Gas chromatography/mass spectrometry (GC/MS) remains a pre-eminent discovery tool in clinical steroid investigations even in the era of fast liquid chromatography tandem mass spectrometry (LC/MS/MS). (Q34139349)

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Gas chromatography/mass spectrometry (GC/MS) remains a pre-eminent discovery tool in clinical steroid investigations even in the era of fast liquid chromatography tandem mass spectrometry (LC/MS/MS)

Language	Label	Description	Also known as
English	Gas chromatography/mass spectrometry (GC/MS) remains a pre-eminent discovery tool in clinical steroid investigations even in the era of fast liquid chromatography tandem mass spectrometry (LC/MS/MS).	scientific article	Gas chromatography/mass spectrometry (GC/MS) remains a pre-eminent discovery tool in clinical steroid investigations even in the era of fast liquid chromatography tandem mass spectrometry (LC/MS/MS)

Statements

scholarly article

1 reference

Europe PubMed Central

31 July 2017

3 references

19 September 2019

13 November 2019

9 October 2020

Gas chromatography/mass spectrometry (GC/MS) remains a pre-eminent discovery tool in clinical steroid investigations even in the era of fast liquid chromatography tandem mass spectrometry (LC/MS/MS). (English)

1 reference

Europe PubMed Central

31 July 2017

biomedical investigative technique

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19 September 2019

polycyclic compound

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13 November 2019

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9 October 2020

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mass spectrometry

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liquid chromatography-tandem mass spectrometry

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based on heuristic

inferred from title

4

object named as

Paul M Stewart

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object named as

Nils Krone

1

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object named as

Wiebke Arlt

5

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Cedric H L Shackleton

6

object named as

Cedric H L Shackleton

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Europe PubMed Central

31 July 2017

Beverly A Hughes

2

object named as

Beverly A Hughes

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Europe PubMed Central

31 July 2017

author name string

Gareth G Lavery

3

1 reference

Europe PubMed Central

31 July 2017

language of work or name

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publication date

22 April 2010

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Europe PubMed Central

31 July 2017

1 August 2010

3 references

19 September 2019

13 November 2019

9 October 2020

The Journal of Steroid Biochemistry and Molecular Biology

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Europe PubMed Central

31 July 2017

19 September 2019

13 November 2019

9 October 2020

121

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Europe PubMed Central

31 July 2017

496-504

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Europe PubMed Central

31 July 2017

3-5

1 reference

Europe PubMed Central

31 July 2017

copyright license

Creative Commons Attribution 3.0 Unported

3 references

Europe PubMed Central

19 September 2019

Europe PubMed Central

13 November 2019

Europe PubMed Central

9 October 2020

copyright status

0 references

Clinical steroid mass spectrometry: a 45-year history culminating in HPLC-MS/MS becoming an essential tool for patient diagnosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2941839

5 July 2018

Steroid hormone analysis by tandem mass spectrometry

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2941839

5 July 2018

Steroid biomarkers and genetic studies reveal inactivating mutations in hexose-6-phosphate dehydrogenase in patients with cortisone reductase deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2941839

5 July 2018

Prenatal diagnosis of P450 oxidoreductase deficiency (ORD): a disorder causing low pregnancy estriol, maternal and fetal virilization, and the Antley-Bixler syndrome phenotype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2941839

5 July 2018

Congenital adrenal hyperplasia caused by mutant P450 oxidoreductase and human androgen synthesis: analytical study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2941839

5 July 2018

Mutant P450 oxidoreductase causes disordered steroidogenesis with and without Antley-Bixler syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2941839

5 July 2018

Apparent pregnene hydroxylation deficiency (APHD): seeking the parentage of an orphan metabolome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2941839

5 July 2018

Maternal urine and serum steroid measurements to identify steroid sulfatase deficiency (STSD) in second trimester pregnancies.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2941839

28 October 2018

Steroid profiling by tandem mass spectrometry improves the positive predictive value of newborn screening for congenital adrenal hyperplasia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2941839

28 October 2018

5alpha-androstane-3alpha,17beta-diol is formed in tammar wallaby pouch young testes by a pathway involving 5alpha-pregnane-3alpha,17alpha-diol-20-one as a key intermediate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2941839

28 October 2018

Validation of a high-throughput liquid chromatography-tandem mass spectrometry method for urinary cortisol and cortisone.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2941839

28 October 2018

The diagnosis of congenital adrenal hyperplasia in the newborn by gas chromatography/mass spectrometry analysis of random urine specimens

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2941839

28 October 2018

A new defect in the peripheral conversion of cortisone to cortisol

1 reference

https://pubmed.ncbi.nlm.nih.gov/20417277

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Male pseudohermaphroditism due to multiple defects in steroid-biosynthetic microsomal mixed-function oxidases. A new variant of congenital adrenal hyperplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/20417277

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Profiling steroid hormones and urinary steroids

1 reference

https://pubmed.ncbi.nlm.nih.gov/20417277

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Apparent cortisone reductase deficiency: a unique form of hypercortisolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/20417277

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Urine steroid hormone profile analysis in cytochrome P450 oxidoreductase deficiency: implication for the backdoor pathway to dihydrotestosterone

1 reference

https://pubmed.ncbi.nlm.nih.gov/20417277

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Newborn screening for congenital adrenal hyperplasia: additional steroid profile using liquid chromatography-tandem mass spectrometry

1 reference

https://pubmed.ncbi.nlm.nih.gov/20417277

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dehydrosteroid measurements in maternal urine or serum for the prenatal diagnosis of Smith-Lemli-Opitz syndrome (SLOS)

1 reference

https://pubmed.ncbi.nlm.nih.gov/20417277

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hormonal diagnosis of 21-hydroxylase deficiency in plasma and urine of neonates using benchtop gas chromatography-mass spectrometry

1 reference

https://pubmed.ncbi.nlm.nih.gov/20417277

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biochemical diagnosis of Antley-Bixler syndrome by steroid analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/20417277

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1016/J.JSBMB.2010.04.010

1 reference

Europe PubMed Central

31 July 2017

1 reference

Europe PubMed Central

31 July 2017

1 reference

Europe PubMed Central

31 July 2017

ResearchGate publication ID

0 references

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