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Clinical Profile and Prognosis of Left Ventricular Apical Aneurysm in Hypertrophic Cardiomyopathy. [electronic resource] by
- Xiao, Yan
- Wang, Lin-Ping
- Yang, Yan-Kun
- Tian, Tao
- Yang, Kun-Qi
- Sun, Xin
- Jiang, Yong
- Liu, Ya-Xin
- Zhou, Xian-Liang
- Li, Jian-Jun
Producer: 20160527
In:
The American journal of the medical sciences vol. 351
Availability: No items available.
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11.
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Hypertension and Brachydactyly Syndrome Associated With Vertebral Artery Malformation Caused by a PDE3A Missense Mutation. [electronic resource] by
- Fan, Peng
- Zhang, Di
- Yang, Kun-Qi
- Zhang, Qiong-Yu
- Luo, Fang
- Lou, Ying
- Liu, Ya-Xin
- Zhang, Hui-Min
- Song, Lei
- Cai, Jun
- Wu, Hai-Ying
- Zhou, Xian-Liang
Producer: 20201221
In:
American journal of hypertension vol. 33
Availability: No items available.
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12.
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Prevalence of Liddle Syndrome Among Young Hypertension Patients of Undetermined Cause in a Chinese Population. [electronic resource] by
- Wang, Lin-Ping
- Yang, Kun-Qi
- Jiang, Xiong-Jing
- Wu, Hai-Ying
- Zhang, Hui-Min
- Zou, Yu-Bao
- Song, Lei
- Bian, Jin
- Hui, Ru-Tai
- Liu, Ya-Xin
- Zhou, Xian-Liang
Producer: 20160905
In:
Journal of clinical hypertension (Greenwich, Conn.) vol. 17
Availability: No items available.
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13.
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A novel PRKAG2 mutation in a Chinese family with cardiac hypertrophy and ventricular pre-excitation. [electronic resource] by
- Yang, Kun-Qi
- Lu, Chao-Xia
- Zhang, Ying
- Yang, Yan-Kun
- Li, Jia-Cheng
- Lan, Tian
- Meng, Xu
- Fan, Peng
- Tian, Tao
- Wang, Lin-Ping
- Liu, Ya-Xin
- Zhang, Xue
- Zhou, Xian-Liang
Producer: 20181218
In:
Scientific reports vol. 7
Availability: No items available.
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14.
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Genetic screening of SCNN1B and SCNN1G genes in early-onset hypertensive patients helps to identify Liddle syndrome. [electronic resource] by
- Yang, Kun-Qi
- Lu, Chao-Xia
- Fan, Peng
- Zhang, Ying
- Meng, Xu
- Dong, Xue-Qi
- Luo, Fang
- Liu, Ya-Xin
- Zhang, Hui-Min
- Wu, Hai-Ying
- Cai, Jun
- Zhang, Xue
- Zhou, Xian-Liang
Producer: 20180627
In:
Clinical and experimental hypertension (New York, N.Y. : 1993) vol. 40
Availability: No items available.
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15.
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A Novel Frameshift Mutation of SCNN1G Causing Liddle Syndrome with Normokalemia. [electronic resource] by
- Fan, Peng
- Zhao, Yu-Mo
- Zhang, Di
- Liao, Ying
- Yang, Kun-Qi
- Tian, Tao
- Lou, Ying
- Luo, Fang
- Ma, Wen-Jun
- Zhang, Hui-Min
- Song, Lei
- Cai, Jun
- Liu, Ya-Xin
- Zhou, Xian-Liang
Producer: 20200727
In:
American journal of hypertension vol. 32
Availability: No items available.
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16.
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Pediatric Liddle Syndrome Caused by a Novel SCNN1G Variant in a Chinese Family and Characterized by Early-Onset Hypertension. [electronic resource] by
- Fan, Peng
- Pan, Xiao-Cheng
- Zhang, Di
- Yang, Kun-Qi
- Zhang, Ying
- Tian, Tao
- Luo, Fang
- Ma, Wen-Jun
- Liu, Ya-Xin
- Wang, Lin-Ping
- Zhang, Hui-Min
- Song, Lei
- Cai, Jun
- Zhou, Xian-Liang
Producer: 20210712
In:
American journal of hypertension vol. 33
Availability: No items available.
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17.
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Genetic diagnosis of Liddle's syndrome by mutation analysis of SCNN1B and SCNN1G in a Chinese family. [electronic resource] by
- Wang, Lin-ping
- Gao, Ling-gen
- Zhou, Xian-liang
- Wu, Hai-ying
- Zhang, Lin
- Wen, Dan
- Li, Yue-hua
- Liu, Ya-xin
- Tian, Tao
- Fan, Xiao-han
- Jiang, Xiong-Jing
- Zhang, Hui-min
- Hui, Ru-tai
Producer: 20120918
In:
Chinese medical journal vol. 125
Availability: No items available.
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18.
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Aortic Dissection in Takayasu Arteritis. [electronic resource] by
- Yang, Kun-Qi
- Yang, Yan-Kun
- Meng, Xu
- Zhang, Ying
- Zhang, Hui-Min
- Wu, Hai-Ying
- Liu, Ya-Xin
- Jiang, Xiong-Jing
- Cai, Jun
- Zhou, Xian-Liang
- Hui, Ru-Tai
- Zheng, De-Yu
- Liu, Li-Sheng
Producer: 20170512
In:
The American journal of the medical sciences vol. 353
Availability: No items available.
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19.
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Liddle syndrome misdiagnosed as primary aldosteronism resulting from a novel frameshift mutation of SCNN1B. [electronic resource] by
- Fan, Peng
- Lu, Chao-Xia
- Zhang, Di
- Yang, Kun-Qi
- Lu, Pei-Pei
- Zhang, Ying
- Meng, Xu
- Hao, Su-Fang
- Luo, Fang
- Liu, Ya-Xin
- Zhang, Hui-Min
- Song, Lei
- Cai, Jun
- Zhang, Xue
- Zhou, Xian-Liang
Publication details: Endocrine connections Dec 2018
In:
Endocrine connections vol. 7
Availability: No items available.
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20.
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A novel phenotype with splicing mutation identified in a Chinese family with desminopathy. [electronic resource] by
- Fan, Peng
- Lu, Chao-Xia
- Dong, Xue-Qi
- Zhu, Di
- Yang, Kun-Qi
- Liu, Ke-Qiang
- Zhang, Di
- Zhang, Ying
- Meng, Xu
- Tan, Hui-Qiong
- Yu, Li-Tian
- Dou, Ke-Fei
- Liu, Ya-Xin
- Zhang, Xue
- Zhou, Xian-Liang
Producer: 20190429
In:
Chinese medical journal vol. 132
Availability: No items available.
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