Myositis with sarcoplasmic inclusions in Nakajo–Nishimura syndrome: a genetic inflammatory myopathy-Reference-Cited by-同舟云学术

Myositis with sarcoplasmic inclusions in Nakajo–Nishimura syndrome: a genetic inflammatory myopathy

Published:2020-03-25 Issue:6 Volume:46 Page:579-587
ISSN:0305-1846
Container-title:Neuropathology and Applied Neurobiology
language:en
Short-container-title:Neuropathol. Appl. Neurobiol.

Author:

Ayaki T.¹^ORCID,Murata K.²,Kanazawa N.³,Uruha A.⁴⁵⁶,Ohmura K.⁷,Sugie K.⁸,Kasagi S.⁹,Li F.¹⁰,Mori M.¹¹,Nakajima R.⁷,Sasai T.⁷,Nishino I.⁴,Ueno S.⁸,Urushitani M.¹²,Furukawa F.³,Ito H.¹¹,Takahashi R.¹

Affiliation:

1. Department of Neurology Kyoto University Graduate School of Medicine KyotoJapan

2. Center for Educational Research and Development Wakayama Medical University WakayamaJapan

3. Department of Dermatology Wakayama Medical University WakayamaJapan

4. Department of Neuromuscular Research National Institute of NeuroscienceNational Center of Neurology and Psychiatry (NCNP) KodairaTokyoJapan

5. Department of Genome Medicine Development Medical Genome Center Kodaira TokyoJapan

6. Department of Neuropathology Charité ‐ Universitätsmedizin Berlin Germany

7. Department of Rheumatology and Clinical Immunology Graduate School of Medicine Kyoto University Sakyo‐ku KyotoJapan

8. Department of Neurology Nara Medical University School of Medicine Kashihara NaraJapan

9. Minato Motomachi Internal Medicine Clinic Kobe Hyogo Japan

10. Department of Neurology Research Center of Neurology in Second Affiliated Hospital Key Laboratory of Medical Neurobiology of Zhejiang Province Zhejiang University School of Medicine Hangzhou China

11. Department of Neurology Wakayama Medical University WakayamaJapan

12. Department of Neurology Shiga University of Medical ScienceSeta Tsukinowa‐cho Otsu City Shiga Japan

Funder

Japan Agency for Medical Research and Development

Wakayama Medical University

Ministry of Education, Culture, Sports, Science and Technology

Publisher

Wiley

Subject

Physiology (medical),Clinical Neurology,Neurology,Histology,Pathology and Forensic Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/nan.12614

Reference20 articles.

1. Proteasome assembly defect due to a proteasome subunit beta type 8 (PSMB8) mutation causes the autoinflammatory disorder, Nakajo-Nishimura syndrome

2. Nakajo-Nishimura Syndrome: An Autoinflammatory Disorder Showing Pernio-Like Rashes and Progressive Partial Lipodystrophy

Nakajo–Nishimura syndrome and related proteasome-associated autoinflammatory syndromes

4. Pluripotent Stem Cell Model of Nakajo-Nishimura Syndrome Untangles Proinflammatory Pathways Mediated by Oxidative Stress

5. Plasma IP-10 level distinguishes inflammatory myopathy

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