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Items: 47

1.

Development of demyelinating lesions in progressive multifocal leukoencephalopathy (PML): Comparison of magnetic resonance images and neuropathology of post-mortem brain.

Ono D, Shishido-Hara Y, Mizutani S, Mori Y, Ichinose K, Watanabe M, Tanizawa T, Yokota T, Uchihara T, Fujigasaki H.

Neuropathology. 2019 Aug;39(4):294-306. doi: 10.1111/neup.12562. Epub 2019 Jun 2.

PMID:
31155757
2.

Functional evaluation of PDGFB-variants in idiopathic basal ganglia calcification, using patient-derived iPS cells.

Sekine SI, Kaneko M, Tanaka M, Ninomiya Y, Kurita H, Inden M, Yamada M, Hayashi Y, Inuzuka T, Mitsui J, Ishiura H, Iwata A, Fujigasaki H, Tamaki H, Tamaki R, Kito S, Taguchi Y, Tanaka K, Atsuta N, Sobue G, Kondo T, Inoue H, Tsuji S, Hozumi I.

Sci Rep. 2019 Apr 5;9(1):5698. doi: 10.1038/s41598-019-42115-y.

3.

Relationship Between Frequency of Spontaneous Swallowing and Salivary Substance P Level in Patients with Acute Stroke.

Niimi M, Hashimoto G, Hara T, Yamada N, Abo M, Fujigasaki H, Ide T.

Dysphagia. 2018 Aug;33(4):414-418. doi: 10.1007/s00455-017-9867-2. Epub 2017 Nov 28.

PMID:
29185035
4.

Significance of Development and Reversion of Collaterals on MRI in Early Neurologic Improvement and Long-Term Functional Outcome after Intravenous Thrombolysis for Ischemic Stroke.

Ichijo M, Iwasawa E, Numasawa Y, Miki K, Ishibashi S, Tomita M, Tomimitsu H, Kamata T, Fujigasaki H, Shintani S, Mizusawa H.

AJNR Am J Neuroradiol. 2015 Oct;36(10):1839-45. doi: 10.3174/ajnr.A4384. Epub 2015 Jul 23.

5.

Embolic stroke during apixaban therapy for left atrial appendage thrombus.

Ohyagi M, Nakamura K, Watanabe M, Fujigasaki H.

J Stroke Cerebrovasc Dis. 2015 Apr;24(4):e101-2. doi: 10.1016/j.jstrokecerebrovasdis.2014.11.031. Epub 2015 Jan 22.

PMID:
25620711
6.

Ocular flutter, generalized myoclonus, and truncal ataxia in a patient with Graves' ophthalmopathy.

Kuwahara H, Suzuki S, Matsumura K, Watanabe M, Yakushiji F, Fujigasaki H.

J Neurol. 2013 Nov;260(11):2906-7. doi: 10.1007/s00415-013-7146-1. Epub 2013 Oct 17. No abstract available.

PMID:
24132672
7.

Intravenous t-PA for the occlusion of an accessory MCA.

Kuwahara H, Matsumura K, Watanabe M, Fujigasaki H.

Intern Med. 2013;52(1):163. Epub 2013 Jan 1. No abstract available.

8.

Posterior cerebral artery laterality on magnetic resonance angiography predicts long-term functional outcome in middle cerebral artery occlusion.

Ichijo M, Miki K, Ishibashi S, Tomita M, Kamata T, Fujigasaki H, Mizusawa H.

Stroke. 2013 Feb;44(2):512-5. doi: 10.1161/STROKEAHA.112.674101. Epub 2012 Nov 27.

PMID:
23192760
9.

Autoimmune polyendocrine syndrome-3 in a patient with late-onset multiple sclerosis.

Yokote H, Nagasawa M, Ichijo M, Amino T, Fujigasaki H.

Neurologist. 2012 Mar;18(2):83-4. doi: 10.1097/NRL.0b013e318248ea2a.

PMID:
22367836
10.

[A 65-year-old man, suspicious of bacterial meningitis with rapid progression of multiple organ failure].

Fujigasaki H, Ohashi K, Fujigasaki J.

Brain Nerve. 2012 Jan;64(1):89-96. Japanese. No abstract available.

PMID:
22223507
11.

Amyloid precursor-like protein 2 cleavage contributes to neuronal intranuclear inclusions and cytotoxicity in spinocerebellar ataxia-7 (SCA7).

Takahashi-Fujigasaki J, Breidert T, Fujigasaki H, Duyckaerts C, Camonis JH, Brice A, Lebre AS.

Neurobiol Dis. 2011 Jan;41(1):33-42. doi: 10.1016/j.nbd.2010.08.016. Epub 2010 Aug 20.

PMID:
20732423
12.

The carboxy-terminal fragment of alpha(1A) calcium channel preferentially aggregates in the cytoplasm of human spinocerebellar ataxia type 6 Purkinje cells.

Ishiguro T, Ishikawa K, Takahashi M, Obayashi M, Amino T, Sato N, Sakamoto M, Fujigasaki H, Tsuruta F, Dolmetsch R, Arai T, Sasaki H, Nagashima K, Kato T, Yamada M, Takahashi H, Hashizume Y, Mizusawa H.

Acta Neuropathol. 2010 Apr;119(4):447-64. doi: 10.1007/s00401-009-0630-0. Epub 2009 Dec 31.

13.

SUMOylation attenuates the aggregation propensity and cellular toxicity of the polyglutamine expanded ataxin-7.

Janer A, Werner A, Takahashi-Fujigasaki J, Daret A, Fujigasaki H, Takada K, Duyckaerts C, Brice A, Dejean A, Sittler A.

Hum Mol Genet. 2010 Jan 1;19(1):181-95. doi: 10.1093/hmg/ddp478.

PMID:
19843541
14.

Brain perfusion abnormalities in a sibship with parkin-linked parkinsonism.

Kobayashi Z, Miake H, Fujigasaki H.

Parkinsonism Relat Disord. 2008 Nov;14(7):581-3. doi: 10.1016/j.parkreldis.2008.01.013. Epub 2008 Mar 10.

PMID:
18331811
15.
16.

Histone deacetylase (HDAC) 4 involvement in both Lewy and Marinesco bodies.

Takahashi-Fujigasaki J, Fujigasaki H.

Neuropathol Appl Neurobiol. 2006 Oct;32(5):562-6. No abstract available.

PMID:
16972890
17.

PML clastosomes prevent nuclear accumulation of mutant ataxin-7 and other polyglutamine proteins.

Janer A, Martin E, Muriel MP, Latouche M, Fujigasaki H, Ruberg M, Brice A, Trottier Y, Sittler A.

J Cell Biol. 2006 Jul 3;174(1):65-76.

18.

SUMOylation substrates in neuronal intranuclear inclusion disease.

Takahashi-Fujigasaki J, Arai K, Funata N, Fujigasaki H.

Neuropathol Appl Neurobiol. 2006 Feb;32(1):92-100.

PMID:
16409557
19.

An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nucleotide substitution in the 5' untranslated region of the gene encoding a protein with spectrin repeat and Rho guanine-nucleotide exchange-factor domains.

Ishikawa K, Toru S, Tsunemi T, Li M, Kobayashi K, Yokota T, Amino T, Owada K, Fujigasaki H, Sakamoto M, Tomimitsu H, Takashima M, Kumagai J, Noguchi Y, Kawashima Y, Ohkoshi N, Ishida G, Gomyoda M, Yoshida M, Hashizume Y, Saito Y, Murayama S, Yamanouchi H, Mizutani T, Kondo I, Toda T, Mizusawa H.

Am J Hum Genet. 2005 Aug;77(2):280-96. Epub 2005 Jul 6.

20.

A clinical and genetic study in a large cohort of patients with spinocerebellar ataxia type 6.

Takahashi H, Ishikawa K, Tsutsumi T, Fujigasaki H, Kawata A, Okiyama R, Fujita T, Yoshizawa K, Yamaguchi S, Tomiyasu H, Yoshii F, Mitani K, Shimizu N, Yamazaki M, Miyamoto T, Orimo T, Shoji S, Kitamura K, Mizusawa H.

J Hum Genet. 2004;49(5):256-64.

PMID:
15362569
21.

Amyotrophic lateral sclerosis with neuronal intranuclear protein inclusions.

Seilhean D, Takahashi J, El Hachimi KH, Fujigasaki H, Lebre AS, Biancalana V, Dürr A, Salachas F, Hogenhuis J, de Thé H, Hauw JJ, Meininger V, Brice A, Duyckaerts C.

Acta Neuropathol. 2004 Jul;108(1):81-7. Epub 2004 Apr 27.

PMID:
15114487
22.

[Two distinct types of neuropathy associated with Sjögren's syndrome developed in one patient. The importance of the selection of an appropriate therapeutic regimen].

Noguchi Y, Tsuchiyama T, Matsumoto T, Fujigasaki H, Inaba A, Yokota T, Kanda T, Mizusawa H.

Rinsho Shinkeigaku. 2003 Sep;43(9):539-43. Japanese.

PMID:
14727559
23.

[Pneumatosis intestinalis in a patient of myasthenia gravis treated with high-dose corticosteroid].

Kameyama K, Noguchi Y, Matsumoto T, Takenawa H, Fujigasaki H, Kanda T, Mizusawa H.

Rinsho Shinkeigaku. 2003 May;43(5):277-80. Japanese.

PMID:
12931635
24.

PML nuclear bodies and neuronal intranuclear inclusion in polyglutamine diseases.

Takahashi J, Fujigasaki H, Iwabuchi K, Bruni AC, Uchihara T, El Hachimi KH, Stevanin G, Dürr A, Lebre AS, Trottier Y, de Thé H, Tanaka J, Hauw JJ, Duyckaerts C, Brice A.

Neurobiol Dis. 2003 Aug;13(3):230-7.

PMID:
12901837
25.

Huntington's disease-like phenotype due to trinucleotide repeat expansions in the TBP and JPH3 genes.

Stevanin G, Fujigasaki H, Lebre AS, Camuzat A, Jeannequin C, Dode C, Takahashi J, San C, Bellance R, Brice A, Durr A.

Brain. 2003 Jul;126(Pt 7):1599-603. Epub 2003 May 6.

PMID:
12805114
26.

Two populations of neuronal intranuclear inclusions in SCA7 differ in size and promyelocytic leukaemia protein content.

Takahashi J, Fujigasaki H, Zander C, El Hachimi KH, Stevanin G, Dürr A, Lebre AS, Yvert G, Trottier Y, de Thé H, Hauw JJ, Duyckaerts C, Brice A.

Brain. 2002 Jul;125(Pt 7):1534-43.

PMID:
12077003
27.

Spinocerebellar ataxia type 10 in the French population.

Fujigasaki H, Tardieu S, Camuzat A, Stevanin G, LeGuern E, Matsuura T, Ashizawa T, Dürr A, Brice A.

Ann Neurol. 2002 Mar;51(3):408-9. No abstract available.

PMID:
11891842
28.

Similarities between spinocerebellar ataxia type 7 (SCA7) cell models and human brain: proteins recruited in inclusions and activation of caspase-3.

Zander C, Takahashi J, El Hachimi KH, Fujigasaki H, Albanese V, Lebre AS, Stevanin G, Duyckaerts C, Brice A.

Hum Mol Genet. 2001 Oct 15;10(22):2569-79.

PMID:
11709544
29.

CAG repeat expansion in the TATA box-binding protein gene causes autosomal dominant cerebellar ataxia.

Fujigasaki H, Martin JJ, De Deyn PP, Camuzat A, Deffond D, Stevanin G, Dermaut B, Van Broeckhoven C, Dürr A, Brice A.

Brain. 2001 Oct;124(Pt 10):1939-47.

PMID:
11571212
30.

Non-expanded polyglutamine proteins in intranuclear inclusions of hereditary ataxias--triple-labeling immunofluorescence study.

Uchihara T, Fujigasaki H, Koyano S, Nakamura A, Yagishita S, Iwabuchi K.

Acta Neuropathol. 2001 Aug;102(2):149-52.

PMID:
11563629
31.

Preferential recruitment of ataxin-3 independent of expanded polyglutamine: an immunohistochemical study on Marinesco bodies.

Fujigasaki H, Uchihara T, Takahashi J, Matsushita H, Nakamura A, Koyano S, Iwabuchi K, Hirai S, Mizusawa H.

J Neurol Neurosurg Psychiatry. 2001 Oct;71(4):518-20.

32.

Cytoplasmic and nuclear polyglutamine aggregates in SCA6 Purkinje cells.

Ishikawa K, Owada K, Ishida K, Fujigasaki H, Shun Li M, Tsunemi T, Ohkoshi N, Toru S, Mizutani T, Hayashi M, Arai N, Hasegawa K, Kawanami T, Kato T, Makifuchi T, Shoji S, Tanabe T, Mizusawa H.

Neurology. 2001 Jun 26;56(12):1753-6.

PMID:
11425948
33.

Ataxin-7 interacts with a Cbl-associated protein that it recruits into neuronal intranuclear inclusions.

Lebre AS, Jamot L, Takahashi J, Spassky N, Leprince C, Ravisé N, Zander C, Fujigasaki H, Kussel-Andermann P, Duyckaerts C, Camonis JH, Brice A.

Hum Mol Genet. 2001 May 15;10(11):1201-13.

PMID:
11371513
34.

Recruitment of nonexpanded polyglutamine proteins to intranuclear aggregates in neuronal intranuclear hyaline inclusion disease.

Takahashi J, Tanaka J, Arai K, Funata N, Hattori T, Fukuda T, Fujigasaki H, Uchihara T.

J Neuropathol Exp Neurol. 2001 Apr;60(4):369-76.

PMID:
11305872
35.

SCA12 is a rare locus for autosomal dominant cerebellar ataxia: a study of an Indian family.

Fujigasaki H, Verma IC, Camuzat A, Margolis RL, Zander C, Lebre AS, Jamot L, Saxena R, Anand I, Holmes SE, Ross CA, Dürr A, Brice A.

Ann Neurol. 2001 Jan;49(1):117-21.

PMID:
11198281
36.

Spinocerebellar ataxia type 6 mutation alters P-type calcium channel function.

Toru S, Murakoshi T, Ishikawa K, Saegusa H, Fujigasaki H, Uchihara T, Nagayama S, Osanai M, Mizusawa H, Tanabe T.

J Biol Chem. 2000 Apr 14;275(15):10893-8.

37.

Ataxin-3 is translocated into the nucleus for the formation of intranuclear inclusions in normal and Machado-Joseph disease brains.

Fujigasaki H, Uchihara T, Koyano S, Iwabuchi K, Yagishita S, Makifuchi T, Nakamura A, Ishida K, Toru S, Hirai S, Ishikawa K, Tanabe T, Mizusawa H.

Exp Neurol. 2000 Oct;165(2):248-56.

PMID:
10993685
38.

Neuronal intranuclear hyaline inclusion disease with polyglutamine-immunoreactive inclusions.

Takahashi J, Fukuda T, Tanaka J, Minamitani M, Fujigasaki H, Uchihara T.

Acta Neuropathol. 2000 May;99(5):589-94.

PMID:
10805106
39.

Neuronal intranuclear inclusions in spinocerebellar ataxia type 2.

Koyano S, Uchihara T, Fujigasaki H, Nakamura A, Yagishita S, Iwabuchi K.

Ann Neurol. 2000 Apr;47(4):550. No abstract available.

PMID:
10762173
40.

Neuronal intranuclear inclusions in spinocerebellar ataxia type 2: triple-labeling immunofluorescent study.

Koyano S, Uchihara T, Fujigasaki H, Nakamura A, Yagishita S, Iwabuchi K.

Neurosci Lett. 1999 Oct 1;273(2):117-20.

PMID:
10505630
41.

Abundant expression and cytoplasmic aggregations of [alpha]1A voltage-dependent calcium channel protein associated with neurodegeneration in spinocerebellar ataxia type 6.

Ishikawa K, Fujigasaki H, Saegusa H, Ohwada K, Fujita T, Iwamoto H, Komatsuzaki Y, Toru S, Toriyama H, Watanabe M, Ohkoshi N, Shoji S, Kanazawa I, Tanabe T, Mizusawa H.

Hum Mol Genet. 1999 Jul;8(7):1185-93.

PMID:
10369863
42.

Murine central neurons express a novel member of the cdc10/SWI6 motif-containing protein superfamily.

Fujigasaki H, Song SY, Kobayashi T, Yamakuni T.

Brain Res Mol Brain Res. 1996 Sep 1;40(2):203-13.

PMID:
8872304
43.

Spastic paraparesis and mutations in the prion protein gene.

Yamada M, Satoh S, Sodeyama N, Fujigasaki H, Kaneko K, Wada Y, Itoh Y, Matsushita M.

J Neurol Sci. 1995 Dec;134(1-2):215-6. No abstract available.

PMID:
8747872
44.

Spastic tetraplegia as an initial manifestation of familial Alzheimer's disease.

Sodeyama N, Shimada M, Uchihara T, Yanagisawa K, Fujigasaki H, Yamaguchi K, Matsushita M, Yamada M.

J Neurol Neurosurg Psychiatry. 1995 Oct;59(4):395-9.

45.

Mutational analysis of the amyloid precursor protein gene in Japanese familial Alzheimer's disease kindreds.

Fujigasaki H, Naruse S, Kaneko K, Hirasawa H, Tsuji S, Miyatake T.

Hum Genet. 1994 Apr;93(4):460-2.

PMID:
8168817
46.

A missense mutation at codon 105 with codon 129 polymorphism of the prion protein gene in a new variant of Gerstmann-Sträussler-Scheinker disease.

Yamada M, Itoh Y, Fujigasaki H, Naruse S, Kaneko K, Kitamoto T, Tateishi J, Otomo E, Hayakawa M, Tanaka J, et al.

Neurology. 1993 Dec;43(12):2723-4. No abstract available.

PMID:
7902972
47.

[Mutation analysis of amyloid precursor protein in early-onset familial Alzheimer's disease].

Naruse S, Fujigasaki H, Miyatake T.

Nihon Rinsho. 1993 Sep;51(9):2445-51. Review. Japanese.

PMID:
8411726

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