Search Results - "Maria G Pascale"

  • Showing 1 - 2 results of 2
Refine Results
  1. 1

    Co-existence of phenylketonuria and Fabry disease on a 3 year-old boy: case report by Concolino, Daniela, Rapsomaniki, Maria, Disabella, Eliana, Sestito, Simona, Pascale, Maria G, Moricca, Maria T, Bonapace, Giuseppe, Arbustini, Elisea, Strisciuglio, Pietro

    Published in BMC pediatrics (17-05-2010)
    “…The co-existence of two genetically distinct metabolic disorders in the same patient has rarely been reported. Phenylketonuria (PKU) is an inborn error of the…”
    Get full text
    Journal Article
  2. 2

    CO-EXISTENCE OF PHENYLKETONURIA AND FABRY DISEASE ON A 3-YEAR-OLD BOY: CASE REPORT by Daniela Concolino, Maria Rapsomaniki, Eliana Disabella, Simona Sestito, Maria G Pascale, Maria T Moricca, Giuseppe Bonapace, Elisea Arbustini, Pietro Strisciuglio

    Published in Revista română de pediatrie (01-06-2010)
    “…Background: The co-existence of two genetically distinct metabolic disorders in the same patient has rarely been reported. Phenylketonuria (PKU) is an inborn…”
    Get full text
    Journal Article