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

^*Corresponding author for this work

Department of Neurology

4 Citations (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.

Original language	English
Journal	European Journal of Neurology
Volume	13
Issue number	10
ISSN	1351-5101
DOIs	https://doi.org/10.1111/j.1468-1331.2006.01393.x
Publication status	Published - 01.10.2006

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SDG 10 Reduced Inequalities

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Academic Focus: Center for Brain, Behavior and Metabolism (CBBM)

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10.1111/j.1468-1331.2006.01393.x

Cite this

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

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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T1 - Different types of intra-saccadic slowing in congenital (RAPSN-mutation) and acquired myasthenic syndromes

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

U2 - 10.1111/j.1468-1331.2006.01393.x

DO - 10.1111/j.1468-1331.2006.01393.x

M3 - Letters

C2 - 16987151

AN - SCOPUS:33748950642

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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