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Connexin32 gene mutations in X-linked dominant Charcot-Marie-Tooth disease (CMTX1).
Hum Genet. 1997 Apr;99(4):501-5. doi: 10.1007/s004390050396.
Hum Genet. 1997.
PMID: 9099841
Variability in nerve biopsy findings in a kinship with dominantly inherited Charcot-Marie-Tooth disease.
Van Weerden TW, Houthoff HJ, Sie O, Minderhoud JM.
Van Weerden TW, et al.
Muscle Nerve. 1982 Mar;5(3):185-96. doi: 10.1002/mus.880050303.
Muscle Nerve. 1982.
PMID: 7088015
No abstract available.
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Dominant inherited distal spinal muscular atrophy with atrophic and hypertrophic calves.
Groen RJ, Sie OG, van Weerden TW.
Groen RJ, et al. Among authors: sie og.
J Neurol Sci. 1993 Jan;114(1):81-4. doi: 10.1016/0022-510x(93)90053-2.
J Neurol Sci. 1993.
PMID: 8433103
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A fatal demyelinating illness in a young woman 10 weeks post partum.
Koch M, den Dunnen W, Sie OG, De Keyser J.
Koch M, et al. Among authors: sie og.
Lancet Neurol. 2005 Feb;4(2):129-34. doi: 10.1016/S1474-4422(05)00994-4.
Lancet Neurol. 2005.
PMID: 15664545
No abstract available.
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The organization and utilization of a case register on epilepsy.
Suurmeije TP, Aldenkamp AP, Heisen TW, Overweg J, Renier WO, Sie OG.
Suurmeije TP, et al. Among authors: sie og.
Int J Adolesc Med Health. 2011 May 18;7(4):281-8. doi: 10.1515/IJAMH.1994.7.4.281.
Int J Adolesc Med Health. 2011.
PMID: 22912204
No abstract available.
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The spasmolytic properties of 5-chloro-4-(2-imidazolin-2-yl-amino)-2, 1,3-benzothiadiazole hydrochloride (DS 103-282): a pilot study.
Sie OG, Lakke JP.
Sie OG, et al.
Clin Neurol Neurosurg. 1980;82(4):273-9. doi: 10.1016/0303-8467(80)90020-7.
Clin Neurol Neurosurg. 1980.
PMID: 6263533
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