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Direct current electrical stimulation of acupuncture needles for peripheral nerve regeneration: an exploratory case series

M Inoue, Y Katsumi, M Itoi, T Hojo… - Acupuncture in …, 2011 - aim.bmj.com
... a distal cathode accelerated peripheral nerve regeneration.1 2 Based on the results of these
basic animal studies, DCEA with the cathode distal to the nerve injury site was applied clinically
in this study to treat seven cases of motor paralysis due to peripheral nerve damage. ...
Cited by 1 - Related articles - All 3 versions

Medium-term outcomes of C3–6 laminoplasty for cervical myelopathy: a prospective study with a minimum 5-year follow-up

H Sakaura, N Hosono, Y Mukai, M Iwasaki… - European Spine …, 2011 - Springer
... achieved widespread acceptance as a safe and effective surgical procedure for multisegmental
cervical compression myelopathy, several problems remain yet to be solved: postoperative axial
neck pain; loss of cer- vical lordosis; and segmental motor paralysis [1]. Regarding ...
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A case of median nerve paralysis after hepatic segmentectomy].

A Yoshimatsu, T Hoshi… - Masui. The Japanese journal …, 2011 - ncbi.nlm.nih.gov
... After surgery, patient complained of motor paralysis and hypesthesia of the left palm side
of the thumb, first finger and radial half of the middle finger. ... Motor paralysis and
hypesthesia gradually disappeared over the two weeks after surgery. ...

Prognosis of Patients with Peripheral Facial Palsy

Y Nunokawa… - Journal of Physical Therapy Science, 2011 - J-STAGE
... Abstract. [Purpose] We analyzed the evaluation of facial motor paralysis employing
Yanagihara's 40-point method for patients diagnosed with Bell's palsy, aiming to
obtain some prognostic findings. [Subjects and Methods] The ...
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Vocal cord paralysis and rapid progressive motor neuron disease by the I113F mutation in SOD1 gene

A Hermann, U Reuner, G Ziethe… - Amyotrophic …, 2011 - informahealthcare.com
Familial cases of amyotrophic lateral sclerosis are most frequently caused by mutation in the
superoxide dismutase-1 (SOD1) gene. We report a heterozygous I113F mutation in a patient
with familial ALS characterized by early and predominant bilateral vocal cord paralysis ...
Cited by 1 - Related articles - All 2 versions

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