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Auteur Sun C

Documents disponibles écrits par cet auteur (23)

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Article

Clinical genetics The clinical and genetic spectrum of mitochondrial diseases in China: A multicenter retrospective cross-sectional study

Zhao Y ; Zhao X ; Ji K ; Wang J ; Zhao Y ; Lin J ; Gang Q ; Yu M ; Yuan Y ; Jiang H ; Sun C ; Fang F ; Yan C ; Wang Z | 09/08/2024

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$Efficacy and safety of tocilizumab in patients with refractory generalized myasthenia gravis$

Article

CNS neuroscience & therapeutics, 30, 6. Efficacy and safety of tocilizumab in patients with refractory generalized myasthenia gravis

Ruan Z ; Tang Y ; Gao T ; Li C ; Guo R ; Sun C ; Huang X ; Li Z ; Chang T | 06/2024

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Article

Neuromuscular disorders : NMD Intrafamilial phenotypic heterogeneity in GIPC1-related oculopharyngodistal myopathy type 2: a case report

Gu X ; Jiao K ; Yue D ; Wang X ; Qiao K ; Gao M ; Lin J ; Sun C ; Zhao C ; Zhu W ; Xi J | 07/07/2023

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Article

Pediatric neurology, 140. Pathogenic PSAT1 Variants and Autosomal Recessive Axonal Charcot-Marie-Tooth Disease With Ichthyosis

Lu Y ; Xing H ; Liu C ; Huang D ; Sun C ; Yu M ; Meng L ; Lv H ; Zhang W ; Wang Z ; Yuan Y ; Xie Z | United States | 24/11/2022

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Article

Journal of neurology Clinical, muscle imaging, and genetic characteristics of dystrophinopathies with deep-intronic DMD variants

Xie Z ; Sun C ; Liu C ; Xie Z ; Wei L ; Yu J ; Ling C ; Guo X ; Liu Y ; Yu M ; Leng Y ; Meng L ; Sun Y ; Deng J ; Leal SM ; Schrauwen I ; Wang Z ; Yuan Y | Germany | 02/11/2022

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Article

Cell stem cell, 29, 4. Human pluripotent stem cell-derived myogenic progenitors undergo maturation to quiescent satellite cells upon engraftment

Sun C ; Kannan S ; Choi IY ; Lim H ; Zhang H ; Chen GS ; Zhang N ; Park SH ; Serra C ; Iyer SR ; Lloyd TE ; Kwon C ; Lovering RM ; Lim SB ; Andersen P ; Wagner KR ; Lee G | 07/04/2022

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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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Article

Neurotherapeutics Thymectomy and Risk of Generalization in Patients with Ocular Myasthenia Gravis: A Multicenter Retrospective Cohort Study

Li H ; Ruan Z ; Gao F ; Zhou H ; Guo R ; Sun C ; Xu Q ; Lu Q ; Zhou Y ; Zhao Z ; Yu L ; Wu S ; Lei T ; Gao T ; Tang Y ; Li C ; Huo F ; Zhu Y ; Sun J ; Tang B ; Zhang M ; Gao Y ; Lu X ; Li Z ; Chang T | United States | 08/10/2021

Correction to: Thymectomy and Risk of Generalization in Patients with Ocular Myasthenia Gravis: a Multicenter Retrospective Cohort Study Li H et al Neurotherapeutics. 2021 Nov 8. doi: 10.1007/s13311-021-01144-0. Correction for the affiliati[...]

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Article

Mitochondrion, 59. Metabolic abnormality in acute stroke-like lesion and its relationship with focal cerebral blood flow in patients with MELAS: Evidence from proton MR spectroscopy and arterial spin labeling

Wang R ; Hu B ; Sun C ; Geng D ; Lin J ; Li Y | Netherlands | 27/06/2021

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Article

Frontiers in medicine, 8. Efficacy and Tolerability of Nintedanib in Idiopathic-Inflammatory-Myopathy-Related Interstitial Lung Disease: A Pilot Study

Liang J ; Cao H ; Yang Y ; Ke Y ; Yu Y ; Sun C ; Yue L ; Lin J | 03/02/2021

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Article

Scientific Reports, 11, 1. Neurofilament light is a novel biomarker for mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes

Zheng YS ; Sun C ; Wang R ; Chen N ; Luo SS ; Xi JY ; Lu JH ; Zhao CB ; Li YX ; Zhou L ; Lin J | 21/01/2021

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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

Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia, 81. The correlation of clinical evaluation with life quality and mental status in a Chinese cohort with dysferlinopathy

Feng X ; Liu C ; Xi J ; Sun C ; Yue D ; Zhu W ; Li J ; Liang Z ; Lu J ; Luo S | Scotland | 11/2020

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Article

JCI insight, 5, 11. Duchenne muscular dystrophy hiPSC-derived myoblast drug screen identifies compounds that ameliorate disease in mdx mice

Sun C ; Choi YI ; Rovira Gonzalez YI ; Andersen P ; Talbot CC Jr ; Iyer SR ; Lovering RM ; Wagner KR ; Lee G | 04/06/2020

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Article

Clinical chemistry Direct Haplotyping-Based Noninvasive Prenatal Test for Myotonic Dystrophy Type 1 with Large CTG Expansion

Lee JS ; Lee KB ; Song H ; Sun C ; Kim MJ ; Cho SI ; Lee YK ; Park SS ; Seong MW | England | 03/2020

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Article

Journal of magnetic resonance imaging : JMRI Altered Dynamic Functional Connectivity in Patients With Mitochondrial Encephalomyopathy With Lactic Acidosis and Stroke-Like Episodes (MELAS) at Acute and Chronic Stages: Shared and Specific Brain Connectivity Abnormalities

Wang R ; Sun C ; Lin J ; Chen N ; Hu B ; Liu X ; Geng D ; Yang L ; Li Y | United States | 2020

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Article

Mitochondrion, 54. Altered spontaneous brain activity at attack and remission stages in patients with mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS): Beyond stroke-like lesions

Wang R ; Li Y ; Lin J ; Sun C ; Chen N ; Xu W ; Hu B ; Liu X ; Geng D ; Yang L | Netherlands | 2020

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Article

Orphanet journal of rare diseases, 14, 1. Value of muscle magnetic resonance imaging in the differential diagnosis of muscular dystrophies related to the dystrophin-glycoprotein complex

Xie Z, Auteur ; Xie Z ; Yu M ; Zheng Y ; Sun C ; Liu Y ; Ling C ; Zhu Y ; Zhang W ; Xiao J ; Wang Z ; Yuan Y | England | 11/2019

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Article

Experimental neurology, 323. Stem cell-based therapies for Duchenne muscular dystrophy.

Sun C, Auteur ; Serra C ; Lee G ; Wagner KR | United States | 10/2019

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Article

JCI insight, 4, 6. Distinct pathological signatures in human cellular models of myotonic dystrophy subtypes

Kim EY, Auteur ; Barefield DY ; Vo AH ; Gacita AM ; Schuster EJ ; Wyatt EJ ; Davis JL ; Dong B ; Sun C ; Page P ; Dellefave-Castillo L ; Demonbreun A ; Zhang HF ; McNally EM | 21/03/2019

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Article

Clinical genetics, 80, 6. Myotonia congenita and myotonic dystrophy in the same family : coexistence of a CLCN1 mutation and expansion in the CNBP (ZNF9) gene

Sun C ; van Ghelue M ; Tranebjaerg L ; Thyssen F ; Nilssen O ; Torbergsen T | 2011

Accès au résumé Pubmed/to pubmed abstract

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Article

Journal of neuroscience (The), 22, 17. The myotonia congenita mutation A331T confers a novel hyperpolarization-activated gate to the muscle chloride channel CIC-1

Warnstedt M ; Sun C ; Poser B ; Escriva MJ ; Tranebjaerg L ; Torbergsen T ; van Ghelue M ; Fahlke C | 1/09/2002

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Article

Clinical genetics, 56, 6. Proximal myotonic myopathy : clinical and molecular investigation of a Norwegian family with PROMM

Sun C ; Henriksen OA ; Tranebjaerg L | 1999

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Détail de l'auteur

Auteur Sun C

Documents disponibles écrits par cet auteur (23)

Clinical genetics The clinical and genetic spectrum of mitochondrial diseases in China: A multicenter retrospective cross-sectional study

CNS neuroscience & therapeutics, 30, 6. Efficacy and safety of tocilizumab in patients with refractory generalized myasthenia gravis

Neuromuscular disorders : NMD Intrafamilial phenotypic heterogeneity in GIPC1-related oculopharyngodistal myopathy type 2: a case report

Pediatric neurology, 140. Pathogenic PSAT1 Variants and Autosomal Recessive Axonal Charcot-Marie-Tooth Disease With Ichthyosis

Journal of neurology Clinical, muscle imaging, and genetic characteristics of dystrophinopathies with deep-intronic DMD variants

Cell stem cell, 29, 4. Human pluripotent stem cell-derived myogenic progenitors undergo maturation to quiescent satellite cells upon engraftment

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

Neurotherapeutics Thymectomy and Risk of Generalization in Patients with Ocular Myasthenia Gravis: A Multicenter Retrospective Cohort Study

Mitochondrion, 59. Metabolic abnormality in acute stroke-like lesion and its relationship with focal cerebral blood flow in patients with MELAS: Evidence from proton MR spectroscopy and arterial spin labeling

Frontiers in medicine, 8. Efficacy and Tolerability of Nintedanib in Idiopathic-Inflammatory-Myopathy-Related Interstitial Lung Disease: A Pilot Study

Scientific Reports, 11, 1. Neurofilament light is a novel biomarker for mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes

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

Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia, 81. The correlation of clinical evaluation with life quality and mental status in a Chinese cohort with dysferlinopathy

JCI insight, 5, 11. Duchenne muscular dystrophy hiPSC-derived myoblast drug screen identifies compounds that ameliorate disease in mdx mice

Clinical chemistry Direct Haplotyping-Based Noninvasive Prenatal Test for Myotonic Dystrophy Type 1 with Large CTG Expansion

Journal of magnetic resonance imaging : JMRI Altered Dynamic Functional Connectivity in Patients With Mitochondrial Encephalomyopathy With Lactic Acidosis and Stroke-Like Episodes (MELAS) at Acute and Chronic Stages: Shared and Specific Brain Connectivity Abnormalities

Mitochondrion, 54. Altered spontaneous brain activity at attack and remission stages in patients with mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS): Beyond stroke-like lesions

Orphanet journal of rare diseases, 14, 1. Value of muscle magnetic resonance imaging in the differential diagnosis of muscular dystrophies related to the dystrophin-glycoprotein complex

Experimental neurology, 323. Stem cell-based therapies for Duchenne muscular dystrophy.

JCI insight, 4, 6. Distinct pathological signatures in human cellular models of myotonic dystrophy subtypes

Clinical genetics, 80, 6. Myotonia congenita and myotonic dystrophy in the same family : coexistence of a CLCN1 mutation and expansion in the CNBP (ZNF9) gene

Journal of neuroscience (The), 22, 17. The myotonia congenita mutation A331T confers a novel hyperpolarization-activated gate to the muscle chloride channel CIC-1

Clinical genetics, 56, 6. Proximal myotonic myopathy : clinical and molecular investigation of a Norwegian family with PROMM