[(1)H] magnetic resonance spectroscopy of urine: diagnosis of a guanidinoacetate methyl transferase deficiency case. (Q46001631)

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28 January 2020

title

[(1)H] magnetic resonance spectroscopy of urine: diagnosis of a guanidinoacetate methyl transferase deficiency case (English)

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13

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author name string

Maria Tassini

1

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28 January 2020

Raffaella Zannolli

2

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28 January 2020

Sabrina Buoni

3

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28 January 2020

Udo Engelke

4

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28 January 2020

Antonio Vivi

5

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28 January 2020

Gianni Valensin

6

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28 January 2020

Gajja S Salomons

7

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28 January 2020

Anna De Nicola

8

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28 January 2020

Mirella Strambi

9

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28 January 2020

Lucia Monti

10

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28 January 2020

Eva Morava

11

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28 January 2020

Ron A Wevers

12

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publication date

21 May 2009

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Journal of Child Neurology

28 January 2020

published in

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volume

25

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28 January 2020

issue

1

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28 January 2020

page(s)

98-101

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Expanded clinical and molecular spectrum of guanidinoacetate methyltransferase (GAMT) deficiency

28 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1177%2F0883073809336120

GAMT deficiency: features, treatment, and outcome in an inborn error of creatine synthesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073809336120

Possibilities of selective screening for inborn errors of metabolism using high-resolution 1H-FT-NMR spectrometry

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073809336120

Improving treatment of guanidinoacetate methyltransferase deficiency: reduction of guanidinoacetic acid in body fluids by arginine restriction and ornithine supplementation

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073809336120

21 January 2018

Identifiers

DOI

10.1177/0883073809336120

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28 January 2020

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