Lan D - Search Results

1

[Clinical and genetic features of limb-girdle muscular dystrophy type 1B: a case report].

Yu XX, Zhong JZ, Guan HL, Zhang M, Lan D. Yu XX, et al. Among authors: lan d. Zhongguo Dang Dai Er Ke Za Zhi. 2018 Dec;20(12):1015-1019. doi: 10.7499/j.issn.1008-8830.2018.12.007. Zhongguo Dang Dai Er Ke Za Zhi. 2018. PMID: 30572990 Free PMC article. Chinese.

2

[Advance in therapy for Duchenne/Becker muscular dystrophy].

Xu TT, Lan D. Xu TT, et al. Among authors: lan d. Zhongguo Dang Dai Er Ke Za Zhi. 2015 Mar;17(3):294-8. Zhongguo Dang Dai Er Ke Za Zhi. 2015. PMID: 25815505 Free article. Review. Chinese.

3

Genetic analysis of the dystrophin gene in children with Duchenne and Becker muscular dystrophies.

Zhong J, Xu T, Chen G, Liao H, Zhang J, Lan D. Zhong J, et al. Among authors: lan d. Muscle Nerve. 2017 Jul;56(1):117-121. doi: 10.1002/mus.25435. Epub 2017 Feb 3. Muscle Nerve. 2017. PMID: 27750387

4

Novel compound heterozygous PLEC mutations lead to early‑onset limb‑girdle muscular dystrophy 2Q.

Zhong J, Chen G, Dang Y, Liao H, Zhang J, Lan D. Zhong J, et al. Among authors: lan d. Mol Med Rep. 2017 May;15(5):2760-2764. doi: 10.3892/mmr.2017.6309. Epub 2017 Mar 9. Mol Med Rep. 2017. PMID: 28447722

5

[Infantile hypophosphatasia caused by a novel compound heterozygous mutation: a case report and pedigree analysis].

Li DF, Lan D, Zhong JZ, Dewan RK, Xie YS, Yang Y. Li DF, et al. Among authors: lan d. Zhongguo Dang Dai Er Ke Za Zhi. 2017 May;19(5):539-544. doi: 10.7499/j.issn.1008-8830.2017.05.012. Zhongguo Dang Dai Er Ke Za Zhi. 2017. PMID: 28506345 Free PMC article. Chinese.

6

Clinical and genetic characteristics of female dystrophinopathy carriers.

Zhong J, Xie Y, Bhandari V, Chen G, Dang Y, Liao H, Zhang J, Lan D. Zhong J, et al. Among authors: lan d. Mol Med Rep. 2019 Apr;19(4):3035-3044. doi: 10.3892/mmr.2019.9982. Epub 2019 Feb 25. Mol Med Rep. 2019. PMID: 30816495 Free PMC article.

7

[Research advances in limb-girdle muscular dystrophy type 2Q].

Zhang M, Lan D. Zhang M, et al. Among authors: lan d. Zhongguo Dang Dai Er Ke Za Zhi. 2019 Aug;21(8):839-844. doi: 10.7499/j.issn.1008-8830.2019.08.019. Zhongguo Dang Dai Er Ke Za Zhi. 2019. PMID: 31416513 Free PMC article. Review. Chinese.

8

[A review on muscle-specific microRNAs as the biomarker for Duchenne muscular dystrophy].

Meng Q, Lan D. Meng Q, et al. Among authors: lan d. Zhongguo Dang Dai Er Ke Za Zhi. 2019 Nov;21(11):1148-1152. doi: 10.7499/j.issn.1008-8830.2019.11.017. Zhongguo Dang Dai Er Ke Za Zhi. 2019. PMID: 31753100 Free PMC article. Review. Chinese.

9

The use of glimepiride for the treatment of neonatal diabetes mellitus caused by a novel mutation of the ABCC8 gene.

Qin X, Zhong J, Lan D. Qin X, et al. Among authors: lan d. J Pediatr Endocrinol Metab. 2020 Oct 9;33(12):1605-1608. doi: 10.1515/jpem-2020-0030. Print 2020 Dec 16. J Pediatr Endocrinol Metab. 2020. PMID: 33035187

10

Serum MyomiRs as Biomarkers for Female Carriers of Duchenne/Becker Muscular Dystrophy.

Zhang J, Meng Q, Zhong J, Zhang M, Qin X, Ni X, Ma J, He Y, Zeng D, Lan D. Zhang J, et al. Among authors: lan d. Front Neurol. 2020 Sep 18;11:563609. doi: 10.3389/fneur.2020.563609. eCollection 2020. Front Neurol. 2020. PMID: 33071947 Free PMC article.

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