT
175. Mutational screening of the pyy3-36 and his receptor in childhood obesity
176. Anthropometric and Biochemical Determinants of Estimated Glomerular Filtration Rate in a Large Cohort of Obese Children
177. 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
178. Clinical and molecular evaluation of non-dominant hereditary spherocytosis
179. EVALUATION OF LEPTIN PROTEIN LEVELS IN PATIENTS WITH COOLEY'S ANAEMIA
180. Polyclonal gammopathy in an adolescent affected by Dent disease 2 and hidradenitis suppurativa
181. The Association of Autoimmune Diseases with Type 1 Diabetes Mellitus in Children Depends Also by the Length of Partial Clinical Remission Phase (Honeymoon)
182. Demystifying the Pizza Bolus: The Effect of Dough Fermentation on Glycemic Response—A Sensor-Augmented Pump Intervention Trial in Children with Type 1 Diabetes Mellitus
183. Pediatric Obesity and the Immune System
184. In children with urinary tract infection reduced kidney length and vesicoureteric reflux predict abnormal DMSA scan
185. Waist‐to‐height ratio is more strongly associated than other weight‐related anthropometric measures with metabolic variables
186. Vitamin D affects insulin sensitivity and β-cell function in obese non-diabetic youths
187. Pilot study showed that poor feeding, especially with leucocyturia, increased the odds of non‐febrile urinary tract infections in children who were not toilet trained
188. Nonalcoholic fatty liver disease and eGFR levels could be linked by the PNPLA3 I148M polymorphism in children with obesity
189. When a secondary form of pediatric non-alcoholic fatty liver disease should be suspected?
190. Acute urinary retention in a 4-year-old girl
191. High frequency of de novo mutations in ankyrin gene (ANK1) in children with hereditary spherocytosis
192. Core promoter mutations 3 years after anti-hepatitis B e seroconversion in patients with chronic hepatitis B or hepatitis B and C infection and cancer remission
193. 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
194. The IRGM rs10065172 variant increases the risk for steatosis but not for liver damage progression in Italian obese children
195. The risk of metabolic derangements is higher in children and adolescents with overweight or obesity born small for gestational age.
196. Acute kidney injury in children hospitalized for acute gastroenteritis: prevalence and risk factors.
197. The rehabilitation of children and adolescents with severe or medically complicated obesity: an ISPED expert opinion document
198. Response to letter to the editor: therapeutic importance of proteinuria classification in children with congenital anomalies of the kidney and urinary tract.
199. Pediatric non-alcoholic fatty liver disease: current perspectives on diagnosis and management
200. Growth Hormone Receptor (GHR)6Ω Pseudoexon Activation: A Novel Cause of Severe Growth Hormone Insensitivity
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.