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Auteur Lin Y

Documents disponibles écrits par cet auteur (19)

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Neuropathology and applied neurobiology, 51, 1. Genotype-Phenotype Correlation in Progressive External Ophthalmoplegia: Insights From a Retrospective Analysis

Wang J ; Lin Y ; Zhuang X ; Zhao D ; Li B ; Zhao Y ; Xu Z ; Liu F ; Dai T ; Li W ; Jiang M ; Yan C ; Zhao Y ; Ji K | 02/2025

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European journal of neurology, Epub. A multicenter, randomized, open-label, phase 2 clinical study of telitacicept in adult patients with generalized myasthenia gravis

Yin J ; Zhao M ; Xu X ; Zhang M ; Xu Z ; Li Z ; Qin X ; Li Z ; Zhao C ; Zhou H ; Ma Y ; Cao W ; Wang G ; Lin Y ; Zhang J ; Zhang X ; Cai H ; Qian W ; Wang Y ; Zhang X ; Liu G ; Wang J ; Qiu W ; Min L ; Li J ; Deng H ; Chu L ; Zhang Y ; Fang J | 10/05/2024

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Clinica chimica acta; international journal of clinical chemistry, 548, Epub. Evaluating the performance of four assays for carrier screening of spinal muscular atrophy

Tan J ; Zhang J ; Sun R ; Jiang Z ; Wang Y ; Ma D ; Jiao J ; Chen H ; Lin Y ; Zhang Q ; Xu Z ; Hu P | 20/07/2023

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Article

Neurology, 101, 3. Association of 4qA-Specific Distal D4Z4 Hypomethylation With Disease Severity and Progression in Facioscapulohumeral Muscular Dystrophy

Zheng F ; Qiu L ; Chen L ; Zheng Y ; Lin X ; He J ; Lin X ; He Q ; Lin Y ; Lin L ; Wang L ; Lin F ; Yang K ; Lin M ; Lin Y ; Fu Y ; Wang N ; Wang Z | 18/07/2023

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Frontiers in neurology, 14. Outcome and clinical features in juvenile myasthenia gravis: A systematic review and meta-analysis

Lin Y ; Kuang Q ; Li H ; Liang B ; Lu J ; Jiang Q ; Yang X | Switzerland | 08/03/2023

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Article

Frontiers in immunology, 14. Characteristics of cardiac involvement in immune-mediated necrotizing myopathy

Liu M ; Lin Y ; Qiao L ; Chen J ; Shi Q | Switzerland | 28/02/2023

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Article

Orphanet journal of rare diseases, 17, 1. Clinical and molecular analysis of four unrelated Chinese families with pathogenic KLHL40 variants causing nemaline myopathy 8

Yuan H ; Wang Q ; Zeng X ; He P ; Xu W ; Guo H ; Liu Y ; Lin Y | 04/04/2022

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Article

Frontiers in neurology, 13. Effect of Fufang Huangqi Decoction on the Gut Microbiota in Patients With Class I or II Myasthenia Gravis

Chen Y ; Lin Y ; Shan C ; Li Z ; Xiao B ; He R ; Huang X ; Wang Z ; Zhang J ; Qiao W | 18/03/2022

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Article

European journal of neurology Association of immunosuppression treatment with generalization among patients with ocular myasthenia gravis: A propensity score analysis

Ruan Z ; Guo R ; Zhou H ; Gao F ; Lin Y ; Xu Q ; Yu L ; Wu S ; Lei T ; Zhang M ; Gao Y ; Lu X ; Li H ; Sun C ; Tang B ; Li Z ; Chang T | England | 21/02/2022

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Orphanet journal of rare diseases, 16, 1. Biochemical and genetic characteristics of patients with primary carnitine deficiency identified through newborn screening

Lin Y ; Lin B ; Chen Y ; Zheng Z ; Fu Q ; Lin W ; Zhang W | 04/12/2021

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Article

The Lancet regional health. Western Pacific, 18. Prevalence and disease progression of genetically-confirmed facioscapulohumeral muscular dystrophy type 1 (FSHD1) in China between 2001 and 2020: a nationwide population-based study

Wang Z ; Qiu L ; Lin M ; Chen L ; Zheng F ; Lin L ; Lin F ; Ye Z ; Lin X ; He J ; Wang L ; Lin X ; He Q ; Chen W ; Lin Y ; Fu Y ; Wang N | 22/11/2021

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Article

Journal of pediatric endocrinology & metabolism : JPEM, 34, 5. Newborn screening and molecular features of patients with multiple acyl-CoA dehydrogenase deficiency in Quanzhou, China

Lin Y ; Lin Y ; Zhang W ; Chen Z ; Lin C ; Lin W ; Fu Q ; Peng W ; Chen D | Germany | 04/2021

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Article

Neuromuscular disorders : NMD A novel nonsense variant in MT-CO3 causes MELAS syndrome

Wang W ; Sun Y ; Lin Y ; Xu X ; Zhao D ; Ji K ; Li W ; Zhao Y ; Yan C | England | 03/03/2021

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Article

Aging Melatonin exerts immunoregulatory effects by balancing peripheral effector and regulatory T helper cells in myasthenia gravis

Chang T ; Niu C ; Sun C ; Ma Y ; Guo R ; Ruan Z ; Gao Y ; Lu X ; Li H ; Lin Y ; Lin J ; Li Z | United States | 02/11/2020

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Article

Clinica chimica acta; international journal of clinical chemistry, 510. Newborn screening and genetic characteristics of patients with short- and very long-chain acyl-CoA dehydrogenase deficiencies

Lin Y ; Zhang W ; Chen D ; Lin C ; Zheng Z ; Fu Q ; Li M ; Peng W | Netherlands | 07/2020

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Article

Frontiers in Genetics, 10. Newborn Screening for Spinal Muscular Atrophy in China Using DNA Mass Spectrometry

Lin Y ; Lin CH ; Yin X ; Zhu L ; Yang J ; Shen Y ; Yang C ; Chen X ; Hu H ; Ma Q ; Shi X ; Shen Y ; Hu Z ; Huang C ; Huang X | Switzerland | 12/2019

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Article

Neurogenetics Whole exome sequencing reveals a broader variant spectrum of Charcot-Marie-Tooth disease type 2

Lin S ; Xu LQ ; Xu GR ; Guo LL ; Lin BJ ; Chen WJ ; Wang N ; Lin Y ; He J | United States | 12/2019

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Article

BMC surgery, 17, 1. Surgical correction of hyperlordosis in facioscapulohumeral muscular dystrophy: A case report

Tan H, Auteur ; Feng F ; Lin Y ; Chen C ; Li Z ; Shen J | 2017

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Article

Neurology, 64, 2. Molecular analysis and prenatal prediction of spinal muscular atrophy in Chinese patients by the combination of restriction fragment length polymorphism analysis, denaturing high-performance liquid chromatography, and linkage analysis

Chen WJ ; Wu ZY ; Lin MT ; Su JF ; Lin Y ; Murong SX ; Wang N | 2007

Accès au résumé PubMed / to PubMed abstract

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Détail de l'auteur

Auteur Lin Y

Documents disponibles écrits par cet auteur (19)

Neuropathology and applied neurobiology, 51, 1. Genotype-Phenotype Correlation in Progressive External Ophthalmoplegia: Insights From a Retrospective Analysis

European journal of neurology, Epub. A multicenter, randomized, open-label, phase 2 clinical study of telitacicept in adult patients with generalized myasthenia gravis

Clinica chimica acta; international journal of clinical chemistry, 548, Epub. Evaluating the performance of four assays for carrier screening of spinal muscular atrophy

Neurology, 101, 3. Association of 4qA-Specific Distal D4Z4 Hypomethylation With Disease Severity and Progression in Facioscapulohumeral Muscular Dystrophy

Frontiers in neurology, 14. Outcome and clinical features in juvenile myasthenia gravis: A systematic review and meta-analysis

Frontiers in immunology, 14. Characteristics of cardiac involvement in immune-mediated necrotizing myopathy

Orphanet journal of rare diseases, 17, 1. Clinical and molecular analysis of four unrelated Chinese families with pathogenic KLHL40 variants causing nemaline myopathy 8

Frontiers in neurology, 13. Effect of Fufang Huangqi Decoction on the Gut Microbiota in Patients With Class I or II Myasthenia Gravis

European journal of neurology Association of immunosuppression treatment with generalization among patients with ocular myasthenia gravis: A propensity score analysis

Orphanet journal of rare diseases, 16, 1. Biochemical and genetic characteristics of patients with primary carnitine deficiency identified through newborn screening

The Lancet regional health. Western Pacific, 18. Prevalence and disease progression of genetically-confirmed facioscapulohumeral muscular dystrophy type 1 (FSHD1) in China between 2001 and 2020: a nationwide population-based study

Journal of pediatric endocrinology & metabolism : JPEM, 34, 5. Newborn screening and molecular features of patients with multiple acyl-CoA dehydrogenase deficiency in Quanzhou, China

Neuromuscular disorders : NMD A novel nonsense variant in MT-CO3 causes MELAS syndrome

Aging Melatonin exerts immunoregulatory effects by balancing peripheral effector and regulatory T helper cells in myasthenia gravis

Clinica chimica acta; international journal of clinical chemistry, 510. Newborn screening and genetic characteristics of patients with short- and very long-chain acyl-CoA dehydrogenase deficiencies

Frontiers in Genetics, 10. Newborn Screening for Spinal Muscular Atrophy in China Using DNA Mass Spectrometry

Neurogenetics Whole exome sequencing reveals a broader variant spectrum of Charcot-Marie-Tooth disease type 2

BMC surgery, 17, 1. Surgical correction of hyperlordosis in facioscapulohumeral muscular dystrophy: A case report

Neurology, 64, 2. Molecular analysis and prenatal prediction of spinal muscular atrophy in Chinese patients by the combination of restriction fragment length polymorphism analysis, denaturing high-performance liquid chromatography, and linkage analysis