Search Results1-20 of  39

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  • Osaka Hitoshi ID: 9000009576891

    Articles in CiNii:1

    • Empirical Analysis on the Economic Effects of Foreign Aid (2001)
  • Osaka Hitoshi ID: 9000014705270

    Articles in CiNii:1

    • The long-term trend of productivity and the determinants of factor inputs since China's economic reform (2009)
  • Osaka Hitoshi ID: 9000261012200

    Articles in CiNii:1

    • Causative novel PNKP mutations and concomitant PCDH15 mutations in a patient with microcephaly with early-onset seizures and developmental delay syndrome and hearing loss (2014)
  • Osaka Hitoshi ID: 9000280538634

    Articles in CiNii:1

    • Mutations in the glutaminyl-tRNA synthetase gene cause early-onset epileptic encephalopathy (2015)
  • Osaka Hitoshi ID: 9000313182347

    Articles in CiNii:1

    • De novo KIF1A mutations cause intellectual deficit, cerebellar atrophy, lower limb spasticity and visual disturbance (2015)
  • Osaka Hitoshi ID: 9000329423402

    Articles in CiNii:1

    • WDR45 mutations in three male patients with West syndrome (2016)
  • Osaka Hitoshi ID: 9000403925143

    Articles in CiNii:1

    • Mitochonic Acid 5 (MA-5) Facilitates ATP Synthase Oligomerization and Cell Survival in Various Mitochondrial Diseases (2017)
  • OSAKA Hitoshi ID: 9000000436227

    Department of pediatrics, Urafune Hospital of Yokohama City University (1996 from CiNii)

    Articles in CiNii:4

    • Tolosa-hunt syndrome with pseudotumor cerebri.report of an unusual case (1995)
    • Pelizaeus-Merzbacher-like disease: female case report (1996)
    • Coefficient of variation of R-R intervals in severe brain damage (1996)
  • OSAKA Hitoshi ID: 9000003654568

    Divisions of Neurology, Kanagawa Children's Medical Center (2013 from CiNii)

    Articles in CiNii:21

    • 同一アレルに複数の遺伝子変異を有した異染性白質ジストロフィーの1男児例 (2007)
    • A Case of GM1-gangliosidosis with Foam Cells in Peripheral Blood and Dysmyelination in Brain-MRI (2009)
    • Outcome assessment in treatment of edaravone in childhood ischemic stroke (2008)
  • OSAKA Hitoshi ID: 9000004139697

    Department of Pediatrics, Urafune Hospital of Yokohama City University, School of Medicine (1996 from CiNii)

    Articles in CiNii:8

    • Plasma Exchange for Treating Childhood Neuromuscular Disorders (1996)
    • Hyperintense Brain Lesions on T_1-Weighted MRI after Parenteral Nutrition (1996)
    • Defects of Pyruvate Metabolism in Cultured Lymjphoblastoid Cells of 20 Patients with Leigh Syndrome (1996)
  • OSAKA Hitoshi ID: 9000004717314

    Department of Degenerative Neurological Diseases, National Institute of Neuroscience, National Center of Neurology and Psychiatry (2001 from CiNii)

    Articles in CiNii:2

    • The ubiquitin-proteasome system and neurodegeneration (2001)
    • P-2B-41 薄束核-軸索変性(gad)マウスの行動解析(日本動物心理学会第61回大会発表要旨) (2001)
  • OSAKA Hitoshi ID: 9000006949522

    Graduate School of Economics, Kyushu University (2007 from CiNii)

    Articles in CiNii:1

    • A research note on the regional trend of income inequality in Asia: Kuznets hypothesis revisited (2007)
  • OSAKA Hitoshi ID: 9000006949536

    Graduate School of Economics, Kyushu University (2008 from CiNii)

    Articles in CiNii:1

    • Environmental issues in economic development: reappraisal of CO2 emissions in Asia (2008)
  • OSAKA Hitoshi ID: 9000016662841

    Division of Neurology, Kanagawa Children's Medical Center (2008 from CiNii)

    Articles in CiNii:1

    • Early onset West syndrome with cerebral hypomyelination and reduced cerebral white matter (2008)
  • OSAKA Hitoshi ID: 9000018467772

    Division of Neurology, Kanagawa Children's Medical Center (2010 from CiNii)

    Articles in CiNii:1

    • Nationwide survey (incidence, clinical course, prognosis) of Rasmussen's encephalitis (2010)
  • OSAKA Hitoshi ID: 9000018467985

    Division of Neurology, Kanagawa Children's Medical Center (2011 from CiNii)

    Articles in CiNii:2

    • Mild phenotype in Pelizaeus-Merzbacher disease caused by a PLP1-specific mutation (2010)
    • 5,10-Methylenetetrahydrofolate reductase deficiency with progressive polyneuropathy in an infant (2011)
  • OSAKA Hitoshi ID: 9000018652906

    Division of Neurology, Kanagawa Children's Medical Center (2010 from CiNii)

    Articles in CiNii:1

    • 1p36 deletion syndrome associated with Prader-Willi-like phenotype (2010)
  • OSAKA Hitoshi ID: 9000107310281

    Division of Neurology, Kanagawa Children's Medical Center (2012 from CiNii)

    Articles in CiNii:1

    • Paradoxical increase in seizure frequency with valproate in nonketotic hyperglycinemia (2012)
  • OSAKA Hitoshi ID: 9000107387965

    Division of Neurology, Clinical Research Institute, Kanagawa Children's Medical Center (2012 from CiNii)

    Articles in CiNii:1

    • A girl with early-onset epileptic encephalopathy associated with microdeletion involving CDKL5 (2012)
  • OSAKA Hitoshi ID: 9000238239818

    Department of Neurology, Kanagawa Children's Medical Center (2011 from CiNii)

    Articles in CiNii:1

    • Acute encephalopathy in two cases with severe congenital hydrocephalus (2011)
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