Different types of intra-saccadic slowing in congenital (RAPSN-mutation) and acquired myasthenic syndromes

H. Rambold; T. Sander; C. Helmchen; W. Heide

doi:10.1111/j.1468-1331.2006.01393.x

Different types of intra-saccadic slowing in congenital (RAPSN-mutation) and acquired myasthenic syndromes

H. Rambold^*, T. Sander, C. Helmchen, W. Heide

^*Korrespondierende/r Autor/-in für diese Arbeit

Klinik für Neurologie

4 Zitate (Scopus)

Abstract

Saccadic slowing and saccadic fatigue is a common clinical finding in myasthenia gravis [1]. However, previous studies on eye movements in myasthenia gravis did not dissociate congenital (CMS) from acquired forms with acetylcholine‐receptor (ACHR) auto‐antibodies [1]. Therefore, saccades of one patient with CMS caused by two compound heterozygote mutations (N88K and 1177 del AA) in the RAPSN gene (2) (one mutation from each parent) were compared with three patients with acquired myasthenia gravis and two healthy controls.

Originalsprache	Englisch
Zeitschrift	European Journal of Neurology
Jahrgang	13
Ausgabenummer	10
ISSN	1351-5101
DOIs	https://doi.org/10.1111/j.1468-1331.2006.01393.x
Publikationsstatus	Veröffentlicht - 01.10.2006

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Forschungsschwerpunkt: Gehirn, Hormone, Verhalten - Center for Brain, Behavior and Metabolism (CBBM)

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10.1111/j.1468-1331.2006.01393.x

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abstract = "Saccadic slowing and saccadic fatigue is a common clinical finding in myasthenia gravis [1]. However, previous studies on eye movements in myasthenia gravis did not dissociate congenital (CMS) from acquired forms with acetylcholine‐receptor (ACHR) auto‐antibodies [1]. Therefore, saccades of one patient with CMS caused by two compound heterozygote mutations (N88K and 1177 del AA) in the RAPSN gene (2) (one mutation from each parent) were compared with three patients with acquired myasthenia gravis and two healthy controls. ",

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AU - Rambold, H.

AU - Sander, T.

AU - Helmchen, C.

AU - Heide, W.

PY - 2006/10/1

Y1 - 2006/10/1

N2 - Saccadic slowing and saccadic fatigue is a common clinical finding in myasthenia gravis [1]. However, previous studies on eye movements in myasthenia gravis did not dissociate congenital (CMS) from acquired forms with acetylcholine‐receptor (ACHR) auto‐antibodies [1]. Therefore, saccades of one patient with CMS caused by two compound heterozygote mutations (N88K and 1177 del AA) in the RAPSN gene (2) (one mutation from each parent) were compared with three patients with acquired myasthenia gravis and two healthy controls.

AB - Saccadic slowing and saccadic fatigue is a common clinical finding in myasthenia gravis [1]. However, previous studies on eye movements in myasthenia gravis did not dissociate congenital (CMS) from acquired forms with acetylcholine‐receptor (ACHR) auto‐antibodies [1]. Therefore, saccades of one patient with CMS caused by two compound heterozygote mutations (N88K and 1177 del AA) in the RAPSN gene (2) (one mutation from each parent) were compared with three patients with acquired myasthenia gravis and two healthy controls.

UR - https://www.scopus.com/pages/publications/33748950642

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DO - 10.1111/j.1468-1331.2006.01393.x

M3 - Letters

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SN - 1351-5101

VL - 13

JO - European Journal of Neurology

JF - European Journal of Neurology

IS - 10

ER -

Different types of intra-saccadic slowing in congenital (RAPSN-mutation) and acquired myasthenic syndromes

Abstract

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