A5084720535- Blood Pressure and Hypertension Studies
- Biotin and Related Studies
- Amino Acid Enzymes and Metabolism
- Thyroid Disorders and Treatments
- Diabetes and associated disorders
- Sodium Intake and Health
- Metabolism and Genetic Disorders
- Renal function and acid-base balance
- Neonatal Health and Biochemistry
- Nutritional Studies and Diet
- Diabetes Management and Research
- Digestive system and related health
- Click Chemistry and Applications
- Vitamin D Research Studies
- Pancreatic function and diabetes
- Orthopedic Infections and Treatments
- Advanced biosensing and bioanalysis techniques
- Case Reports on Hematomas
- Obesity, Physical Activity, Diet
- Infectious Diseases and Tuberculosis
- Health and Lifestyle Studies
- Cardiovascular and exercise physiology
Ospedale di Santo Spirito
2020-2022
Azienda USL di Pescara
2020-2021
University of Chieti-Pescara
2002
Abstract Aims Associated autoimmune phenomena might influence metabolic control in children and adolescents with Type 1 diabetes mellitus. A retrospective case study was performed order to explore the effect of subclinical hypothyroidism on Patients methods For this purpose each patient (cases) matched for age, duration disease and, if possible, sex, two three diabetic patients without (controls). Parameters such as HbA 1c , total insulin requirement frequency symptomatic hypoglycaemia were...
Biotinidase deficiency (BD) is an autosomal recessive inherited disorder in which the enzyme biotinidase totally or partially defective and vitamin biotin not recycled. BD meets major criteria for a population screening program. Newborn bloodspot (NBS) allows early diagnosis of BD, thus preventing high morbidity mortality associated with untreated disease. Both profound partial variant can be detected by NBS test, serum activity and/or mutational analysis are required definitive diagnosis....
Phenylketonuria (PKU) is a rare autosomal recessive condition affecting about 1 in 10,000 people the Europe, with higher rate some countries, like Ireland and Italy. In Italy, newborn screening (NBS) by MS/MS allows diagnostic suspicion of PKU its variants (Hyperphenylalaninemia (HPA), Tetrahydrobiopterin (BH4) synthesis deficiency, recycling deficiency) through quantification Phenylalanine (Phe) Phenylalanine/Tyrosine (Phe/Tyr) ratio dried blood Spot (DBS) samples. Here, we report case an...
Biotinidase (BTD) deficiency is an autosomal recessive inherited neurocutaneous disorder. BTD recycles the vitamin biotin, a coenzyme essential for function of four biotin-dependent carboxylases, including propionyl-CoA carboxylase, 3-methylcrotonyl-CoA pyruvate and acetyl-CoA carboxylase. Due to deficient activities also recognized as late-onset multiple carboxylase associated with secondary alterations in metabolism amino acids, carbohydrates, fatty acids. can be classified “profound”,...
Background: Sodium intake is known to contribute the development of hypertension. The reduction sodium currently a cornerstone in prevention and management Inducing an increase renal excretion might represent further potential preventive and/or therapeutic opportunity.Methods: SPA Project multicenter, observational, cohort study aimed at investigating blood pressure relation fluid with working hypothesis that increased can improve handling towards decreased pressure. Children were...
Sodium intake is known to contribute the development of hypertension, thus reduction a cornerstone in prevention and management hypertension. The increase renal sodium excretion might represent further potential preventive and/or therapeutic opportunity.To explore working hypothesis that an increased fluid can improve handling towards decrease blood pressure.The SPA Project multicenter, observational, cross-sectional, cohort study investigating healthy children, aged 5-8 years as by means...