Cong L - Search Results

1

How to interpret low human chorionic gonadotropin levels in cerebrospinal fluid of patients with intracranial germinoma?

Cong L, Tian CL, Wang XQ, Dong Z, Zhang JT, Yu SY. Cong L, et al. Chin Med J (Engl). 2013;126(24):4809-10. Chin Med J (Engl). 2013. PMID: 24342338 No abstract available.

2

[Clinical, pathological and genetic characteristics of 8 patients with distal hereditary motor neuropathy].

Liu MG, Fang P, Wang Y, Cong L, Fan YY, Yuan Y, Xu Y, Zhang J, Hong DJ. Liu MG, et al. Among authors: cong l. Beijing Da Xue Xue Bao Yi Xue Ban. 2021 Oct 18;53(5):957-963. doi: 10.19723/j.issn.1671-167X.2021.05.025. Beijing Da Xue Xue Bao Yi Xue Ban. 2021. PMID: 34650302 Free PMC article. Chinese.

3

Clinical and muscle magnetic resonance image findings in patients with late-onset multiple acyl-CoA dehydrogenase deficiency.

Hong DJ, Zhu M, Zhu ZJ, Cong L, Zhong SS, Liu L, Zhang J. Hong DJ, et al. Among authors: cong l. Chin Med J (Engl). 2019 Feb 5;132(3):275-284. doi: 10.1097/CM9.0000000000000032. Chin Med J (Engl). 2019. PMID: 30681493 Free PMC article.

4

Clonazepam improves the symptoms of two siblings with novel variants in the SYNJ1 gene.

Hong D, Cong L, Zhong S, He Y, Xin L, Gao X, Zhang J. Hong D, et al. Among authors: cong l. Parkinsonism Relat Disord. 2019 May;62:221-225. doi: 10.1016/j.parkreldis.2018.11.020. Epub 2018 Nov 19. Parkinsonism Relat Disord. 2019. PMID: 30473187 Review.

5

A novel KIF5A gene variant causes spastic paraplegia and cerebellar ataxia.

Qiu Y, Zhong S, Cong L, Xin L, Gao X, Zhang J, Hong D. Qiu Y, et al. Among authors: cong l. Ann Clin Transl Neurol. 2018 Sep 17;5(11):1415-1420. doi: 10.1002/acn3.650. eCollection 2018 Nov. Ann Clin Transl Neurol. 2018. PMID: 30480035 Free PMC article.

6

Clinical findings and autophagic pathology in neutral lipid storage disease with myopathy.

Hong D, Zheng J, Xin L, Xiang Y, Luan X, Cao L, Cong L, Fang P, Zhang J. Hong D, et al. Among authors: cong l. Clin Neuropathol. 2019 Jul/Aug;38(4):157-167. doi: 10.5414/NP301159. Clin Neuropathol. 2019. PMID: 30738494

7

A novel CPT1C variant causes pure hereditary spastic paraplegia with benign clinical course.

Hong D, Cong L, Zhong S, Liu L, Xu Y, Zhang J. Hong D, et al. Among authors: cong l. Ann Clin Transl Neurol. 2019 Jan 4;6(3):610-614. doi: 10.1002/acn3.717. eCollection 2019 Mar. Ann Clin Transl Neurol. 2019. PMID: 30911584 Free PMC article.

8

Variants in MME are associated with autosomal-recessive distal hereditary motor neuropathy.

Hong D, Fang P, Yao S, Chen J, Zhang X, Chen S, Zhang J, Tan D, Wang L, Han X, Xin L, Wang Y, Liu M, Cong L, Zhong S, Ouyang H, Gao X, Zhang J. Hong D, et al. Among authors: cong l. Ann Clin Transl Neurol. 2019 Sep;6(9):1728-1738. doi: 10.1002/acn3.50868. Epub 2019 Aug 20. Ann Clin Transl Neurol. 2019. PMID: 31429185 Free PMC article.

9

Diagnostic indicators for adult-onset neuronal intranuclear inclusion disease.

Wang Y, Wang B, Wang L, Yao S, Zhao J, Zhong S, Cong L, Liu L, Zhang J, Zhang J, Hong D. Wang Y, et al. Among authors: cong l. Clin Neuropathol. 2020 Jan/Feb;39(1):7-18. doi: 10.5414/NP301203. Clin Neuropathol. 2020. PMID: 31661069

10

A novel heterozygous HTRA1 mutation is associated with autosomal dominant hereditary cerebral small vessel disease.

Zhuo ZL, Cong L, Zhang J, Zhao XT. Zhuo ZL, et al. Among authors: cong l. Mol Genet Genomic Med. 2020 Jun;8(6):e1111. doi: 10.1002/mgg3.1111. Epub 2020 Apr 2. Mol Genet Genomic Med. 2020. PMID: 32239807 Free PMC article.

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