(Q33637060)

28 July 2017

1 reference

title

Application of electrospray tandem mass spectrometry to neonatal screening (English)

1 reference

28 July 2017

Rashed MS

1

1 reference

PubMed ID

10331469

28 July 2017

Rahbeeni Z

series ordinal

2

1 reference

PubMed ID

10331469

28 July 2017

Ozand PT

series ordinal

3

1 reference

28 July 2017

1 April 1999

1 reference

28 July 2017

Seminars in Perinatology

1 reference

28 July 2017

23

1 reference

28 July 2017

2

1 reference

28 July 2017

183-193

1 reference

NEWBORN PHENYLKETONURIA DETECTION PROGRAM IN MASSACHUSETTS

28 July 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980050-0

7 January 2021

Microfilter paper method for 17 alpha-hydroxyprogesterone radioimmunoassay: its application for rapid screening for congenital adrenal hyperplasia

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980050-0

7 January 2021

Organic acidurias: a review. Part 1.

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980050-0

7 January 2021

Suberylglycine excretion in the urine from a patient with dicarboxylic aciduria

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980050-0

7 January 2021

In vitro fibroblast studies in a patient with C6-C10-dicarboxylic aciduria: evidence for a defect in general acyl-CoA dehydrogenase

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980050-0

7 January 2021

Disorders of mitochondrial long-chain fatty acid oxidation

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980050-0

7 January 2021

Isovaleric acidemia: a new genetic defect of leucine metabolism

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980050-0

7 January 2021

Medium-chain acyl-CoA dehydrogenase deficiency. Diagnosis by stable-isotope dilution measurement of urinary n-hexanoylglycine and 3-phenylpropionylglycine

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980050-0

7 January 2021

Rapid diagnosis of medium-chain acyl CoA dehydrogenase deficiency by measurement of cis-4-decenoic acid in plasma

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980050-0

7 January 2021

New defect in fatty-acid metabolism with hypoglycemia and organic aciduria

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980050-0

7 January 2021

Diagnosis of Smith-Lemli-Opitz syndrome by gas chromatography/mass spectrometry of 7-dehydrocholesterol in plasma, amniotic fluid and cultured skin fibroblasts

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980050-0

7 January 2021

Stable isotope dilution analysis of very long chain fatty acids in plasma, urine and amniotic fluid by electron capture negative ion mass fragmentography

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980050-0

7 January 2021

Automated screening of urine samples for carbohydrates, organic and amino acids after treatment with urease

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980050-0

7 January 2021

The routine investigation of urinary organic acids in selected paediatric patients: results over a 2 1/2-year period

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980050-0

7 January 2021

Screening newborns for multiple organic acidurias in dried filter paper urine samples: method development

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980050-0

7 January 2021

Positive-ion thermospray liquid chromatography—mass spectrometry: detection of organic acidurias

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980050-0

7 January 2021

Screening techniques for the detection of inborn errors of bile acid metabolism by direct injection and micro-high performance liquid chromatography-continuous flow/fast atom bombardment mass spectrometry

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980050-0

7 January 2021

Thermospray liquid chromatography/mass spectrometry for the analysis of L-carnitine and its short-chain acyl derivatives

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980050-0

7 January 2021

Biomedical applications of high-performance liquid chromatography-mass spectrometry with continuous-flow fast atom bombardment

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980050-0

7 January 2021

Electrospray mass spectrometry in the clinical diagnosis of variant hemoglobins

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980050-0

7 January 2021

Oligopeptide sequence analysis by collision-activated dissociation of multiply charged ions

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980050-0

7 January 2021

On-line capillary electrophoresis-electrospray ionization mass spectrometry of nucleotides

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980050-0

7 January 2021

Sequencing of peptides by tandem mass spectrometry and high-energy collision-induced dissociation

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980050-0

7 January 2021

Capillary electrophoresis and capillary electrophoresis-mass spectrometry in drug and metabolite analysis

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980050-0

7 January 2021

Urinary excretion of l-carnitine and acylcarnitines by patients with disorders of organic acid metabolism: evidence for secondary insufficiency of l-carnitine

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980050-0

7 January 2021

Tandem mass spectrometry: a new method for acylcarnitine profiling with potential for neonatal screening for inborn errors of metabolism

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980050-0

7 January 2021

[22] Electrospray ionization mass spectrometry

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980050-0

7 January 2021

Diagnosis of inborn errors of metabolism from blood spots by acylcarnitines and amino acids profiling using automated electrospray tandem mass spectrometry

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980050-0

7 January 2021

A disease, probably hereditary characterised by severe mental deficiency and a constant gross abnormality of aminoacid metabolism.

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980050-0

7 January 2021

Glutaric acidemia type 1: First Saudi patient diagnosed by tandem mass spectrometry-based neonatal screening

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980050-0

7 January 2021

The use of automated electrospray ionization tandem MS for the diagnosis of inborn errors of metabolism from dried blood spots

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980050-0

7 January 2021

Stability of amino acids and galactose in the newborn screening filter paper blood specimen

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980050-0

7 January 2021

10.1016/S0146-0005(99)80050-0

Identifiers

DOI

1 reference

28 July 2017

1 reference

PubMed ID

10331469