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

Clinic 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

Research Areas and Centers

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

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

Access to Document

10.1111/j.1468-1331.2006.01393.x

Cite this

@article{2888e016d8434c799784ccf3c4ab4603,

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. ",

author = "H. Rambold and T. Sander and C. Helmchen and W. Heide",

year = "2006",

month = oct,

day = "1",

doi = "10.1111/j.1468-1331.2006.01393.x",

language = "English",

volume = "13",

journal = "European Journal of Neurology",

issn = "1351-5101",

publisher = "Wiley-Blackwell Publishing Ltd",

number = "10",

}

TY - JOUR

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

Research Areas and Centers

UN SDGs

Access to Document

Other files and links

Fingerprint

Cite this