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Sung Yeol Joo

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Neuromuscular Disorders : NMD|April 22, 2004
A novel point mutation in PMP22 gene associated with a familial case of Charcot-Marie-Tooth disease type 1A with sensorineural deafnessIn Soo Joo, Chang-Seok Ki, Sung Yeol Joo, et al.
Annals of Neurology|August 2, 2003
Frequency and mechanisms of stroke recurrence after cryptogenic strokeOh Young Bang, Phil Hyu Lee, Sung Yeol Joo, et al.
Archives of Neurology|April 21, 2004
The course of patients with lacunar infarcts and a parent arterial lesion: similarities to large artery vs small artery diseaseOh Young Bang, Sung Yeol Joo, Phil Hyu Lee, et al.
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Showing results (1-10 of 3) with videos related to

Sort By:
Pageof 1
Neuromuscular Disorders : NMD|April 22, 2004
A novel point mutation in PMP22 gene associated with a familial case of Charcot-Marie-Tooth disease type 1A with sensorineural deafnessIn Soo Joo, Chang-Seok Ki, Sung Yeol Joo, et al.
Annals of Neurology|August 2, 2003
Frequency and mechanisms of stroke recurrence after cryptogenic strokeOh Young Bang, Phil Hyu Lee, Sung Yeol Joo, et al.
Archives of Neurology|April 21, 2004
The course of patients with lacunar infarcts and a parent arterial lesion: similarities to large artery vs small artery diseaseOh Young Bang, Sung Yeol Joo, Phil Hyu Lee, et al.
Pageof 1