它们也都缺省了皮下组织的关键部分——如进行动作协调的小脑，控制情绪的扁桃体以及控制肌肉组织的脊髓。
They are also missing essential subcortical structures, -such as the cerebellum that organizes movements, the amygdala that creates emotional states and the spinal cord that runs the musculature.
目的研究遗传性脊髓小脑性共济失调7型（SCA7）的基因突变和临床特征。
Objective To study the gene mutation and clinical characteristic of hereditary spinocerebellar ataxia type 7 (SCA7).
目的研究细胞凋亡在脊髓小脑性共济失调3型(SCA3)分子发病机制中的作用。
Objective to study the role of cell apoptosis in the molecular pathogenesis of spinocerebellar ataxia type 3 (SCA3).
主要分布于脑桥、小脑、苍白球壳核、延髓白质纤维束，脊髓外侧束，且与髓鞘变性脱失的分布一致。
Their main distributions were transverse fibers of the basis pontine, the white matter of the cerebellum, striatopallidal fibers and lateral column of the spinal cord.
目的分析泛素依赖的蛋白水解通路(UPP)在转染了脊髓小脑性共济失调3型(SCA3)基因的PC 12细胞中的定位及作用。
Objective To analyze the role and location of ubiquitin-dependent proteolysis pathway (UPP) in PC12 cells transfected by plasmids with spinocerebellar ataxia type 3 (SCA3) gene.
后脑由延髓和桥脑组成，连接脊髓和脑的高级部分，也包含将讯息从大脑皮质传到小脑的神经细胞。
The hindbrain comprises the medulla oblongata and the pons, which connects the spinal cord with higher Brain levels and transfers information from the cerebral cortex to the cerebellum.
结论：大鼠脊髓颈段有向小脑中央核的投射，与腰髓的投射相比较，存在一定的定位关系。
CONCLUSION: The cervical segments of spinocerebellar tract project to the cerebellar nuclei in rats and locate somatotopically as compared with the lumbar spinal cord.
回顾小脑性共济失调的研究历史、分类，介绍脊髓小脑共济失调的病因机制和治疗方法。
The history of the research of cerebellar ataxia, and the different classifications of ataxia were reviewed. The pathogenesis and treatments of spinocerebellar ataxia were summarizd.
主要病变包括大脑皮质、丘脑、海马、小脑和脊髓的神经细胞尼氏体溶解、核浓缩和细胞表面结痂。
The major lesions included dissolution of Nissl bodies, pyknosis, and incrustation of neuronal surface in the cerebral cortex, thalamus, hippocampus, cerebellum and spinal cord.
本研究采用放射自显影顺行追踪法研究了家兔脊髓中央颈核向小脑的投射。
The experiment is to trace the projection from the central cervical nucleus(CCN)to the cerebellum in the rabbits with the method of autoradiography anterogradely.
异常步态包括偏瘫步态、脑瘫步态、小脑损害步态、周围神经损伤所致异常步态、前冲步态、疼痛步态、脊柱疾患所致异常步态以及脊髓损伤的步态等。
Abnormal gait included hemiplegia gait, brain paralysis gait, cerebella gait, peripheral nervous system injury gait, festination, pain gait and spinal column and spinal cord injury gait and so on.
用荧光素双标记法研究了36只大鼠蓝斑向前额叶皮质、海马、丘脑、小脑和脊髓的分支投射。
The divergent axon collaterals from neurons in locus coeruleus have been investigated by means of fluorescent double labeling technique in 36 rats.
方法对14例先天性小脑扁桃体下疝畸形合并脊髓空洞症患者，根据不同的病情采用相应的手术方式进行治疗。
Methods 14 patients with congenital tonsillar hernia deformity associated with syringomyelia had been treated with correspondent surgery depending on their case condition.
它们也都缺省了皮下组织的关键部分——如进行动作协调的小脑，控制情绪的扁桃体以及控制肌肉组织的脊髓。
They are also missing essential subcortical structures, - such as the cerebellum that organizes movements, the amygdala that creates emotional states and the spinal cord that runs the musculature.
小脑后下动脉梗死：一例先天性脊柱侧凸青少年病人脊髓后路融合术的罕见并发症。
Posterior Inferior Cerebellar Artery Infarction: an Unusual Complication of Posterior Spinal Fusion Surgery in an Adolescent with Idiopathic Scoliosis.
只有5% - 30%的小脑血管母细胞瘤是归因于VHL病，但是80%的脊髓血管母细胞瘤发生在VHL病中。
Only 5%-30% of all cerebellar hemangioblastomas are attributed to VHL disease, whereas 80% of spinal cord hemangioblastomas occur with the disease.
只有5% - 30%的小脑血管母细胞瘤是归因于VHL病，但是80%的脊髓血管母细胞瘤发生在VHL病中。
Only 5%-30% of all cerebellar hemangioblastomas are attributed to VHL disease, whereas 80% of spinal cord hemangioblastomas occur with the disease.
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