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CARUSO U

Last name: CARUSO U

    Recent uploads

  • 1999 (v1)
    Publication
    Metadata-only
    Minor facial anomalies in combined methylmalonic aciduria and homocystinuria due to a defect in cobalamin metabolism
    CERONE, ROBERTO SCHIAFFINO MC CARUSO U

    No description

    Uploaded on: April 14, 2023
  • 2007 (v1)
    Publication
    Metadata-only
    Neonatal screening for congenital errors of metabolism by means of Tandem Mass: Italian experience
    CERONE, ROBERTO LORINI, RENATA GIUSEPPINA CASSANELLO M

    No description

    Uploaded on: April 14, 2023
  • 2003 (v1)
    Publication
    Metadata-only
    Rivisitazione degli screening neonatali di massa per le malattie metaboliche alla luce delle nuove esperienze diagnostiche.
    CERONE, ROBERTO LORINI, RENATA GIUSEPPINA SCHIAFFINO MC

    No description

    Uploaded on: March 31, 2023
  • 1993 (v1)
    Publication
    Metadata-only
    Role of haematological, pulmonary and renal complications in the long-term prognosis of patients with lysinuric protein intolerance.
    DIROCCO M ROSSI GA CARUSO U

    No description

    Uploaded on: December 2, 2022
  • 1999 (v1)
    Publication
    Metadata-only
    15 years of screening for BH4 deficiency in the Ligurian Region, Italy
    CERONE, ROBERTO LORINI, RENATA GIUSEPPINA SCHIAFFINO MC

    No description

    Uploaded on: December 4, 2022
  • 2001 (v1)
    Publication
    Metadata-only
    Cobalamin (Cbl)C/D deficiency: clinical, neurophysiological and neuroradiologic finding in 14 cases
    BIANCHERI R. SCHIAFFINO MC CARUSO U

    No description

    Uploaded on: March 31, 2023
  • 1996 (v1)
    Publication
    Metadata-only
    Combined deficiency of xanthine oxidase and sulphite oxidase due to a deficiency of molybdenum cofactor.
    BONIOLI, EUGENIO DI STEFANO, ANTONIO PALMIERI A

    No description

    Uploaded on: April 14, 2023
  • 2007 (v1)
    Publication
    Metadata-only
    Severe epilepsy in X-linked creatine transporter defect (CRTR-D)
    MANCARDI MM CARUSO U SCHIAFFINO MC

    Disorders of creatine synthesis or its transporter resulting in neurological impairment with mental retardation and epilepsy have only been recognized in recent years. To date, the epileptic disorder observed in creatine transporter deficiency (CRTR-D) has been described as a mild phenotype with infrequent seizures and favorable response to...

    Uploaded on: April 14, 2023
  • 2008 (v1)
    Publication
    Metadata-only
    Peroxisomal acyl-CoA-oxidase deficiency: two new cases
    CARROZZO R BELLINI C LUCIOLI S

    No description

    Uploaded on: March 5, 2024
  • 2001 (v1)
    Publication
    Metadata-only
    Programmi svolti dalla II Clinica Pediatrica.
    LORINI, RENATA GIUSEPPINA CERONE, ROBERTO COTELLESSA, MARIO

    No description

    Uploaded on: March 25, 2023

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