Bi FF - Search Results

1

Expanding the clinicopathological-genetic spectrum of GNE myopathy by a Chinese neuromuscular centre.

Zhang KY, Duan HQ, Li QX, Luo YB, Bi FF, Huang K, Yang H. Zhang KY, et al. Among authors: bi ff. J Cell Mol Med. 2021 Nov;25(22):10494-10503. doi: 10.1111/jcmm.16978. Epub 2021 Oct 22. J Cell Mol Med. 2021. PMID: 34676965 Free PMC article.

2

Expanding the Clinico-Genetic Spectrum of Myofibrillar Myopathy: Experience From a Chinese Neuromuscular Center.

Luo YB, Peng Y, Lu Y, Li Q, Duan H, Bi F, Yang H. Luo YB, et al. Front Neurol. 2020 Sep 15;11:1014. doi: 10.3389/fneur.2020.01014. eCollection 2020. Front Neurol. 2020. PMID: 33041974 Free PMC article.

3

[Clinical, pathological and genetic studies of two cases of childhood-onset nemaline myopathy].

Huang K, Luo YE, Li QX, Duan HQ, Bi FF, Yang H, Luo YB. Huang K, et al. Among authors: bi ff. Zhongguo Dang Dai Er Ke Za Zhi. 2018 Oct;20(10):804-808. doi: 10.7499/j.issn.1008-8830.2018.10.004. Zhongguo Dang Dai Er Ke Za Zhi. 2018. PMID: 30369353 Free PMC article. Chinese.

4

Clinicopathological features of titinopathy from a Chinese neuromuscular center.

Huang K, Duan HQ, Li QX, Luo YB, Bi FF, Yang H. Huang K, et al. Among authors: bi ff. Neuropathology. 2021 Oct;41(5):349-356. doi: 10.1111/neup.12761. Epub 2021 Sep 22. Neuropathology. 2021. PMID: 34553419

5

Findings of limb-girdle muscular dystrophy R7 telethonin-related patients from a Chinese neuromuscular center.

Huang K, Li QX, Duan HQ, Luo YB, Bi FF, Yang H. Huang K, et al. Among authors: bi ff. Neurogenetics. 2022 Jan;23(1):37-44. doi: 10.1007/s10048-021-00681-2. Epub 2022 Jan 4. Neurogenetics. 2022. PMID: 34982307

6

Clinicopathological-genetic features of congenital myasthenic syndrome from a Chinese neuromuscular centre.

Huang K, Duan HQ, Li QX, Luo YB, Bi FF, Yang H. Huang K, et al. Among authors: bi ff. J Cell Mol Med. 2022 Jul;26(14):3828-3836. doi: 10.1111/jcmm.17417. Epub 2022 Jun 6. J Cell Mol Med. 2022. PMID: 35670010 Free PMC article.

7

Expanding the clinicopathological-genetic spectrum of glycogen storage disease type IXd by a Chinese neuromuscular center.

Huang K, Duan HQ, Li QX, Luo YB, Bi FF, Yang H. Huang K, et al. Among authors: bi ff. Front Neurol. 2022 Aug 11;13:945280. doi: 10.3389/fneur.2022.945280. eCollection 2022. Front Neurol. 2022. PMID: 36034300 Free PMC article.

8

Corrigendum: Expanding the Clinico-Genetic Spectrum of Myofibrillar Myopathy: Experience From a Chinese Neuromuscular Center.

Luo YB, Peng Y, Lu Y, Li Q, Duan H, Bi F, Yang H. Luo YB, et al. Front Neurol. 2021 Jan 8;11:636981. doi: 10.3389/fneur.2020.636981. eCollection 2020. Front Neurol. 2021. PMID: 33488509 Free PMC article.

9

Limb-girdle Muscular Dystrophy Type 2A with Muscular Eosinophilic Infiltration in a Chinese Patient.

Luo YB, Li QX, Duan HQ, Bi FF, Yang H. Luo YB, et al. Among authors: bi ff. Chin Med J (Engl). 2018 Sep 5;131(17):2133-2134. doi: 10.4103/0366-6999.239307. Chin Med J (Engl). 2018. PMID: 30127231 Free PMC article. No abstract available.

10

The association between myositis-specific autoantibodies and muscle pathologies in idiopathic inflammatory myopathies.

Xu Q, Li QX, Bi FF, Duan HQ, Luo YB, Yang H. Xu Q, et al. Among authors: bi ff. Clin Rheumatol. 2021 Feb;40(2):613-624. doi: 10.1007/s10067-020-05274-2. Epub 2020 Jul 15. Clin Rheumatol. 2021. PMID: 32671659

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