Huang P - Search Results

1

Clinical and genetic characteristics of myotonia congenita in Chinese population.

He Y, Qiu Y, Xiong Y, Shen Y, Jiang K, Yi H, Huang P, Zhu Y, Zhu M, Zhou M, Hong D, Tan D. He Y, et al. Among authors: huang p. Channels (Austin). 2024 Dec;18(1):2349823. doi: 10.1080/19336950.2024.2349823. Epub 2024 May 8. Channels (Austin). 2024. PMID: 38720415 Free PMC article.

2

Pathological changes of the sural nerve in patients with familial episodic pain syndrome.

Zheng Y, Huang P, Li S, Jiang K, Zhou B, Fang X, Zhou M, Hong D, Zhu M. Zheng Y, et al. Among authors: huang p. Neurol Sci. 2022 Sep;43(9):5605-5614. doi: 10.1007/s10072-022-06107-7. Epub 2022 May 7. Neurol Sci. 2022. PMID: 35524925

3

TMEM151A phenotypic spectrum includes paroxysmal kinesigenic dyskinesia with infantile convulsions.

Wang H, Huang P, Zhu M, Fang X, Wu C, Hong D. Wang H, et al. Among authors: huang p. Neurol Sci. 2022 Oct;43(10):6095-6099. doi: 10.1007/s10072-022-06208-3. Epub 2022 Jun 21. Neurol Sci. 2022. PMID: 35727387

4

Juvenile-onset PSAT1-related neuropathy: A milder phenotype of serine deficiency disorder.

Shen Y, Peng Y, Huang P, Zheng Y, Li S, Jiang K, Zhou M, Deng J, Zhu M, Hong D. Shen Y, et al. Among authors: huang p. Front Genet. 2022 Aug 16;13:949038. doi: 10.3389/fgene.2022.949038. eCollection 2022. Front Genet. 2022. PMID: 36061210 Free PMC article.

5

Urine cytological study in patients with clinicopathologically confirmed neuronal intranuclear inclusion disease.

Zhou Y, Huang P, Huang Z, Peng Y, Zheng Y, Yu Y, Zhu M, Deng J, Wang Z, Hong D. Zhou Y, et al. Among authors: huang p, huang z. Front Aging Neurosci. 2022 Sep 12;14:977604. doi: 10.3389/fnagi.2022.977604. eCollection 2022. Front Aging Neurosci. 2022. PMID: 36172483 Free PMC article.

6

Subclinical peripheral neuropathy is common in neuronal intranuclear inclusion disease with dominant encephalopathy.

Hong D, Wang H, Zhu M, Peng Y, Huang P, Zheng Y, Yu M, Meng L, Li F, Yu J, Zhou M, Deng J, Wang Z, Yuan Y. Hong D, et al. Among authors: huang p. Eur J Neurol. 2023 Feb;30(2):527-537. doi: 10.1111/ene.15606. Epub 2022 Nov 1. Eur J Neurol. 2023. PMID: 36263606

7

Whole Exome Sequencing Indicating GGCCTG Hexanucleotide Repeat in Patients with Spinocerebellar Ataxia Type 36.

Chen R, Zhou C, Peng Y, Huang P, Yu Y, Zhu M, Zhou M, Hong D, Tan D. Chen R, et al. Among authors: huang p. Neurodegener Dis. 2024;24(2):71-79. doi: 10.1159/000540006. Epub 2024 Jun 26. Neurodegener Dis. 2024. PMID: 38934198

8

Clinical and pathological characteristics of OPDM4 patients in advanced disease.

Tang H, Xiong Y, Jiang K, Shen Y, Yu Y, Huang P, Zhu M, Li X, Zheng Y, Zhou M, Yu J, Deng J, Wang Z, Hong D, Qiu Y, Tan D. Tang H, et al. Among authors: huang p. Muscle Nerve. 2024 Oct;70(4):744-752. doi: 10.1002/mus.28200. Epub 2024 Jul 23. Muscle Nerve. 2024. PMID: 39044557

9

[Effects on the amount of total hemolytic complement levels(CH50) and immunoglobulin in serum induced by the implantation of biomaterials into rats].

Zhu M, Zeng Y, Jiang L, Huang P, Wu Z. Zhu M, et al. Among authors: huang p. Sheng Wu Yi Xue Gong Cheng Xue Za Zhi. 1999 Sep;16(3):275-8. Sheng Wu Yi Xue Gong Cheng Xue Za Zhi. 1999. PMID: 12552743 Chinese.

10

[Experimental safety study using rats and mice irradiated with the complex field cure instrument].

Zhu MH, Zeng Y, Jiang L, Huang PH, Wu ZS, Fu XZ, Wang DQ, Lu JW. Zhu MH, et al. Among authors: huang ph. Zhongguo Yi Liao Qi Xie Za Zhi. 2000 Jan;24(1):29-32. Zhongguo Yi Liao Qi Xie Za Zhi. 2000. PMID: 12583110 Chinese.

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