Cargando…

Muscular Tuberculosis: A New Case and a Review of the Literature

Objective: To investigate the clinical manifestations, underlying diseases, pathological features, and therapeutic responses in patients with muscular tuberculosis (MT), which is rare and often misdiagnosed in clinical practice. Methods: This study describes a rare MT case that was recently diagnose...

Descripción completa

Detalles Bibliográficos
Autores principales:	Zeng, Yanping, Liu, Yin, Xie, Yanchun, Liang, Jingjing, Kuang, Jiabing, Lu, Zuneng, Zhou, Yu
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2019
Materias:	Neurology
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6779781/ https://www.ncbi.nlm.nih.gov/pubmed/31632334 http://dx.doi.org/10.3389/fneur.2019.01031

Ejemplares similares

Effect of Muscular Exercise on Patients With Muscular Dystrophy: A Systematic Review and Meta-Analysis of the Literature
por: Gianola, Silvia, et al.
Publicado: (2020)

SCN4A p.R675Q Mutation Leading to Normokalemic Periodic Paralysis: A Family Report and Literature Review
por: Shi, Jiejing, et al.
Publicado: (2019)

Can the Large-Scale Decrement in Repetitive Nerve Stimulation Be Used as an Exclusion Criterion for Amyotrophic Lateral Sclerosis?
por: Shang, Li, et al.
Publicado: (2020)

Novel compound heterozygous mutations of LAMA2-limb–girdle muscular dystrophy: A case report and literature review
por: Wang, Duo-Zi, et al.
Publicado: (2023)

Case Report: Acute Bulbar Palsy Plus Syndrome: A Guillain-Barré Syndrome Variant More Prone to Be a Subtype Than Overlap of Distinct Subtypes
por: Cao, Qian, et al.
Publicado: (2020)

Intracarotid Transplantation of Skin-Derived Precursor Schwann Cells Promotes Functional Recovery After Acute Ischemic Stroke in Rats
por: Liang, Jingjing, et al.
Publicado: (2021)

Treatment of Facioscapulohumeral Muscular Dystrophy (FSHD): A Systematic Review
por: Aguirre, Alex S, et al.
Publicado: (2023)

Cerebral infarction in centrum semiovale presenting with hemichorea: a case report and literature review
por: Yi, Jingjing, et al.
Publicado: (2023)

Novel miRNA Biomarkers for Patients With Duchenne Muscular Dystrophy
por: Meng, Qi, et al.
Publicado: (2022)

Anti-homer-3 Antibody Encephalitis in a 10-Year-Old Child: Case Report and Review of the Literature
por: Kuang, Zuying, et al.
Publicado: (2022)

A blended neurostimulation protocol to delineate cortico-muscular and spino-muscular dynamics following neuroplastic adaptation
por: Stefanovic, Filip, et al.
Publicado: (2023)

Role of circulating biomarkers in spinal muscular atrophy: insights from a new treatment era
por: Giorgia, Querin, et al.
Publicado: (2023)

Longitudinal Study of Three microRNAs in Duchenne Muscular Dystrophy and Becker Muscular Dystrophy
por: Trifunov, Selena, et al.
Publicado: (2020)

Fukuyama Congenital Muscular Dystrophy
por: Agarwal, Amit, et al.
Publicado: (2022)

Genetic Modifiers of Duchenne Muscular Dystrophy in Chinese Patients
por: Chen, Menglong, et al.
Publicado: (2020)

A rare case of intracranial solitary fibrous tumor that is still alive after multiple surgical resections: a case report and review of the literature
por: Gao, YiMeng, et al.
Publicado: (2023)

Effectiveness of pharmacological treatments in Duchenne muscular dystrophy: a protocol for a systematic review and meta-analysis
por: Pascual Morena, Carlos, et al.
Publicado: (2019)

Spinal Muscular Atrophy: The Treatment Approved
por: Tabet, Rabih, et al.
Publicado: (2017)

A New Method for Measuring Bell-Shaped Chest Induced by Impaired Ribcage Muscles in Spinal Muscular Atrophy Children
por: LoMauro, Antonella, et al.
Publicado: (2018)

Serum MyomiRs as Biomarkers for Female Carriers of Duchenne/Becker Muscular Dystrophy
por: Zhang, Jiapeng, et al.
Publicado: (2020)

Pilot Study on Quantitative Cervical Cord and Muscular MRI in Spinal Muscular Atrophy: Promising Biomarkers of Disease Evolution and Treatment?
por: Savini, Giovanni, et al.
Publicado: (2021)

Encephalic Schistosoma japonicum resembles brainstem neoplasm: Case report and literature review
por: Wu, Kang, et al.
Publicado: (2022)

The Tadpole Pupil: Case Series With Review of the Literature and New Considerations
por: Udry, Morgane, et al.
Publicado: (2019)

Cardiac Involvement in Facioscapulohumeral Muscular Dystrophy (FSHD)
por: Ducharme-Smith, Allison, et al.
Publicado: (2021)

Impairment of muscular endothelial cell regeneration in dermatomyositis
por: Lemmer, D., et al.
Publicado: (2022)

Corrigendum: Serum MyomiRs as Biomarkers for Female Carriers of Duchenne/Becker Muscular Dystrophy
por: Zhang, Jiapeng, et al.
Publicado: (2020)

Shifting Valproic Acid to Levetiracetam in Women of Childbearing Age With Epilepsy: A Retrospective Investigation and Review of the Literature
por: Kuo, Cheng-Yen, et al.
Publicado: (2020)

Biomarkers and the Development of a Personalized Medicine Approach in Spinal Muscular Atrophy
por: Kariyawasam, Didu S. T., et al.
Publicado: (2019)

Machine learning-based radiomics to differentiate immune-mediated necrotizing myopathy from limb-girdle muscular dystrophy R2 using MRI
por: Wei, Ping, et al.
Publicado: (2023)

Clinical Phenotyping and Biomarkers in Spinal and Bulbar Muscular Atrophy
por: Millere, Elina, et al.
Publicado: (2021)

Posterior Circulation ASPECTS on CT Angiography Predicts Futile Recanalization of Endovascular Thrombectomy for Acute Basilar Artery Occlusion
por: Ouyang, Keni, et al.
Publicado: (2022)

The Refinement of Home Exercise Program for Children and Adolescents With Muscular Dystrophy in the Present COVID-19 Pandemic Scenario: A Scoping Review
por: Harjpal, Pallavi, et al.
Publicado: (2022)

A Novel SACS Variant Identified in a Chinese Patient: Case Report and Review of the Literature
por: Chen, Yuchao, et al.
Publicado: (2022)

Atypical Teratoid/Rhabdoid Tumor Originated From the Trigeminal Nerve in a Young Male Adult: Case Report and Review of the Literature
por: Chen, Fuxiang, et al.
Publicado: (2020)

Editorial: Spinal Muscular Atrophy: Evolutions and Revolutions of Modern Therapy
por: Finkel, Richard S., et al.
Publicado: (2020)

The Impact of COVID-19 on Families With Pediatric Muscular Dystrophy Patients
por: Zubair, Adeel S, et al.
Publicado: (2023)

A Patient With CAD Deficiency Responsive to Uridine and Literature Review
por: Zhou, Ling, et al.
Publicado: (2020)

Outcome and clinical features in juvenile myasthenia gravis: A systematic review and meta-analysis
por: Lin, Yangtao, et al.
Publicado: (2023)

Cognitive impairment in Chinese adult patients with type III spinal muscular atrophy without disease-modifying treatment
por: Hu, Ying, et al.
Publicado: (2023)

A rare cervical dystonia mimic in adults: congenital muscular torticollis (fibromatosis colli)
por: Gonzalez-Usigli, Hector, et al.
Publicado: (2013)

Cannot write session to /tmp/vufind_sessions/sess_qu3rnu9sl7j26p12d2m3amt6oq