順天堂大学脳神経内科

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〒113-8431 東京都文京区本郷3-1-3 TEL03-3813-3111(大代表)
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原著・症例報告【順天堂医院 脳神経内科】

 
Arai T, Fujishima K, Kobayashi H, Yamamoto T, Mori K, Maeda M, Mizuno Y, Okuma Y. Pseudoathetosis caused by migrated cervical disc. Parkinsonism Rel Disord 13:59-61,2007
Ephraty L, Porat O, Israeli D, Cohen OS, Tunkel O, Yael S, Hatano Y, Hattori N, Hassin-Baer S. Neuropsychiatric and cognitive features in autosomal-recessive early parkinsonism due to PINK1 mutations. Mov Disord. (in press)
Fukae J, Noda K, Fujishima K, Wada R, Yoshiike T, Hattori N, Okuma Y. Successful treatment of relapsing neuro-Sweet's disease with corticosteroid and dapsone combination therapy. Clin Neurol Neurosurg. 2007 Dec;109(10):910-3
Fukae J, Mizuno Y, Hattori N. Mitochondrial dysfunction in Parkinson's disease. Mitochondrion 7:58-62, 2007
Fujita E, Kouroku Y, Isoai A, Kumagai H, Misutani A, Matsuda C, Hayashi YK, Momoi T. Two endoplasmic reticulum-associated degradation (ERAD) systems for the novel variant of the mutant dysferlin: ubiquitin/proteasome ERAD(I) and autophagy/lysosome ERAD(II). Hum Mol Genet 2007;16:618-629
Funayama M, Li Y, Tomiyama H, Yoshino H, Imamichi Y, Yamamoto M, Murata M, Toda T, Mizuno Y, and Hattori N. LRRK2 G2385R is susceptible to sporadic Parkinson's disease in Asian population. Neuroreport 2007;18(3):273-275
Hara K, Momose Y, Tokiguchi S, Shimohata M, Terajima K, Onodera O, Kakita A, Yamada M, Takahashi H, Hirasawa M, Mizuno Y, Ogata K, Goto J, Kanazawa I, Nishizawa M, Tsuji S ;Multiplex families with multiple system atrophy. Arch Neurol. 2007 ;64(4):545-51
Hatano T, Kubo S, Imai S, Maeda M, Ishikawa K, Mizuno Y, Hattori N. Leucine-rich repeat kinase 2 associates with lipid rafts. Hum Mol Genet. 16:678-690, 2007
Hyakawa H, Hayashita-Kinoh H, Nihira T, Mizuno Y, Mochizuki H, The isolation of neural stem cells from olfactory bulb of Parkinson's disease model. Neurosci Res 57:393-398, 2007
Kawajiri S, Tani M, Noda K, Fujishima K, Hattori N, Okuma Y. Segmental zoster paresis of limbs: Report of three cases and review of literature. Neurologist 13:313-317,2007
Kasai S, Urushibata S, Hozumi K, Yokoyama F, Ichikawa N, Kadoya Y, Nishi N, Watanabe N, Yamada Y, Nomizu M. Identification of multiple amyloidogenic sequences in laminin-1. Biochemistry. 2007 Apr 3;46(13):3966-74. Epub 2007 Mar 10
Kerever A, Schnack J, Vellinga D, Ichikawa N, Moon C, Arikawa-Hirasawa E, Efird JT, Mercier F. Novel extracellular matrix structures in the neural stem cell niche capture the neurogenic factor fibroblast growth factor 2 from the extracellular milieu. Stem Cells. 2007 Sep;25(9):2146-57. Epub 2007 Jun 14
Kono S, Shirakawa K, Ouchi Y, Sakamoto M, Ida H, Sugiura T, Tomiyama H, Suzuki H, Takahashi Y, Miyajima H, Hattori N, Mizuno Y. Dopaminergic neuronal dysfunction associated with parkinsonism in both a Gaucher disease patient and a carrier. .J Neurol Sci. 252:181-184, 2007
Kumazawa R, Tomiyama H, Li Y, Imamichi Y, Funayama M, Yoshino H, Yokochi F, Fukusako T, Takehisa Y, Kashihara K, Kondo T, Elibol B, Bostantjopoulou S, Toda T, Takahashi H, Yoshii F, Mizuno Y, Hattori N.Mutation analysis of the PINK1 gene in 395 patients with Parkinson's disease. Arch Neurol. In press
Ichikawa N, Iwabuchi K, Kurikara H, Hozumi K, Yamada Y, Arikawa-Hirasawa E. Ganglioside GM1 plays important role in laminin-1 induced-neurite outgrowth. 7th Pan Pacific Connective Tissue Societies Symposium. 28th October - 1st November 2007
Shangri-La Resort, Cairns, Australia
Ichikawa N, Iwabuchi K, Kurikara H, Hozumi K, Yamada Y, Arikawa-Hirasawa E. Laminin-1 directly binds GM1 in lipid rafts to activate cellular signaling to promote neurite outgrowth. 第54回マトリックス研究会大会・第39回日本結合組織学会学術大会、東京、5月9-11日、2007 Japan Matrix Club Young Investigator Award受賞
Ihara M, Yamasaki N, Hagiwara A, Tanigaki A, Kitano A, Hikawa R, Tomimoto H, Noda M, Takanashi M, Mori H, Hattori N, Miyakawa T, Kinoshita M. Sept4, a Component of Presynaptic Scaffold and Lewy Bodies, Is Required for the Suppression of alpha-Synuclein Neurotoxicity. Neuron 2007;53:519-33
Ishihara L, Gibson RA, Warren L, Amouri R, Lyons K, Wielinski C, Hunter C, Swartz JE, Elango R, Akkari PA, Leppert D, Surh L, Reeves KH, Thomas S, Ragone L, Hattori N, Pahwa R, Jankovic J, Nance M, Freeman A, Gouider-Khouja N, Kefi M, Zouari M, Ben Sassi S, Ben Yahmed S, El Euch-Fayeche G, Middleton L, Burn DJ, Watts RL, Hentati F. Screening for Lrrk2 G2019S and clinical comparison of Tunisian and North American Caucasian Parkinson's disease families. Mov Disord. 2007;22:55-61
Itoh M, Ide S, Takashima S, Kudo S, Nomura Y, Segawa M, Kubota T, Mori H, Tanaka S, Horie H, Tanabe Y, Goto Y. :Methyl CpG-Binding Protein 2(a Mutation of Which Causes Rett Syndrome) Directly Regulates Insulin-Like Growth Factor Binding Protein 3 in Mouse and Human Brains. J Neuropathol Exp Neurol vol66, No2,2007,pp117-123
Iguchi Y, Kimura K, Kobayashi K, Ueno Y, Shibazaki K, Inoue T. Microembolic signals at 48 hours of stroke onset contribute to new ischemia within a week. J Neurol Neurosurg Psychiatry 2007;Sep 10. Epub
Iguchi Y, Kimura K, Kobayashi K, Ueno Y, Shibazaki K, Iwanaga T, Inoue T. In-hospital onset ischemic stroke may be associated with atrial fibrillation and right-to-left shunt. J Neurol Sci 2007;254:39-43
Iguchi Y, Kimura K, Inoue T, Wada K, Ueno Y, Sunada Y. Diffusion-weighted MR images in patient with neuropsychiatric lupus: A case report. J Clin Neurosci 2007;14:273-275
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Kawakami T, Kanazawa H, Satoh T, Ieda M, Ieda Y, Kimura K, Mochizuki H, Shimada T, Yokoyama C, Ogawa S, Tanabe T, Fukuda K.AAV-PGIS gene transfer improves hypoxia-induced pulmonary hypertension in mice. Biochem Biophys Res Commun. 2007 23;363(3):656-61
Kagohashi M, Nakazato T, Yoshimi K, Moizumi S, Hattori N, Kitazawa S.Wireless voltammetry recording in unanesthetised behaving rats.Neurosci Res. 2008;60(1):120-7
Kawahara G, Okada M, Morone N, Ibarra CA, Nonaka I, Noguchi S, Hayashi YK, Nishino I. Reduced cell anchorage may cause sarcolemma-specific collagen VI deficiency in Ullrich disease. Neurology 2007;69:1043-1049
Kawajiri S,Tani M,Noda K,Fujishima K,Nobutaka H,Okuma Y Segmental zoster paresis of limbs: report of three cases and review of literature.Neurologist. 2007;13(5):313-7
Keira Y, Noguchi S, Kurokawa R, Fujita M, Minami N, Hayashi YK, Kato T, Nishino I. Characterization of lobulated fibers in limb girdle muscular dystrophy type 2A by gene expression profiling. Neurosci Res 2007;57:513-521
Kimura K, Ieda M, Kanazawa H, Yagi T, Tsunoda M, Ninomiya S, Kurosawa H, Yoshimi K, Mochizuki H, Yamazaki K, Ogawa S, Fukuda K. Cardiac sympathetic rejuvenation: a link between nerve function and cardiac hypertrophy. Circ Res. 2007;100(12):1755-64
Kimura K, Masaki Ieda M, Hideaki KanazawaH, Yagi T, Tsunoda, Ninomiya S, Kurosawa H, Yoshimi K, Mochizuki H, Yamazaki K, Ogawa S, Fukuda K Cardiac Sympathetic Rejuvenation: A Link between Nerve Function and Cardiac Hypertrophy. Circulation Res. 22: 1755-1764, 2007
Kono S, Shirakawa K, Ouchi Y, Sakamoto M, Ida H, Sugiura T, Tomiyama H, Suzuki H, Takahashi Y, Miyajima H, Hattori N, Mizuno Y. Dopaminergic neuronal dysfunction associated with parkinsonism in both a Gaucher disease patient and a carrier. .J Neurol Sci. 2007;252:181-184
Kubo SI, Iwatake A, Ebihara N, Murakami A, Hattori N. Visual impairment in Parkinson's disease treated with amantadine: Case report and review of the literature. Parkinsonism Relat Disord. 2007 May 15; [Epub ahead of print]
Kumazawa R, Tomiyama H, Li Y, Imamichi Y, Funayama M, Yoshino H, Yokochi F, Fukusako T, Takehisa Y, Kashihara K, Kondo T, Elibol B, Bostantjopoulou S, Toda T, Takahashi H, Yoshii F, Mizuno Y, Hattori N. Mutation analysis of the PINK1 gene in 391 patients with Parkinson's disease. Archives of Neurology (in press).
Kono S, Shirakawa K, Ouchi Y, Sakamoto M, Ida H, Sugiura T, Tomiyama H, Suzuki H, Takahashi Y, Miyajima H, Hattori N, Mizuno Y. Dopaminergic neuronal dysfunction associated with parkinsonism in both a Gaucher disease patient and a carrier. J Neurol Sci. 2007 Jan 31;252(2):181-184
Kumazawa R, Tomiyama H, Li Y, Imamichi Y; Funayama M, Yoshino H, Yokochi F, Fukusako T, Takehisa Y, Kashihara K, Kondo T, Elibol B, Bostantjopoulou S, Toda T, Takahashi H, Yoshii F, Mizuno Y, Hattori N. Mutation analysis of the PINK1 gene in 391 patients with Parkinson's disease. Arch Neurol (in press)
Lee J, Kagamihara Y, Kakei S.Development of a quantitative evaluation system for motor control using wrist movement. -An analysis of movement disorders in patients with cerebellar diseases-Journal of Japanese Society of Laboratory Medicine, 55(10); 912-921, 2007
Liewluck T, Hayashi YK, Ohsawa M, Kurokawa R, Fujita M, Noguchi S, Nonaka I, Nishino I. Unfolded protein response and aggresome formation in hereditary reducing-body myopathy. Muscle Nerve 2007;35:322-326
Liang W-C, You C-Y, Liu C-Y, Lee C-S, Goto K, Hayashi YK, Jong YJ. Novel LMNA mutation in a Taiwanese family with autosomal dominant Emery-Dreifuss muscular dystrophy. J Formos Med Assoc 2007;106:S27-S31
Lin YC, Murakami T, Hayashi YK, Nishino I, Nonaka I, Yuo CY, Jong YJ. A novel FKRP gene mutation in a Taiwanese patient with limb-girdle muscular dystrophy 2I. Brain Dev 2007;29:234-238
Liu M, Eguchi N, Yamasaki Y, Urade Y, Hattori N, Urabe T: Focal cerebral ischemia/reperfusion injury in mice induces hematopoietic prostaglandin D synthase in microglia and macrophages. Neuroscience 145: 520-529, 2007
Malicdan MC, Noguchi S, Nonaka I, Hayashi YK, Nishino I. A Gne knockout mouse expressing human GNE D176V mutation develops features similar to distal myopathy with rimmed vacuoles or hereditary inclusion body myopathy. Hum Mol Genet 2007;16:2669-2682
Fukae J, Noda K, Fujishima K, Wada R, Yoshiike T, Hattori N, Okuma Y. Successful treatment of relapsing neuro-Sweet's disease with corticosteroids and dapsone combination therapy. Clin Neurol Neurosurg 109:910-913,2007
Funayama M Li Y, Tomiyama H, Yoshino H, Imamichi Y, Yamamoto M, Murata M, Toda T, Mizuno Y, Hattori N: LRRK2 G2385R variant is a risk factor for Parkinson disease in Asian population NeuroReport 18:273-275, 2007
Mellick GD, Siebert GA, Funayama M, Buchanan DD, Li Y, Imamichi Y, Yoshino H, Silburn PA, Hattori N. Screening PARK Genes for Mutations in Early Onset Parkinson's Disease Patients from Queensland, Australia. Parkinsonism & Related Disorders. In press
Mizuno Y, Kanazawa I, Kuno S, Yanagisawa N, Yamamoto M, Kondo T, Japanese Parkinson-Entacapone Study Group. Placebo-controlled, double-blind dose-finding study of entacapone in fluctuating parkinsonian patients. Mov Disord 2007;22:75-80
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Mizuno Y, Hattori N, Kubo S, Sato S, Nishioka K, Hatano T, Tomiyama H, Funayama M, Machida Y, Mochizuki H. Progress in the Pathogenesis and Genetics of Parkinson's Disease (Review). Royal Soc of Med Man (in press).
Mori K, Nakao Y, Yamamoto T, Okuma Y, Osada H, Esaki T. Partial (one-third) side-to-end hypoglossal-facial anastomosis ensures facial reanimation without tongue dysfunction. Neurosurg Q 17:180-184,2007
Muchir A, Pavlidis P, Bonne G, Hayashi YK, Worman HJ. Activation of MAPK in hearts of EMD null mice: similarities between mouse models of X-linked and autosomal dominant Emery Dreifuss muscular dystrophy. Hum Mol Genet 2007;16:1884-1895
Namba T, Mochizuki H, Onodera M, Namiki H, SekiT Postnatal neurogenesis in hippocampal slicecultures: early in vitro labeling of neuronal precursor cells leads to efficient neuronal production. J Neurosci Res, 85: 1704-1712, 2007
Nakashima I, Fukazawa T, Ota K, Nohara C, Warabi Y, Ohashi T, Miyazawa I, Fujihara K, Itoyama Y. Two subtype of optic-spinal form of multiple sclerosis in Japan: Clinical and laboratory features. J Neurol. 2007 Apr;254(4) 488-92
Ning YP, Kanai K, Tomiyama H, Li Y, Funayama M, Yoshino H, Sato S, Asahina M, Kuwabara S, Takeda A, Hattori T, Mizuno Y, Hattori N. PARK9-linked parkinsonism in Eastern Asia: Mutation detection in ATP13A2 and clinical phenotype. Neurology (in press).
Obi K, Akiyama H, Kondo H, Shimomura Y, Hasegawa M, Iwatsubo T, Mizuno Y, Mochizuki H.Relationship of phosphorylated alpha-synuclein and tau accumulation to Abeta deposition in the cerebral cortex of dementia with Lewy bodies.Exp Neurol. 2008 in press
Obi T, Nishioka K, Owen A. Ross OA, Terada T, Yamazaki K, Sugiura, A, Takanashi M, Mizoguchi K, Mori H, Mizuno Y, Hattori N. Clinicopathological study of a SNCA gene duplication patient with Parkinson disease and dementia Neurology (in press)
Ohsawa M, Liewluck T, Ogata K, Iizuka T, Hayashi Y, Nonaka I, Sasaki M, Nishino I. Familial reducing body myopathy. Brain Dev 2007;29:112-116
Ohshima T, Hirasawa M, Tabata H, Mutoh T, Adachi T, Suzuki H, Saruta K, Iwasato T, Itohara S, Hashimoto M, Nakajima K, Ogawa M, Kulkarni AB, Mikoshiba K. :Cdk5 is required for multipolar-to-bipolar transition during radial neuronal migration and proper dendrite development of pyramidal neurons in the cerebral cortex. Development.2007;134(12):2273-82
Oizumi H, Hayashita-Kinoh H, Hayakawa H, Arai H, Furuya T, Ren YR, Yasuda T, Miura M, Mizuno Y, Mochizuki H Alteration in the differentiation-related molecular expression in the subventricular zone in a mouse model of Parkinson's disease. Neurosci Res 60, 15-21, 2008
Okada M, Kawahara G, Noguchi S, Sugie K, Murayama K, Nonaka I, Hayashi YK, Nishino I. Primary collagen VI deficiency is the second most common congenital muscular dystrophy in Japan. Neurology 2007;69:1035-1042
SekiT, Namba T, Mochizuki H, Onodera M, Clustering, migration and neurite formation of neural precusor cells in the adult rat hippocampus . J Comp Neurol, 10; 502: 275-290, 2007
Saiki M, Saiki S, Sakai K, Matsunari I, Higashi K, Murata KY, Hattori N, Hirose G. Neurological deficits are associated with increased brain calcinosis, hypoperfusion, and hypometabolism in idiopathic basal ganglia calcification. Mov Disord. 2007 May 15;22(7):1027-30
Satake W, Mizuta I, Suzuki S, Nakabayashi Y, Ito C, Watanabe M, Takeda A, Hasegawa K, Sakoda S, Yamamoto M, Hattori N, Murata M, Toda T.Fibroblast growth factor 20 gene and Parkinson's disease in the Japanese population. NeuroReport 18937-40, 2007
Setsuie R,Wang YL, Mochizuki H, Osaka H, Hayakawa H, Ichihara N, Li H, Furuta A, Sato Y, Sun YJ, Kwon J, Kabuta T, Yoshimi K, Mizuno Y, Aoki S, Noda M, Wada K, Dopaminergic cell loss in transgenic mice expressing the Parkinson's disease-associated UCH-L1 I93M mutant. Neurochemistry International 50(1):119-29, 2007
Shimizu Y, Yokoyama K, Misu T, Takahashi T, Fujihara K, Kikuchi S, Itoyama Y, Iwata M. Development of extensive brain lesions following interferon beta therapy in relapsing neuromyelitis optica and longitudinally extensive myelitis. November 2007 DOI 10.1007/s00415-007-0730-5
Satake W, Mizuta I, Suzuki S, Nakabayashi Y, Ito C, Watanabe M, Takeda A, Hasegawa K, Sakoda S, Yamamoto M, Hattori N, Murata M, Toda T. Fibroblast growth factor 20 gene and Parkinson's disease in the Japanese population. NeuroReport 18937-40, 2007
Setsuie R, Wang YL, Mochizuki H, Osaka H, Hayakawa H, Ichihara N, Li H, Furuta A, Sano Y, Sun YJ, Kwon J, Kabuta T, Yoshimi K, Aoki S, Mizuno Y, Noda M, Wada K. Dopaminergic neuronal loss in transgenic mice expressing the Parkinson's disease-associated UCH-L1 I93M mutant. Neurochem Int. 2007;50(1):119-29
Shibazaki K, Iguchi Y, Kimura K, Ueno Y, Inoue T. New asymptomatic ischemic lesions on diffusion-weighted imaging after cerebral angiography. J Neurol Sci 2007;Oct 23. Epub
Shibazaki K, Iguchi Y, Kimura K, Wada K, Ueno Y, Sunada Y. Paradoxical brain embolism associated with HCV-related type II mixed cryoglobulinemia. J Clin Neurosci 2007;14:780-782
Shibazaki K, Iguchi Y, Inoue T, Ueno Y, Kimura K. Serial contrast saline transcranial Doppler examination in a patient with paradoxical brain embolism associated with pulmonary embolism. J Clin Neurosci 2007;14:788-791
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Suzuki K, Okuma Y, Hattori N, Kamei S, Yoshii F, Utsumi H, Iwasaki Y, Iijima M, Miyamoto T, Miyamoto M, Hirata K. Characteristics of sleep disturbances in Japanese patients with Parkinson's disease. A study using Parkinson's Disease Sleep Scale. Mov Disord 22:1245-1251,2007
Tani M, Natori S, Noda K, Fujishima K, Hattori N, Mizuno Y, Okuma Y. Isolated reversible splenial lesion in adult meningitis: a case report and review of the literature. Intern Med. 2007;46(18):1597-600. Epub 2007 Sep 14. Review
Tamura Y, Ogihara T, Uchida T, Ikeda F, Kumashiro N, Nomiyama T, Sato F, Hirose T, Tanaka Y, Mochizuki H, Kawamori R, Watada H Amelioration of glucose tolerance by hepatic inhibition of nuclear factor κB in db/db mice. Diabetologia 50(1):131-41, 2007
Tomiyama H, Funayama M, Mizuno Y, Hattori N. LRRK2 in neurodegenerative disorders (Review). CNS drugs 2007;21 Spec. issue 1:63-71
Ueno Y, Kimura K, Iguchi Y, Shibazaki K, Inoue T, Hattori N, Urabe T. Mobile aortic plaques are a cause of multiple brain infarcts seen on diffusion-weighted imaging. Stroke 2007;38:2470-2476
Ueno Y, Iguchi Y, Shibazaki K, Inoue T, Hattori N, Urabe, T, Kimura K. Paradoxical brain embolism may not be uncommon-Prospective study in acute ischemic stroke. J Neurol 2007;254:763-766
Ueno Y, Kimura K, Iguchi Y, Shibazaki K, Inoue T, Urabe T. Right-to-left shunt and lacunar stroke in patients without hypertension and diabetes. Neurology 2007;68:528-531
Ura S, Hayashi YK, Goto K, Astejada MN, Murakami T, Nagato M, Ohta S, Daimon Y, Takekawa H, Hirata K, Nonaka I, Noguchi S, Nishino I. Limb-girdle muscular dystrophy due to emerin gene mutations. Archives of neurology 2007;64:1038-1041
Yamashiro K, Liu R, Maeda M, Hattori N, Urabe T. Induction and selective accumulation of mutant ubiquitin in CA1 pyramidal neurons after transient global ischemia. Neuroscience 2007;147:71-9
Yasuda T, Fukuda-Tani M, Nihira T, Wada K, Hattori N, Mizuno Y, Mochizuki H. Correlation between levels of pigment epithelium-derived factor and vascular endothelial growth factor in the striatum of patients with Parkinson's disease. Exp Neurol 2007;206:308-317
Yasuda T, Miyachi S, Kitagawa R, Wada K, Nihira T, Ren YR, Hirai Y, Ageyama N, Terao K, Shimada T, Takada M, Mizuno Y, Mochizuki H. Neuronal specificity of alpha-synuclein toxicity and effect of Parkin co-expression in primates. Neuroscience 2007;144:743-753
Yasuda T, Momo F-T, Nihira T, Wada K, Mizuno Y, Mochizuki H Correlation between levels of pigment epithelium-derived factor and vascular endothelial growth factor in the striatum of patients with Parkinson's disease. Exp Neurol.206, 308-317, 2007
安野 みどり. 性格変化 ―特に脳血管障害と頭部外傷を中心としてー. 総合リハビリテーション;35(5)、2007
今井壽正:導入から5年で明らかとなった電子カルテの光と影.病院活性化に直結するIT導入.院長が語る電子カルテ有用論、新医療 2007年7月号、pp 76-78, 2007
小尾公美子、土谷邦秋、安野みどり、太田 聡、中村亮介、秋山治彦. Fisher斑を伴った髄膜血管型神経梅毒の1剖検例. BRAIN and NERVE : 59(7),797-803,2007
風間(鈴木)明日香,中村範行,後藤啓五.特徴的な延髄萎縮を認めた52歳男性例.越谷市立病院年報
神戸泰紀, 深江治郎, 野田和幸, 藤島健次, 大熊泰之. 頭痛で発症し、初期診断が困難であったVogt-小柳-原田病の1例. 神経内科 2007;66(6):598-600
高田由希子, 野田和幸, 藤島健次, 服部信孝, 水野美邦, 大熊泰之. 下肢に生じたneralgic amyotrophy(lumbosacral radiculoplexus neuropathy)の一例. BRAIN and NERVE 59(4):435-438, 2007
富山弘幸,服部信孝.PAPK6 (PINK1) (総説). Clinical neuroscience 2007;25(1):77-78
富山弘幸,波田野琢,服部信孝.PARK8 (LRRK2) の臨床分子遺伝学(総説). Brain and Nerve神経研究の進歩 2007;59(8): 839-850
中村真一郎.脳内報酬系において報酬の質と量は異なる脳領域で処理されている.PD Today 19号,pp14-15,アルタ出版,東京
平澤基之、金澤 章:評価基準と評価スケール EBMのコンセプトを取り入れた パーキンソン病ハンドブック改定第2版 水野美邦編 中外医学社2007
舟辺さやか, 深江治郎, 野田和幸, 藤島健次, 大熊泰之. 胃切除後にビタミンB1欠乏性ニューロパチーおよびWernicke-Korsakoff症候群をきたした1例. 内科 2007;99(5):948-950
宮元伸和, 伊澤奈々, 本井ゆみ子, 服部信孝, 卜部貴夫.頭部MRI所見による延髄梗塞の臨床分類の検討. 脳卒中.2007;295;617-623
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