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Experimental estimation of the spin diffusion length in undoped p-Ge on Fe3Si using vertical spin-valve devices

Journal of applied physics, 2021-01, Vol.129 (1)

2021

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Cytokine-related and sodium channel polymorphism as candidate predisposing factors for childhood encephalopathy FIRES/AERRPS

Journal of the neurological sciences, 2016-09, Vol.368, p.272-276

2016

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Epitaxial growth of Sb-doped Ge layers on ferromagnetic Fe3Si for vertical semiconductor spintronic devices

Semiconductor science and technology, 2018-09, Vol.33 (10)

2018

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Expansion of the first PolyA tract of ARX causes infantile spasms and status dystonicus

Neurology, 2007-07, Vol.69 (5), p.427

2007

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Widening Spectrum of a Reversible Splenial Lesion with Transiently Reduced Diffusion

American Journal of Neuroradiology, 2006-04, Vol.27 (4), p.836-838

2006

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Epitaxial growth of Sb-doped Ge layers on ferromagnetic Fe 3 Si for vertical semiconductor spintronic devices

Semiconductor science and technology, 2018-10, Vol.33 (10), p.104008

2018

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Fluctuation of Computed Tomographic Findings in White Matter in Alexander's Disease

Journal of child neurology, 2002-03, Vol.17 (3), p.227-230

2002

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A nationwide survey of opsoclonus–myoclonus syndrome in Japanese children

Brain & development (Tokyo. 1979), 2015-08, Vol.37 (7), p.656-660

2015

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Hypomyelination with atrophy of the basal ganglia and cerebellum: further delineation of the phenotype and genotype―phenotype correlation

Brain (London, England : 1878), 2014-07, Vol.137 (Pt 7), p.1921-1930

2014

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Clinical characteristics and visual outcomes of work-related open globe injuries in Japanese patients

Scientific reports, 2020-01, Vol.10 (1), p.1208-1208, Article 1208

2020

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Clinical characteristics of SARS-CoV-2-associated encephalopathy in children: Nationwide epidemiological study

Journal of the neurological sciences, 2024-02, Vol.457, p.122867-122867, Article 122867

2024

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Clinical characteristics and outcomes of fall-related open globe injuries in Japan

Graefe's archive for clinical and experimental ophthalmology, 2018-07, Vol.256 (7), p.1347-1352

2018

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A Standard Set of Value-Based Patient-Centered Outcomes for Pancreatic Carcinoma: An International Delphi Survey

Annals of surgical oncology, 2021-02, Vol.28 (2), p.1069-1078

2021

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Phenotypic consequences of genetic variation at hemizygous alleles: Sotos syndrome is a contiguous gene syndrome incorporating coagulation factor twelve (FXII) deficiency

Genetics in medicine, 2005-09, Vol.7 (7), p.479-483

2005

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Clinically mild encephalitis/encephalopathy with a reversible splenial lesion

Neurology, 2005-04, Vol.64 (8), p.1487; author reply 1487

2005

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Asymptomatic hereditary Alexander's disease caused by a novel mutation in GFAP

Journal of the neurological sciences, 2004-10, Vol.225 (1), p.125-127

2004

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Costello Syndrome Showing Moyamoya-like Vasculopathy

Pediatric neurology, 2005-05, Vol.32 (5), p.361-363

2005

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Craniosynostosis with extra copy of MSX2 in a patient with partial 5q-trisomy

American journal of medical genetics, 2004-07, Vol.128A (2), p.214-216

2004

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Preferential Paternal Origin of Microdeletions Caused by Prezygotic Chromosome or Chromatid Rearrangements in Sotos Syndrome

American journal of human genetics, 2003-05, Vol.72 (5), p.1331-1337

2003

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Microcephaly, Cerebellar Atrophy, and Focal Segmental Glomerulosclerosis in Two Brothers: A Possible Mild Form of Galloway-Mowat Syndrome

Journal of child neurology, 2003-02, Vol.18 (2), p.147-149

2003

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Accurate motion-produced distance and direction under systematically distorted perception

Japanese psychological research, 2005-09, Vol.47 (3), p.163-174

2005

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Progressive Sliding Hiatal Hernia as a Complication of Menkes' Syndrome

Journal of child neurology, 2002-05, Vol.17 (5), p.401-402

2002

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Spondyloepimetaphyseal dysplasia with joint laxity leptodactylic form: Clinical course and phenotypic variations in four patients

American journal of medical genetics, 2003-03, Vol.117A (2), p.147-153

2003

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Sonic hedgehog signal peptide mutation in a patient with holoprosencephaly

Annals of neurology, 2000-04, Vol.47 (4), p.514-516

2000

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Experimental estimation of the spin diffusion length in undoped p-Ge on Fe3Si using vertical spin-valve devices

Cytokine-related and sodium channel polymorphism as candidate predisposing factors for childhood encephalopathy FIRES/AERRPS

Epitaxial growth of Sb-doped Ge layers on ferromagnetic Fe3Si for vertical semiconductor spintronic devices

Expansion of the first PolyA tract of ARX causes infantile spasms and status dystonicus

Widening Spectrum of a Reversible Splenial Lesion with Transiently Reduced Diffusion

Epitaxial growth of Sb-doped Ge layers on ferromagnetic Fe 3 Si for vertical semiconductor spintronic devices

Fluctuation of Computed Tomographic Findings in White Matter in Alexander's Disease

A nationwide survey of opsoclonus–myoclonus syndrome in Japanese children

Hypomyelination with atrophy of the basal ganglia and cerebellum: further delineation of the phenotype and genotype―phenotype correlation

Clinical characteristics and visual outcomes of work-related open globe injuries in Japanese patients

Fifty microdeletions among 112 cases of Sotos syndrome: Low copy repeats possibly mediate the common deletion

Clinical characteristics of SARS-CoV-2-associated encephalopathy in children: Nationwide epidemiological study

Clinical characteristics and outcomes of fall-related open globe injuries in Japan

A Standard Set of Value-Based Patient-Centered Outcomes for Pancreatic Carcinoma: An International Delphi Survey

Phenotypic consequences of genetic variation at hemizygous alleles: Sotos syndrome is a contiguous gene syndrome incorporating coagulation factor twelve (FXII) deficiency

Clinically mild encephalitis/encephalopathy with a reversible splenial lesion

Asymptomatic hereditary Alexander's disease caused by a novel mutation in GFAP

Costello Syndrome Showing Moyamoya-like Vasculopathy

Craniosynostosis with extra copy of MSX2 in a patient with partial 5q-trisomy

Preferential Paternal Origin of Microdeletions Caused by Prezygotic Chromosome or Chromatid Rearrangements in Sotos Syndrome

Microcephaly, Cerebellar Atrophy, and Focal Segmental Glomerulosclerosis in Two Brothers: A Possible Mild Form of Galloway-Mowat Syndrome

Accurate motion-produced distance and direction under systematically distorted perception

Progressive Sliding Hiatal Hernia as a Complication of Menkes' Syndrome

Spondyloepimetaphyseal dysplasia with joint laxity leptodactylic form: Clinical course and phenotypic variations in four patients

Sonic hedgehog signal peptide mutation in a patient with holoprosencephaly

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