0000000000626819

AUTHOR

D. Domianello

showing 5 related works from this author

Tryptophan Fortification of Adapted Formula Increases Plasma Tryptophan Concentrations to Levels Not Different from Those Found in Breast-Fed Infants

1992

Several recent studies have demonstrated significantly lower plasma total tryptophan concentrations in formula-fed than in breast-fed infants. We have measured preprandial plasma amino acid concentrations in infants breast-fed or fed a formula with a protein concentration of 1.57 g/dl and with a whey/casein ratio of 60:40 or a formula with a protein concentration of 1.37 g/dl and a whey/casein ratio of 40:60 and fortified with 10 mg/dl (15 mg/100 kcal) of tryptophan. Healthy term infants (10 per group) were either breast-fed from birth or randomly assigned to one of the two study formulas. At 4 and 12 weeks of age, anthropometric measurements were performed and blood samples were obtained. …

medicine.medical_specialtyPhenylalanineWeight Gainchemistry.chemical_compoundAnimal scienceDouble-Blind MethodValineInternal medicineCaseinmedicineHumansAnalysis of VarianceMethionineMilk Humanbusiness.industryInfant NewbornTryptophanGastroenterologyTryptophanInfantBody HeightBreast FeedingEndocrinologychemistryPediatrics Perinatology and Child HealthInfant FoodAmino Acids EssentialLeucineIsoleucinebusinessBreast feedingJournal of Pediatric Gastroenterology and Nutrition
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PROFILO DI RISCHIO DEL NEONATO LATE PRETERM: DISTURBI DEL NEUROSVILUPPO E RUOLO DEL FOLLOWUP

2015

Settore MED/38 - Pediatria Generale E SpecialisticaLATE PRETERM NEUROSVILUPPO
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Sorveglianza dello sviluppo in soggetti con anomalie del setto pellucido. descrizione di un caso con agenzia isolata.

2015

malformazioni cerebrali, anomalie setto pellucido

Settore MED/38 - Pediatria Generale E Specialisticamalformazioni cerebrali anomalie setto pellucido
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Malformations of central nervous system: General issues

2013

Malformations of the central nervous system (CNS) encompass a heterogeneous group of congenital anomalies that may be isolated or appear as part of a genetic syndrome. Advances in identifying the genetic etiology underlying many CNS malformation and syndromes have led to the current genetic-based classifications that allows us to better estimate prognosis and potential complications. Herein, we discuss the main genetic, clinical and radiological features and their implications for diagnostic testing and disease management

Settore MED/38 - Pediatria Generale E SpecialisticaSettore MED/31 - OtorinolaringoiatriaCNS malformations genetic investigations developmental delay.
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ENCEFALOPATIA NEONATALE. IL RUOLO DELLA INFEZIONE. ANALISI DI UN CAMPIONE DI 1107 NEONATI RICOVERATI IN UTIN E TERAPIA SEMINTENSIVA

2012

encefalopatia neonatale, infezione

encefalopatia neonatale infezione
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