نتائج البحث

The chromosome 16q-linked autosomal dominant cerebellar ataxia (16q-ADCA): A newly identified degenerative ataxia in Japan showing peculiar morphological changes of the Purkinje cell.

• Authors : Ishikawa, Kinya; Mizusawa, Hidehiro

Subjects: CEREBELLAR ataxia; CEREBELLUM diseases; IMMUNOHISTOCHEMISTRYJAPAN

• Source: Neuropathology; Oct2010, Vol. 30 Issue 5, p490-494, 5p, 4 Color Photographs

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A mutation in the low voltage-gated calcium channel CACNA1G alters the physiological properties of the channel, causing spinocerebellar ataxia.

• Authors : Morino H; Department of Epidemiology, Research Institute for Radiation Biology and Medicine, Hiroshima University, Hiroshima, 1-2-3, Kasumi, Minami-ku, Hiroshima, 734-8553, Japan. .; Matsuda Y

Subjects: Calcium Channels, T-Type/Calcium Channels, T-Type/Calcium Channels, T-Type/*genetics ; Spinocerebellar Ataxias/Spinocerebellar Ataxias/Spinocerebellar Ataxias/*genetics; Adolescent

• Source: Molecular brain [Mol Brain] 2015 Dec 29; Vol. 8, pp. 89. Date of Electronic Publication: 2015 Dec 29.Publisher: BioMed Central Country of Publication: England NLM ID: 101468876 Publication Model: Electronic Cited Medium: Internet ISSN: 1756-6606

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Progressive myoclonus epilepsy: extraneuronal brown pigment deposition and system neurodegeneration in the brains of Japanese patients with novel SCARB2 mutations.

• Authors : Fu YJ; Department of Pathology, Brain Research Institute, University of Niigata, Niigata, Japan.; Aida I

Subjects: Mutation*; Astrocytes/Astrocytes/Astrocytes/*ultrastructure ; Brain/Brain/Brain/*ultrastructure

• Source: Neuropathology and applied neurobiology [Neuropathol Appl Neurobiol] 2014 Aug; Vol. 40 (5), pp. 551-63.Publisher: Blackwell Scientific Publications Country of Publication: England NLM ID: 7609829 Publication Model: Print Cited Medium: Internet ISSN:

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On autosomal dominant cerebellar ataxia (ADCA) other than polyglutamine diseases, with special reference to chromosome 16q22.1-linked ADCA.

• Authors : Ishikawa K; Department of Neurology and Neurological Science, Graduate School, Tokyo Medical and Dental University, Japan. ; Mizusawa H

Subjects: Chromosomes, Human, Pair 16*; Brain/Brain/Brain/*pathology ; Cerebellar Ataxia/Cerebellar Ataxia/Cerebellar Ataxia/*genetics

• Source: Neuropathology : official journal of the Japanese Society of Neuropathology [Neuropathology] 2006 Aug; Vol. 26 (4), pp. 352-60.Publisher: Blackwell Science Asia Country of Publication: Australia NLM ID: 9606526 Publication Model: Print Cited Medium: Print ISSN: 0919-6544

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Neuropathology of spinocerebellar ataxia type 8: Common features and unique tauopathy.

• Authors : Yonenobu, Yuki¹ (AUTHOR); Beck, Goichi¹ (AUTHOR) ; Kido, Kansuke² (AUTHOR)

• Source: Neuropathology. Oct2023, Vol. 43 Issue 5, p351-361. 11p.

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Minamata disease.

• Authors : Eto, Komyo¹

• Source: Neuropathology. Sep2000 Supplement, Vol. 20, pS14-S19. 6p.

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Autosomal recessive spastic ataxia of Charlevoix-Saguenay.

• Authors : Takiyama Y; Division of Neurology, Department of Internal Medicine, Jichi Medical School, Tochigi, Japan.

Subjects: Brain/Brain/Brain/*pathology ; Cerebellar Ataxia/Cerebellar Ataxia/Cerebellar Ataxia/*genetics ; Cerebellar Ataxia/Cerebellar Ataxia/Cerebellar Ataxia/*pathology

• Source: Neuropathology : official journal of the Japanese Society of Neuropathology [Neuropathology] 2006 Aug; Vol. 26 (4), pp. 368-75.Publisher: Blackwell Science Asia Country of Publication: Australia NLM ID: 9606526 Publication Model: Print Cited Medium: Print ISSN: 0919-6544

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