(Q46411758)

22 December 2017

title

1H MR spectroscopy as a diagnostic tool for cerebral creatine deficiency (English)

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22 December 2017

author

Jiri Zeman

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22 December 2017

Milan Jirsa

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22 December 2017

Věra Malinová

object named as

Vera Malinova

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author name string

Monika Dezortova

1

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22 December 2017

Filip Jiru

2

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22 December 2017

Jan Petrasek

3

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22 December 2017

Milan Hajek

7

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22 December 2017

publication date

26 August 2008

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22 December 2017

Magnetic Resonance Materials in Physics, Biology and Medicine

published in

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22 December 2017

volume

21

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22 December 2017

issue

5

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22 December 2017

page(s)

327-332

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22 December 2017

https://scigraph.springernature.com/pub.10.1007/s10334-008-0137-z

exact match

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cites work

Biochemical and clinical characteristics of creatine deficiency syndromes.

1 reference

12 December 2020

X-linked creatine deficiency syndrome: a novel mutation in creatine transporter gene SLC6A8.

1 reference

12 December 2020

Detection of low-level somatic and germline mosaicism by denaturing high-performance liquid chromatography in a EURO-MRX family with SLC6A8 deficiency.

1 reference

12 December 2020

1H chemical shift imaging of the brain in guanidino methyltransferase deficiency, a creatine deficiency syndrome; guanidinoacetate accumulation in the gray matter

1 reference

12 December 2020

Quantitative analysis of short echo time1H-MRSI of cerebral gray and white matter

1 reference

12 December 2020

Creatine deficiency syndromes

1 reference

12 December 2020

Irreversible brain creatine deficiency with elevated serum and urine creatine: a creatine transporter defect?

1 reference

12 December 2020

Lack of creatine in muscle and brain in an adult with GAMT deficiency

1 reference

12 December 2020

Congenital creatine transporter deficiency

1 reference

12 December 2020

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

1 reference

12 December 2020

X-linked creatine-transporter gene (SLC6A8) defect: a new creatine-deficiency syndrome.

1 reference

12 December 2020

Creatine deficiency syndromes

1 reference

12 December 2020

Magnetic resonance spectroscopy in a 9-day-old heterozygous female child with creatine transporter deficiency

1 reference

12 December 2020

Normalisation of metabolite images in 1H NMR spectroscopic imaging

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12 December 2020

Laboratory diagnosis of defects of creatine biosynthesis and transport

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12 December 2020

Proton T2 relaxation of cerebral metabolites of normal human brain over large TE range

1 reference

12 December 2020

Estimation of metabolite concentrations from localized in vivo proton NMR spectra

1 reference

12 December 2020

X-linked creatine transporter defect: an overview

1 reference

12 December 2020

Guanidinoacetate methyltransferase deficiency: differences of creatine uptake in human brain and muscle

1 reference

12 December 2020

X-linked creatine transporter defect: a report on two unrelated boys with a severe clinical phenotype

1 reference

12 December 2020

AGAT, GAMT and SLC6A8 distribution in the central nervous system, in relation to creatine deficiency syndromes: a review

1 reference

12 December 2020

Application of LCModel for quality control and quantitative in vivo 1H MR spectroscopy by short echo time STEAM sequence

1 reference

12 December 2020

Error images for spectroscopic imaging by LCModel using Cramer-Rao bounds.

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12 December 2020

10.1007/S10334-008-0137-Z

Identifiers

DOI

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22 December 2017

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22 December 2017