Constraint-induced movement therapy promotes brain functional reorganization in stroke patients with hemiplegia
2012-01-04WenqingWangAihuiWangLiminYuXuesongHanGuiyunJiangChangshuiWengHongweiZhangZhiqiangZhou
Wenqing Wang, Aihui Wang, Limin Yu, Xuesong Han, Guiyun Jiang, Changshui Weng, Hongwei Zhang, Zhiqiang Zhou
1 Department of Rehabilitation Medicine, Affiliated Hospital of Chengde Medical College, Chengde 067000, Hebei Province, China
2 Department of Computer Tomography, Affiliated Hospital of Chengde Medical College, Chengde 067000, Hebei Province, China
3 Department of Anatomy, Chengde Nursing Vocational College, Chengde 067000, Hebei Province, China
4 Department of Computer & Information Engineering, Chengde Petroleum College, Chengde 067000, Hebei Province, China
5 Department of Rehabilitation Medicine, General Hospital of Chinese PLA, Beijing 100853, China
Constraint-induced movement therapy promotes brain functional reorganization in stroke patients with hemiplegia
Wenqing Wang1, Aihui Wang2, Limin Yu3, Xuesong Han4, Guiyun Jiang1, Changshui Weng5, Hongwei Zhang1, Zhiqiang Zhou1
1Department of Rehabilitation Medicine, Affiliated Hospital of Chengde Medical College, Chengde 067000, Hebei Province, China
2Department of Computer Tomography, Affiliated Hospital of Chengde Medical College, Chengde 067000, Hebei Province, China
3Department of Anatomy, Chengde Nursing Vocational College, Chengde 067000, Hebei Province, China
4Department of Computer & Information Engineering, Chengde Petroleum College, Chengde 067000, Hebei Province, China
5Department of Rehabilitation Medicine, General Hospital of Chinese PLA, Beijing 100853, China
Stroke patients with hemiplegia exhibit flexor spasms in the upper limb and extensor spasms in the lower limb, and their movement patterns vary greatly. Constraint-induced movement therapy is an upper limb rehabilitation technique used in stroke patients with hemiplegia; however, studies of lower extremity rehabilitation are scarce. In this study, stroke patients with lower limb hemiplegia underwent conventional Bobath therapy for 4 weeks as baseline treatment, followed by constraint-induced movement therapy for an additional 4 weeks. The 10-m maximum walking speed and Berg balance scale scores significantly improved following treatment, and lower extremity motor function also improved. The results of functional MRI showed that constraint-induced movement therapy alleviates the reduction in cerebral functional activation in patients, which indicates activation of functional brain regions and a significant increase in cerebral blood perfusion. These results demonstrate that constraint-induced movement therapy promotes brain functional reorganization in stroke patients with lower limb hemiplegia.
stroke; constraint-induced movement therapy; functional MRI; lower extremity; maximum walking speed; Berg balance scale; central nervous injury; neuroimaging; regeneration; neural regeneration
Research Highlights
(1) The maximum walking speed and Berg balance scale scores were assessed to evaluate the influence of constraint-induced movement therapy on the walking speed and balance function of stroke patients.
(2) Functional MRI examination demonstrated new activation in the lower limb dominant area on the affected side and functional reorganization of the cerebral cortex on the healthy side.
(3) We speculate that constraint-induced movement therapy promotes functional reorganization following brain injury.
INTRODUCTION
Existing functional imaging studies, such as positron emission tomography and single photon emission computed tomography, are mainly applied to the upper extremities. Functional MRI studies have revealed that the number of newly activated foci in the motor cortex or premotor cortex on the contralateral side (affected side) and the number of activated foci in the motor cortex and supplementary motor area on the ipsilateral side (unaffected side) are significantly increased[1-9]. Constraint-induced movement therapy is a new technique for upper limb rehabilitation in hemiplegic patients[3-4].There is limited information from functional MRI studies on the mechanism of cerebral cortical recovery associated with lower extremity motor functional improvement[10]. It has been reported that rehabilitation treatment is more effective for the recovery of lower limb function than for upper limb function[11].
Hemiplegic patients exhibit flexor spasms in the upper limb and extensor spasms in the lower limb; thus, these movement patterns differ. The upper limb is chiefly used for grasping and protrusive movements, while the lower limb is primarily used for standing and walking; thus, the mechanism of cerebral cortical recovery associated with the upper limb cannot completely underlie recovery of lower limb function[12]. At present, the effect of constraint-induced movement therapy in stroke patients with hemiplegia is unclear, especially for lower limb function. This study aimed to examine cerebral cortical changes in hemiplegic patients before and after constraint-induced movement therapy using functional MRI.
RESULTS
Quantitative analysis of subjects
Five stroke patients were involved in this study, and all of them were entered into the final analysis without any dropout or loss.
Baseline data of subjects
Five stroke patients, aged 34–75 years, with a mean of 54.3±11.8 years, consisted of four men and one woman. The disease course ranged between 2–6 months, with a mean of 4.2±1.6 months. There were three cases of cerebral infarction and two cases of cerebral hemorrhage.
Distribution of brain functional activation zones in stroke patients
All five patients were subjected to functional MRI examination before and after constraint-induced movement therapy. Regions of functional activation were located in the postcentral gyrus and precentral gyrus, paracentral lobule and contralateral superior parietal gyrus in the left hemisphere of two patients; in the postcentral gyrus and precentral gyrus, as well as the ipsilateral paracentral lobule in the left hemisphere of one patient; in the postcentral gyrus and precentral gyrus, as well as the ipsilateral paracentral lobule in the right hemisphere of one patient; and in the postcentral gyrus and precentral gyrus in the right hemisphere of one patient.
After constraint-induced movement therapy, the areas of functional activation were enlarged to varying degrees, and the reduction in activation of regions was alleviated (Figure 1), compared with before treatment.
Figure 1 Functional MRI images of brain functional activation in a stroke patient before (A) and after (B) constraint-induced movement therapy for 4 weeks.
Complications during constraint-induced movement therapy
One male with hypertension displayed transient dizziness during the first and fifth treadmill exercises, and resumed training after a 2-day period of oral administration of antihypertensive drugs. One female with knee osteoarthritis complained of pain at 5 weeks, which was relieved by intra-articular injection of 20 mg Triamcinolone Acetonide. The other patients completed the treatment regimen as scheduled.
After neurodevelopmental treatment, mainly lower extremity physical therapy during the baseline period, the maximum walking speed and Berg balance scale scores were unchanged in five patients (P>0.05). After 4 weeks of constraint-induced movement therapy, the maximum walking speed and Berg balance scale scores were significantly increased when compared with those before treatment (P<0.01; Table 1).
Table 1 Effect of constraint-induced movement therapy on lower extremity motor function in hemiplegic patients after stroke
DISCUSSION
Constraint-induced movement therapy is an increasingly popular rehabilitation technique based on the principle of learned non-use[13], and mainly involves training the affected limbs while restricting the healthy ones. A recent study showed that constraint-induced movement therapy has a training effect on the upper limbs similar to that achieved with bilateral training[14], which suggests that the intensity of exercise is the most critical factor in constraint-induced movement therapy. Kwakkelet al[15]performed a meta-analysis and found that weekly training of more than 16 hours within 6 months after stroke significantly improved activities of daily living. Even several months or years after stroke, rehabilitation treatment is still effective in improving motor function and activities of daily living[16]. However, rehabilitation has greatest efficacy within 6 months of stroke[17]. In this study, the 10-m maximum walking speed and Berg balance scale scores demonstrated that constraint-induced movement therapy can apparently increase walking speed and promote functional recovery of balance in stroke patients. The functional MRI observations revealed new activation in the lower limb functional innervation area and functional reorganization in the contralateral cortex. Presumably, this is due to the ability of constraint-induced movement therapy to promote functional reorganization following brain injury. Three examinations of functional MRI and TMS-induced pyramidal tract reaction test were applied to determine the motor function of the upper limb in stroke patients. The results demonstrated that activation patterns in the cerebral cortex did not contribute to the recovery of motor function in the affected limb, nor were they associated with pyramidal tract Wallerian degeneration[18-19]. However, the degree of functional recovery of the affected limbs appears to be associated with Wallerian degeneration.
In the study of Priceet al[20], the white matter tract anomalies displayed by conventional MRI and diffusion tensor imaging were compared using the FA value, and results showed that diffusion tensor imaging can provide more comprehensive information about white matter tract damage, consistent with the results of Schonberget al[21]. We hypothesize that the correlation between the functional recovery of the affected hands and brain activation patterns is determined by the number of intact nerve fibers in the impaired corticospinal tract; if the number of remaining nerve fibers is insufficient, no activation pattern can promote the functional recovery of the affected hands. Further research is required to clarify the neural basis of recovery mediated by constraint-induced movement therapy. Constraint-induced movement therapy needs no drug application, and is safe, with no risk of adverse reaction[22]. The shortcomings of this study include small sample size and lack of long-term follow-up. Lin and Sutcliffe[23-24]obtained satisfactory therapeutic effects in a randomized controlled study. However, while functional MRI can reveal cerebral cortical activation patterns and allow clinicians to follow the recovery of motor cortical function, it cannot display the trajectory or structure of subcortical white matter fiber tracts. In contrast, diffusion tensor imaging allows imaging of white matter tracts. Thus, functional MRI and diffusion tensor imaging suitably complement each other[25-28], thereby providing a more reliable assessment of the recovery of motor function after stroke[29-30]. The combination of these two imaging techniques promises to advance basic and clinical research, and encourage an increasing number of detailed studies.
In summary, constraint-induced movement therapy of the lower extremity can promote the recovery of motor function after stroke and alter brain neuronal plasticity; this conclusion still needs to be confirmed by large-sample clinical studies. Further research is necessary to clarify the mechanisms underlying the reorganization of motor function to permit the selection of effective treatment strategies.
SUBJECTS AND METHODS
Design
A self-controlled experiment.
Time and setting
Experiments were performed from March 2008 to July 2009 in the Department of Rehabilitation Medicine, Affiliated Hospital of Chengde Medical College, China.
Subjects
Five patients with lower limb hemiplegia after stroke were selected from the Department of Rehabilitation Medicine, Affiliated Hospital of Chengde Medical College, China between March 2008 and July 2009.
Inclusion criteria
(1) All cases were diagnosed in accordance with the standards revised in the Fourth National Cerebrovascular Disease Conference, and verified by skull CT or MRI as lower limb hemiplegia after cerebral stroke. (2) Cases aged 60–80 years were included. (3) The duration of disease was less than or equal to 6 months. (4) Cases exhibited clear awareness, with no aphasia, and action instruction was acceptable. (5) Blood pressure and heart rate within the normal range. (6) The hemiplegic lower extremity was graded ≥ II stage by the Brunnstrom classification system[31]. (7) The muscle strength of lower limb iliopsoas and quadriceps femoris was ≥ III grade[32]. (8) The standing balance and sitting balance were ≥ II grade[33-34]. (9) The ability to stand with the assistance of one person and the ability for assisted walking for a distance of 10 m, at a speed of <36 m/min (half less than normal walking speed).
Exclusion criteria
Patients with severe lower limb bone or joint disease were excluded, as well as those with dementia or severe cognitive impairment.
The clinical experiment complied with the “Declaration of Helsinki”. Before the experiment, all subjects and their relatives were informed of the experimental scheme and risk, and they agreed to sign informed consent.
Methods
Baseline treatment
Baseline treatment included lower extremity loading exercise using the Bobath technique[35], hip adduction and abduction, both lower limbs supporting hip extension, affected limb alone supporting hip extension, gravity center transfer to the paretic side and return to the normal side at the sitting position, anterior-posterior and lateral sitting balance, upper limb loading, and extending and stability training on the affected side. The above treatment was performed twice per day, 2 hours each, 5 times per week, for a total of 4 weeks. Following Bobath treatment, the patients were forced to exercise for an additional 2 weeks. To avoid the overlapping effect of constraint-induced movement therapy and Bobath treatment, constraint-induced movement therapy was performed when the maximum walking speed and Berg balance scale scores were reduced.
Constraint-induced movement therapy
Patients were trained on the 3108 Performance Series treadmill (electric; Taiwan, China) for treadmill exercise; the speed was initially slow and was gradually increased. It is a mandatory ambulation training for patients, with the aim to enhance the walking speed and improve the gait pattern. Treadmill exercise training was given six times, each 5 minutes, totaling 30 minutes, twice per day. In addition, constraint-induced movement therapy also included quadriceps femoris training for 1 hour, rehabilitation treadmill for 50 minutes, upstairs and downstairs training for 30 minutes, balance training for 30 minutes, single leg loading for 30 minutes, and lower limb compulsory training for 4 hours per day, five times per week, for 4 weeks.
Evaluation of rehabilitation
The motor function of the lower limbs was assessed before and after treatment by a therapist who was blinded to the experiment. 10-m maximum walking speed was used to evaluate the walking speed of stroke patients with hemiplegia[36]. In brief, the ground was marked with color rubber at the start point, at 3.0 m, at 13.0 m, and at the end point. The time the patients took to walk from 3.0 m to 13.0 m was recorded using a stopwatch, accurate to 0.1 second. The patients were tested three times with a rest interval, and the fastest walking speed of three measurements was taken as the maximum walking speed. Data were expressed as m/min. Berg balance scale was used to evaluate the balance ability of patients[37]. There were a total of 14 movements; from sitting to standing, continued standing without support, standing without support, from standing to sitting, transferring, standing without support and with eyes closed, feet and standing without support, standing and extending upper limb, standing and fetching from the ground, standing and turning back, standing and turning 360°, alternating feet on the bench with continued support, continuous standing on one foot, and standing on a leg. In the Berg test, each action was classified into five grades, ranging from 0–4. The maximum score was 56 points and the lowest score was 0 point; a lower score indicated a more severe balance impairment.
Functional MRI
Dynamic changes in blood perfusion in brain functional areas were detected using blood oxygen level-dependent contrast technique, which assesses local neuronal functional recovery. 1.5T superconducting magnetic resonance instrument (Toshiba, Tokyo, Japan) was used for oxygen level-dependent functional MRI sequence scanning; in Single shot SEEPI sequences, TR=2 000 ms, TE=20 ms, slice thickness=5 mm, space=0 mm, matrix=128×128, NEX=1; the scanning was performed from 7 cm above the canthomeatal line to the calvaria. Patients were forced to maintain immobility and performed advance training. The head and waist were fixed using a strap. Image preprocessing was performed used a head correction technique. Patients in the supine position, with the head fixed, were kept motionless and scanned for 30 seconds, and then the patients were forced to consecutively raise and strengthen their leg, and simultaneous scanning was conducted for an additional 30 seconds. 30-second systemic motionless scanning was performed; 30 seconds of raising and strengthening of the affected legs was repeated six times for successive scanning. Data were analyzed and processed into functional MRI images. In the functional MRI images, red color represented normal blood perfusion, indicating normal functional activation, while yellow and green colors represented different levels of decreased blood perfusion, indicating abnormal functional activation. Scanning was performed before and after the 4-week period of constraint-induced movement therapy.
Statistical analysis
Measurement data were expressed as mean±SD and were processed using SPPS version 13.0 (SPSS, Chicago, IL, USA). Measurement data were compared using the pairedt-test. A value ofP<0.05 indicated a significant difference.
Author contributions:Wenqing Wang had full access to study concept and design, provided technical information, wrote the manuscript, and validated the study. Aihui Wang was responsible for CT projection, data acquisition and integration. Limin Yu analyzed the cerebral cortical innervation area. Xuesong Han participated in functional MRI image processing and supervised the manuscript. Hongwei Zhang performed statistical processing. Guiyun Jiang and Zhiqiang Zhou, rehabilitation therapists, conducted routine rehabilitation training and constraint-induced movement therapy. Changshui Weng was involved in validation and data analysis.
Conflicts of interest:None declared.
Ethical approval:The experiment was approved by the Ethics Committee of Affiliated Hospital of Chengde Medical College in China.
Author statements:The manuscript is original, has not been submitted to or is not under consideration by another publication, has not been previously published in any language or any form, including electronic, and contains no disclosure of confidential information or authorship/patent application disputations.
[1] Page SJ, Szaflarski JP, Eliassen JC, et al. Cortical plasticity following motor skill learning during mental practice in stroke. Neurorehabil Neural Repair. 2009;23(4):382-388.
[2] Isozaki M, Arai Y, Kudo T, et al. Clinical implication and prognosis of normal baseline cerebral blood flow with impaired vascular reserve in patients with major cerebral artery occlusive disease. Ann Nucl Med. 2010;24(5): 371-377.
[3] Hayner K, Gibson G, Giles GM. Comparison of constraint-induced movement therapy and bilateral treatment of equal intensity in people with chronic upper-extremity dysfunction after cerebrovascular accident. Am J Occup Ther. 2010;64(4):528-539.
[4] Sheng B, Lin M. A longitudinal study of functional magnetic resonance imaging in upper-limb hemiplegia after stroke treated with constraint-induced movement therapy. Brain Inj. 2009;23(1):65-70.
[5] Kin YH, Park JW, Ko MH, et al. Plastic changes of motor network after constraint-induced movement therapy. Yonsei Med J. 2004;45(2):241-246.
[6] Sutcliffe TL, Gaetz WC, Logan WJ, et al. Cortical reorganization after modified CIMT in pediatric hemiplegic cerebral palsy. J Child Neurol. 2007;22(11): 1281-1287.
[7] Juenger H, Linder-Lucht M, Wacther M, et al. Cortical neuromodulation by CIMT in congenital hemiparedis:an fMRI study. Neuropediatrics. 2007;38(3):130-136.
[8] Wu CY, Hsieh YW, Lin KC, et al. Brain reorganization after bilateral arm training and distributed constraintinduced therapy in stroke patients: a preliminary functional magnetic resonance imaging study. Chang Gung Med J. 2010;33(6):628-638.
[9] Murayama T, Numata K, Kawakami T, et al. Changes in the brain activation balance in motor-related areas after constraint-induced movement therapy; a longitudinal fMRI study. Brain Inj. 2011;25(11):1047-1057.
[10] Richards LG, Stewart KC, Woodbury ML, et al. Movement-dependent stroke recovery: a systematic review and mate-analysis of TMS and fMRI evidence. Neuropsychologia. 2008;46(1):3-11.
[11] Marklund I, Klässbo M. Effects of lower limb intensive mass practice in post-stroke patients:Single subject experimental design with long-term follow-up. Clinical Rehabilitation. 2006;20(7):568-576.
[12] Luft AR, Forrester L, Macko RF, et al. Brain activation of lower extremity movement in chronically impaire stroksurvivous. Neuroimage. 2005;26(1):184-194.
[13] Wittenberg GF, Schaechter JD. The neural basis of constraint-induced movement therapy. Curr Opin Neurol. 2009;22(6):582-588.
[14] Hayner K, Gibson G, Giles GM. Comparison of constraint-induced movement therapy and bilateral treatment of equal intensity in people with chronic upper-extremity dysfunction after cerebrovascular accident. Am J Occup Ther. 2010;64(4):528-539.
[15] Kwakkel G, Van Peppen R, Wagenarr RC, et al. Effects of augmented exercise therapy time after stroke: a meta-analysis. Stroke. 2004;35(11):2529-2539.
[16] Wolf SL, Thompson PA, Winstein CJ, et al. The excite stroke trial: comparing early and delayed constraintinduced movement therapy. Stroke. 2010;41(10): 2309-2315.
[17] Maulden SA, Gassaway J, Horn SD, et al. Timing of initiation of rehabilitation after stroke. Arch Phys Med Rehabil. 2005;86(12 Suppl 2):34-40.
[18] Feydy A, Carlier R, Roby-Brami A, et al. Longitudinal study of motor recovery after stroke: recruitment and focusing of brain activation. Stroke. 2002;33(6): 1610-1617.
[19] Könönen M, Tarkka IM, Niskanen E, et al. Functional MRI and motor behavioral changes obtained with constraintinduced movement therapy in chronic stroke. Eur J Neurol. 2012;19(4):578-586.
[20] Price SJ, Burnet NG, Donovan T, et al. Diffusion tensor imaging of brain tumours at 3T: a potential tool for assessing white matter tract invasion? Clin Radiol. 2003;58(6):455-462.
[21] Schonberg T, Pianka P, Hendler T, et al. Characterization of displaced white matter by brain tumors using combined DTI and fMRI. Neuroimage. 2006;30(4):1100-1111.
[22] Taub E, Uswatt G, Morris DM. Improved motor recovery after stroke and massive cortical reorganization following Constraint-Induced Movement therapy. Phys Med Rehabil Clin N Am. 2003;14(1 Suppl):S77-91.
[23] Lin KC, Chung HY, Wu CY, et al. Constraint-induced therapy versus control intervention in patients with stroke: a functional magnetic resonance imaging study. Am J Phys Med Rehabil. 2010;89(3):177-185.
[24] Sutcliffe TL, Logan WJ, Fehlings DL. Pediatric constraintinduced movement therapy is associated with increased contralateral cortical activity on functional magnetic resonance imaging. J Child Neurol. 2009;24(10): 1230-1235.
[25] Parmar H, Sitoh YY, Yeo TT. Combined magnetic resonance tractography and functional magnetic resonance imaging in evaluation of brain tumors involving the motor system. J Comput Assist Tomogr. 2004,28(4): 551-556.
[26] Holodny AI, Ollenschleger MD, Liu WC, et al. Identification of the corticospinal tracts achieved using blood-oxygen leveldependent and diffusion functional MR imaging in patients with brain tumors. AJNR Am J Neuroradiol. 2001;22(1):83-88.
[27] Schonberg T, Pianka P, Hendler T, et al. Characterization of disp laced white matter by brain tumors using combined DTI and fMRI. Neuroimage. 2006;30(4):1100-1111.
[28] Gumprecht H, Ebel GK, Auer DP, et al. Neuronavgation and functional MRI for surgery in patients with lesion in eloquent brain areas. Minim Invasive Neurosur. 2002; 45(3):151-153.
[29] Ahn YH, You SH, Randolph M, et al. Peri-infarct reorganization of motor function in patients with pontine infarct. NeuroRehabilitation. 2006;21(3):233-237.
[30] Akai H, Mori H, Aoki S, et al. Diffusion tensor tractography of gliomatosis cerebri: fiber tracking through the tumor. J Comput Assist Tomogr. 2005;29(1):127-129.
[31] Dajpratham P, Kuptniratsaikul V, Kovindha A, et al. Prevalence and management of poststroke spasticity in Thai stroke patients: a multicenter study. J Med Assoc Thai. 2009;92(10):1354-1360.
[32] Lucas JT, Ducker TB. Motor classification of spinal cord injuries with mobility, morbidity and recovery indices. Am Surg. 1979;45(3):151-158.
[33] Blum L, Korner-Bitensky N. Usefulness of the berg balance scale in stroke rehabilitation: a systematic review. Phys Ther. 2008;88(5):559-566.
[34] Ng SS, Hui-Chan CW. The timed up & go test: Its reliability and association with lower-limb impairments and locomotor capacities in people with chronic stroke. Arch Phys Med Rehabil. 2005;86(8):1641-1647.
[35] Yagura H, Hatakenaka M, Miyai I. Does therapeutic facilitation add to locomotor outcome of body weight--supported treadmill training in nonambulatory patients with stroke? A randomized controlled trial. Arch Phys Med Rehabil. 2006;87(4):529-535.
[36] Salbach NM, Mayo NE, Wood-Dauphinee S, et al. A task-orientated intervention enhances walking distance and speed in the first year post stroke: a randomized controlled trial. Clin Rehabil. 2004;18(5):509-519.
[37] Kim YH, You SH, Kwon YH, et al. Longitudinal fMRI study for locomotor recovery in patients with stroke. Neurology. 2006;67(2):330-333.
10.3969/j.issn.1673-5374.2012.32.010 [http://www.crter.org/nrr-2012-qkquanwen.html]
Wang WQ, Wang AH, Yu LM, Han XS, Jiang GY, Weng CS, Zhang HW, Zhou ZQ. Constraint-induced movement therapy promotes brain functional reorganization in stroke patients with hemiplegia. Neural Regen Res. 2012;7(32):2548-2553.
Wenqing Wang, Associate chief physiotherapist, Department of Rehabilitation Medicine, Affiliated Hospital of Chengde Medical College, Chengde 067000, Hebei Province, China
Wenqing Wang, Department of Rehabilitation Medicine, Affiliated Hospital of Chengde Medical College, Chengde 067000, Hebei Province, China Wangwenqing186@163.com
2012-07-06
2012-09-24 (N20111126004/WJ)
We would like to thank Shenglin Wang, Zhixin Cui and Liye Wan from the Department of Computer Tomography, Affiliated Hospital of Chengde Medical College, China, for providing technical help.
(Edited by Huang YJ, Yin JZ/Yang Y/Song LP)
杂志排行
中国神经再生研究(英文版)的其它文章
- Characteristics of vascular lesions in patients with posterior circulation infarction according to age and region of infarct*☆
- Morphological differences in skeletal muscle atrophy of rats with motor nerve and/or sensory nerve injury*★
- A standardized method to create peripheral nerve injury in dogs using an automatic non-serrated forceps***★
- Rapid genetic screening of Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies patients**★
- Ultrasound guided neural stem cell transplantation through the lateral ventricle for treatment of cerebral palsy in children☆
- Correlation between spina bifida manifesta in fetal rats and c-Jun N-terminal kinase signaling**★