T. Fukuda

发表

Are MuSK antibodies the primary cause of myasthenic symptoms?

A. Engel, D. Selcen, Xin-Ming Shen, 2004, Neurology.

Acetylcholine receptors loss and postsynaptic damage in MuSK antibody–positive myasthenia gravis

A. Vincent, K. Eguchi, M. Tsujihata, 2005, Annals of neurology.

Congenital myasthenia-related AChR delta subunit mutation interferes with intersubunit communication essential for channel gating.

K. Ohno, S. Sine, A. Engel, 2008, The Journal of clinical investigation.

Apheresis treatment in Lambert-Eaton myasthenic syndrome.

M. Motomura, S. Nakane, T. Fukuda, 2000, Therapeutic apheresis : official journal of the International Society for Apheresis and the Japanese Society for Apheresis.

Rheumatoid vasculitis of crural muscles confirmed by muscle biopsy in the absence of inflammatory myopathy: histologic and MRI study

S. Yamasaki, K. Eguchi, K. Satoh, 2010, Rheumatology International.

Structural Abnormalities at Neuromuscular Synapses Lacking Multiple Syntrophin Isoforms

A. Engel, S. Froehner, M. Adams, 2004, The Journal of Neuroscience.

Efficacy of tacrolimus in Sjögren’s syndrome-associated CNS disease with aquaporin-4 autoantibodies

K. Eguchi, M. Motomura, Hideki Nakamura, 2009, Journal of Neurology.

A case of mixed connective tissue disease complicated with hypertrophic obstructive cardiomyopathy

K. Eguchi, S. Seto, Hideki Nakamura, 2008, Rheumatology International.

A case of Japanese spotted fever complicated with central nervous system involvement and multiple organ failure.

M. Motomura, A. Kawakami, A. Tsujino, 2012, Internal medicine.

K. Eguchi, K. Iwanaga, M. Tsujihata, 2003 .

Novel congenital myasthenic syndromes associated with defects in quantal release

M. Milone, A. Engel, J. Brengman, 2006, Neurology.

Myasthenic syndrome caused by mutation of the SCN4A sodium channel

S. Cannon, K. Ohno, A. Engel, 2003, Proceedings of the National Academy of Sciences of the United States of America.

Antibodies against the main immunogenic region of the acetylcholine receptor correlate with disease severity in myasthenia gravis

M. Tsujihata, M. Motomura, A. Kawakami, 2012, Journal of Neurology, Neurosurgery & Psychiatry.

A CLCN1 mutation in dominant myotonia congenita impairs the increment of chloride conductance during repetitive depolarization

H. Hayashi, K. Taniyama, A. Kawakami, 2011, Neuroscience Letters.

Neurogenic bladder in Lambert–Eaton myasthenic syndrome and its response to 3,4-diaminopyridine

K. Eguchi, M. Motomura, K. Satoh, 2001, Journal of the Neurological Sciences.

Pentosan polysulfate treatment ameliorates motor function with increased serum soluble vascular cell adhesion molecule-1 in HTLV-1-associated neurologic disease

H. Sasaki, Tadahiro Nakamura, K. Satoh, 2014, Journal of NeuroVirology.

Efficacy of prosultiamine treatment in patients with human T lymphotropic virus type I-associated myelopathy/tropical spastic paraparesis: results from an open-label clinical trial

H. Sasaki, K. Satoh, Hideki Nakamura, 2013, BMC Medicine.

Thymus histology and concomitant autoimmune diseases in Japanese patients with muscle‐specific receptor tyrosine kinase‐antibody‐positive myasthenia gravis

M. Tsujihata, M. Motomura, A. Kawakami, 2013, European journal of neurology.

Seronegative Lambert-Eaton myasthenic syndrome

M. Tsujihata, M. Motomura, K. Eguchi, 2002, Neurology.

Reduction of P/Q‐type calcium channels in the postmortem cerebellum of paraneoplastic cerebellar degeneration with Lambert‐Eaton myasthenic syndrome

H. Dosaka-akita, K. Eguchi, K. Iwanaga, 2003, Annals of neurology.

Interferon‐alpha and dexamethasone inhibit adhesion of T cells to endothelial cells and synovial cells

S. Nagataki, K. Eguchi, Y. Kawabe, 1992, Clinical and experimental immunology.

Thymus histology and concomitant autoimmune diseases in Japanese patients with muscle‐specific receptor tyrosine kinase‐antibody‐positive myasthenia gravis

T. Fukuda, H. Shiraishi, R. Nakata, 2013, European journal of neurology.