Stroke-like pattern in DTI and MRS of childhood mitochondrial leukoencephalopathy.

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Stroke-like pattern in DTI and MRS of childhood mitochondrial leukoencephalopathy. / Brockmann, K; Finsterbusch, Jürgen; Schara, U; Wilichowski, E; Frahm, J; Hanefeld, F.

In: NEURORADIOLOGY, Vol. 46, No. 4, 4, 2004, p. 267-271.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

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Brockmann K, Finsterbusch J, Schara U, Wilichowski E, Frahm J, Hanefeld F. Stroke-like pattern in DTI and MRS of childhood mitochondrial leukoencephalopathy. NEURORADIOLOGY. 2004;46(4):267-271. 4.

Bibtex

@article{ece871a8edf346fc873cfd4efa4f6339,
title = "Stroke-like pattern in DTI and MRS of childhood mitochondrial leukoencephalopathy.",
abstract = "In a 13-month-old boy with recurrent motor deterioration provoked by fever MRI and proton MRS detected a leukoencephalopathy with reduced cerebral metabolites and elevated lactate. At follow-up 6 and 16 months later these abnormalities improved gradually. Serial diffusion tensor imaging revealed a stroke-like pattern with an initial strong reduction of the apparent diffusion coefficient followed by elevated values 6 months later. The relative diffusion anisotropy remained reduced. Muscle biopsy confirmed a mitochondrial encephalomyopathy.",
author = "K Brockmann and J{\"u}rgen Finsterbusch and U Schara and E Wilichowski and J Frahm and F Hanefeld",
year = "2004",
language = "Deutsch",
volume = "46",
pages = "267--271",
journal = "NEURORADIOLOGY",
issn = "0028-3940",
publisher = "Springer",
number = "4",

}

RIS

TY - JOUR

T1 - Stroke-like pattern in DTI and MRS of childhood mitochondrial leukoencephalopathy.

AU - Brockmann, K

AU - Finsterbusch, Jürgen

AU - Schara, U

AU - Wilichowski, E

AU - Frahm, J

AU - Hanefeld, F

PY - 2004

Y1 - 2004

N2 - In a 13-month-old boy with recurrent motor deterioration provoked by fever MRI and proton MRS detected a leukoencephalopathy with reduced cerebral metabolites and elevated lactate. At follow-up 6 and 16 months later these abnormalities improved gradually. Serial diffusion tensor imaging revealed a stroke-like pattern with an initial strong reduction of the apparent diffusion coefficient followed by elevated values 6 months later. The relative diffusion anisotropy remained reduced. Muscle biopsy confirmed a mitochondrial encephalomyopathy.

AB - In a 13-month-old boy with recurrent motor deterioration provoked by fever MRI and proton MRS detected a leukoencephalopathy with reduced cerebral metabolites and elevated lactate. At follow-up 6 and 16 months later these abnormalities improved gradually. Serial diffusion tensor imaging revealed a stroke-like pattern with an initial strong reduction of the apparent diffusion coefficient followed by elevated values 6 months later. The relative diffusion anisotropy remained reduced. Muscle biopsy confirmed a mitochondrial encephalomyopathy.

M3 - SCORING: Zeitschriftenaufsatz

VL - 46

SP - 267

EP - 271

JO - NEURORADIOLOGY

JF - NEURORADIOLOGY

SN - 0028-3940

IS - 4

M1 - 4

ER -