E-LIB Suche - Ergebnisse für: Xiao, SX

1

Quality of life in patients with lepromatous leprosy in Chi..:

An, J‐G ; Ma, J‐H ; Xiao, S‐X..
Journal of the European Academy of Dermatology and Venereology. 24 (2010) 7 - p. 827-832 , 2010

Link: https://doi.org/10.1111/..

2

A recurrent keratin 14 mutation in Dowling–Meara epidermoly..:

Wu, JW ; Xiao, SX
Journal of the European Academy of Dermatology and Venereology. 23 (2009) 4 - p. 484-486 , 2009

Link: https://doi.org/10.1111/..

3

Identification of two recurrent mutations in keratin genes ..:

Wu, JW ; Xiao, SX ; Liu, Y...
Journal of the European Academy of Dermatology and Venereology. 23 (2009) 2 - p. 174-176 , 2009

Link: https://doi.org/10.1111/..

4

A Chinese family with lipoid proteinosis resulting from a h..:

Wang, XP ; Huo, J ; Liu, Y...
Journal of the European Academy of Dermatology and Venereology. 23 (2009) 11 - p. 1336-1338 , 2009

Link: https://doi.org/10.1111/..

5

Mutations of KRT6A are more frequent than those of KRT16 in..:

Bai, Z-L. ; Feng, Y-G. ; Tan, S-S....
British Journal of Dermatology. 159 (2008) 1 - p. 238-240 , 2008

Link: https://doi.org/10.1111/..

6

Novel frameshift mutation of theDSRADgene in a Chinese fami..:

Ren, JW ; Luo, SJ ; Peng, ZH...
Journal of the European Academy of Dermatology and Venereology. 22 (2008) 11 - p. 1375-1376 , 2008

Link: https://doi.org/10.1111/..

7

A mutation in exon 1 of keratin 14 resulting in a Chinese f..:

Li, XL ; Xiao, SX ; Peng, ZH...
Journal of the European Academy of Dermatology and Venereology. 21 (2007) 7 - p. 979-981 , 2007

Link: https://doi.org/10.1111/..

8

A novel deletion mutation of the ATP2C1 gene in Chinese pat..:

Li, XL ; Peng, ZH ; Xiao, SX...
Journal of the European Academy of Dermatology and Venereology. 22 (2007) 2 - p. 253-254 , 2007

Link: https://doi.org/10.1111/..

9

Two frameshift mutations of the double-stranded RNA-specifi..:

Liu, Y. ; Xiao, S-X. ; Peng, Z-H....
British Journal of Dermatology. 155 (2006) 2 - p. 473-476 , 2006

Link: https://doi.org/10.1111/..

10

Unusual psoriasiform lesions in a patient with Hyper‐IgE sy..:

Li, XL ; Geng, SM ; Lei, XB...
Journal of the European Academy of Dermatology and Venereology. 21 (2006) 3 - p. 424-426 , 2006

Link: https://doi.org/10.1111/..

11

Keratin 17 mutation in pachyonychia congenita type 2 with e..:

Feng, Y-G. ; Xiao, S-X. ; Ren, X-R....
British Journal of Dermatology. 148 (2003) 3 - p. 452-455 , 2003

Link: https://doi.org/10.1046/..

12

Genetic Polymorphisms in NLRP3 Inflammasome-Associated Gene..:

Liu ZH ; Zhang L ; Jing FJ...
https://www.dovepress.com/genetic-polymorphisms-in-nlrp3-inflammasome-associated-genes-in-patien-peer-reviewed-fulltext-article-JIR. , 2021

Link: https://doaj.org/article..

13

The familial risk of acne vulgaris in Chinese Hans – a case..:

Xu, SX ; Wang, HL ; Fan, X...
Journal of the European Academy of Dermatology and Venereology. 21 (2007) 5 - p. 602-605 , 2007

Link: https://doi.org/10.1111/..

14

The use status of anticoagulation drugs for inpatients with..:

Zheng HJ ; Ouyang SK ; Zhao Y...
https://www.dovepress.com/the-use-status-of-anticoagulation-drugs-for-inpatients-with-nonvalvula-peer-reviewed-article-IJGM. , 2017

Link: https://doaj.org/article..

15

Combined acoustic radiation force impulse, aminotransferase..:

Liu, J ; Li, SX ; Le, XH...
World Journal of Hepatology. , 2016

Link: https://doi.org/10.4254/..