Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Chen Liang"'
Autor:
Cheng-Chang Lu, Wen-Chen Liang, Zi-Miao Liu, Shih-Hsiang Chou, Po-Chih Shen, Yin-Chun Tien, Yen-Mou Lu, Chia-Lung Shih, Yuh-Jyh Jong
Publikováno v:
Clinical Spine Surgery
Study Design: This was a single-center, retrospective study. Objective: The objective of this study was to assess the risk factors for deformity progression after scoliosis correction surgery in spinal muscular atrophy (SMA) patients. Summary of Back
Publikováno v:
Ophthalmic Research. 63:358-368
Background: The purpose of this study is to determine the mutation frequencies of key driver genes in uveal melanoma (UM) in Chinese patients and to detect associations between metastasis and the mutation of these genes. Method: A total of 85 patient
Autor:
Ling‐di Qin, Qing‐jiao Zhang, Xiao‐lin Shi, Xiao‐hong Liu, Zi‐ming Zhou, Xiao‐yi Ding, Chen Liang, Lei Jiang
Publikováno v:
Orthopaedic Surgery, Vol 11, Iss 4, Pp 628-634 (2019)
Orthopaedic Surgery
Orthopaedic Surgery
Objective To find new clues to reduce postoperative recurrence after intralesional curettage by studying MRI and pathological features of giant tumor of bone (GCTB) boundaries. Methods A retrospective study was performed in the departments of orthopa
Autor:
Shulian Chen, Yigeng Cao, Sizhou Feng, Erlie Jiang, Chen Liang, Aiming Pang, Jianfeng Yao, Qiaoling Ma, Zhe Ding, Xiao-Yu Zhang, Mingzhe Han, Jialin Wei
Publikováno v:
Chinese Medical Journal, Vol 128, Iss 15, Pp 2065-2071 (2015)
Chinese Medical Journal
Chinese Medical Journal
Background: The postremission therapies for adult patients generally contain consolidation chemotherapy, allogeneic hematopoietic stem cell transplantation and autologous hematopoietic stem cell transplantation (auto-HSCT). Because of the various res
Autor:
Chen Zhao Yang, Chen Liang-long, Chen Wan Hua, Chen Qiang, Fan Lin, Xiong Chang, Cao Hua, Ma Yuan Ji, Pan Wen Zhi, Ge Jun Bo
Publikováno v:
The Annals of Thoracic Surgery. 99:1664-1670
Transfemoral and perventricular device occlusions are performed for doubly committed subarterial ventricular septal defect (dcVSD) to reduce the invasiveness of the conventional surgical repair through a median sternotomy. Few comparative studies hav
Autor:
Tzu-Hua Chen-Liang, Marta Guinot, Jose Javier Sanchez-Blanco, Anabel Teruel, Carolina Villegas, Rosa Fernández-López, Guillermo Rodríguez-García, Jorge Mucientes, Fatima De la Cruz, Jose Contreras, Laura Frutos, Joaquín Gómez-Espuch, Francisco José Ortuño, Javier López-Jiménez, Mayte Orero, Carolina Igua, Elena Pérez-Ceballos, Taida Martín-Santos, Jon Uña, Maria del Puig Cozar, Cristina Martínez-Millán, José María Raya, Carmen Benet, Alejandro Martín, Marta Fernández-González, Isabel Ballester, Raquel Sánchez-Vañó, María Moya, Kyra Kennedy, Pilar Tamayo, Leonor Senent, Mónica Baile, Andres Jerez, J. L. Navarro, Begoña Muiña
Publikováno v:
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Cancer Medicine
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Consejería de Sanidad de la Comunidad de Madrid
Cancer Medicine
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Several studies have reported uneven results when evaluating the prognostic value of bone marrow biopsy (BMB) and PET/CT as part of the staging of diffuse large B‐cell lymphoma (DLBCL). The heterogeneity of the inclusion criteria and not taking int
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48f85496bb1426c9dfbb5a8571cae31d
https://hdl.handle.net/20.500.12530/42117
https://hdl.handle.net/20.500.12530/42117
Publikováno v:
Pediatrics and Neonatology, Vol 59, Iss 2, Pp 176-183 (2018)
Background: Duchenne muscular dystrophy (DMD) is the most common hereditary muscular dystrophy and caused by DMD gene mutation. In addition to progressive proximal muscle weakness, respiratory, orthopedic, and gastrointestinal complications are often
Autor:
Xia Tian, Chung-Yee Yuo, Yuh-Jyh Jong, Lee-Jun C. Wong, Yi-Ning Su, Ichizo Nishino, Wen-Chen Liang, Tsu-Min Kan, Wan-Zi Chen
Publikováno v:
PLoS ONE
PLoS ONE, Vol 12, Iss 2, p e0170517 (2017)
PLoS ONE, Vol 12, Iss 2, p e0170517 (2017)
Purpose Congenital muscular dystrophy (CMD) is a heterogeneous disease entity. The detailed clinical manifestation and causative gene for each subgroup of CMD are quite variable. This study aims to analyze the phenotypes and genotypes of Taiwanese pa
Autor:
Yuh-Jyh Jong, Ichizo Nishino, Chien-Hua Wang, Yukiko K. Hayashi, Wen-Chen Liang, Wan-Ting Huang, Megumu Ogawa
Publikováno v:
Neuromuscular Disorders. 23:675-681
Alpha-dystroglycanopathy is caused by the glycosylation defects of α-dystroglycan (α-DG). The clinical spectrum ranges from severe congenital muscular dystrophy (CMD) to later-onset limb girdle muscular dystrophy (LGMD). Among all α-dystroglycanop
Publikováno v:
American Journal of Hospice and Palliative Medicine®. 29:53-59
To evaluate the relationship between pain and quality of life (QoL) in patients newly admitted to Wuhan Hospice Center, China. A total of 1,634 patients were analyzed in this retrospective study. A Numerical Rating Scale and Chinese-QoL instrument we