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Ada Consalvo

Biographic Data

ID7860391
NAMEAda Consalvo
GIVEN NAMESAda
FAMILY NAMEConsalvo
SIGNATURECONSALVO A
AFFILIATIONSUniversity of Chieti-Pescara
ORCID0000-0003-3860-9404
VERIFIEDYes
TOTAL WORKS1
TOTAL CITATIONS0
WORKS AS AUTHOR1
WORKS AS EDITOR0
FIRST PUBLICATION YEAR2020
LATEST PUBLICATION YEAR2020
H-INDEX0
  • A False-Positive Case of Methylmalonic Aciduria by Tandem Mass Spectrometry Newborn Screening Dependent on Maternal Malnutrition in Pregnancy

    Open Access•Cláudia Rossi, Ilaria Cicalini et al.•ARTICLE•International Journal of…•2020

    Methylmalonic Acidurias (MMAs) are a group of inborn errors of metabolism (IEMs), specifically of propionate catabolism characterized by gastrointestinal and neurometabolic manifestations resulting from a deficiency in the function of methylmalonyl-CoA mutase, methylmalonyl-CoA epimerase, and cobalamin metabolism. In Expanded Newborn Screening (NBS), increased levels of propionylcarnitine (C3) and/or of its ratios by MS/MS analysis of dried blood…

No prominent works on this page.

  • A False-Positive Case of Methylmalonic Aciduria by Tandem Mass Spectrometry Newborn Screening Dependent on Maternal Malnutrition in Pregnancy

    Open Access•Cláudia Rossi, Ilaria Cicalini et al.•ARTICLE•International Journal of…•2020

    Methylmalonic Acidurias (MMAs) are a group of inborn errors of metabolism (IEMs), specifically of propionate catabolism characterized by gastrointestinal and neurometabolic manifestations resulting from a deficiency in the function of methylmalonyl-CoA mutase, methylmalonyl-CoA epimerase, and cobalamin metabolism. In Expanded Newborn Screening (NBS), increased levels of propionylcarnitine (C3) and/or of its ratios by MS/MS analysis of dried blood…

Biology (1 work) · Chemistry (1 work) · cobalamin (1 work) · Endocrinology (1 work) · Folate and B Vitamins Research (1 work) · Genetics (1 work) · Internal Medicine (1 work) · Mass spectrometry (1 work) · Medicine (1 work) · Metabolism and Genetic Disorders (1 work)

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