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 - http://www.scopus.com/inward/record.url?scp=33748950642&partnerID=8YFLogxK
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 -
