J. Fujitake

发表

Natural history of transthyretin Val30Met familial amyloid polyneuropathy: analysis of late-onset cases from non-endemic areas

G. Sobue, Takeo Kato, T. Kawanami, 2012, Journal of Neurology, Neurosurgery & Psychiatry.

rt-PA with Antithrombotic Therapies in a Case with Capsular Warning Syndrome

J. Fujitake, M. Kawamura, Yasuhiro Fuseya, 2017, Internal medicine.

Distinct characteristics of amyloid deposits in early- and late-onset transthyretin Val30Met familial amyloid polyneuropathy

G. Sobue, Y. Ando, M. Katsuno, 2009, Journal of the Neurological Sciences.

Immunohistochemical evaluation of the neurotoxic effects of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) on dopaminergic nigrostriatal neurons of young adult mice using dopamine and tyrosine hydroxylase antibodies

J. Fujitake, Y. Sano, S. Kuno, 1988, Neuroscience Letters.

Atypical Familial Amyotrophic Lateral Sclerosis with Slowly Progressing Lower Extremities-predominant Late-onset Muscular Weakness and Atrophy

S. Tsuji, H. Ishiura, J. Mitsui, 2019, Internal medicine.

Identification of a new homozygous frameshift insertion mutation in the SIL1 gene in 3 Japanese patients with Marinesco–Sjögren syndrome

J. Fujitake, M. Eriguchi, Y. Kuroda, 2008, Journal of the Neurological Sciences.

Four Cases of Cerebral Venous Sinus Thrombosis

K. Hayakawa, J. Fujitake, K. Takasu, 2002, European Neurology.

Leber's hereditary optic neuropathy with intracranial arteriovenous malformation: a case report.

I. Nonaka, Yu‐ichi Goto, J. Fujitake, 2002, Acta neurologica Belgica.

[Neuroleptic malignant syndrome-like state in eight patients with parkinsonism].

J. Fujitake, S. Kuno, H. Nishitani, 1984, Rinsho shinkeigaku = Clinical neurology.

GCH1 mutations in dopa-responsive dystonia and Parkinson’s disease

Y. Shimo, G. Oyama, N. Hattori, 2018, Journal of Neurology.

[Imported trichinellosis with severe myositis--report of a case].

J. Fujitake, N. Arizono, Y. Tatsuoka, 1999, Kansenshogaku zasshi. The Journal of the Japanese Association for Infectious Diseases.

Idiopathic hypertrophic cranial pachymeningitis associated with hydrocephalus and myocarditis

J. Fujitake, M. Tanaka, Y. Tatsuoka, 1996, Neurology.

A case of Marinesco-Sjögren syndrome: MRI observations of skeletal muscles, bone metabolism, and treatment with testosterone and risedronate.

Y. Hataya, Y. Komatsu, J. Fujitake, 2011, Internal medicine.

Late-onset familial amyloid polyneuropathy: An autopsy study of two Japanese brothers

J. Fujitake, K. Takasu, K. Saida, 2003, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

[A case of phenytoin intoxication induced by hypothyroidism].

J. Fujitake, S. Shimbo, K. Horii, 1991, Rinsho shinkeigaku = Clinical neurology.

l-2-Hydroxyglutaric aciduria: two Japanese adult cases in one family

K. Hayakawa, N. Terada, J. Fujitake, 1999, Journal of Neurology.

[Two brother cases of late-onset familial amyloidotic polyneuropathy in Kyoto].

J. Fujitake, K. Saida, K. Horii, 1991, Rinshō shinkeigaku Clinical neurology.

[A case of anti-MuSK antibody-positive myasthenia gravis with dropped head as the initial presenting symptom].

Kaori Suzuki, J. Fujitake, S. Nakane, 2006, Rinsho shinkeigaku = Clinical neurology.

Localized polymyositis associated with chronic thyroiditis.

J. Fujitake, Y. Tatsuoka, Y. Ishikawa, 1994, The Journal of rheumatology.