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Auteur Huang X

Documents disponibles écrits par cet auteur (27)

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Article

Neurological research, 46, 7. microRNA-mRNA expression profiles in the skeletal muscle of myotonic dystrophy type 1

Li M ; Li Y ; Wang Z ; Cui F ; Yang F ; Wang H ; Shi Q ; Huang X | 07/2024

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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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$Bispecific BCMA/CD19 targeted CAR-T cell therapy forces sustained disappearance of symptoms and anti-acetylcholine receptor antibodies in refractory myasthenia gravis: a case report$

Article

Journal of neurology, Epub. Bispecific BCMA/CD19 targeted CAR-T cell therapy forces sustained disappearance of symptoms and anti-acetylcholine receptor antibodies in refractory myasthenia gravis: a case report

Zhang Y ; Liu D ; Zhang Z ; Huang X ; Cao J ; Wang G ; Du X ; Wang Z ; Yang M ; Luo T ; Liu S ; Zhang W ; Sheng Y ; Li H ; Zhang W ; Chen H ; Zhang S ; Wang X ; Meng W ; Zong S ; Shi M ; Zheng J ; Cui G | 11/04/2024

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$Refractory generalized myasthenia gravis treated successfully with telitacicept: two cases report$

Article

Journal of neurology, Epub. Refractory generalized myasthenia gravis treated successfully with telitacicept: two cases report

Zhang Z ; Wang Z ; Du X ; Huang X ; Zhang Y | 07/10/2023

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Article

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology Circulating miRNAs drive personalized medicine based on subgroup classification in myasthenia gravis patients

Huang X ; Zhang Z ; Wang Y ; Xu M ; Du X ; Zhang Y | 05/07/2023

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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

Frontiers in bioscience (Landmark edition), 27, 1. The protective role of mesencephalic astrocyte-derived neurotrophic factor in endoplasmic reticulum stress in RT4-D6P2T schwannoma sells with the S63del MPZ mutation

Sun B ; Wang H ; Li Y ; He Z ; Cui F ; Yang F ; Huang X | Singapore | 04/01/2022

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Article

British journal of pharmacology A new therapeutic effect of fenofibrate in Duchenne muscular dystrophy: The promotion of myostatin degradation

Sun Z ; Xu D ; Zhao L ; Li X ; Li S ; Huang X ; Li C ; Sun L ; Liu B ; Jiang Z ; Zhang L | England | 22/09/2021

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Article

Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences, 50, 4. Screening of multiple acyl-CoA dehydrogenase deficiency in newborns and follow-up of patients

Zhou D ; Ye M ; Hu Z ; Zhang Y ; Zhu L ; Yang R ; Huang X | China | 25/08/2021

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Article

Acta neurologica Belgica Clinical evaluation of efficacy of leflunomide combined with low-dose prednisone for treatment of myasthenia gravis

Huang X ; Qiu L ; Lu Y ; Chen J ; Yang W ; Ou C ; Ran H ; Liu W | Italy | 19/08/2021

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Article

Stem cell research, 54. Generation of an induced pluripotent stem cell line (TRNDi012-B) from Fibrodysplasia Ossificans Progressiva (FOP) patient carrying a heterozygous mutation c. 617G > A in the ACVR1 gene

Huang X ; Roeder A ; Li R ; Beers J ; Liu C ; Zou J ; Yu PB ; Zheng W | England | 07/2021

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Article

JCI insight Saracatinib is an efficacious clinical candidate for fibrodysplasia ossificans progressiva

Williams EP ; Bagarova J ; Kerr G ; Xia DD ; Place ES ; Dey D ; Shen Y ; Bocobo GA ; Mohedas AH ; Huang X ; Sanderson PE ; Lee A ; Zheng W ; Economides AN ; Smith JC ; Yu PB ; Bullock AN | United States | 11/03/2021

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Article

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 42, 3. AChRAb and MuSKAb double-seropositive myasthenia gravis: a distinct subtype?

Zhang J ; Chen Y ; Chen J ; Huang X ; Wang H ; Li Y ; Liu W ; Feng H | 01/2021

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Article

Journal of cachexia, sarcopenia and muscle TAK1 inhibition improves myoblast differentiation and alleviates fibrosis in a mouse model of Duchenne muscular dystrophy

Xu D ; Li S ; Wang L ; Jiang J ; Zhao L ; Huang X ; Sun Z ; Li C ; Sun L ; Li X ; Jiang Z ; Zhang L | Germany | 25/11/2020

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Article

Chinese medical journal A case of de novo dynamin 2-related centronuclear myopathy with electrical but not clinical myotonia

Huang X ; Liu XY ; Chen L ; Sun AP ; Zhang YS ; Zheng DF ; Zhong YF ; Fan DS | China | 2020

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Article

Journal of cachexia, sarcopenia and muscle A potential therapeutic effect of catalpol in Duchenne muscular dystrophy revealed by binding with TAK1

Xu D ; Zhao L ; Jiang J ; Li S ; Sun Z ; Huang X ; Li C ; Wang T ; Sun L ; Li X ; Jiang Z ; Zhang L | Germany | 2020

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Article

Prenatal diagnosis, 40, 8. Noninvasive prenatal diagnosis for Duchenne muscular dystrophy based on the direct haplotype phasing

Chen M ; Chen C ; Huang X ; Sun J ; Jiang L ; Li Y ; Zhu Y ; Tian C ; Li Y ; Lu Z ; Wang Y ; Zeng F ; Yang Y ; Song X ; Peng Z ; Yin C ; Chen D | England | 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

Italian journal of Pediatrics, 45, 1. Comprehensive approach to weaning in difficult-to-wean infantile and juvenile-onset glycogen-storage disease type II patients: a case series

Xu L, Auteur ; Ba H ; Pei Y ; Huang X ; Liang Y ; Zhang L ; Huang H ; Zhang C ; Tang W | England | 08/2019

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Article

Journal of cachexia, sarcopenia and muscle, 10, 3. Hemojuvelin is a novel suppressor for Duchenne muscular dystrophy and age-related muscle wasting

Zhang P, Auteur ; He J ; Wang F ; Gong J ; Wang L ; Wu Q ; Li W ; Liu H ; Wang J ; Zhang K ; Li M ; Huang X ; Pu C ; Li Y ; Jiang F ; Wang F ; Min J ; Chen X | 06/2019

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Article

European journal of obstetrics, gynecology, and reproductive biology, 240. Haplotype-Based noninvasive prenatal diagnosis for duchenne muscular dystrophy: A pilot study in South China.

Chen M, Auteur ; Chen C ; Li Y ; Yuan Y ; Lai Z ; Guo F ; Wang Y ; Huang X ; Li S ; Wu R ; Peng Z ; Sun J ; Chen D | Ireland | 05/2019

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Article

Frontiers in neurology, 9. Clinical Characteristics of Juvenile Myasthenia Gravis in Southern China

Huang X, Auteur ; Li Y ; Feng H ; Chen P ; Liu W | 2018

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Article

Frontiers in neurology, 9. Myasthenia Gravis With Thymoma, Manifesting as AChR-Ab-Positive, Distinct Bulbar Palsy Accompanied by Dysgeusia: A Case Series and Review of Literature

Zhu K, Auteur ; Chen J ; Li J ; Wang H ; Huang X ; Li Y ; Feng H | 2018

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Article

Neurological sciences, 38, 10. Thymectomy is a beneficial therapy for patients with non-thymomatous ocular myasthenia gravis: a systematic review and meta-analysis

Zhu K, Auteur ; Li J ; Huang X ; Xu W ; Liu W ; Chen J ; Chen P ; Feng H | 2017

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Article

Brain & development, 38, 7. Infantile spinal muscular atrophy with respiratory distress type I presenting without respiratory involvement: Novel mutations and review of the literature

Luan X, Auteur ; Huang X ; Liu X ; Zhou H ; Chen S ; Cao L | 2016

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Détail de l'auteur

Auteur Huang X

Documents disponibles écrits par cet auteur (27)

Neurological research, 46, 7. microRNA-mRNA expression profiles in the skeletal muscle of myotonic dystrophy type 1

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

Journal of neurology, Epub. Bispecific BCMA/CD19 targeted CAR-T cell therapy forces sustained disappearance of symptoms and anti-acetylcholine receptor antibodies in refractory myasthenia gravis: a case report

Journal of neurology, Epub. Refractory generalized myasthenia gravis treated successfully with telitacicept: two cases report

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology Circulating miRNAs drive personalized medicine based on subgroup classification in myasthenia gravis patients

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

Frontiers in bioscience (Landmark edition), 27, 1. The protective role of mesencephalic astrocyte-derived neurotrophic factor in endoplasmic reticulum stress in RT4-D6P2T schwannoma sells with the S63del MPZ mutation

British journal of pharmacology A new therapeutic effect of fenofibrate in Duchenne muscular dystrophy: The promotion of myostatin degradation

Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences, 50, 4. Screening of multiple acyl-CoA dehydrogenase deficiency in newborns and follow-up of patients

Acta neurologica Belgica Clinical evaluation of efficacy of leflunomide combined with low-dose prednisone for treatment of myasthenia gravis

Stem cell research, 54. Generation of an induced pluripotent stem cell line (TRNDi012-B) from Fibrodysplasia Ossificans Progressiva (FOP) patient carrying a heterozygous mutation c. 617G > A in the ACVR1 gene

JCI insight Saracatinib is an efficacious clinical candidate for fibrodysplasia ossificans progressiva

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 42, 3. AChRAb and MuSKAb double-seropositive myasthenia gravis: a distinct subtype?

Journal of cachexia, sarcopenia and muscle TAK1 inhibition improves myoblast differentiation and alleviates fibrosis in a mouse model of Duchenne muscular dystrophy

Chinese medical journal A case of de novo dynamin 2-related centronuclear myopathy with electrical but not clinical myotonia

Journal of cachexia, sarcopenia and muscle A potential therapeutic effect of catalpol in Duchenne muscular dystrophy revealed by binding with TAK1

Prenatal diagnosis, 40, 8. Noninvasive prenatal diagnosis for Duchenne muscular dystrophy based on the direct haplotype phasing

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

Italian journal of Pediatrics, 45, 1. Comprehensive approach to weaning in difficult-to-wean infantile and juvenile-onset glycogen-storage disease type II patients: a case series

Journal of cachexia, sarcopenia and muscle, 10, 3. Hemojuvelin is a novel suppressor for Duchenne muscular dystrophy and age-related muscle wasting

European journal of obstetrics, gynecology, and reproductive biology, 240. Haplotype-Based noninvasive prenatal diagnosis for duchenne muscular dystrophy: A pilot study in South China.

Frontiers in neurology, 9. Clinical Characteristics of Juvenile Myasthenia Gravis in Southern China

Frontiers in neurology, 9. Myasthenia Gravis With Thymoma, Manifesting as AChR-Ab-Positive, Distinct Bulbar Palsy Accompanied by Dysgeusia: A Case Series and Review of Literature

Neurological sciences, 38, 10. Thymectomy is a beneficial therapy for patients with non-thymomatous ocular myasthenia gravis: a systematic review and meta-analysis

Brain & development, 38, 7. Infantile spinal muscular atrophy with respiratory distress type I presenting without respiratory involvement: Novel mutations and review of the literature