Výsledky vyhledávání - "Keiko Shishikura"

Benefits of FK 506 for refractory eye symptoms in a young child with ocular myasthenia gravis

Autor: Yoshito Hirayama, Keiko Shishikura, Makiko Osawa, Haruko Suzuki, Keiko Ishigaki, Terumi Murakami

Publikováno v: Brain and Development. 31:634-637

Recently, there have been many reports on the efficacy and safety of tacrolimus (FK506) treatment for adult patients with intractable generalized myasthenia gravis (MG). There have also been a few reports of successful FK506 therapy in patients with

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4cdab731d71b7faf1b38ca9f7c16a6bd
https://doi.org/10.1016/j.braindev.2008.08.016

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[Pre-evening meal administration of tacrolimus improved refractory ocular symptoms in two young children with latent general myasthenia gravis]

Autor: Yoko, Yoshikawa, Keiko, Ishigaki, Keiko, Shishikura, Kyoko, Hirasawa, Takatoshi, Sato, Haruko, Suzuki, Yoshito, Hirayama, Makiko, Osawa

Publikováno v: No to hattatsu = Brain and development. 45(4)

We report two patients with latent general myasthenia gravis (MG) with refractory ocular symptoms who were successfully treated with pre-evening meal administration of tacrolimus. Patient 1 was a 4-year-old girl with persistent ocular symptoms despit

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::38aa96d15ddda43d222908c50f79b871
https://pubmed.ncbi.nlm.nih.gov/23951946

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Clinical variability of congenital myopathy with type I fiber atrophy: A long-term observation of three cases

Autor: Keiko Shishikura, Haruko Suzuki, Makiko Osawa, Rieko Takahashi, Sawako Sumida, Yumi Arai, Yoshito Hirayama, Yukio Fukuyama

Publikováno v: Pediatrics International. 36:186-193

The variable clinical courses of three cases of congenital fiber type disproportion (CFTD) over a period of 10 years are presented. All showed improvement in early childhood, but subsequently, varying degrees of deterioration were noted: specifically

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::bce30a42ceee3b62297e630f26c7c1b4
https://doi.org/10.1111/j.1442-200x.1994.tb03159.x

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Computed tomography and magnetic resonance imaging of affected muscle in childhood acid α-glucosidase deficiency: a case report

Autor: Kayoko Saito, Hideo Sugie, Yumi Arai, Yukio Fukuyama, Keiko Shishikura, Makiko Osawa, Haruko Suzuki

Publikováno v: Brain and Development. 15:147-152

A 13-year-old boy with the juvenile type of acid α-glucosidase deficiency is presented. Muscle CT scans performed before muscle biopsy revealed high image density over the entire rectus femoris, and partial high density over the iliopsoas, adductor

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c835f01c2370d1b83825795e6797913
https://doi.org/10.1016/0387-7604(93)90053-b

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High-density areas on muscle CT in childhood-onset Pompe disease are caused by excess calcium accumulation

Autor: Makiko Osawa, Keiko Ishigaki, Ryohei Kuwatsuru, Ikuya Nonaka, Satomi Mitsuhashi, Haruko Suzuki, Yoshito Hirayama, Terumi Murakami, Keiko Shishikura

Publikováno v: Acta neuropathologica. 120(4)

We report two patients with childhood-onset Pompe disease showing striking changes with high-density areas on skeletal muscle CT, not seen in adult- or infantile-onset forms of this disease. While the anterior compartment of the thigh muscles was les

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba99f82a1a62a1474a4db063b415e0a1
https://pubmed.ncbi.nlm.nih.gov/20680637

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[Treatment approach to congenital myasthenic syndrome in a patient with acetylcholine receptor deficiency]

Autor: Keiko, Ishigaki, Terumi, Murakami, Yasushi, Ito, Akiko, Yanagisawa, Kayano, Kodaira, Keiko, Shishikura, Haruko, Suzuki, Yoshito, Hirayama, Makiko, Osawa

Publikováno v: No to hattatsu = Brain and development. 41(1)

Congenital myasthenic syndromes (CMS) are rare heterogeneous disorders of neurotransmission caused by genetic defects of neuromuscular junction molecules. While CMS patients have been reported worldwide, in Japan there have been only a few descriptio

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::5996fb946defcde08a3f14b9a593e851
https://pubmed.ncbi.nlm.nih.gov/19172815

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Fukuyama Type Congenital Progressive Muscular Dystrophy

Autor: Noriko Okada, Kyoko Hirasawa, Yukio Fukuyama, Sawako Sumida, Keiko Shishikura, Yoshito Hirayama, Makiko Osawa, Harumi Ikenaka, Hiroko Murasugi, Haruko Suzuki, Atsuko Tsutsumi, Yumi Arai, Nobuko Sugahara, Keiko Ito, Yukio Uchida

Publikováno v: Pediatrics International. 33:261-269

Clincopathological features of Fukuyama type congenital muscular dystrophy (FCMD), a combination of brain malformation and muscular dystrophy with facial muscle and CNS involvement and high prevalence in Japan, are reviewed. Evidence of progressive d

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e0737d3b5d706f29688958b23ef835c
https://doi.org/10.1111/j.1442-200x.1991.tb01552.x

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Improvement of action myoclonus by an administration of 5-hydroxytryptophan and carbidopa in a child with muscular subsarcolemmal hyperactivity

Autor: Yukio Fukuyama, Keiko Shishikura, Kazutoshi Nakano, Taketoshi Hayakawa, Makiko Ohsawa, Haruko Suzuki

Publikováno v: Brain and Development. 12:516-520

We report a 3-year-11-month-old boy who manifested action myoclonus only. Histochemical analysis of the quadriceps muscle revealed subsarcolemmal hyperactivity. The administration of 5-hydroxytryptophan and carbidopa dramatically improved the action

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d45afdbe329ed775ff82f4e3f3432978
https://doi.org/10.1016/s0387-7604(12)80218-x

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[Carry over: practical experience of persons with severe motor and intellectual disabilities]

Autor: Keiko, Shishikura

Publikováno v: No to hattatsu = Brain and development. 37(3)

Tomo clinic is a special clinic for the handicapped. We have supported a day care center and a group home for persons with severe motor and intellectual disabilities (SMID) for over ten years. It seems that physical well-being declines dramatically i

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::b78824a76d52820393e97be4d3c8d447
https://pubmed.ncbi.nlm.nih.gov/15915738

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