Li M - Search Results

1

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: li c, li m. 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.

2

LUMBAR syndrome: A case manifesting as cutaneous infantile hemangiomas of the lower extremity, perineum and gluteal region, and a review of published work.

Yu X, Zhang J, Wu Z, Liu M, Chen R, Gu Y, Li M, Yao Z. Yu X, et al. Among authors: li m. J Dermatol. 2017 Jul;44(7):808-812. doi: 10.1111/1346-8138.13763. Epub 2017 Feb 13. J Dermatol. 2017. PMID: 28191659 Review.

3

Ankyloblepharon-ectodermal dysplasia-clefting syndrome misdiagnosed as epidermolysis bullosa and congenital ichthyosiform erythroderma: Case report and review of published work.

Zhang Z, Cheng R, Liang J, Lu Z, Wang Y, Li M, Yu H, Yao Z. Zhang Z, et al. Among authors: li m. J Dermatol. 2019 May;46(5):422-425. doi: 10.1111/1346-8138.14837. Epub 2019 Feb 27. J Dermatol. 2019. PMID: 30809829 Review.

4

Family of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis caused by a novel FAM111B mutation.

Zhang Z, Zhang J, Chen F, Zheng L, Li H, Liu M, Li M, Yao Z. Zhang Z, et al. Among authors: li h, li m. J Dermatol. 2019 Nov;46(11):1014-1018. doi: 10.1111/1346-8138.15045. Epub 2019 Aug 7. J Dermatol. 2019. PMID: 31392773

5

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. Among authors: li m. Eur J Dermatol. 2019 Dec 1;29(6):641-646. doi: 10.1684/ejd.2019.3673. Eur J Dermatol. 2019. PMID: 31903955

6

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: li m. 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.

7

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: li m. 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.

8

Molecular screening strategies for NF1-like syndromes with café-au-lait macules (Review).

Zhang J, Li M, Yao Z. Zhang J, et al. Among authors: li m. Mol Med Rep. 2016 Nov;14(5):4023-4029. doi: 10.3892/mmr.2016.5760. Epub 2016 Sep 22. Mol Med Rep. 2016. PMID: 27666661 Free PMC article. Review.

9

A novel KRT5 mutation associated with generalized severe epidermolysis bullosa simplex in a 2-year-old Chinese boy.

Zhang J, Yan M, Liang J, Li M, Yao Z. Zhang J, et al. Among authors: li m. Exp Ther Med. 2016 Nov;12(5):2823-2826. doi: 10.3892/etm.2016.3717. Epub 2016 Sep 20. Exp Ther Med. 2016. PMID: 27882080 Free PMC article.

10

Two Novel Mutations in the ERCC8 Gene in a Patient with Ultraviolet-sensitive Syndrome.

Li Y, Zheng L, Chen F, Yao Z, Li M. Li Y, et al. Among authors: li m. Acta Derm Venereol. 2019 Jan 1;99(1):117-118. doi: 10.2340/00015555-3032. Acta Derm Venereol. 2019. PMID: 30182135 Free article. No abstract available.

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