K. Arimura

K. Arimura, M. Nakagawa, S. Izumo, 1996, Journal of acquired immune deficiency syndromes and human retrovirology : official publication of the International Retrovirology Association.

Voltage-gated potassium channel antibodies associated limbic encephalitis in a patient with invasive thymoma

K. Arimura, H. Kawakami, T. Kohriyama, 2006, Journal of the Neurological Sciences.

HTLV‐I viral escape and host genetic changes in the development of adult T cell leukemia

K. Arimura, S. Izumo, M. Osame, 2006, International journal of cancer.

Chronic sensory ataxic neuropathy and ophthalmoplegia with oculomotor nerve hypertrophy associated with IgM antibodies against gangliosides containing disialosyl groups.

K. Arimura, M. Osame, F. Umehara, 1997, Journal of neurology, neurosurgery, and psychiatry.

Different manners of sarcoglycan expression in genetically proven α-sarcoglycan deficiency and γ-sarcoglycan deficiency

K. Arimura, M. Nakagawa, M. Osame, 1998, Acta Neuropathologica.

Different manners of sarcoglycan expression in genetically proven alpha-sarcoglycan deficiency and gamma-sarcoglycan deficiency.

K. Arimura, M. Nakagawa, M. Osame, 1998, Acta Neuropathologica.

Eosinophilic pneumonia with eosinophilic gastroenteritis.

K. Arimura, M. Osame, I. Higashimoto, 1999, Internal medicine.

Abnormal expression of proteoglycans in Ullrich's disease with collagen VI deficiency

K. Arimura, M. Osame, I. Higuchi, 2006, Muscle & nerve.

Vacuolar myositis with expression of both MHC class I and class II antigens on skeletal muscle fibers

M. Nerenberg, K. Arimura, M. Osame, 1991, Journal of the Neurological Sciences.

Therapeutic trials in 200 patients with HTLV-I-associated myelopathy/ tropical spastic paraparesis.

K. Arimura, M. Nakagawa, S. Izumo, 1996, Journal of neurovirology.

Longer dinucleotide repeat polymorphism in matrix metalloproteinase-9 (MMP-9) gene promoter which correlates with higher HTLV-I Tax mediated transcriptional activity influences the risk of HTLV-I associated myelopathy/tropical spastic paraparesis (HAM/TSP)

K. Arimura, S. Izumo, M. Osame, 2004, Journal of Neuroimmunology.

Clinical symptoms and the odds of human T-cell lymphotropic virus type 1-associated myelopathy/ tropical spastic paraparesis (HAM/TSP) in healthy virus carriers: Application of best-fit logistic regression equation based on host genotype, age, and provirus load

K. Arimura, S. Izumo, M. Osame, 2006, Journal of NeuroVirology.

Pathological changes in skeletal muscle in HTLV-I-associated myelopathy

K. Arimura, M. Osame, I. Higuchi, 1992, Journal of the Neurological Sciences.

Killer cell immunoglobulin‐like receptor/3DL2 expression in adult T‐cell leukaemia

K. Arimura, M. Osame, R. Kubota, 2007, British journal of haematology.

Clinical electrophysiologic studies of HTLV-I-associated myelopathy.

K. Arimura, R. Rosales, M. Osame, 1987, Archives of neurology.

Neuro-ophthalmological abnormalities in HTLV-I associated myelopathy

K. Arimura, Y. Arimura, A. Igata, 1987 .

Skeletal muscle abnormalities in two patients with dystonia

K. Arimura, M. Osame, I. Higuchi, 2002, Acta Neuropathologica.

IgM‐containing fraction suppressed voltage‐gated potassium channels in acquired neuromyotonia

K. Arimura, M. Kameyama, M. Osame, 2006, Acta neurologica Scandinavica.

Experimental simvastatin-induced myopathy in rabbits

K. Arimura, M. Nakagawa, M. Osame, 1992, Journal of the Neurological Sciences.

Polyneuropathy with minifascicle formation in a patient with 46XY mixed gonadal dysgenesis

K. Arimura, M. Osame, F. Umehara, 1999, Acta Neuropathologica.

Increased frequency of CD4+T cells expressing fractalkine receptor CX3CR1 in patients with HTLV-1 associated myelopathy/tropical spastic paraparesis (HAM/TSP), but its AIDS susceptible polymorphisms are not associated with the disease

K. Arimura, Y. Ohara, S. Izumo, 2008, Journal of the Neurological Sciences.

Diseases among men living in human T-lymphotropic virus type I endemic areas in Japan.

K. Arimura, M. Osame, T. Matsuzaki, 1993, Internal medicine.

Electroencephalographic abnormalities in human T-cell lymphotropic virus type I-associated myelopathy.

K. Arimura, M. Osame, Y. Arimura, 1989, Archives of neurology.

Characteristic expression of cell adhesion molecules in adhalin deficiency

K. Arimura, M. Nakagawa, M. Osame, 1996, Journal of the Neurological Sciences.

Expression of vascular endothelial growth factor in sera and lymph nodes of the plasma cell type of Castleman's disease

A. Utsunomiya, I. Kitajima, K. Arimura, 1999, British journal of haematology.

Effects of omega-3 polyunsaturated fatty acids on inflammatory markers in COPD.

K. Arimura, M. Osame, W. Matsuyama, 2005, Chest.

A prospective uncontrolled trial of fermented milk drink containing viable Lactobacillus casei strain Shirota in the treatment of HTLV-1 associated myelopathy/tropical spastic paraparesis

K. Arimura, S. Izumo, M. Osame, 2005, Journal of the Neurological Sciences.

Treatment for POEMS (polyneuropathy, organomegaly, endocrinopathy, M-protein, and skin changes) syndrome.

A. Dispenzieri, K. Arimura, C. Nakaseko, 2012, The Cochrane database of systematic reviews.

Predictive value of serial platelet count and VEGF determination for the management of DIC in the Crow-Fukase (POEMS) syndrome.

I. Maruyama, K. Arimura, T. Hashiguchi, 2003, Internal medicine.

Circulating levels of MMP-1, -2, -3, -9, and TIMP-1 are increased in POEMS syndrome

K. Arimura, E. Matsuura, T. Hashiguchi, 2001, Neurology.

Treatment for POEMS (polyneuropathy, organomegaly, endocrinopathy, M-protein, and skin changes) syndrome.

A. Dispenzieri, K. Arimura, S. Kuwabara, 2008, The Cochrane database of systematic reviews.

Diagnostic value of serum peptidome analyses for protease activated pathological conditions beyond cancer diagnosis.

S. Natsugoe, I. Maruyama, K. Arimura, 2009, Medical hypotheses.

Histopathological and ultrastructural features of feline hereditary cerebellar cortical atrophy: a novel animal model of human spinocerebellar degeneration

K. Arimura, Y. Isashiki, S. Izumo, 1998, Acta Neuropathologica.

Notice of retraction: Increased expression of TRAIL receptor 3 on eosinophils in Churg-Strauss syndrome (Arthritis Rheum 2007;56:662-73).

K. Arimura, T. Wada, M. Osame, 2008, Arthritis & Rheumatism.

Hermansky-Pudlak syndrome with a novel mutation.

K. Arimura, M. Osame, W. Matsuyama, 2005, Internal medicine.

Neurologic manifestations of Kanzaki disease

K. Arimura, Y. Kurono, M. Osame, 2004, Neurology.

The effects of shounousui on the three responses of the blink reflex in man

S. Suwazono, K. Arimura, M. Osame, 1997, Muscle & nerve.

Different pattern of HSP47 expression in skeletal muscle of patients with neuromuscular diseases

K. Arimura, E. Matsuura, M. Osame, 2007, Neuromuscular Disorders.

Enlarged, multifocal upper limb neuropathy with HTLV-I associated myelopathy in a patient with chronic adult T-cell leukemia

K. Arimura, F. Umehara, K. Higashi, 2008, Journal of the Neurological Sciences.

Role of Kenae/CCDC125 in cell motility through the deregulation of RhoGTPase.

A. Fukamizu, J. Ishida, S. Aratani, 2009, International journal of molecular medicine.

Fine mapping of 16q-linked autosomal dominant cerebellar ataxia type III in Japanese families

K. Arimura, M. Nakagawa, R. Hirano, 2004, Neurogenetics.

Autosomal dominant early onset dementia and leukoencephalopathy in a Japanese family: clinical, neuroimaging and genetic studies

K. Arimura, M. Nakagawa, M. Nagai, 1997, Journal of the Neurological Sciences.

Highly accumulated platelet vascular endothelial growth factor in coagulant thrombotic region

I. Maruyama, K. Arimura, T. Hashiguchi, 2003, Journal of thrombosis and haemostasis : JTH.

The main HTLV-I-harboring cells in the muscles of viral carriers with polymyositis are not macrophages but CD4+ lymphocytes

K. Arimura, M. Nakagawa, R. Rosales, 1996, Acta Neuropathologica.

Detection of HTLV‐I provirus by in situ polymerase chain reaction in mononuclear inflammatory cells in skeletal muscle of viral carriers with polymyositis

K. Arimura, M. Nakagawa, S. Izumo, 1995, Muscle & nerve.

Involvement of enhanced sensitivity of N-methyl-d-aspartate receptors in vulnerability of developing cortical neurons to methylmercury neurotoxicity

H. Nakanishi, K. Murao, S. Moriguchi, 2001, Brain Research.

Capillary changes in skeletal muscle of patients with Ullrich's disease with collagen VI deficiency

K. Arimura, M. Nakagawa, T. Hashiguchi, 2003, Acta Neuropathologica.

Cross-Sectional Analysis of Neurological Findings among Healthy Elderly: Study in a Remote Island in Kagoshima, Japan

S. Akiba, K. Arimura, M. Nakagawa, 2001, Neuroepidemiology.

MRI studies of spinal visceral larva migrans syndrome

K. Arimura, E. Matsuura, M. Osame, 2006, Journal of the Neurological Sciences.

HTLV-I-associated myelopathy (HAM): epidemiology, clinical features, and pathomechanism

I. Maruyama, K. Arimura, M. Nakagawa, 1992 .

Frameshift mutation in the collagen VI gene causes Ullrich's disease

K. Arimura, M. Nakagawa, T. Hashiguchi, 2001, Annals of neurology.

Molecular mechanism of rigid spine with muscular dystrophy type 1 caused by novel mutations of selenoprotein N gene

K. Arimura, M. Nakagawa, R. Hirano, 2006, Neurogenetics.

Serum levels of vascular endothelial growth factor dependent on the stage progression of lung cancer.

K. Arimura, T. Hashiguchi, M. Osame, 2000, Chest.

Reference values for voluntary and stimulated single-fibre EMG using concentric needle electrodes: A multicentre prospective study

T. Komori, M. Sonoo, N. Kokubun, 2012, Clinical Neurophysiology.

Guidelines for single fiber EMG

Donald B. Sanders, Erik Stålberg, Kimiyoshi Arimura, 2019, Clinical Neurophysiology.

Spinocerebellar ataxia with axonal neuropathy.

Kimiyoshi Arimura, Hiroshi Takashima, J. Champoux, 2010, Advances in experimental medicine and biology.

A new type of hereditary motor and sensory neuropathy linked to chromosome 3

K. Arimura, M. Nakagawa, S. Izumo, 1997, Annals of neurology.

SET binding factor 2 (SBF2) mutation causes CMT4B with juvenile onset glaucoma

M Nakagawa, J. Lupski, C. Boerkoel, 2004, Neurology.

Genetically Confirmed Patients with Merosin-deficient Congenital Muscular Dystrophy in China

K. Arimura, H. Takashima, I. Higuchi, 2008, Neuropediatrics.

Genetic Stability of Human T Lymphotropic Virus Type I despite Antiviral Pressures by CTLs1

T. Gojobori, Kousuke Hanada, K. Arimura, 2007, The Journal of Immunology.

Association of AKT1 haplotype with the risk of schizophrenia in Iranian population

M. R. Sargolzaee, K. Arimura, H. Najmabadi, 2006, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

A new phenotype of mitochondrial disease characterized by familial late-onset predominant axial myopathy and encephalopathy

K. Arimura, H. Takashima, Y. Okamoto, 2011, Acta Neuropathologica.

Pathological characteristics of skeletal muscle in Ullrich's disease with collagen VI deficiency

K. Arimura, M. Nakagawa, M. Osame, 2003, Neuromuscular Disorders.

ApaI polymorphism of vitamin D receptor gene is associated with susceptibility to HTLV-1-associated myelopathy/tropical spastic paraparesis in HTLV-1 infected individuals

K. Arimura, S. Izumo, M. Osame, 2005, Journal of the Neurological Sciences.

Necrotising vasculitis with conduction block in mononeuropathy multiplex with cold agglutinins

K. Arimura, M. Osame, F. Umehara, 1999, Journal of neurology, neurosurgery, and psychiatry.

In vivo expression of the HBZ gene of HTLV-1 correlates with proviral load, inflammatory markers and disease severity in HTLV-1 associated myelopathy/tropical spastic paraparesis (HAM/TSP)

Kousuke Saito, M. Matsuoka, J. Yasunaga, 2009, Retrovirology.

Microvascular endothelial abnormality in skeletal muscle from a patient with gastric cancer without dermatomyositis

K. Arimura, M. Nakagawa, M. Osame, 2000, Acta Neuropathologica.

Genetic variability in the extracellular matrix protein as a determinant of risk for developing HTLV-I-associated neurological disease

K. Arimura, S. Izumo, C. Bangham, 2006, Immunogenetics.

Early clinical signs and imaging findings in Gerstmann–Sträussler–Scheinker syndrome (Pro102Leu)

K. Arimura, R. Hirano, H. Takashima, 2006, Neurology.

Polymorphism in the interleukin-10 promoter affects both provirus load and the risk of human T lymphotropic virus type I-associated myelopathy/tropical spastic paraparesis.

Mitsuhiro Osame, Kimiyoshi Arimura, Alun L Lloyd, 2004, The Journal of infectious diseases.

An overexpression of fibroblast growth factor (FGF) and FGF receptor 4 in a severe clinical phenotype of facioscapulohumeral muscular dystrophy

K. Arimura, M. Osame, I. Higuchi, 2000, Muscle & nerve.

Mechanomyographic determination of post-activation potentiation in myopathies

K. Arimura, M. Osame, I. Higuchi, 2006, Clinical Neurophysiology.

New missense mutation in the alpha-sarcoglycan gene in a Japanese patient with severe childhood autosomal recessive muscular dystrophy with incomplete alpha-sarcoglycan deficiency

K. Arimura, M. Nakagawa, M. Osame, 1997, Journal of the Neurological Sciences.

Alteration of cytokine levels by fosfomycin and prednisolone in spontaneous proliferation of cultured lymphocytes from patients with HTLV-I-associated myelopathy (HAM/TSP)

K. Arimura, Y. Yamano, M. Osame, 1997, Journal of the Neurological Sciences.

Predictive value of the prolonged exercise test in hypokalemic paralytic attack

S. Suwazono, K. Arimura, M. Osame, 1995, Muscle & nerve.

[Crow-Fukase (POEMS) syndrome].

K. Arimura, T. Hashiguchi, M. Osame, 2000, Ryoikibetsu shokogun shirizu.

[Recent advance in neuroimmunology].

K. Arimura, M. Osame, 1998, Rinsho shinkeigaku = Clinical neurology.

Deletion in chromosome 17p11.2 including the peripheral myelin protein-22 (PMP-22) gene in hereditary neuropathy with liability to pressure palsies

K. Arimura, M. Nakagawa, S. Izumo, 1995, Journal of the Neurological Sciences.

Clinical electrophysiologic tests and genotype correlations in muscle channelopathies.

K. Arimura, Y. Arimura, 2004, Supplements to Clinical neurophysiology.

[The electrophysiologic diagnosis for muscle ion channelopathies].

K. Arimura, Tomonori Nakamura, H. Takashima, 2012, Rinsho shinkeigaku = Clinical neurology.

Statistically significant differences in the number of CD24 positive muscle fibers and satellite cells between sarcoglycanopathy and age-matched Becker muscular dystrophy patients.

K. Arimura, M. Nakagawa, M. Osame, 1999, Internal medicine.

Serum VEGF increases in diabetic polyneuropathy, particularly in the neurologically active symptomatic stage

K. Arimura, T. Hashiguchi, T. Deguchi, 2009, Diabetic medicine : a journal of the British Diabetic Association.

Cerebrovascular disorders and genetic polymorphisms: mitochondrial DNA5178C is predominant in cerebrovascular disorders

S. Akiba, K. Arimura, M. Nakagawa, 2002, Journal of the Neurological Sciences.

Posterior interosseous nerve syndrome with hourglass-like fascicular constriction of the nerve

K. Arimura, S. Yoshino, M. Osame, 2003, Journal of the Neurological Sciences.

Long-term follow-up study of health status in population living in methylmercury-polluted area.

T. Inaoka, T. Kitano, M. Nagano, 2005, Environmental sciences : an international journal of environmental physiology and toxicology.

[n-Hexane polyneuropathy presenting with CIDP-like features].

K. Arimura, E. Matsuura, M. Osame, 2006, Nihon Naika Gakkai zasshi. The Journal of the Japanese Society of Internal Medicine.

Short communication Enlarged, multifocal upper limb neuropathy with HTLV-I associated myelopathy in a patient with chronic adult T-cell leukemia

K. Arimura, F. Umehara, K. Higashi, 2008 .

[Sensory function test and Achilles tendon reflex for the diagnosis and staging of diabetic neuropathies].

K. Arimura, T. Deguchi, 2005, Nihon rinsho. Japanese journal of clinical medicine.

Satoyoshi syndrome has antibody against brain and gastrointestinal tissue

K. Arimura, E. Matsuura, W. Matsuyama, 2007, Muscle & nerve.

Electrophysiological studies in cerebrotendinous xanthomatosis.

K. Arimura, Y. Tokimura, M. Osame, 1992, Journal of neurology, neurosurgery, and psychiatry.

Reversible F‐wave hyperexcitability associated with antibodies to potassium channels in Isaacs' syndrome

K. Arimura, M. Baba, M. Matsunaga, 1999, European journal of neurology.

Adult‐type metachromatic leukodystrophy with compound heterozygous ARSA mutations: A case report and phenotypic comparison with a previously reported case

K. Arimura, A. Sano, Y. Okamoto, 2011, Psychiatry and clinical neurosciences.

Electron microscopic abnormalities of skeletal muscle in patients with collagen VI deficiency in Ullrich's disease

I. Maruyama, K. Arimura, M. Nakagawa, 2002, Acta Neuropathologica.

[Two lung adenocarcinoma patients with multiple brain metastasis treated with Gefitinib and surviving more than 2 years].

K. Arimura, M. Osame, W. Matsuyama, 2006, Nihon Kokyuki Gakkai zasshi = the journal of the Japanese Respiratory Society.

Case of Morvan syndrome with anti‐Ma2/Ta antibodies

N. Hattori, T. Nakazato, K. Arimura, 2016 .

[Increased vascular endothelial growth factor (VEGF) is causative in Crow-Fukase syndrome].

K. Arimura, 1999, Rinsho shinkeigaku = Clinical neurology.

Isaacs' syndrome successfully treated by immunoadsorption plasmapheresis

S. Sakoda, Y. Nakatsuji, K. Arimura, 2000, Acta neurologica Scandinavica.

Reduced Foxp3 expression with increased cytomegalovirus-specific CTL in HTLV-I-associated myelopathy

Yuetsu Tanaka, K. Arimura, R. Hirano, 2008, Journal of Neuroimmunology.

Contralateral early blink reflex in patients with HTLV-I associated myelopathy/tropical spastic paraparesis

K. Arimura, M. Osame, Y. Arimura, 1995, Journal of the Neurological Sciences.

[Pathomechanism of autoantibody production in neurological disorders].

K. Arimura, O. Watanabe, 2008, Nihon rinsho. Japanese journal of clinical medicine.

Antibodies to potassium channels pc12 in serum of Isaacs' syndrome: Western blot and immunohistochemical studies

I. Kitajima, K. Arimura, M. Osame, 1997, Muscle & nerve.

Botulinum neurotoxin injections for muscle-based (dystonia and spasticity) and non-muscle-based (neuropathic pain) pain disorders: a meta-analytic study

P. Kaňovský, D. Dressler, H. Fernandez, 2020, Journal of Neural Transmission.

Median neuropathy at the wrist as an early manifestation of diabetic neuropathy

K. Arimura, Tomonori Nakamura, H. Takashima, 2014, Journal of diabetes investigation.

Effects of thymectomy on late-onset myasthenia gravis without thymoma

K. Arimura, S. Kuwabara, T. Fukutake, 2007, Clinical Neurology and Neurosurgery.

Mechanism of action of voltage‐gated K+ channel antibodies in acquired neuromyotonia

K. Arimura, M. Kameyama, M. Osame, 2004, Annals of neurology.

[Immune-mediated neuromyotonia (Isaacs' syndrome)--clinical aspects and pathomechanism].

K. Arimura, O. Watanabe, 2010, Brain and nerve = Shinkei kenkyu no shinpo.

Protective effect of MK-801 in methyl mercury induced neuronal injury

K. Murao, K. Arimura, K. Eto, 1998, Neuroscience Research.

Clinical investigation of the lesions responsible for sensory disturbance in Minamata disease.

K. Arimura, M. Nakagawa, Y. Ando, 2001, The Tohoku journal of experimental medicine.

[A patient of ADEM with central and peripheral conduction block improved with ultra-high-dose methylprednisolone].

K. Arimura, M. Osame, A. Uehara, 2002, Rinsho shinkeigaku = Clinical neurology.

PS-19-10 Antibodies to potassium channel in Isaacs syndrome and other neurological disorders

Osamu Watanabe, Mitsuhiro Osame, Kimiyoshi Arimura, 1995 .

A null mutation in basigin, an immunoglobulin superfamily member, indicates its important roles in peri-implantation development and spermatogenesis.

K. Yamamura, K. Arimura, T. Senda, 1998, Developmental biology.

Outbreak of Bronchiolitis obliterans Associated with Consumption of Sauropus androgynus in Japan – Alert of Food-Associated Pulmonary Disorders from Japan

K. Arimura, K. Imaizumi, T. Ogura, 2005, Respiration.

Comparative electrophysiological study of response to botulinum toxin type B in Japanese and Caucasians

R. Kaji, K. Arimura, Tomonori Nakamura, 2008, Movement disorders : official journal of the Movement Disorder Society.

[Crow-Fukase syndrome and VEGF].

K. Arimura, T. Hashiguchi, O. Watanabe, 2008, Brain and nerve = Shinkei kenkyu no shinpo.

[Two cases of POEMS syndrome with increased vascular endothelial growth factor (VEGF)].

I. Maruyama, K. Arimura, O. Watanabe, 1997, Rinsho shinkeigaku = Clinical neurology.

A hemophiliac with human immunodeficiency virus (HIV)-1-associated dementia complex.

K. Arimura, M. Osame, Y. Maruyama, 1995, Internal medicine.

Prevalence and incidence rates of chronic inflammatory demyelinating polyneuropathy in the Japanese population

G. Sobue, N. Hattori, A. Tamakoshi, 2008, Journal of Neurology, Neurosurgery, and Psychiatry.

[A case of bronchiolitis obliterans syndrome successfully treated by Tiotropium bromide].

K. Arimura, M. Osame, W. Matsuyama, 2006, Nihon Kokyuki Gakkai zasshi = the journal of the Japanese Respiratory Society.

Accumulation of human T-lymphotropic virus type I (HTLV-I)-infected cells in the cerebrospinal fluid during the exacerbation of HTLV-I-associated myelopathy

K. Arimura, Tomonori Nakamura, S. Izumo, 2011, Journal of NeuroVirology.

Recent studies on the epidemiology, clinical features and pathogenic mechanisms of HTLV-I associated myelopathy (HAM/TSP) and other diseases associated to HTLV.

K. Arimura, M. Nakagawa, S. Izumo, 1997, Journal of neurovirology.

[A case of myasthenia gravis associated with systemic lupus erythematosus and pemphigus erythematosus].

K. Arimura, F. Umehara, K. Itoh, 1997, Rinsho shinkeigaku = Clinical neurology.

The effects of tobacco smoking on the short, middle, and long latency responses of the blink reflex in humans.

S. Suwazono, K. Arimura, S. Takenaga, 1997, Journal of clinical neurophysiology : official publication of the American Electroencephalographic Society.

Spinocerebellar ataxia with axonal neuropathy: consequence of a Tdp1 recessive neomorphic mutation?

K. Choi, K. Arimura, R. Hirano, 2007, The EMBO journal.

Novel mutations identified in patients with a mild phenotype of Ullrich congenital muscular dystrophy through targeted next‐generation sequencing

K. Arimura, E. Matsuura, H. Takashima, 2013 .

Diagnostic value of serum peptidome analyses for protease activated pathological conditions beyond cancer diagnosis.

S. Natsugoe, I. Maruyama, K. Arimura, 2009, Medical hypotheses.

Intraepidermal nerve fiber density and nerve conduction study parameters correlate with clinical staging of diabetic polyneuropathy.

S. Yagihashi, K. Sugimoto, K. Arimura, 2013, Diabetes research and clinical practice.

Rippling muscle syndrome.

K. Arimura, 2002, Internal medicine.

Safety and efficacy of interferon-α in 167 patients with human T-cell lymphotropic virus type 1-associated myelopathy

Y. Itoyama, J. Kira, K. Arimura, 2007, Journal of NeuroVirology.

Activation of discoidin domain receptor 1 on CD14-positive bronchoalveolar lavage fluid cells induces chemokine production in idiopathic pulmonary fibrosis (Journal of Immunology (2005) 174, (6490-6498))

K. Arimura, T. Yoshimura, M. Osame, 2008 .

This information is current as Inflammation by RNA Interference Attenuates Lung Suppression of Discoidin Domain Receptor 1 Mistuhiro Osame and

K. Arimura, R. Hirano, M. Osame, 2006 .