K. Fukushima

A. Nakamura, T. Tokuda, S. Ikeda, 2005, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Intravenous immunoglobulin (IVIg) with methylprednisolone pulse therapy for motor impairment of neuralgic amyotrophy: clinical observations in 10 cases.

H. Morita, S. Kusunoki, S. Ikeda, 2012, Internal medicine.

Imbalanced expression of dysfunctional regulatory T cells and T-helper cells relates to immunopathogenesis in polyarteritis nodosa

S. Ikeda, Y. Shimojima, W. Ishii, 2017, Modern rheumatology.

A 73-year-old patient with adult-onset type II citrullinemia successfully treated by sodium pyruvate and arginine

T. Saheki, S. Ikeda, M. Yazaki, 2013, Clinical Neurology and Neurosurgery.

Leukoencephalopathy induced by low-dose methotrexate in a patient with rheumatoid arthritis.

S. Ikeda, Y. Shimojima, M. Matsuda, 2011, Internal medicine.

Muscle CD31(-) CD45(-) side population cells promote muscle regeneration by stimulating proliferation and migration of myoblasts.

A. Uezumi, K. Imaizumi, S. Takeda, 2008, The American journal of pathology.

Differential roles of MMP-9 in early and late stages of dystrophic muscles in a mouse model of Duchenne muscular dystrophy.

A. Nakamura, S. Takeda, K. Koike, 2015, Biochimica et biophysica acta.

Follow-up of three patients with a large in-frame deletion of exons 45–55 in the Duchenne muscular dystrophy (DMD) gene

A. Nakamura, J. Koyama, Kunihiro Yoshida, 2008, Journal of Clinical Neuroscience.

Perforation of rectal diverticulum with amyloidosis secondary to rheumatoid arthritis: case report and review of the literature

N. Koide, Daisuke Takeuchi, S. Miyagawa, 2010, Clinical journal of gastroenterology.

Reversible cerebral vasoconstriction syndrome with cardiac involvement during treatment for iron deficiency anemia: caser report

A. Nakamura, Y. Takei, K. Fukushima, 2021, BMC Neurology.

[Dropped head sign and tongue atrophy in systemic sclerosis-associated myopathy: a case report].

S. Ikeda, Y. Shimojima, M. Matsuda, 2010, Rinsho shinkeigaku = Clinical neurology.

Characterization of deletion breakpoints in patients with dystrophinopathy carrying a deletion of exons 45–55 of the Duchenne muscular dystrophy (DMD) gene

A. Nakamura, Kunihiro Yoshida, S. Takeda, 2009, Journal of Human Genetics.

Corpus callosum atrophy in patients with hereditary diffuse leukoencephalopathy with neuroaxonal spheroids: an MRI-based study.

J. Kira, N. Araki, Kunihiro Yoshida, 2014, Internal medicine.

Early involvement of the corpus callosum in a patient with hereditary diffuse leukoencephalopathy with spheroids carrying the de novo K793T mutation of CSF1R.

Kunihiro Yoshida, S. Ikeda, K. Fukushima, 2013, Internal medicine.

Reversible extensive leukoencephalopathy in Sweet disease: A case report

H. Morita, Kunihiro Yoshida, S. Ikeda, 2008, Journal of the Neurological Sciences.

[A case of Wernicke-Korsakoff syndrome caused by gastrojejunostomy--specific findings of MRI and SPECT].

K. Sakajiri, M. Takamori, K. Fukushima, 1993, Rinsho shinkeigaku = Clinical neurology.

Hereditary rimmed vacuole myopathy showing interstitial amyloid deposition in muscle tissue

F. Kametani, M. Yazaki, M. Yamada, 2009, Muscle & nerve.

Activation and localization of matrix metalloproteinase-2 and -9 in the skeletal muscle of the muscular dystrophy dog (CXMDJ)

A. Nakamura, Kunihiro Yoshida, H. Ueda, 2007, BMC musculoskeletal disorders.

Like a Rolling Stone: Year-Over-Year Growth of a Rectal Fecalith

K. Fukushima, Hidenori Tomida, S. Imai, 2022, Case Reports in Gastroenterology.

Pure red cell aplasia developing after treatment of pleural recurrence of thymoma, successfully treated with cyclosporin A but not with tacrolimus.

S. Ikeda, M. Yazaki, T. Gono, 2006, Internal medicine.

Patient with adult‐onset type II citrullinemia beginning 2 years after operation for duodenal malignant somatostatinoma: Indication for liver transplantation

M. Makuuchi, Y. Iwasaki, S. Ikeda, 2013, Hepatology research : the official journal of the Japan Society of Hepatology.

Matrix metalloproteinase-2 ablation in dystrophin-deficient mdx muscles reduces angiogenesis resulting in impaired growth of regenerated muscle fibers.

A. Nakamura, Kunihiro Yoshida, S. Takeda, 2011, Human molecular genetics.

Mutations in MME cause an autosomal‐recessive Charcot–Marie–Tooth disease type 2

S. Tsuji, J. Kira, S. Morishita, 2016, Annals of neurology.

Isaacs’ syndrome associated with myasthenia gravis, showing remission after cytoreductive surgery of pleural recurrence of thymoma

T. Hashimoto, S. Ikeda, M. Yazaki, 2006, Neuromuscular Disorders.

First two cases of adult‐onset type II citrullinemia successfully treated by deceased‐donor liver transplantation in Japan

S. Ikeda, M. Yazaki, S. Miyagawa, 2012, Hepatology research : the official journal of the Japan Society of Hepatology.

USE OF MANY CELL TYPES TO DELIVER GENES IN THE JOINT

Freddie H. Fu, M. Moreland, K. Fukushima, 2000 .

Characteristic spinal MRI findings of HIV-associated myelopathy in an AIDS patient.

H. Morita, T. Hashimoto, S. Ikeda, 2005, Internal medicine.

Elderly-Onset Multiple System Atrophy with Lewy Body Pathology: A Case Report

S. Ohara, M. Yamada, Y. Takei, 2021, Case Reports in Neurology.

Migrating osteoarthralgia: a rare initial manifestation of adult leukemia.

S. Ikeda, Toshiro Ito, M. Matsuda, 2006, Internal medicine.

Reversible extensive leukoencephalopathy in Sweet disease: A case report

H. Morita, Kunihiro Yoshida, S. Ikeda, 2008, Journal of the Neurological Sciences.