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Volumn 34, Issue 9, 2012, Pages 784-786

Childhood-onset anti-MuSK antibody positive myasthenia gravis demonstrates a distinct clinical course

Author keywords

Muscle specific tyrosine kinase; Myasthenia gravis; Seronegative myasthenia gravis

Indexed keywords

ANTIBIOTIC AGENT; IMMUNOGLOBULIN; METHYLPREDNISOLONE; MUSCLE SPECIFIC TYROSINE KINASE ANTIBODY; PREDNISONE; UNCLASSIFIED DRUG;

EID: 84865587059     PISSN: 03877604     EISSN: 18727131     Source Type: Journal    
DOI: 10.1016/j.braindev.2011.12.014     Document Type: Article
Times cited : (18)

References (10)
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    • Auto-antibodies to the receptor tyrosine kinase MuSK in patients with myasthenia gravis without acetylcholine receptor antibodies
    • Hoch W., McConville J., Newsom-Davis J., Melms A., Vincent A. Auto-antibodies to the receptor tyrosine kinase MuSK in patients with myasthenia gravis without acetylcholine receptor antibodies. Nat Med 2001, 7:365-368.
    • (2001) Nat Med , vol.7 , pp. 365-368
    • Hoch, W.1    McConville, J.2    Newsom-Davis, J.3    Melms, A.4    Vincent, A.5
  • 2
    • 33847175506 scopus 로고    scopus 로고
    • Clinical comparison of anti-MuSK- vs anti-AChR-positive and seronegative myasthenia gravis
    • Deymeer F., Gungor-Tuncer O., Yilmaz V., Parman Y., Serdaroglu P., Ozdemir C., et al. Clinical comparison of anti-MuSK- vs anti-AChR-positive and seronegative myasthenia gravis. Neurology 2007, 68:609-611.
    • (2007) Neurology , vol.68 , pp. 609-611
    • Deymeer, F.1    Gungor-Tuncer, O.2    Yilmaz, V.3    Parman, Y.4    Serdaroglu, P.5    Ozdemir, C.6
  • 5
    • 65449136244 scopus 로고    scopus 로고
    • Long remission in muscle-specific kinase antibody-positive juvenile myasthenia
    • Anlar B., Yilmaz V., Saruhan-Direskeneli G. Long remission in muscle-specific kinase antibody-positive juvenile myasthenia. Pediatr Neurol 2009, 40:455-456.
    • (2009) Pediatr Neurol , vol.40 , pp. 455-456
    • Anlar, B.1    Yilmaz, V.2    Saruhan-Direskeneli, G.3
  • 6
    • 54949121804 scopus 로고    scopus 로고
    • A mouse model for congenital myasthenic syndrome due to MuSK mutations reveals defects in structure and function of neuromuscular junctions
    • Chevessier F., Girard E., Molgo J., Bartling S., Koenig J., Hantai D., et al. A mouse model for congenital myasthenic syndrome due to MuSK mutations reveals defects in structure and function of neuromuscular junctions. Hum Mol Genet 2008, 17:3577-3595.
    • (2008) Hum Mol Genet , vol.17 , pp. 3577-3595
    • Chevessier, F.1    Girard, E.2    Molgo, J.3    Bartling, S.4    Koenig, J.5    Hantai, D.6
  • 7
    • 33746266452 scopus 로고    scopus 로고
    • Concentric-needle single-fiber electromyography for the diagnosis of myasthenia gravis
    • Benatar M., Hanmad M., Doss-Riney H. Concentric-needle single-fiber electromyography for the diagnosis of myasthenia gravis. Muscle Nerve 2006, 34:163-168.
    • (2006) Muscle Nerve , vol.34 , pp. 163-168
    • Benatar, M.1    Hanmad, M.2    Doss-Riney, H.3
  • 9
    • 44949142964 scopus 로고    scopus 로고
    • Reference jitter values for concentric needle electrodes in voluntarily activated extensor digitorum communis and orbicularis oculi muscles
    • Kouyoumdjian J.A., Stålberg E.V. Reference jitter values for concentric needle electrodes in voluntarily activated extensor digitorum communis and orbicularis oculi muscles. Muscle Nerve 2008, 37:694-699.
    • (2008) Muscle Nerve , vol.37 , pp. 694-699
    • Kouyoumdjian, J.A.1    Stålberg, E.V.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.