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P.12.3 Do congenital myasthenic syndromes in childhood have a common face? Clinical profile of slow channel, CHRNE and RAPSYN mutations
by
Ekker, M.S
,
Rietveld, A
,
Eymard, B
,
Erasmus, C.E
,
Sie, L.T.L
Published in
Neuromuscular disorders : NMD
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P.12.1 Diagnostic pitfalls in congenital myasthenic syndromes in children: Clinical experience in an academic neuromuscular centre
by
Ekker, M.S
,
Rietveld, A
,
Kamsteeg, E.J
,
van Alfen, N
,
Sie, L.T.L
,
Erasmus, C.E
Published in
Neuromuscular disorders : NMD
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Response to: On the role of visual electrophysiology in parkinson's disease
by
S, Janssen
,
Ekker, M.S.
,
Poewe, W.
,
van Wezel, R.J.A.
,
Nonnekes, J.
,
Bloem, B.R.
Published in
Parkinsonism & related disorders
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