Search Results1-20 of  54

  • 1 / 3
  • Saito Kayoko ID: 9000010198973

    Articles in CiNii:1

    • The Political Matter and the Domestic Tragedy in The Secret Agent (2006)
  • Saito Kayoko ID: 9000291890515

    Articles in CiNii:1

    • A new method for SMN1 and hybrid SMN gene analysis in spinal muscular atrophy using long-range PCR followed by sequencing (2015)
  • Saito Kayoko ID: 9000337069749

    Articles in CiNii:1

    • Target resequencing of neuromuscular disease-related genes using next-generation sequencing for patients with undiagnosed early-onset neuromuscular disorders (2016)
  • SAITO Kayoko ID: 9000402269411

    Articles in CiNii:1

    • Diagnosis and Genetic Counseling for Mitochondrial Disease at the Institute of Medical Genetics, Tokyo Women's Medical University (2018)
  • SAITO KAYOKO ID: 9000254213046

    Articles in CiNii:1

    • Studies on the Metabolic Products of a Strain of Aspergillus fumigatus DH 413. VI. Metabolic Position of 3, 4-Dihydroxytoluquinone and Fumigatin Chlorohydrin in Fumigatin Biosynthesis (1974)
  • SAITO Kayoko ID: 9000000421264

    Institute of Medical Genetics, Tokyo Women's medical University (2010 from CiNii)

    Articles in CiNii:7

    • Fukuyama congenital muscular dystrophy: Cortical dysplasia of the cerebrum in a 20 week fetus (1996)
    • Polymorphism analysis of Fukuyama type congenital muscular dystrophy(FCMD) siblings with different phenotypes (1997)
    • Pial-glial barrier abnormalities in fetuses with Fukuyama congenital muscular dystrophy (1997)
  • SAITO Kayoko ID: 9000000435958

    Dpartment of Pediatrics, Tokyo Women's Medical College (1995 from CiNii)

    Articles in CiNii:1

    • Abnormality of cerebral gangliosides in Fukuyama type congenital muscular dystrophy (1995)
  • SAITO Kayoko ID: 9000000728389

    聖マリアンナ医科大学第2内科 (1996 from CiNii)

    Articles in CiNii:2

    • Ultrasound diagnosis of cerebral vascular disease : Supplementary presentation with special reference to intracranial vessels (1995)
    • Difference of efficacy of various antihypercholesterolemic therapies in human dry dock (1996)
  • SAITO Kayoko ID: 9000001083250

    Department of Pediatrics, Tokyo Women's Medical University (2003 from CiNii)

    Articles in CiNii:1

    • Bibliography of congenital muscular dystrophies : Series V (2001) (2003)
  • SAITO Kayoko ID: 9000001758711

    Institute of Medical Genetics, Tokyo Women's Medical University (2006 from CiNii)

    Articles in CiNii:1

    • Unified method for Bayesian calculation of genetic risk (2006)
  • SAITO Kayoko ID: 9000001891331

    Institute of Medical Genetics, Tokyo Women's Medical University (2006 from CiNii)

    Articles in CiNii:1

    • The mildest known case of Fukuyama-type congenital muscular dystrophy (2006)
  • SAITO Kayoko ID: 9000006158225

    Institute of Medical Genetics, Tokyo Women's Medical University (2011 from CiNii)

    Articles in CiNii:6

    • Thalamic lesions in a long-surviving child with spinal muscular atrophy type I : MRI and EEG findings (2004)
    • A 1-year-old infant with McArdle disease associated with hyper-creatine kinase-emia during febrile episodes (2003)
    • TRH therapy in a patient with juvenile Alexander disease (2006)
  • SAITO Kayoko ID: 9000006498501

    Articles in CiNii:28

    • Study on surgical treatment of intractable childhood epilepsy (1998)
    • Genetic abnormalities underlying familial epilepsy syndromes (2002)
    • Electroclinical Picture of Autosomal Dominant Nocturnal Frontal Lobe Epilepsy in a Japanese Family (2000)
  • SAITO Kayoko ID: 9000016823389

    Institute of Medical Genetics, Tokyo Women's Medical University (2009 from CiNii)

    Articles in CiNii:1

    • An autopsy case of spinal muscular atrophy type III (Kugelberg-Welander disease) (2009)
  • SAITO Kayoko ID: 9000018530655

    Tokyo Women's Medical University Institute for Integrated Medical Sciences (2011 from CiNii)

    Articles in CiNii:4

    • A Case of Fukuyama Congenital Muscular Dystrophy Associated with Negative Electroretinograms (2010)
    • Loss-of-function mutation of collybistin is responsible for X-linked mental retardation associated with epilepsy (2011)
    • Tandem configurations of variably duplicated segments of 22q11.2 confirmed by fiber-FISH analysis (2011)
  • SAITO Kayoko ID: 9000019148253

    Institute of Medical Genetics, Tokyo Women's Medical University (2012 from CiNii)

    Articles in CiNii:1

    • Mutations in PRRT2 responsible for paroxysmal kinesigenic dyskinesias also cause benign familial infantile convulsions (2012)
  • SAITO Kayoko ID: 9000019187466

    Institute of Medical Genetics, Tokyo Women's Medical University (2009 from CiNii)

    Articles in CiNii:1

    • Neurofilament light chain polypeptide gene mutations in Charcot-Marie-Tooth disease : nonsense mutation probably causes a recessive phenotype (2009)
  • SAITO Kayoko ID: 9000019187736

    Institute of Medical Genetics, Tokyo Women's Medical University, School of Medicine (2009 from CiNii)

    Articles in CiNii:1

    • Nevoid basal cell carcinoma syndrome with cleft lip and palate associated with the novel PTCH gene mutations (2009)
  • SAITO Kayoko ID: 9000021309219

    <I>Second Department of Internal Medicine, St. Marianna University School of Medicine</I> (1993 from CiNii)

    Articles in CiNii:1

    • Spectral Analysis of Blood Pressure and Blood Flow Velocity in the Middle Cerebral Artery Using the Maximum Entropy Method (MEM) (1993)
  • SAITO Kayoko ID: 9000256113195

    Department of Pediatrics, Tokyo Women's Medical College (1980 from CiNii)

    Articles in CiNii:1

    • Usefulness of Percutaneous Needle Muscle Biopsy in the Diagnosis of Neuromuscular Disorders in Children:Histological, Histochemical and Electron Microscopic Studies (1980)
  • 1 / 3
Page Top