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Rapid Reduction of pH and CaCO3 Saturation State in the Tsugaru Strait by the Intensified Tsugaru Warm Current During 2012–2019

Geophysical research letters, 2021-05, Vol.48 (10), p.n/a

2021

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Implantable CMOS image sensor with incident-angle-selective pixels

Electronics letters, 2019-06, Vol.55 (13), p.729-731

2019

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Effects of CO2 and iron availability on rbcL gene expression in Bering Sea diatoms

Biogeosciences, 2015-04, Vol.12 (7), p.2247-2259

2015

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Reactive-gas-flow sputter deposition of amorphous WO3 films for electrochromic devices

Thin solid films, 2013-04, Vol.532, p.1-6

2013

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Myositis with sarcoplasmic inclusions in Nakajo–Nishimura syndrome: a genetic inflammatory myopathy

Neuropathology and applied neurobiology, 2020-10, Vol.46 (6), p.579-587

2020

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looking within – implantable image sensors

Electronics letters, 2019-06, Vol.55 (13), p.718-718

2019

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Primary collagen VI deficiency is the second most common congenital muscular dystrophy in Japan

Neurology, 2007-09, Vol.69 (10), p.1035-1042

2007

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Clinical features of knee osteoarthritis in patients with sporadic inclusion body myositis

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S202-S202

2016

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Resting spore formation in the marine diatom Thalassiosira nordenskioeldii under iron- and nitrogen-limited conditions

Journal of plankton research, 2008-11, Vol.30 (11), p.1245-1255

2008

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Clinicopathological features of genetically confirmed Danon disease

Neurology, 2002-06, Vol.58 (12), p.1773-1778

2002

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Characteristic MRI findings of upper limb muscle involvement in myotonic dystrophy type 1

Neuromuscular disorders : NMD, 2015-10, Vol.25, p.S272-S272

2015

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Serum and muscular kl-6/muc1 are useful biomarker for gne-myopathy

Journal of the neurological sciences, 2015-10, Vol.357, p.e338-e338

2015

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Distal myopathy with rimmed vacuoles is allelic to hereditary inclusion body myopathy

Neurology, 2002-12, Vol.59 (11), p.1689-1693

2002

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Ullrich disease due to deficiency of collagen VI in the sarcolemma

Neurology, 2004-02, Vol.62 (4), p.620-623

2004

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Synergistic effects of pCO2 and iron availability on nutrient consumption ratio of the Bering Sea phytoplankton community

Biogeosciences, 2013-10, Vol.10 (10), p.6309-6321

2013

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Ullrich disease: collagen VI deficiency: EM suggests a new basis for muscular weakness

Neurology, 2002-09, Vol.59 (6), p.920-923

2002

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Thioredoxin-binding protein-2 (TBP-2 VDUP1 TXNIP) regulates T-cell sensitivity to glucocorticoid during HTLV-I-induced transformation

Leukemia, 2011-03, Vol.25 (3), p.440-448

2011

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G.P.53

Neuromuscular disorders : NMD, 2014-10, Vol.24 (9), p.810-811

2014

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Coexistence of chronic inflammatory demyelinating polyneuropathy and camptocormia

Journal of neurology, neurosurgery and psychiatry, 2009-11, Vol.80 (11), p.1296-1297

2009

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P.3.3 MUC1 is associated with the pathogenesis of GNE-myopathy

Neuromuscular disorders : NMD, 2013-10, Vol.23 (9), p.756-756

2013

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589P Nanopore CRISPR/Cas9-targeted sequencing reveals genetic characteristics and a possible haplotype in oculopharyngodistal myopathy

Neuromuscular disorders : NMD, 2024-10, Vol.43, p.104441, Article 104441.344

2024

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Teaching NeuroImages: Hemiatrophy as a clinical presentation in facioscapulohumeral muscular dystrophy

Neurology, 2009-08, Vol.73 (5), p.e24

2009

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586P Visualization of degenerative processes of the myofibers on muscle pathology in OPDM based on single nucleus RNA-seq data

Neuromuscular disorders : NMD, 2024-10, Vol.43, p.104441, Article 104441.341

2024

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A new congenital form of X-linked autophagic vacuolar myopathy

Neurology, 2005-10, Vol.65 (7), p.1132-1134

2005

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HP18: Analysis of functional connectivity in non-motor symptoms in Parkinson’s Disease

Clinical neurophysiology, 2022-03, Vol.135, p.e5-e5

2022

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Rapid Reduction of pH and CaCO3 Saturation State in the Tsugaru Strait by the Intensified Tsugaru Warm Current During 2012–2019

Implantable CMOS image sensor with incident-angle-selective pixels

Effects of CO2 and iron availability on rbcL gene expression in Bering Sea diatoms

Reactive-gas-flow sputter deposition of amorphous WO3 films for electrochromic devices

Myositis with sarcoplasmic inclusions in Nakajo–Nishimura syndrome: a genetic inflammatory myopathy

looking within – implantable image sensors

Primary collagen VI deficiency is the second most common congenital muscular dystrophy in Japan

Clinical features of knee osteoarthritis in patients with sporadic inclusion body myositis

Resting spore formation in the marine diatom Thalassiosira nordenskioeldii under iron- and nitrogen-limited conditions

Clinicopathological features of genetically confirmed Danon disease

Characteristic MRI findings of upper limb muscle involvement in myotonic dystrophy type 1

Serum and muscular kl-6/muc1 are useful biomarker for gne-myopathy

Distal myopathy with rimmed vacuoles is allelic to hereditary inclusion body myopathy

Ullrich disease due to deficiency of collagen VI in the sarcolemma

Synergistic effects of pCO2 and iron availability on nutrient consumption ratio of the Bering Sea phytoplankton community

Ullrich disease: collagen VI deficiency: EM suggests a new basis for muscular weakness

Thioredoxin-binding protein-2 (TBP-2 VDUP1 TXNIP) regulates T-cell sensitivity to glucocorticoid during HTLV-I-induced transformation

G.P.53

Coexistence of chronic inflammatory demyelinating polyneuropathy and camptocormia

P.3.3 MUC1 is associated with the pathogenesis of GNE-myopathy

589P Nanopore CRISPR/Cas9-targeted sequencing reveals genetic characteristics and a possible haplotype in oculopharyngodistal myopathy

Teaching NeuroImages: Hemiatrophy as a clinical presentation in facioscapulohumeral muscular dystrophy

586P Visualization of degenerative processes of the myofibers on muscle pathology in OPDM based on single nucleus RNA-seq data

A new congenital form of X-linked autophagic vacuolar myopathy

HP18: Analysis of functional connectivity in non-motor symptoms in Parkinson’s Disease

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