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PIERO RINALDO, MD
MD
Student in an Organized Health Care Education/Training Program
NPI: 1720121536Individual
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training ProgramPrimary
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Research & Publications (20)
Newborn screening of metabolic disorders: recent progress and future developments.
PMID 18626194·Nestle Nutr Workshop Ser Pediatr Program·2008
6-review
Making the case for objective performance metrics in newborn screening by tandem mass spectrometry.
PMID 17183573·Ment Retard Dev Disabil Res Rev·2006
8-other
Recent developments and new applications of tandem mass spectrometry in newborn screening.
PMID 15273505·Curr Opin Pediatr·2004
6-review
Clinical biochemical genetics in the twenty-first century.
PMID 15176715·Acta Paediatr Suppl·2004
8-other
Fatty acid transport and mitochondrial oxidation disorders.
PMID 11745037·Semin Liver Dis·2001
6-review
Prenatal diagnosis of disorders of fatty acid transport and mitochondrial oxidation.
PMID 11180241·Prenat Diagn·2001
6-review
Gene expression and functional analyses of primary rat hepatocytes on nanofiber matrices.
PMID 19494481·Cells Tissues Organs·2010
7-preclinical
Rat hepatocyte spheroids formed by rocked technique maintain differentiated hepatocyte gene expression and function.
PMID 19085959·Hepatology·2009
7-preclinical
National academy of clinical biochemistry laboratory medicine practice guidelines: follow-up testing for metabolic disease identified by expanded newborn screening using tandem mass spectrometry; executive summary.
PMID 19574465·Clin Chem·2009
6-review
Combined newborn screening for succinylacetone, amino acids, and acylcarnitines in dried blood spots.
PMID 18281422·Clin Chem·2008
8-other
The ACADS gene variation spectrum in 114 patients with short-chain acyl-CoA dehydrogenase (SCAD) deficiency is dominated by missense variations leading to protein misfolding at the cellular level.
PMID 18523805·Hum Genet·2008
4-observational
Second-tier test for quantification of alloisoleucine and branched-chain amino acids in dried blood spots to improve newborn screening for maple syrup urine disease (MSUD).
PMID 18178665·Clin Chem·2008
8-other
Essential fatty acid profiling for routine nutritional assessment unmasks adrenoleukodystrophy in an infant with isovaleric acidaemia.
PMID 19089597·J Inherit Metab Dis·2008
5-case
Committee Report: advancing the current recommended panel of conditions for newborn screening.
PMID 18007148·Genet Med·2007
8-other
Expanded newborn screening identifies maternal primary carnitine deficiency.
PMID 17126586·Mol Genet Metab·2007
8-other
Reduction of the false-positive rate in newborn screening by implementation of MS/MS-based second-tier tests: the Mayo Clinic experience (2004-2007).
PMID 17643193·J Inherit Metab Dis·2007
8-other
Metabolism of gamma-hydroxybutyrate to d-2-hydroxyglutarate in mammals: further evidence for d-2-hydroxyglutarate transhydrogenase.
PMID 16483879·Metabolism·2006
7-preclinical
Teaching pediatric laboratory medicine to pathology residents.
PMID 16831030·Arch Pathol Lab Med·2006
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 200 1ST ST SW
ROCHESTER, MN 55905 - Phone
- (507) 284-2511
Quick Facts
- NPI
- 1720121536
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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