N. Ito

发表

The role of premotor cortex and the supplementary motor area in the temporal control of movement in man.

J. Tanji, H. Freund, U. Halsband, 1993, Brain : a journal of neurology.

Histopathologic Analysis of Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CARASIL): A Report of a New Genetically Confirmed Case and Comparison to 2 Previous Cases

N. Ito, T. Niki, M. Fukayama, 2016, Journal of neuropathology and experimental neurology.

Extensive loss of arterial medial smooth muscle cells and mural extracellular matrix in cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL)

K. Arima, N. Ito, S. Ikeda, 2008, Neuropathology : official journal of the Japanese Society of Neuropathology.

Cerebral arterial pathology of CADASIL and CARASIL (Maeda syndrome)

K. Arima, N. Ito, S. Ikeda, 2003, Neuropathology : official journal of the Japanese Society of Neuropathology.

Spinal cord vascular and leptomeningeal amyloid β-protein deposition in a case with cerebral amyloid angiopathy

N. Ito, T. Tokuda, N. Yanagisawa, 2004, Acta Neuropathologica.

Identification and functional characterization of novel mutations including frameshift mutation in exon 4 of CSF1R in patients with adult-onset leukoencephalopathy with axonal spheroids and pigmented glia

David T. Jones, D. Dickson, N. Ito, 2018, Journal of Neurology.

Clinical and Pathological Studies of Familial Amyloid Polyneuropathy (FAP), with Special Reference to Nephropathy and Cardiopathy

N. Ito, N. Yanagisawa, S. Ikeda, 1986 .

Vagus nerve and celiac ganglion lesions in generalized amyloidosis A correlative study of familial amyloid polyneuropathy and AL-amyloidosis

N. Ito, N. Yanagisawa, S. Ikeda, 1987, Journal of the Neurological Sciences.

A novel CLCN1 mutation: P480T in a Japanese family with Thomsen's myotonia congenita

N. Ito, M. Uchino, E. Uyama, 2001, Muscle & nerve.

Hereditary generalized amyloidosis with polyneuropathy. Clinicopathological study of 65 Japanese patients.

N. Ito, N. Yanagisawa, H. Tsukagoshi, 1987, Brain : a journal of neurology.

AH amyloidosis associated with lymphoplasmacytic lymphoma secreting a monoclonal gamma heavy chain carrying an unusual truncated D segment.

N. Ito, F. Kametani, S. Ikeda, 2006, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy.

K. Arima, N. Ito, S. Ikeda, 2002, Neurology.

A case of autosomal dominant osteopetrosis type II with a severe bone phenotype but no amino acid converting mutation in the CLCN7 gene

N. Ito, A. Evdokiou, P. Roschger, 2021, medRxiv.

Recurrent transient topographical amnesia: a patient with frequent episodes

N. Ito, M. Satoh, H. Tomimoto, 2011, Journal of Neurology.