N. Hattori

发表

Type I (transthyretin Met30) familial amyloid polyneuropathy in Japan: early- vs late-onset form.

G. Sobue, S. Ikeda, M. Nakazato, 2002, Archives of neurology.

Wide range of lineages of cells expressing nerve growth factor mRNA in the nerve lesions of patients with vasculitic neuropathy: An implication of endoneurial macrophage for nerve regeneration

G. Sobue, N. Mitsuma, F. Tanaka, 2004, Neuroscience.

Nonmyelinating Schwann Cell Involvement With Well-Preserved Unmyelinated Axons in Charcot-Marie-Tooth Disease Type 1A

G. Sobue, H. Yoshikawa, M. Katsuno, 2007, Journal of neuropathology and experimental neurology.

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.

The significance of carpal tunnel syndrome in transthyretin Val30Met familial amyloid polyneuropathy

G. Sobue, S. Ikeda, Y. Ando, 2009, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Mortality and morbidity in peripheral neuropathy associated Churg-Strauss syndrome and microscopic polyangiitis.

G. Sobue, H. Koike, K. Misu, 2002, The Journal of rheumatology.

Spatial Distribution of Nerve Fiber Pathology and Vasculitis in Microscopic Polyangiitis-Associated Neuropathy

G. Sobue, M. Tomita, M. Katsuno, 2011, Journal of neuropathology and experimental neurology.

A novel missense mutation in the early growth response 2 gene associated with late-onset Charcot–Marie–Tooth disease type 1

G. Sobue, K. Chihara, K. Misu, 2001, Journal of the Neurological Sciences.

Expression of glial cell line-derived neurotrophic factor and GDNFR-α mRNAs in human peripheral neuropathies

G. Sobue, N. Mitsuma, M. Nagamatsu, 1998, Brain Research.

Differential response to intravenous immunoglobulin (IVIg) therapy among multifocal and polyneuropathy types of painful diabetic neuropathy

G. Sobue, Hirohisa Watanabe, H. Koike, 2010, Journal of Clinical Neuroscience.

Paradoxical brain embolism induced by Mycoplasma pneumoniae infection with deep venous thrombus.

G. Sobue, N. Atsuta, Hirohisa Watanabe, 2010, Internal medicine.

Expression of mRNAs for Ciliary Neurotrophic Factor (CNTF), Leukemia Inhibitory Factor (LIF), Interleukin-6 (IL-6), and Their Receptors (CNTFRα, LIFRβ, IL-6Rα, and gp130) in Human Peripheral Neuropathies

G. Sobue, N. Mitsuma, Masahiko Yamamoto, 2004, Neurochemical Research.

A case of azygos anterior cerebral artery dissection with subarachnoid hemorrhage and hemorrhagic infarct during treatment for cerebral infarction

M. Tomita, N. Hattori, Shohei Ikeda, 2021, Japanese Journal of Stroke.

Glu528del in NEFL is a polymorphic variant rather than a disease-causing mutation for Charcot-Marie-Tooth disease in Japan

G. Sobue, Masahiko Yamamoto, N. Hattori, 2004, Neurogenetics.

Identification of novel sequence variants in the neurofilament‐light gene in a Japanese population: analysis of Charcot‐Marie‐Tooth disease patients and normal individuals

G. Sobue, H. Koike, K. Misu, 2002, Journal of the peripheral nervous system : JPNS.

Parallel expression of neurotrophic factors and their receptors in chronic inflammatory demyelinating polyneuropathy

G. Sobue, N. Mitsuma, Masahiko Yamamoto, 2002, Muscle & nerve.

Clinicopathologic features of nonsystemic vasculitic neuropathy and microscopic polyangiitis-associated neuropathy: A comparative study

G. Sobue, M. Katsuno, F. Tanaka, 2006, Journal of the Neurological Sciences.

Nerve excitability properties in Charcot-Marie-Tooth disease type 1A.

G. Sobue, K. Asanuma, R. Kaji, 2004, Brain : a journal of neurology.

Mutations in the peripheral myelin protein zero and connexin32 genes detected by non‐isotopic RNase cleavage assay and their phenotypes in Japanese patients with Charcot‐Marie‐Tooth disease

G. Sobue, M. Doyu, Masahiko Yamamoto, 2000, Human mutation.

Clinicopathological features of chronic inflammatory demyelinating polyradiculoneuropathy in childhood

G. Sobue, Koji Yamamoto, M. Nagamatsu, 1998, Journal of the Neurological Sciences.

Myopathy in thiamine deficiency: Analysis of a case

G. Sobue, Hirohisa Watanabe, H. Koike, 2006, Journal of the Neurological Sciences.

Intravenous immunoglobulin treatment for painful sensory neuropathy associated with Sjögren's syndrome

G. Sobue, M. Katsuno, F. Tanaka, 2009, Journal of the Neurological Sciences.

Slowly progressive autonomic neuropathy with antiganglionic acetylcholine receptor antibody

G. Sobue, M. Katsuno, H. Koike, 2010, Journal of Neurology, Neurosurgery & Psychiatry.

G. Sobue, N. Mitsuma, Masahiko Yamamoto, 2003, Internal medicine.

G. Sobue, N. Mitsuma, Masahiko Yamamoto, 2001, Muscle & nerve.

The wide spectrum of clinical manifestations in Sjögren's syndrome-associated neuropathy.

Fumiaki Tanaka, Mari Yoshida, Gen Sobue, 2005, Brain : a journal of neurology.

Clinicopathologic and genetic features of early- and late-onset FAP type I (FAP ATTR Val30Met) in Japan

G. Sobue, S. Ikeda, M. Nakazato, 2003, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Rapidly developing weakness mimicking Guillain-Barré syndrome in beriberi neuropathy: two case reports.

G. Sobue, F. Tanaka, H. Koike, 2008, Nutrition.

Alcoholic neuropathy is clinicopathologically distinct from thiamine‐deficiency neuropathy

G. Sobue, M. Hirayama, H. Koike, 2003, Annals of neurology.

Single nucleotide polymorphism of TAG-1 influences IVIg responsiveness of Japanese patients with CIDP

G. Sobue, N. Hattori, M. Katsuno, 2009, Neurology.

Postgastrectomy polyneuropathy with thiamine deficiency is identical to beriberi neuropathy.

G. Sobue, M. Hirayama, H. Koike, 2004, Nutrition.

International ward rounds Rapidly developing weakness mimicking Guillain-Barré syndrome in beriberi neuropathy: Two case reports

G. Sobue, F. Tanaka, H. Koike, 2008 .

Demyelinating and axonal features of Charcot-Marie-Tooth disease with mutations of myelin-related proteins (PMP22, MPZ and Cx32): a clinicopathological study of 205 Japanese patients.

G. Sobue, K. Nakashima, J. Kira, 2003, Brain : a journal of neurology.