Ni C - Search Results

1

Severe dermatitis, multiple allergies and metabolic wasting (SAM) syndrome caused by de novo mutation in the DSP gene misdiagnosed as generalized pustular psoriasis and treatment of acitretin with gabapentin.

Liang J, Li C, Zhang Z, Ni C, Yu H, Li M, Yao Z. Liang J, et al. Among authors: ni c. J Dermatol. 2019 Jul;46(7):622-625. doi: 10.1111/1346-8138.14925. Epub 2019 May 20. J Dermatol. 2019. PMID: 31106887

2

Report of Chinese family with severe dermatitis, multiple allergies and metabolic wasting syndrome caused by novel homozygous desmoglein-1 gene mutation.

Cheng R, Yan M, Ni C, Zhang J, Li M, Yao Z. Cheng R, et al. Among authors: ni c. J Dermatol. 2016 Oct;43(10):1201-1204. doi: 10.1111/1346-8138.13431. J Dermatol. 2016. PMID: 27154412

3

Coinheritance of generalized pustular psoriasis and familial Behçet-like autoinflammatory syndrome with variants in IL36RN and TNFAIP3 in the heterozygous state.

Liang J, Zhang H, Guo Y, Yang K, Ni C, Yu H, Kong X, Li M, Lu Z, Yao Z. Liang J, et al. Among authors: ni c. J Dermatol. 2019 Oct;46(10):907-910. doi: 10.1111/1346-8138.15034. Epub 2019 Jul 29. J Dermatol. 2019. PMID: 31353537

4

A novel mutation in TRPV3 gene causes atypical familial Olmsted syndrome.

Ni C, Yan M, Zhang J, Cheng R, Liang J, Deng D, Wang Z, Li M, Yao Z. Ni C, et al. Sci Rep. 2016 Feb 23;6:21815. doi: 10.1038/srep21815. Sci Rep. 2016. PMID: 26902751 Free PMC article.

5

Identification of a PTPN11 hot spot mutation in a child with atypical LEOPARD syndrome.

Zhang J, Shen J, Cheng R, Ni C, Liang J, Li M, Yao Z. Zhang J, et al. Among authors: ni c. Mol Med Rep. 2016 Sep;14(3):2639-43. doi: 10.3892/mmr.2016.5547. Epub 2016 Jul 27. Mol Med Rep. 2016. PMID: 27484170 Review.

6

Mutations in IL36RN are associated with geographic tongue.

Liang J, Huang P, Li H, Zhang J, Ni C, Wang Y, Shen J, Li C, Kang L, Chen J, Zhang H, Wang Z, Zhang Z, Li M, Yao Z. Liang J, et al. Among authors: ni c. Hum Genet. 2017 Feb;136(2):241-252. doi: 10.1007/s00439-016-1750-y. Epub 2016 Nov 29. Hum Genet. 2017. PMID: 27900482 Free PMC article.

7

A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis.

Yu X, Chen F, Ni C, Zhang G, Zheng L, Zhang J, Li C, Sandilands A, Yao Z, Li M. Yu X, et al. Among authors: ni c. J Invest Dermatol. 2018 Jan;138(1):230-233. doi: 10.1016/j.jid.2017.08.035. Epub 2017 Sep 9. J Invest Dermatol. 2018. PMID: 28899683 Free article. No abstract available.

8

Novel and recurrent PHGDH and PSAT1 mutations in Chinese patients with Neu-Laxova syndrome.

Ni C, Cheng RH, Zhang J, Liang JY, Wei RQ, Li M, Yao ZR. Ni C, et al. Eur J Dermatol. 2019 Dec 1;29(6):641-646. doi: 10.1684/ejd.2019.3673. Eur J Dermatol. 2019. PMID: 31903955

9

Next-generation sequencing through multi-gene panel testing for diagnosis of hereditary ichthyosis in Chinese.

Cheng R, Liang J, Li Y, Zhang J, Ni C, Yu H, Kong X, Li M, Yao Z. Cheng R, et al. Among authors: ni c. Clin Genet. 2020 May;97(5):770-778. doi: 10.1111/cge.13704. Epub 2020 Feb 9. Clin Genet. 2020. PMID: 31953843

10

Nagashima-type palmoplantar keratosis in a Chinese Han population.

Zhang J, Zhang G, Ni C, Cheng R, Liang J, Li M, Yao Z. Zhang J, et al. Among authors: ni c. Mol Med Rep. 2016 Nov;14(5):4049-4054. doi: 10.3892/mmr.2016.5757. Epub 2016 Sep 21. Mol Med Rep. 2016. PMID: 27666198 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

1,825 results

Search Page