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Ikuya Nonaka

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Takatoshi Sato; Kazuma Sugie; Ichiro Yabe; Yukiko K Hayashi; Hideki Houzen; Daita Kaneda; Tomoyoshi Kondo; Satoru Noguchi; Ikuya Nonaka; Makiko Osawa; Yasushi Oya; Hidenao Sasaki; Ichizo Nishino
DNAJB6 myopathy in an Asian cohort and cytoplasmic/nuclear inclusions.
Rie S Tsuburaya; Ikuya Nonaka; Yasushi Oya; Hideo Sugie; Tokiko Fukuda; Yukiko K Hayashi; Kazunari Monma; Takahiro Nakayama; Ichizo Nishino
Acid phosphatase-positive globular inclusions is a good diagnostic marker for two patients with adult-onset Pompe disease lacking disease specific pathology.
Etsuko Keduka; Hiroaki Mitsuhashi; Satoru Noguchi; Ikuya Nonaka; Sherine Shalaby; Yukiko K Hayashi; Ichizo Nishino
In vivo characterization of mutant myotilins.

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All Publications

2013: Takatoshi Sato; Kazuma Sugie; Ichiro Yabe; Yukiko K Hayashi; Hideki Houzen; Daita Kaneda; Tomoyoshi Kondo; Satoru Noguchi; Ikuya Nonaka; Makiko Osawa; Yasushi Oya; Hidenao Sasaki; Ichizo Nishino
DNAJB6 myopathy in an Asian cohort and cytoplasmic/nuclear inclusions.
Neuromuscular disorders : NMD 2013;23(3):269-76.
2012: Rie S Tsuburaya; Ikuya Nonaka; Yasushi Oya; Hideo Sugie; Tokiko Fukuda; Yukiko K Hayashi; Kazunari Monma; Takahiro Nakayama; Ichizo Nishino
Acid phosphatase-positive globular inclusions is a good diagnostic marker for two patients with adult-onset Pompe disease lacking disease specific pathology.
Neuromuscular disorders : NMD 2012;22(5):389-93.
2012: Etsuko Keduka; Hiroaki Mitsuhashi; Satoru Noguchi; Ikuya Nonaka; Sherine Shalaby; Yukiko K Hayashi; Ichizo Nishino
In vivo characterization of mutant myotilins.
The American journal of pathology 2012;180(4):1570-80.
2012: Ayako Hattori; Yukiko K Hayashi; Masao Kawatani; Hirofumi Komaki; Eiji Nakagawa; Ikuya Nonaka; Yoshiaki Saito; Hiroshi Sakuma; Masayuki Sasaki; Kenji Sugai; Ichizo Nishino
A novel mutation in the LMNA gene causes congenital muscular dystrophy with dropped head and brain involvement.
Neuromuscular disorders : NMD 2012;22(2):149-51.
2012: Kazunari Momma; Satoru Noguchi; Ikuya Nonaka; Yukiko K Hayashi; Keiko Kamakura; May Christine V Malicdan; Narihiro Minami; Ichizo Nishino
Rimmed vacuoles in Becker muscular dystrophy have similar features with inclusion myopathies.
PloS one 2012;7(12):e52002.
2011: Tomoko Mizuno; Eiji Nakagawa; Ikuya Nonaka; Yoshiaki Saito; Yuko Saito; Hiroshi Sakuma; Masayuki Sasaki; Hirofumi Komaki; Kenji Sugai; Yukio Sawaishi
A case of congenital axonal neuropathy associated with West syndrome.
Brain & development 2011;33(8):692-6.
2011: Rie Tsuburaya; Yukiko K Hayashi; Ikuya Nonaka; Ken Saiki; Hideo Sugita; Takateru Suzuki; Ichizo Nishino
Lobulated fibers in a patient with 46-year history of limb-girdle muscle weakness.
Neuropathology : official journal of the Japanese Society of Neuropathology 2011;31(4):455-7.
2011: Yoshiaki Saito; Masayuki Sasaki; Fumi Takeuchi; Kayo Tominaga; Ayako Hattori; Yukiko K Hayashi; Ken Kawabata; Hirofumi Komaki; Nigel G Laing; Satomi Mitsuhashi; Ikuya Nonaka; Kristen J Nowak; Ichizo Nishino
Extramuscular manifestations in children with severe congenital myopathy due to ACTA1 gene mutations.
Neuromuscular disorders : NMD 2011;21(7):489-93.
2011: Wen-Chen Liang; Hiroaki Mitsuhashi; Ichizo Nishino; Satoru Noguchi; Ikuya Nonaka; Etsuko Keduka; Yukiko K Hayashi
TMEM43 mutations in Emery-Dreifuss muscular dystrophy-related myopathy.
Annals of neurology 2011;69(6):1005-13.
2010: Kiyoko Ishii; Hirofumi Komaki; Aya Ohkuma; Ichizo Nishino; Ikuya Nonaka; Masayuki Sasaki
Central nervous system and muscle involvement in an adolescent patient with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency.
Brain & development 2010;32(8):669-72.
2010: Kayo Tominaga; Yukiko K Hayashi; Kanako Goto; Narihiro Minami; Satoru Noguchi; Ikuya Nonaka; Tetsuro Miki; Ichizo Nishino
Congenital myotonic dystrophy can show congenital fiber type disproportion pathology.
Acta neuropathologica 2010;119(4):481-6.
2010: Ayako Miyahara-Katayama; Yasushi Ohya; Tsuyoshi Omi; Hirofumi Komaki; Ikuya Nonaka; Noriko Sato; Masayuki Sasaki
A case of intraneural perineurioma presenting with monomelic atrophy in a child.
Brain & development 2010;32(4):338-41.
2009: Yukiko K Hayashi; Chie Matsuda; Megumu Ogawa; Kanako Goto; Kayo Tominaga; Satomi Mitsuhashi; Young-Eun Park; Ikuya Nonaka; Naomi Hino-Fukuyo; Kazuhiro Haginoya; Hisashi Sugano; Ichizo Nishino
Human PTRF mutations cause secondary deficiency of caveolins resulting in muscular dystrophy with generalized lipodystrophy.
The Journal of clinical investigation 2009;119(9):2623-33.
2009: Young-Eun Park; Yukiko K Hayashi; Gisèle Bonne; Takuro Arimura; Satoru Noguchi; Ikuya Nonaka; Ichizo Nishino
Autophagic degradation of nuclear components in mammalian cells.
Autophagy 2009;5(6):795-804.
2009: Asako Arai; Satomi Mitsuhashi; Yoshiaki Saito; Hirofumi Komaki; Hiroshi Sakuma; Eiji Nakagawa; Kenji Sugai; Masayuki Sasaki; Stephen P Robertson; Gen Nishimura; Toshiyuki Yamamoto; Ikuya Nonaka; Ichizo Nishino
Nemaline (actin) myopathy with myofibrillar dysgenesis and abnormal ossification.
Neuromuscular disorders : NMD 2009;19(7):485-8.
2009: Sherine Shalaby; Hiroaki Mitsuhashi; Chie Matsuda; Narihiro Minami; Satoru Noguchi; Ikuya Nonaka; Ichizo Nishino; Yukiko K Hayashi
Defective myotilin homodimerization caused by a novel mutation in MYOT exon 9 in the first Japanese limb girdle muscular dystrophy 1A patient.
Journal of neuropathology and experimental neurology 2009;68(6):701-7.
2009: May Christine Malicdan; Satoru Noguchi; Yukiko K Hayashi; Ikuya Nonaka; Ichizo Nishino
Prophylactic treatment with sialic acid metabolites precludes the development of the myopathic phenotype in the DMRV-hIBM mouse model.
Nature medicine 2009;15(6):690-5.
2009: Terumi Murakami; Yukiko K Hayashi; Megumu Ogawa; Satoru Noguchi; Kevin P Campbell; Masami Togawa; Takehiko Inoue; Akira Oka; Kousaku Ohno; Ikuya Nonaka; Ichizo Nishino
A novel POMT2 mutation causes mild congenital muscular dystrophy with normal brain MRI.
Brain & development 2009;31(6):465-8.
2009: Wen-Chen Liang; Aya Ohkuma; Yukiko K Hayashi; Luis Lopez; Michio Hirano; Ikuya Nonaka; Satoru Noguchi; Liang-Hui Chen; Yuh-Jyh Jong; Ichizo Nishino
ETFDH mutations, CoQ10 levels, and respiratory chain activities in patients with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency.
Neuromuscular disorders : NMD 2009;19(3):212-6.
2009: Aya Ohkuma; Satoru Noguchi; Hideo Sugie; May Christine Malicdan; Tokiko Fukuda; Kunio Shimazu; Luis Lopez; Michio Hirano; Yukiko K Hayashi; Ikuya Nonaka; Ichizo Nishino
Clinical and genetic analysis of lipid storage myopathies.
Muscle & nerve 2009;39(3):333-42.
2009: S Shalaby; Yukiko K Hayashi; Ikuya Nonaka; Satoru Noguchi; Ichizo Nishino
Novel FHL1 mutations in fatal and benign reducing body myopathy.
Neurology 2009;72(4):375-6.
2009: Young-Eun Park; Yukiko K Hayashi; Kanako Goto; Hirofumi Komaki; Yuichi Hayashi; Takashi Inuzuka; Satoru Noguchi; Ikuya Nonaka; Ichizo Nishino
Nuclear changes in skeletal muscle extend to satellite cells in autosomal dominant Emery-Dreifuss muscular dystrophy/limb-girdle muscular dystrophy 1B.
Neuromuscular disorders : NMD 2009;19(1):29-36.
2008: Sherine Shalaby; Yukiko K Hayashi; Kanako Goto; Megumu Ogawa; Ikuya Nonaka; Satoru Noguchi; Ichizo Nishino
Rigid spine syndrome caused by a novel mutation in four-and-a-half LIM domain 1 gene (FHL1).
Neuromuscular disorders : NMD 2008;18(12):959-61.
2008: Aya Ohkuma; Ikuya Nonaka; May Christine Malicdan; Satoru Noguchi; Satoru Ohji; Kyoichi Nomura; Hideo Sugie; Yukiko K Hayashi; Ichizo Nishino
Distal lipid storage myopathy due to PNPLA2 mutation.
Neuromuscular disorders : NMD 2008;18(8):671-4.
2008: May Christine Malicdan; Ikuya Nonaka
Distal myopathies a review: highlights on distal myopathies with rimmed vacuoles.
Neurology India 2008;56(3):314-24.
2008: May Christine Malicdan; Satoru Noguchi; Ikuya Nonaka; Paul Saftig; Ichizo Nishino
Lysosomal myopathies: an excessive build-up in autophagosomes is too much to handle.
Neuromuscular disorders : NMD 2008;18(7):521-9.
2008: I Sato; S Wu; M C A Ibarra; Yukiko K Hayashi; H Fujita; M Tojo; S J Oh; Ikuya Nonaka; Satoru Noguchi; Ichizo Nishino
Congenital neuromuscular disease with uniform type 1 fiber and RYR1 mutation.
Neurology 2008;70(2):114-22.
2007: M N Astejada; Kanako Goto; A Nagano; S Ura; Satoru Noguchi; Ikuya Nonaka; Ichizo Nishino; Yukiko K Hayashi
Emerinopathy and laminopathy clinical, pathological and molecular features of muscular dystrophy with nuclear envelopathy in Japan.
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology / edited by the Gaetano Conte Academy for the study of striated muscle diseases 2007;26(3):159-64.
2007: May Christine Malicdan; Satoru Noguchi; Ikuya Nonaka; Yukiko K Hayashi; Ichizo Nishino
A Gne knockout mouse expressing human GNE D176V mutation develops features similar to distal myopathy with rimmed vacuoles or hereditary inclusion body myopathy.
Human molecular genetics 2007;16(22):2669-82.
2007: Genri Kawahara; M Okada; N Morone; C A Ibarra; Ikuya Nonaka; Satoru Noguchi; Yukiko K Hayashi; Ichizo Nishino
Reduced cell anchorage may cause sarcolemma-specific collagen VI deficiency in Ullrich disease.
Neurology 2007;69(10):1043-9.
2007: M Okada; Genri Kawahara; Satoru Noguchi; Kazuma Sugie; Kumiko Murayama; Ikuya Nonaka; Yukiko K Hayashi; Ichizo Nishino
Primary collagen VI deficiency is the second most common congenital muscular dystrophy in Japan.
Neurology 2007;69(10):1035-42.
2007: Shigehisa Ura; Yukiko K Hayashi; Kanako Goto; Mina Nolasco Astejada; Terumi Murakami; Masako Nagato; Shigeru Ohta; Yasuhisa Daimon; Hidehiro Takekawa; Koichi Hirata; Ikuya Nonaka; Satoru Noguchi; Ichizo Nishino
Limb-girdle muscular dystrophy due to emerin gene mutations.
Archives of neurology 2007;64(7):1038-41.
2007: Teerin Liewluck; Yukiko K Hayashi; Maki Ohsawa; Rumi Kurokawa; Masako Fujita; Satoru Noguchi; Ikuya Nonaka; Ichizo Nishino
Unfolded protein response and aggresome formation in hereditary reducing-body myopathy.
Muscle & nerve 2007;35(3):322-6.
2007: Maki Ohsawa; Teerin Liewluck; Katuhisa Ogata; Takahiro Iizuka; Yukiko Hayashi; Ikuya Nonaka; Masayuki Sasaki; Ichizo Nishino
Familial reducing body myopathy.
Brain & development 2007;29(2):112-6.
2007: May Christine Malicdan; Satoru Noguchi; Ikuya Nonaka; Yukiko K Hayashi; Ichizo Nishino
A Gne knockout mouse expressing human V572L mutation develops features similar to distal myopathy with rimmed vacuoles or hereditary inclusion body myopathy.
Human molecular genetics 2007;16(2):115-28.
2006: Terumi Murakami; Yukiko K Hayashi; Satoru Noguchi; Megumu Ogawa; Ikuya Nonaka; Yuzo Tanabe; Mieko Ogino; Fumio Takada; Makoto Eriguchi; Norihiko Kotooka; Kevin P Campbell; Makiko Osawa; Ichizo Nishino
Fukutin gene mutations cause dilated cardiomyopathy with minimal muscle weakness.
Annals of neurology 2006;60(5):597-602.
2006: Shiwen Wu; M Carlos A Ibarra; May Christine Malicdan; Kumiko Murayama; Yasuko Ichihara; Hirosato Kikuchi; Ikuya Nonaka; Satoru Noguchi; Yukiko K Hayashi; Ichizo Nishino
Central core disease is due to RYR1 mutations in more than 90% of patients.
Brain : a journal of neurology 2006;129(Pt 6):1470-80.
2006: Ritsuko Ozawa; Yukiko K Hayashi; Megumu Ogawa; Rumi Kurokawa; Hiroshi Matsumoto; Satoru Noguchi; Ikuya Nonaka; Ichizo Nishino
Emerin-lacking mice show minimal motor and cardiac dysfunctions with nuclear-associated vacuoles.
The American journal of pathology 2006;168(3):907-17.
2005: Ichizo Nishino; Satoru Noguchi; Kumiko Murayama; Aya Ohkuma; Naoki Kasahata; May Christine Malicdan; Yukiko K Hayashi; Ikuya Nonaka
[Molecular pathomechanism of distal myopathy with rimmed vacuoles].
Rinshō shinkeigaku = Clinical neurology 2005;45(11):943-5.
2005: C Yan; M Tanaka; Kazuma Sugie; T Nobutoki; M Woo; N Murase; Y Higuchi; Satoru Noguchi; Ikuya Nonaka; Yukiko K Hayashi; Ichizo Nishino
A new congenital form of X-linked autophagic vacuolar myopathy.
Neurology 2005;65(7):1132-4.
2005: Ichizo Nishino; May Christine Malicdan; Kumiko Murayama; Ikuya Nonaka; Yukiko K Hayashi; Satoru Noguchi
Molecular pathomechanism of distal myopathy with rimmed vacuoles.
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology / edited by the Gaetano Conte Academy for the study of striated muscle diseases 2005;24(2):80-3.
2005: Kazuma Sugie; Satoru Noguchi; Yoshimichi Kozuka; Eri Arikawa-Hirasawa; Mikihito Tanaka; Chuanzhu Yan; Paul Saftig; Kurt von Figura; Michio Hirano; Satoshi Ueno; Ikuya Nonaka; Ichizo Nishino
Autophagic vacuoles with sarcolemmal features delineate Danon disease and related myopathies.
Journal of neuropathology and experimental neurology 2005;64(6):513-22.
2005: Hiroshi Matsumoto; Yukiko K Hayashi; Dae-Son Kim; Megumu Ogawa; Terumi Murakami; Satoru Noguchi; Ikuya Nonaka; Tomoyuki Nakazawa; Takiko Matsuo; Satoshi Futagami; Kevin P Campbell; Ichizo Nishino
Congenital muscular dystrophy with glycosylation defects of alpha-dystroglycan in Japan.
Neuromuscular disorders : NMD 2005;15(5):342-8.
2005: Tzung-Chang Tsai; Hideo Horinouchi; Satoru Noguchi; Narihiro Minami; Kumiko Murayama; Yukiko K Hayashi; Ikuya Nonaka; Ichizo Nishino
Characterization of MTM1 mutations in 31 Japanese families with myotubular myopathy, including a patient carrying 240 kb deletion in Xq28 without male hypogenitalism.
Neuromuscular disorders : NMD 2005;15(3):245-52.
2004: Kazuma Sugie; Kumiko Murayama; Satoru Noguchi; Nobuyuki Murakami; Mika Mochizuki; Yukiko K Hayashi; Ikuya Nonaka; Ichizo Nishino
Two novel CAV3 gene mutations in Japanese families.
Neuromuscular disorders : NMD 2004;14(12):810-4.
2004: Y Ohashi; Y Hasegawa; Kumiko Murayama; Megumu Ogawa; T Hasegawa; M Kawai; N Sakata; K Yoshida; H Yarita; K Imai; I Kumagai; K Murakami; H Hasegawa; Satoru Noguchi; Ikuya Nonaka; S Yamaguchi; Ichizo Nishino
A new diagnostic test for VLCAD deficiency using immunohistochemistry.
Neurology 2004;62(12):2209-13.
2004: D S Kim; Yukiko K Hayashi; Hiroshi Matsumoto; Megumu Ogawa; Satoru Noguchi; N Murakami; R Sakuta; M Mochizuki; Daniel Michele; Kevin P Campbell; Ikuya Nonaka; Ichizo Nishino
POMT1 mutation results in defective glycosylation and loss of laminin-binding activity in alpha-DG.
Neurology 2004;62(6):1009-11.
2004: Satoru Noguchi; Yoko Keira; Kumiko Murayama; Megumu Ogawa; Masako Fujita; Genri Kawahara; Yasushi Oya; Masaoki Imazawa; Yu-Ichi Goto; Yukiko K Hayashi; Ikuya Nonaka; Ichizo Nishino
Reduction of UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase activity and sialylation in distal myopathy with rimmed vacuoles.
The Journal of biological chemistry 2004;279(12):11402-7.
2004: H Ishikawa; Kazuma Sugie; Kumiko Murayama; A Awaya; Y Suzuki; Satoru Noguchi; Yukiko K Hayashi; Ikuya Nonaka; Ichizo Nishino
Ullrich disease due to deficiency of collagen VI in the sarcolemma.
Neurology 2004;62(4):620-3.
2003: Tetsuro Nagasawa; Akira Sudo; Michio Fukumizu; Shigeru Hanaoka; Masayuki Sasaki; Kenji Sugai; Ikuya Nonaka
Congenital monomelic neurogenic disorder with calf muscle hypertrophy.
Brain & development 2003;25(8):571-3.
2003: Kazuma Sugie; Tateo Koori; Ayaka Yamamoto; Megumu Ogawa; Michio Hirano; Kiyoharu Inoue; Ikuya Nonaka; Ichizo Nishino
Characterization of Danon disease in a male patient and his affected mother.
Neuromuscular disorders : NMD 2003;13(9):708-11.
2003: Kazuhiko Tagawa; Megumu Ogawa; Kiyokazu Kawabe; Gaku Yamanaka; Tsuyoshi Matsumura; Kanako Goto; Ikuya Nonaka; Ichizo Nishino; Yukiko K Hayashi
Protein and gene analyses of dysferlinopathy in a large group of Japanese muscular dystrophy patients.
Journal of the neurological sciences 2003;211(1-2):23-8.
2003: Ken-ichi Yamada; Kenji Sugai; Michio Fukumizu; Shigeru Hanaoka; Masayuki Sasaki; Ikuya Nonaka
[The parents' assessment and needs for home mechanical ventilation in patients with pediatric neurological disorders].
No to hattatsu. Brain and development 2003;35(2):147-52.
2003: Toshikuni Sasaoka; Michihiro Imamura; Kenji Araishi; Satoru Noguchi; Yuji Mizuno; Naomi Takagoshi; Hiroshi Hama; Eriko Wakabayashi-Takai; Yukiko Yoshimoto-Matsuda; Ikuya Nonaka; Kiyotoshi Kaneko; Mikiharu Yoshida; Eijiro Ozawa
Pathological analysis of muscle hypertrophy and degeneration in muscular dystrophy in gamma-sarcoglycan-deficient mice.
Neuromuscular disorders : NMD 2003;13(3):193-206.
2002: Ichizo Nishino; Satoru Noguchi; Kumiko Murayama; Adel Driss; Kazuma Sugie; Yasushi Oya; T Nagata; K Chida; T Takahashi; Y Takusa; T Ohi; J Nishimiya; N Sunohara; E Ciafaloni; M Kawai; M Aoki; Ikuya Nonaka
Distal myopathy with rimmed vacuoles is allelic to hereditary inclusion body myopathy.
Neurology 2002;59(11):1689-93.
2002: H Ishikawa; Kazuma Sugie; Kumiko Murayama; M Ito; Narihiro Minami; Ichizo Nishino; Ikuya Nonaka
Ullrich disease: collagen VI deficiency: EM suggests a new basis for muscular weakness.
Neurology 2002;59(6):920-3.
2002: Eri Arikawa-Hirasawa; Alexander H Le; Ichizo Nishino; Ikuya Nonaka; Nicola C. Ho; Clair A Francomano; Prasanthi Govindraj; John R Hassell; Joseph M Devaney; Jürgen Spranger; Roger E Stevenson; Susan Iannaccone; Marinos C Dalakas; Yoshihiko Yamada
Structural and functional mutations of the perlecan gene cause Schwartz-Jampel syndrome, with myotonic myopathy and chondrodysplasia.
American journal of human genetics 2002;70(5):1368-75.
2001: Chie Matsuda; Yukiko K Hayashi; M Ogawa; M Aoki; K Murayama; I Nishino; Ikuya Nonaka; Kiichi Arahata; Robert H Brown
The sarcolemmal proteins dysferlin and caveolin-3 interact in skeletal muscle.
Human molecular genetics 2001;10(17):1761-6.
2001: Yukiko K Hayashi; Megumu Ogawa; K Tagawa; Satoru Noguchi; T Ishihara; Ikuya Nonaka; Kiichi Arahata
Selective deficiency of alpha-dystroglycan in Fukuyama-type congenital muscular dystrophy.
Neurology 2001;57(1):115-21.
2001: Yukiko K Hayashi; Z Tezak; T Momoi; Ikuya Nonaka; C A Garcia; Eric Hoffman; Kiichi Arahata
Massive muscle cell degeneration in the early stage of merosin-deficient congenital muscular dystrophy.
Neuromuscular disorders : NMD 2001;11(4):350-9.
2000: Yasuko Hagiwara; Toshikuni Sasaoka; Kenji Araishi; Michihiro Imamura; H Yorifuji; Ikuya Nonaka; Eijiro Ozawa; T Kikuchi
Caveolin-3 deficiency causes muscle degeneration in mice.
Human molecular genetics 2000;9(20):3047-54.
2000: Yasuko Ichihara; Junji Sasaki; Hirosato Kikuchi; M Ozawa; Y Goto; Ikuya Nonaka
[Preliminary report: first identification of known mutation in the ryanodine receptor gene in a Japanese malignant hyperthermia pedigree].
Masui. The Japanese journal of anesthesiology 2000;49(4):404-6.
1999: Masayuki Sasaki; E Kondo; Y Yamashita; T Toda; Ikuya Nonaka
[A patient of Walker-Warburg syndrome with a haplotype different from that in Fukuyama-type congenital muscular dystrophy].
No to hattatsu. Brain and development 1999;31(5):445-51.
1999: A Ishii; Yasuko Hagiwara; Y Saito; K Yamamoto; K Yuasa; Y Sato; K Arahata; S Shoji; Ikuya Nonaka; I Saito; Y Nabeshima; S Takeda
Effective adenovirus-mediated gene expression in adult murine skeletal muscle.
Muscle & nerve 1999;22(5):592-9.
1998: Hidenori Suzuki; Asako Hase; B Y Kim; Y Miyata; Ikuya Nonaka; Kiichi Arahata; C Akazawa
Up-regulation of glial cell line-derived neurotrophic factor (GDNF) expression in regenerating muscle fibers in neuromuscular diseases.
Neuroscience letters 1998;257(3):165-7.
1998: S Kubo; Toshifumi Tsukahara; M Takemitsu; K B Yoon; H Utsumi; Ikuya Nonaka; Kiichi Arahata
Presence of emerinopathy in cases of rigid spine syndrome.
Neuromuscular disorders : NMD 1998;8(7):502-7.
1998: Yukiko K Hayashi; F L Chou; E Engvall; M Ogawa; Chie Matsuda; S Hirabayashi; K Yokochi; Barry L Ziober; Randall H Kramer; Stephen J Kaufman; Eijiro Ozawa; Y Goto; Ikuya Nonaka; T Tsukahara; J Z Wang; Eric Hoffman; Kiichi Arahata
Mutations in the integrin alpha7 gene cause congenital myopathy.
Nature genetics 1998;19(1):94-7.
1997: B L Hodges; Yukiko K Hayashi; Ikuya Nonaka; W Wang; Kiichi Arahata; Stephen J Kaufman
Altered expression of the alpha7beta1 integrin in human and murine muscular dystrophies.
Journal of cell science 1997;110 ( Pt 22)():2873-81.
1997: Y Miyagoe; K Hanaoka; Ikuya Nonaka; M Hayasaka; Y Nabeshima; Kiichi Arahata; Y Nabeshima; S Takeda
Laminin alpha2 chain-null mutant mice by targeted disruption of the Lama2 gene: a new model of merosin (laminin 2)-deficient congenital muscular dystrophy.
FEBS letters 1997;415(1):33-9.
1997: Y Saito; Kenji Sugai; Masayuki Sasaki; S Hirano; Shigeru Hanaoka; Toshiaki Hashimoto; Ikuya Nonaka; T Nagai
[A case of congenital hypomyelination neuropathy with type I Chiari malformation and mental retardation].
No to hattatsu. Brain and development 1997;29(5):378-83.
1997: H Ishii; Yukiko K Hayashi; Ikuya Nonaka; Kiichi Arahata
Electron microscopic examination of basal lamina in Fukuyama congenital muscular dystrophy.
Neuromuscular disorders : NMD 1997;7(3):191-7.
1997: S Tanaka; S Osari; M Ozawa; H Yamanouchi; Y Goto; H Matsuda; Ikuya Nonaka
Recurrent pain attacks in a 3-year-old patient with myoclonus epilepsy associated with ragged-red fibers (MERRF): a single-photon emission computed tomographic (SPECT) and electrophysiological study.
Brain & development 1997;19(3):205-8.
1997: H Kinoshita; Norio Sakuragawa; H Tada; E Naito; Yasuhiro Kuroda; Ikuya Nonaka
Recurrent muscle weakness and ataxia in thiamine-responsive pyruvate dehydrogenase complex deficiency.
Journal of child neurology 1997;12(2):141-4.
1996: E Nakagawa; S Osari; H Yamanouchi; H Matsuda; Y Goto; Ikuya Nonaka
Long-term therapy with cytochrome c, flavin mononucleotide and thiamine diphosphate for a patient with Kearns-Sayre syndrome.
Brain & development 1996;18(1):68-70.
1996: E Nakagawa; M Ozawa; H Yamanouchi; Kenji Sugai; Y Goto; Ikuya Nonaka
Severe central nervous system involvement in a patient with congenital fiber-type disproportion myopathy.
Journal of child neurology 1996;11(1):71-3.
1995: H Kinoshita; Kenji Sugai; Y Goto; Ikuya Nonaka
Early onset distal muscular dystrophy.
Brain & development 1995;17(3):206-9.
1995: H Kinoshita; Y Goto; M Ishikawa; T Uemura; K Matsumoto; Y K Hayashi; K Arahata; Ikuya Nonaka
A carrier of Duchenne muscular dystrophy with dilated cardiomyopathy but no skeletal muscle symptom.
Brain & development 1995;17(3):202-5.