Cargando…

Dermatomyositis: Muscle Pathology According to Antibody Subtypes

BACKGROUND AND OBJECTIVES: Discoveries of dermatomyositis-specific antibodies (DMSAs) in patients with dermatomyositis raised awareness of various myopathologic features among antibody subtypes. However, only perifascicular atrophy and perifascicular myxovirus resistant protein A (MxA) overexpressio...

Descripción completa

Detalles Bibliográficos
Autores principales:	Tanboon, Jantima, Inoue, Michio, Saito, Yoshihiko, Tachimori, Hisateru, Hayashi, Shinichiro, Noguchi, Satoru, Okiyama, Naoko, Fujimoto, Manabu, Nishino, Ichizo
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Lippincott Williams & Wilkins 2022
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8865893/ https://www.ncbi.nlm.nih.gov/pubmed/34873015 http://dx.doi.org/10.1212/WNL.0000000000013176

Ejemplares similares

Muscle pathology of antisynthetase syndrome according to antibody subtypes
por: Tanboon, Jantima, et al.
Publicado: (2023)

A 53‐year‐old man with a 16‐year history of asymmetrical proximal muscle weakness, facial muscle weakness, and scapular winging
por: Tanboon, Jantima, et al.
Publicado: (2023)

Cutaneous manifestations of dermatomyositis characterized by myositis-specific autoantibodies
por: Okiyama, Naoko, et al.
Publicado: (2019)

Editorial: Inflammatory muscle diseases: an update
por: Tanboon, Jantima, et al.
Publicado: (2023)

Causative variant profile of collagen VI-related dystrophy in Japan
por: Inoue, Michio, et al.
Publicado: (2021)

HLA-DRB1 allele and autoantibody profiles in Japanese patients with inclusion body myositis
por: Oyama, Munenori, et al.
Publicado: (2020)

A Continuous Increase in CXC-Motif Chemokine Ligand 10 in a Case of Anti-Nuclear Matrix Protein-2-Positive Juvenile Dermatomyositis
por: Nagamori, Tsunehisa, et al.
Publicado: (2022)

Inflammatory features in sporadic late‐onset nemaline myopathy are independent from monoclonal gammopathy
por: Tanboon, Jantima, et al.
Publicado: (2021)

Clinical Features and Cutaneous Manifestations of Juvenile and Adult Patients of Dermatomyositis Associated with Myositis-Specific Autoantibodies
por: Okiyama, Naoko
Publicado: (2021)

Exon skipping induced by nonsense/frameshift mutations in DMD gene results in Becker muscular dystrophy
por: Okubo, Mariko, et al.
Publicado: (2020)

Two novel VCP missense variants identified in Japanese patients with multisystem proteinopathy
por: Inoue, Michio, et al.
Publicado: (2018)

Lomentospora prolificans vertebral osteomyelitis with spinal epidural abscess in an immunocompetent woman: Case report and literature review
por: Wangchinda, Walaiporn, et al.
Publicado: (2018)

Anti-SAE autoantibody-positive Japanese patient with juvenile dermatomyositis complicated with interstitial lung disease - a case report
por: Kishi, Takayuki, et al.
Publicado: (2021)

A novel LMNA mutation identified in a Japanese patient with LMNA-associated congenital muscular dystrophy
por: Ishiyama, Akihiko, et al.
Publicado: (2018)

A recurrent homozygous ACTN2 variant associated with core myopathy
por: Inoue, Michio, et al.
Publicado: (2021)

A Cavernous Venous Malformation of the Orbit Mimicking an Idiopathic Orbital Inflammation
por: Chirapapaisan, Niphon, et al.
Publicado: (2020)

Intranuclear inclusions in muscle biopsy can differentiate oculopharyngodistal myopathy and oculopharyngeal muscular dystrophy
por: Ogasawara, Masashi, et al.
Publicado: (2022)

Successful Treatment of Acrodermatitis Continua of Hallopeau with an Anti-IL-17A Agent
por: Inoue, Sae, et al.
Publicado: (2021)

A Novel Mutation of the GNE Gene in Distal Myopathy with Rimmed Vacuoles: A Case with Inflammation
por: Tanboon, Jantima, et al.
Publicado: (2014)

Three novel MTM1 pathogenic variants identified in Japanese patients with X‐linked myotubular myopathy
por: Nishikawa, Atsuko, et al.
Publicado: (2019)

Association between a C8orf13–BLK Polymorphism and Polymyositis/Dermatomyositis in the Japanese Population: An Additive Effect with STAT4 on Disease Susceptibility
por: Sugiura, Tomoko, et al.
Publicado: (2014)

A 7‐year‐old female with hypotonia and scoliosis
por: Saito, Yoshihiko, et al.
Publicado: (2022)

Successful treatment of frequent premature ventricular contractions and non-sustained ventricular tachycardia with verapamil and flecainide in RYR1-related myopathy: a case report
por: Maruo, Yuji, et al.
Publicado: (2023)

Clinically amyopathic dermatomyositis associated with anti-nuclear matrix protein 2 antibody
por: Abe, Saori, et al.
Publicado: (2021)

Nodulocystic Basal Cell Carcinoma Arising Directly from a Seborrheic Keratosis: A Rare Case Report
por: Shibao, Kana, et al.
Publicado: (2016)

A Case of Cardiogenic Stroke With a Novel LMNA Variant (c. 1135C>A; p.Leu379Ile)
por: Tokuda, Naoki, et al.
Publicado: (2023)

Whole-body MRI revealed generalized subcutaneous oedema in a patient with juvenile dermatomyositis
por: Fujita, Yuji, et al.
Publicado: (2023)

Allele-specific Gene Silencing of Mutant mRNA Restores Cellular Function in Ullrich Congenital Muscular Dystrophy Fibroblasts
por: Noguchi, Satoru, et al.
Publicado: (2014)

Muscle Weakness and Fibrosis Due to Cell Autonomous and Non-cell Autonomous Events in Collagen VI Deficient Congenital Muscular Dystrophy
por: Noguchi, Satoru, et al.
Publicado: (2016)

Disclosure of cancer diagnosis and prognosis: a survey of the general public's attitudes toward doctors and family holding discretionary powers
por: Miyata, Hiroaki, et al.
Publicado: (2004)

Honey and Chamomile Activate Keratinocyte Antioxidative Responses via the KEAP1/NRF2 System
por: Ogawa, Tatsuya, et al.
Publicado: (2020)

PD-1 Regulates Passive Anaphylaxis: A Possible Role of the Mast Cell Intracellular Inhibitory Signal
por: Ogawa, Tatsuya, et al.
Publicado: (2021)

Activation of CD8 T cells accelerates anti-PD-1 antibody-induced psoriasis-like dermatitis through IL-6
por: Tanaka, Ryota, et al.
Publicado: (2020)

Oropharyngeal Dysphagia in Dermatomyositis: Associations with Clinical and Laboratory Features Including Autoantibodies
por: Mugii, Naoki, et al.
Publicado: (2016)

Simultaneous measurement of the size and methylation of chromosome 4qA-D4Z4 repeats in facioscapulohumeral muscular dystrophy by long-read sequencing
por: Hiramuki, Yosuke, et al.
Publicado: (2022)

Providing support to psychiatric patients living in the community in Japan: patient needs and care providers perceptions
por: Miyata, Hiroaki, et al.
Publicado: (2008)

Rimmed Vacuoles in Becker Muscular Dystrophy Have Similar Features with Inclusion Myopathies
por: Momma, Kazunari, et al.
Publicado: (2012)

A nationwide survey on Marinesco-Sjögren syndrome in Japan
por: Goto, Masahide, et al.
Publicado: (2014)

Cutaneous Angiosarcoma: The Possibility of New Treatment Options Especially for Patients with Large Primary Tumor
por: Fujisawa, Yasuhiro, et al.
Publicado: (2018)

Consultation-liaison psychiatry in Japan: a nationwide retrospective observational study
por: Shinjo, Daisuke, et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_dt7u2ueqmgs7fmjvakbb4hd8da