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Application of cross-migration theory in limb rehabilitation of stroke patients with hemiplegia
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作者 yan-hong lu Yi Fu +2 位作者 Jin Shu Li-Yan Yan Hai-Jian Shen 《World Journal of Clinical Cases》 SCIE 2023年第19期4531-4543,共13页
BACKGROUND Stroke is a common cause of neurological dysfunction,often resulting in hemiplegia.Thus,rehabilitation of limb function in stroke patients is an important step towards accelerating recovery and improving qu... BACKGROUND Stroke is a common cause of neurological dysfunction,often resulting in hemiplegia.Thus,rehabilitation of limb function in stroke patients is an important step towards accelerating recovery and improving quality of life.AIM To investigate whether unilateral strength training in hemiplegic stroke patients could lead to cross-migration,an increase in bilateral muscle strength,and an improvement in lower limb motor function.METHODS We randomly divided 120 patients with hemiplegic stroke into two groups:Eexperimental and control groups,with 60 patients in each group.Both groups received routine rehabilitation treatment,while the experimental group additional-ly received ankle dorsiflexion resistance training on the healthy side for 6 wk.We measured the maximum voluntary contract(MVC),changes in surface electromyography(EMG),and the lower limb motor function using the simplified Fugl Meyer Motor Function Assessment Scale(FMA)before and within 1 wk after training.RESULTS The FMA score in the experimental group improved significantly compared to both their pre-training score and the control group's post-training score(P<0.05).The integrated EMG of the anterior tibialis muscle and pulmonary intestine muscle in the experimental group were significantly different after training than before(P<0.05).Furthermore,the MVC of the anterior tibialis muscle on both the healthy and affected sides and the MVC of the pulmonary intestine muscle on both sides showed significant improvement compared with before training and the control group(P<0.05).CONCLUSION Our findings suggest that ankle dorsiflexion resistance training on the healthy side in hemiplegic stroke patients can increase strength in the opposite tibialis anterior muscle and antagonist's muscle,indicating a cross-migration phenomenon of strength training.Furthermore,this type of training can also improve lower limb motor function,providing a new exercise method for improving early ankle dorsiflexion dysfunction. 展开更多
关键词 Stroke hemiplegia Cross migration Strength training Lower limb function Resistance training
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c.753_754delAG, a novel CFTR mutation found in a Chinese patient with cystic fibrosis: A case report and review of the literature 被引量:1
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作者 Yu-Qing Wang Chuang-Li Hao +4 位作者 Wu-Jun Jiang yan-hong lu Hui-Quan Sun Chun-Yan Gao Min Wu 《World Journal of Clinical Cases》 SCIE 2019年第15期2110-2119,共10页
BACKGROUND Cystic fibrosis(CF)is rare in Asian populations relative to the Caucasian population.In this paper,we report the cystic fibrosis transmembrane conductance regulator(CFTR)variation in a family of Chinese CF ... BACKGROUND Cystic fibrosis(CF)is rare in Asian populations relative to the Caucasian population.In this paper,we report the cystic fibrosis transmembrane conductance regulator(CFTR)variation in a family of Chinese CF patients,and systematically review the previous literature.CASE SUMMARY Here we report a 30-month-old Chinese girl who was diagnosed with CF based on her history and symptoms such as recurrent productive cough,wheezing with repeated infection of Pseudomonas aeruginosa,and parasinusitis.Chest computed tomography(CT)scanning revealed obvious exudative lesions and bilateral bronchiectasis.Liver CT scanning revealed a low-density lesion in the left lobe of the liver.A diagnosis of CF was made based upon CFTR gene tests.The CFTR gene was sequenced using the blood samples of her and her parents and showed a heterozygous novel missense mutation of c.753_754delAG in exon 7.In addition,a heterozygous c.1240 C>T mutation was found in exon 10 of the CFTR.The mutation c.753_754delAG was verified to have been inherited from her mother,and the c.1240 C>T mutation was from her father who was diagnosed with congenital absence of vas deferens.CONCLUSION A novel mutation of CFTR,c.753_754delAG,was found in a Chinese CF child.c.2909G>A is the most common mutation among Chinese CF patients. 展开更多
关键词 CYSTIC FIBROSIS CYSTIC FIBROSIS TRANSMEMBRANE conductance regulator MUTATION CHINESE children Case report
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Multisystem smooth muscle dysfunction syndrome in a Chinese girl:A case report and review of the literature 被引量:1
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作者 Sai-Nan Chen Yu-Qing Wang +4 位作者 Chuang-Li Hao yan-hong lu Wu-Jun Jiang Chun-Yan Gao Min Wu 《World Journal of Clinical Cases》 SCIE 2019年第24期4355-4365,共11页
BACKGROUND Multisystemic smooth muscle dysfunction syndrome(MSMDS) is a rare genetic disease worldwide. The main mutation is the actin alpha 2(ACTA2) gene p.R179 H. In this paper, we report a Chinese MSMDS patient and... BACKGROUND Multisystemic smooth muscle dysfunction syndrome(MSMDS) is a rare genetic disease worldwide. The main mutation is the actin alpha 2(ACTA2) gene p.R179 H. In this paper, we report a Chinese MSMDS patient and systematically review the previous literature.CASE SUMMARY Here, we report a 9.6-month-old Chinese girl who was diagnosed with MSMDS based on her history and symptoms, such as recurrent cough, wheezing, and complications with congenital fixed dilated pupils. Chest high-resolution computed tomography revealed inhomogeneous lung transparency, obvious exudative lesions, and some lung fissures that were markedly thickened. Cranial magnetic resonance imaging excluded bleeding and infarction but showed abnormal signals in the centrum ovale majus and bilateral periventricular regions. Echocardiography only showed patent foramen ovale, and no patent ductus arteriosus, pulmonary artery dilatation, or pulmonary hypertension was found. Bronchoscopy indicated moderate bronchial malacia. These examinations in conjunction with the typical eye abnormality suggested a diagnosis of MSMDS, and sequencing of exon 6 of the ACTA2 gene demonstrated the heterozygous mutation c.536 G>A, p.R179 H. However, her parents' gene analyses were normal.CONCLUSION MSMDS is a rare genetic disease mainly caused by the mutation of the ACTA2 gene p.R179 H. Early genetic diagnosis should be performed for children presenting with congenital fixed dilated pupils and patent ductus arteriosus.During the process of diagnosis and treatment, clinicians should be on high alert for cerebrovascular, cardiovascular, and pulmonary complications. 展开更多
关键词 Multisystem smooth muscle dysfunction syndrome Gene mutation Congenital mydriasis Patent ductus arteriosus Case report
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Heterogeneous layered structure in thermal barrier coatings by plasma spray-physical vapor deposition
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作者 yan-hong lu lu HUANG +2 位作者 Mei-Jun LIU Guan-Jun YANG Chang-Jiu LI 《Journal of Advanced Ceramics》 SCIE EI CAS CSCD 2023年第2期386-398,共13页
The unique columnar structure endows thermal barrier coatings(TBCs)prepared by plasma spray-physical vapor deposition(PS-PVD)with high thermal insulation and long lifetime.However,the coating delamination failure resu... The unique columnar structure endows thermal barrier coatings(TBCs)prepared by plasma spray-physical vapor deposition(PS-PVD)with high thermal insulation and long lifetime.However,the coating delamination failure resulting from an intra-column fracture(within a column rather than between columns)is a bottleneck in the solid dust particle impact environment for aero-engine.To clarify the intra-column fracture mechanism,a basic layer deposition model is developed to explore a heterogeneous weak-to-strong layered structure formed by a local transient in-situ deposit temperature.During the PS-PVD,an in-situ deposit surface is continuously updated due to constantly being covered by vapor condensation,showing a transient temperature,which means that the in-situ deposit surface temperature rises sharply in short period of 0.2 s of depositing a thin layer during a single pass.Meanwhile,the increasing temperature of the in-situ deposit surface results in an experimentally observed heterogeneous weak-to-strong structure,showing a continuous transition from a porous weak structure at the bottom region to a dense strong structure at the top region.This structure easily makes the intra-column fracture at the porous weak region.The results shed light on improving TBC lifetime by restraining the intra-column fracture. 展开更多
关键词 transient temperature in-situ deposit surface heterogeneous layered structure fracture mechanism plasma spray-physical vapor deposition(PS-PVD)
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Plasma spray-physical vapor deposition toward advanced thermal barrier coatings:a review 被引量:6
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作者 Mei-Jun Liu Gao Zhang +5 位作者 yan-hong lu Jia-Qi Han Guang-Rong Li Cheng-Xin Li Chang-Jiu Li Guan-Jun Yang 《Rare Metals》 SCIE EI CAS CSCD 2020年第5期479-497,共19页
Plasma spray–physical vapor deposition(PS–PVD)is a unique technology that enables highly tailorable functional films and coatings with various rare metal elements to be processed.This technology bridges the gap betw... Plasma spray–physical vapor deposition(PS–PVD)is a unique technology that enables highly tailorable functional films and coatings with various rare metal elements to be processed.This technology bridges the gap between conventional thermal spray and vapor deposition and provides a variety of coating microstructures composed of vapor,liquid,and solid deposition units.The PS–PVD technique serves a broad range of applications in the fields of thermal barrier coatings(TBCs),environmental barrier coatings(EBCs),oxygen permeable films,and electrode films.It also represents the development direction of high-performance TBC/EBC preparation technologies.With the PS–PVD technique,the composition of the deposition unit determines the microstructure of the coating and its performance.When coating materials are injected into a nozzle and transported into the plasma jet,the deposition unit generated by a coating material is affected by the plasma jet characteristics.However,there is no direct in situ measurement method of material transfer and deposition processes in the PS–PVD plasma jet,because of the extreme conditions of PS–PVD such as a low operating pressure of*100 Pa,temperatures of thousands of degrees,and a thin and high-velocity jet.Despite the difficulties,the transport and transformation behaviors of the deposition units were also researched by optical emission spectroscopy,observation of the coating microstructure and other methods.This paper reviews the progress of PS–PVD technologies considering the preparation of advanced thermal barrier coatings from the perspective of the transport and transformation behaviors of the deposition units.The development prospects of new high-performance TBCs using the PS–PVD technique are also discussed. 展开更多
关键词 Plasma spray–physical vapor deposition (PSPVD) Deposition unit Cross-domain behavior Deposition mechanism Thermal barrier coatings (TBCs)
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A new species of Aequales,genus Gieysztoria(Rhabdocoela:Dalyelliidae) from China 被引量:6
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作者 Xiao-Jie Xia yan-hong lu An-Tai Wang 《动物分类学报》 CSCD 北大核心 2014年第2期229-235,共7页
A new species of Aequales group, namely Gieysztoria shiyanensis Wang & Xia, sp. nov., is described from China. The new species is diagnosed by a sclerotic stylet with a belt attaching 15 fang-like spines. A worldwide... A new species of Aequales group, namely Gieysztoria shiyanensis Wang & Xia, sp. nov., is described from China. The new species is diagnosed by a sclerotic stylet with a belt attaching 15 fang-like spines. A worldwide list of Aequales group and a key to species of Gieysztoria in China are provided. 展开更多
关键词 Turbellarian RHABDOCOELA Gieysztoria new species China.
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