(Q43645138)

25 November 2017

title

Analysis of guanidinoacetate and creatine by isotope dilution electrospray tandem mass spectrometry (English)

1 reference

25 November 2017

Bodamer OA

1

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25 November 2017

Bloesch SM

2

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25 November 2017

Gregg AR

3

1 reference

25 November 2017

Stockler-Ipsiroglu S

4

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25 November 2017

O'Brien WE

5

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25 November 2017

publication date

1 June 2001

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25 November 2017

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25 November 2017

volume

308

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25 November 2017

issue

1-2

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25 November 2017

page(s)

173-178

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Creatine deficiency syndrome caused by guanidinoacetate methyltransferase deficiency: diagnostic tools for a new inborn error of metabolism.

25 November 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2801%2900480-6

Guanidinoacetate methyltransferase deficiency: new clinical features.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2801%2900480-6

Guanidino compounds in serum, urine, liver, kidney, and brain of man and some ureotelic animals

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2801%2900480-6

An accurate stable isotope dilution gas chromatographic-mass spectrometric approach to the diagnosis of guanidinoacetate methyltransferase deficiency

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2801%2900480-6

GC-MS determination of guanidinoacetate in urine and plasma

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2801%2900480-6

Simultaneous determination of creatinine, creatine, and guanidinoacetic acid in human serum and urine using liquid chromatography-atmospheric pressure chemical ionization mass spectrometry

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2801%2900480-6

Guanidino compounds in guanidinoacetate methyltransferase deficiency, a new inborn error of creatine synthesis.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2801%2900480-6

Guanidinoacetate methyltransferase (GAMT) deficiency: non-invasive enzymatic diagnosis of a newly recognized inborn error of metabolism

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2801%2900480-6

10.1016/S0009-8981(01)00480-6

7 January 2021

Identifiers

DOI

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25 November 2017

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