Výsledky vyhledávání - "Yoshiro Nishikawa"

A case of central nervous system relapse in acute promyelocytic leukemia

Autor: Yoshiro Nishikawa, Hideki Mitsui, Yuhei Hasuike, Fuminobu Sugai, Hiroshi Yamaguchi

Publikováno v: Rinsho shinkeigaku = Clinical neurology. 56(4)

A 70-year-old woman who have achieved complete remission (CR) of acute promyelocytic leukemia (APL) with all-trans retinoic acid and chemotherapy presented with abnormal sensation in the right lateral thigh and the bilateral legs. In addition, neurol

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20598e337b608911a2433b697eaf8b6a
https://pubmed.ncbi.nlm.nih.gov/27025992

Zobrazit plný text záznamu

Late-onset Alexander disease with a V87L mutation in glial fibrillary acidic protein (GFAP) and calcifying lesions in the sub-cortex and cortex

Autor: Juri Ichihashi, Yoshiyuki Mistui, Masanori Nakagawa, Hidekazu Suzuki, Mari Kitada, Hiroshi Sasayama, Susumu Kusunoki, Tomokatsu Yoshida, Yoshiro Nishikawa

Publikováno v: Journal of Neurology. 259:457-461

Glial fibrillary acidic protein (GFAP) mutation has been reported in Alexander disease. We report a 31-year-old woman suffering from Alexander disease with a V87L mutation in GFAP. She showed psychomotor regression and a history of seizures, in addit

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c92b257956e7f9e0f168310712f1948f
https://doi.org/10.1007/s00415-011-6201-z

Zobrazit plný text záznamu

Increased expression of MUC1 in advanced pancreatic cancer

Autor: Masaaki Oka, Shinji Waki, Suguru Yonezawa, Yuji Hinoda, Mikiko Fukui, Yoshiro Nishikawa, Hideo Kida, Shuji Sato, Yuichiro Hamanaka, Kohzoh Imai, Tomoko Nakano, Kotaro Yamamoto, Yutaka Suehiro, Yoshito Ikematsu, Michiko Horinochi

Publikováno v: Journal of Gastroenterology. 38:1162-1166

MUC1 is associated with tumor invasion and metastasis, and is expressed in pancreatic cancer with a high frequency. This study explored whether MUC1 expression affected the survival of patients with pancreatic cancer. Tissue specimens obtained from 7

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::611e48744ff8a514b472dc61aa68c260
https://doi.org/10.1007/s00535-003-1224-6

Zobrazit plný text záznamu

Adult-onset multiple acyl CoA dehydrogenation deficiency associated with an abnormal isoenzyme pattern of serum lactate dehydrogenase

Autor: Wen-Chen Liang, Harutoshi Fujimura, Ichizo Nishino, Kousuke Baba, Yoshiro Nishikawa, Fuminobu Sugai, Hisae Sumi, Misaki Yamadera, Keiko Toyooka

Publikováno v: Neuromuscular Disorders. 22:159-161

We report a case of a 37 year-old male with multiple acyl-CoA dehydrogenation deficiency (MADD). The patient had suffered from exercise intolerance in his hip and thigh muscles for one year. Then, restriction of carbohydrates for a diet made his symp

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1b79497bfe4c03957836663c2f2e791
https://doi.org/10.1016/j.nmd.2011.08.004

Zobrazit plný text záznamu

Marked reduction in CSF lactate and pyruvate levels after CoQ therapy in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS)

Autor: Shiro Yorifuji, Yoshiro Nishikawa, Masakuni Kameyama, N. Hirono, Harutoshi Fujimura, N. Nishitani, Kazuo Abe, T. Mezaki

Publikováno v: Acta Neurologica Scandinavica. 83:356-359

Many CoQ trials for mitochondrial encephalomyopathy are reported, however, the action of CoQ in the central nervous system is unknown. We administered CoQ to a patient with MELAS, and decreasing CSF lactate and pyruvate levels were revealed. This red

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62f3d4f9efebf37463cf18ba31445179
https://doi.org/10.1111/j.1600-0404.1991.tb03962.x

Zobrazit plný text záznamu

Clinical and magnetic resonance image correlation in idiopathic cerebellar ataxia

Autor: Harutoshi Fujimura, Yoshiro Nishikawa, Keiko Toyooka, Takehiko Yanagihara, Kazuo Abe, Shiro Yorifuji, Misako Kaido

Publikováno v: Journal of the neurological sciences. 133(1-2)

Sixty-one patients who fulfilled the clinical criteria for idiopathic cerebellar ataxia and who had symptoms at least for 3 years were examined clinically and by magnetic resonance imaging (MRI). Based on the clinical signs, they were divided into pa

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d732d77ce0988e441db572ba94a9d961
https://pubmed.ncbi.nlm.nih.gov/8583232

Zobrazit plný text záznamu

Involvement of the central nervous system in myotonic dystrophy

Autor: T. Hazama, Takehiko Yanagihara, Yoshiro Nishikawa, Kazuo Abe, Harutoshi Fujimura, Keiko Toyooka, Shiro Yorifuji

Publikováno v: Journal of the neurological sciences. 127(2)

To investigate the etiological factors responsible for intellectual impairment and mood changes in patients with myotonic dystrophy (DM), we evaluated 14 patients with DM by means of neuropsychological evaluation and magnetic resonance images (MRI).

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72a56ceeb4f3351334feec76d982b288
https://pubmed.ncbi.nlm.nih.gov/7707077

Zobrazit plný text záznamu

Dopamine metabolism in the central nervous system after discontinuation of l-dopa therapy in patients with Parkinson disease

Autor: Saburo Ogasahara, Yoshiro Nishikawa, Seiichiro Tarui, M. Takahashi, Yusaku Nakamura, Keiji Wada, Shiro Yorifuji

Publikováno v: Journal of the Neurological Sciences. 66:151-163

The dopamine turnover rate in the central nervous system (CNS) of parkinsonian patients was studied by means of the intravenous probenecid test during drug holiday (DH) and alternate day L-dopa therapy (ADDT). After L-dopa therapy was stopped, the do

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c5c6a2c4cff6b776ad38b4f7bdbe239
https://doi.org/10.1016/0022-510x(84)90003-0

Zobrazit plný text záznamu

Long-term coenzyme Q10 therapy for a mitochondrial encephalomyopathy with cytochrome c oxidase deficiency: a 31P NMR study

Autor: S. Ueno, Yusaku Nakamura, M. Takahashi, Shiro Yorifuji, T. Kozuka, T. Nishimura, Seiichiro Tarui, Yoshiro Nishikawa

Publikováno v: Neurology. 39(3)

For 2 years we administered high doses of coenzyme Q10 (CoQ) to a patient having mitochondrial encephalomyopathy with cytochrome c oxidase deficiency. Abnormal elevation of the serum lactate per pyruvate ratio and the increased concentration of serum

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e2bda3937411ac7069689f9c78ec8b9
https://pubmed.ncbi.nlm.nih.gov/2538775

Zobrazit plný text záznamu

Treatment of Kearns-Sayre syndrome with coenzyme Q10

Autor: Saburo Ogasahara, Yusaku Nakamura, Norio Kono, Fumihisa Soga, Mitsuo Takahashi, Shigeo Hashimoto, Yoshiro Nishikawa, Shiro Yorifuji, Seiichiro Tarui

Publikováno v: Neurology. 36(1)

We studied the metabolism of coenzyme Q10 (CoQ) and the effects of CoQ therapy in five patients with Kearns-Sayre syndrome (KSS). Although the mitochondrial fraction was increased in muscles from KSS patients, CoQ content was slightly low. CoQ synthe

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76a75b2aee822bf1993894de680cf366
https://pubmed.ncbi.nlm.nih.gov/3941783

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání