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Clinical, electrophysiological and immunological remissions after thymectomy in myasthenia gravis.
Clin Neurophysiol. 2002 Apr;113(4):615-9. doi: 10.1016/s1388-2457(02)00035-4.
Clin Neurophysiol. 2002.
PMID: 11956007
[A case of the Lambert-Eaton syndrome of non-neoplastic origin. Ten-year follow-up].
Emeryk-Szajewska B, Strugalska-Cynowska H, Zakrzewska-Pniewska B, Szyluk B, Kostera-Pruszczyk A.
Emeryk-Szajewska B, et al. Among authors: strugalska cynowska h.
Neurol Neurochir Pol. 2006 May-Jun;40(3):243-7.
Neurol Neurochir Pol. 2006.
PMID: 16794965
Polish.
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L239F founder mutation in GDAP1 is associated with a mild Charcot-Marie-Tooth type 4C4 (CMT4C4) phenotype.
Kabzińska D, Strugalska-Cynowska H, Kostera-Pruszczyk A, Ryniewicz B, Posmyk R, Midro A, Seeman P, Báranková L, Zimoń M, Baets J, Timmerman V, Guergueltcheva V, Tournev I, Sarafov S, De Jonghe P, Jordanova A, Hausmanowa-Petrusewicz I, Kochański A.
Kabzińska D, et al. Among authors: strugalska cynowska h.
Neurogenetics. 2010 Jul;11(3):357-66. doi: 10.1007/s10048-010-0237-6. Epub 2010 Mar 16.
Neurogenetics. 2010.
PMID: 20232219
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Dysmyelinating and demyelinating Charcot-Marie-Tooth disease associated with two myelin protein zero gene mutations.
Drac H, Kabzińska D, Moszyńska I, Strugalska-Cynowska H, Hausmanowa-Petrusewicz I, Kochański A.
Drac H, et al. Among authors: strugalska cynowska h.
J Appl Genet. 2011 May;52(2):177-83. doi: 10.1007/s13353-010-0003-3. Epub 2010 Nov 3.
J Appl Genet. 2011.
PMID: 21107784
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Histochemical studies on normal and diseased human and chick muscle in tissue culture.
Gallup B, Strugalska-Cynowska H, Dubowitz V.
Gallup B, et al. Among authors: strugalska cynowska h.
J Neurol Sci. 1972 Oct;17(2):109-25. doi: 10.1016/0022-510x(72)90134-7.
J Neurol Sci. 1972.
PMID: 4340931
No abstract available.
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