1,392 results on '"del Giudice Emanuele"'
Search Results
202. Influence of genetic variants in FADS2 and ELOVL2 genes on BMI and PUFAs homeostasis in children and adolescents with obesity
203. Addome acuto come presentazione di imene imperforato con idrometrocolpo nel neonato
204. How to interpret symptoms, signs and investigations of dehydration in children with gastroenteritis
205. High Dietary Salt Intake in Pediatric Patients with Type 1 Diabetes Mellitus Not Related to Overweight and Obesity
206. A Particular Form of “Urolithiasis” in a Toddler
207. Genetic Evaluation of Patients With Delayed Puberty and Congenital Hypogonadotropic Hypogonadism: Is it Worthy of Consideration?
208. Pretreatment Endocrine Disorders Due to Optic Pathway Gliomas in Pediatric Neurofibromatosis Type 1: Multicenter Study
209. The rs72613567:TA Variant in the Hydroxysteroid 17-beta Dehydrogenase 13 Gene Reduces Liver Damage in Obese Children
210. Effects of a Mixed Meal on Hemodynamics and Autonomic Control of the Heart in Patients with Type 1 Diabetes
211. The N-terminal 11 amino acids of human erythrocyte band 3 are critical for aldolase binding and protein phosphorylation: implications for band 3 function
212. Hepcidin in Obese Children as a Potential Mediator of the Association between Obesity and Iron Deficiency
213. Effect of the rs997509 Polymorphism on the Association between Ectonucleotide Pyrophosphatase Phosphodiesterase 1 and Metabolic Syndrome and Impaired Glucose Tolerance in Childhood Obesity
214. 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
215. A Single-Nucleotide Polymorphism in the p110β Gene Promoter Is Associated with Partial Protection from Insulin Resistance in Severely Obese Adolescents
216. Insulin Gene Variable Number of Tandem Repeats (INS VNTR) Genotype and Metabolic Syndrome in Childhood Obesity
217. Abnormal myocardial deformation properties in obese, non-hypertensive children: an ambulatory blood pressure monitoring, standard echocardiographic, and strain rate imaging study
218. Growth acceleration in prepubertal obese children: Role of hyperinsulinaemia
219. The Leu34Phe ProCART Mutation Leads to Cocaine- and Amphetamine-Regulated Transcript (CART) Deficiency: A Possible Cause for Obesity in Humans
220. A Novel Hyperekplexia-causing Mutation in the Pre-transmembrane Segment 1 of the Human Glycine Receptor α1 Subunit Reduces Membrane Expression and Impairs Gating by Agonists
221. Growth Hormone Receptor (GHR) 6O Pseudoexon Activation: A Novel Cause of Severe Growth Hormone Insensitivity.
222. An Insertional Polymorphism of the Proopiomelanocortin Gene Is Associated with Fasting Insulin Levels in Childhood Obesity
223. WEIGHT LOSS IN OBESE CHILDREN WITH THE POMC R236G VARIANT
224. CART Peptides: Modulators of Mesolimbic Dopamine, Feeding, and Stress
225. Mutational screening of the pyy3-36 and his receptor in childhood obesity
226. MC3R GENE VARIANT AFFECTS BOBY FAT LOSS DURING A WEIGHT REDUCTION PROGRAM FOR CHILDHOOD OBESITY
227. Anthropometric and Biochemical Determinants of Estimated Glomerular Filtration Rate in a Large Cohort of Obese Children
228. 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
229. Clinical and molecular evaluation of non-dominant hereditary spherocytosis
230. 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. (Brief Genetics Report)
231. Gilbert's syndrome accounts for the phenotypic variability of congenital dyserythropoietic anemia type II (CDA-II)
232. Acute kidney injury in children hospitalized for community acquired pneumonia.
233. The American Academy of Pediatrics hypertension guidelines identify obese youth at high cardiovascular risk among individuals non-hypertensive by the European Society of Hypertension guidelines
234. EVALUATION OF LEPTIN PROTEIN LEVELS IN PATIENTS WITH COOLEY'S ANAEMIA
235. Bilirubin levels in the acute hemolytic crisis of G6PD deficiency are related to Gilbert's syndrome
236. Polyclonal gammopathy in an adolescent affected by Dent disease 2 and hidradenitis suppurativa
237. Transmembrane 6 superfamily member 2 167K allele improves renal function in children with obesity
238. The Association of Autoimmune Diseases with Type 1 Diabetes Mellitus in Children Depends Also by the Length of Partial Clinical Remission Phase (Honeymoon)
239. A novel GHR pseudoexon mutation causing frameshift and severe postnatal growth failure
240. 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
241. Pediatric Obesity and the Immune System
242. In children with urinary tract infection reduced kidney length and vesicoureteric reflux predict abnormal DMSA scan
243. Three novel Growth Hormone Receptor (GHR) splicing mutations causing a spectrum of Growth Hormone Insensitivity
244. Contribution of a genetic risk score to clinical prediction of hepatic steatosis in obese children and adolescents
245. Waist‐to‐height ratio is more strongly associated than other weight‐related anthropometric measures with metabolic variables
246. Vitamin D affects insulin sensitivity and β-cell function in obese non-diabetic youths
247. 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
248. Nonalcoholic fatty liver disease and eGFR levels could be linked by the PNPLA3 I148M polymorphism in children with obesity
249. Asthma, exercise and metabolic dysregulation in paediatrics
250. Micturition Syncope in Childhood
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