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The basis examination of leukocyte-platelet aggregates with CD45 gating as a novel platelet activation marker

International journal of laboratory hematology, 2013-10, Vol.35 (5), p.534-541

2013

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Demyelinating and axonal features of Charcot–Marie–Tooth disease with mutations of myelin‐related proteins (PMP22, MPZ and Cx32): a clinicopathological study of 205 Japanese patients

Brain (London, England : 1878), 2003-01, Vol.126 (1), p.134-151

2003

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Clinical and electrophysiologic correlates of IVIg responsiveness in CIDP

Neurology, 2005-04, Vol.64 (8), p.1471

2005

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Microbiota as Predictor of Mortality in Allogeneic Hematopoietic-Cell Transplantation

The New England journal of medicine, 2020-02, Vol.382 (9), p.822-834

2020

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Age associated axonal features in HNPP with 17p11.2 deletion in Japan

Journal of neurology, neurosurgery and psychiatry, 2005-08, Vol.76 (8), p.1109-1114

2005

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Chimerism analyses by sex-chromosome analysis confused relapse with donor cell leukemia after sex-mismatched allo-SCT

Bone marrow transplantation (Basingstoke), 2012-12, Vol.47 (12), p.1583-1584

2012

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Mitochondrial GTPase mitofusin 2 mutation in Charcot-Marie-Tooth neuropathy type 2A

Human genetics, 2005-01, Vol.116 (1-2), p.23-27

2005

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Neurofilament light chain polypeptide gene mutations in Charcot-Marie-Tooth disease: nonsense mutation probably causes a recessive phenotype

Journal of human genetics, 2009-02, Vol.54 (2), p.94-97

2009

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Prevalence and incidence rates of chronic inflammatory demyelinating polyneuropathy in the Japanese population

Journal of neurology, neurosurgery and psychiatry, 2008-09, Vol.79 (9), p.1040-1043

2008

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Periaxin mutation causes early-onset but slow-progressive Charcot-Marie-Tooth disease

Journal of human genetics, 2004-07, Vol.49 (7), p.376-379

2004

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Mutational and structural analysis of Japanese patients with mucopolysaccharidosis type II

Journal of human genetics, 2005-09, Vol.50 (8), p.395-402

2005

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Isolation and Sequence Determination of cDNA Encoding Human T-Protein of the Glycine Cleavage System

Biochemical and biophysical research communications, 1993-04, Vol.192 (2), p.766-771

1993

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Age-related Increases in Plasma Phosphatidylcholine Hydroperoxide Concentrations in Control Subjects and Patients with Hyperlipidemia

Clinical chemistry (Baltimore, Md.), 2000-06, Vol.46 (6), p.822-828

2000

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Tissue distribution of mutant mitochondrial DNA in mitochondrial myopathy, encephalopathy, lactic acidosis and stroke‐like episodes (MELAS)

Journal of inherited metabolic disease, 1993-01, Vol.16 (1), p.27-30

1993

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Sensitive Detection of Polyalanine Expansions in PHOX2B by Polymerase Chain Reaction Using Bisulfite-Converted DNA

The Journal of molecular diagnostics : JMD, 2005-11, Vol.7 (5), p.638-640

2005

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Charcot-Marie-Tooth families in Japan with MPZ Thr124Met mutation

Journal of neurology, neurosurgery and psychiatry, 2004-10, Vol.75 (10), p.1492-1494

2004

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Screening of the early growth response 2 gene in Japanese patients with Charcot–Marie–Tooth disease type 1

Journal of the neurological sciences, 2003-06, Vol.210 (1), p.61-64

2003

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Successful unrelated donor bone marrow transplantation for Shwachman-Diamond syndrome with leukemia

International journal of hematology, 2004-02, Vol.79 (2), p.189-192

2004

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Cisplatin Combination Chemotherapy in Squamous Cell Carcinoma and Adenoid Cystic Carcinoma of the Skin

Journal of dermatology, 1989-06, Vol.16 (3), p.227-230

1989

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Association of the uteroglobin gene polymorphism with IgA nephropathy

American journal of kidney diseases, 2002-01, Vol.39 (1), p.36-41

2002

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Polymorphisms of Heme Oxygenase-1 and Bilirubin UDP-Glucuronosyltransferase Genes are not Associated with Kawasaki Disease Susceptibility

The Tohoku Journal of Experimental Medicine, 2003, Vol.200(3), pp.155-159

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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Abnormality of PMP-22 gene in Japanese patients with Charcot-Marie-Tooth disease--comparison between Southern blot and polymerase chain reaction analysis in the detection of PMP-22 gene duplication

No To Shinkei, 1995-07, Vol.47 (7), p.687

1995

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Restriction fragment length polymorphisms among Japanese detected with a dihydropteridine reductase cDNA gene probe

Journal of inherited metabolic disease, 1990-11, Vol.13 (6), p.873-878

1990

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Treatment and prognostic factors of stage I and II non-Hodgkin's lymphoma

[Hokkaido igaku zasshi] The Hokkaido journal of medical science, 1994-03, Vol.69 (2), p.347

1994

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The basis examination of leukocyte-platelet aggregates with CD45 gating as a novel platelet activation marker

Demyelinating and axonal features of Charcot–Marie–Tooth disease with mutations of myelin‐related proteins (PMP22, MPZ and Cx32): a clinicopathological study of 205 Japanese patients

Clinical and electrophysiologic correlates of IVIg responsiveness in CIDP

Microbiota as Predictor of Mortality in Allogeneic Hematopoietic-Cell Transplantation

Age associated axonal features in HNPP with 17p11.2 deletion in Japan

Chimerism analyses by sex-chromosome analysis confused relapse with donor cell leukemia after sex-mismatched allo-SCT

Mitochondrial GTPase mitofusin 2 mutation in Charcot-Marie-Tooth neuropathy type 2A

Neurofilament light chain polypeptide gene mutations in Charcot-Marie-Tooth disease: nonsense mutation probably causes a recessive phenotype

Prevalence and incidence rates of chronic inflammatory demyelinating polyneuropathy in the Japanese population

Periaxin mutation causes early-onset but slow-progressive Charcot-Marie-Tooth disease

Mutational and structural analysis of Japanese patients with mucopolysaccharidosis type II

Isolation and Sequence Determination of cDNA Encoding Human T-Protein of the Glycine Cleavage System

Age-related Increases in Plasma Phosphatidylcholine Hydroperoxide Concentrations in Control Subjects and Patients with Hyperlipidemia

Tissue distribution of mutant mitochondrial DNA in mitochondrial myopathy, encephalopathy, lactic acidosis and stroke‐like episodes (MELAS)

Sensitive Detection of Polyalanine Expansions in PHOX2B by Polymerase Chain Reaction Using Bisulfite-Converted DNA

Charcot-Marie-Tooth families in Japan with MPZ Thr124Met mutation

Screening of the early growth response 2 gene in Japanese patients with Charcot–Marie–Tooth disease type 1

Successful unrelated donor bone marrow transplantation for Shwachman-Diamond syndrome with leukemia

Cisplatin Combination Chemotherapy in Squamous Cell Carcinoma and Adenoid Cystic Carcinoma of the Skin

Association of the uteroglobin gene polymorphism with IgA nephropathy

Polymorphisms of Heme Oxygenase-1 and Bilirubin UDP-Glucuronosyltransferase Genes are not Associated with Kawasaki Disease Susceptibility

Sonic hedgehog signal peptide mutation in a patient with holoprosencephaly

Abnormality of PMP-22 gene in Japanese patients with Charcot-Marie-Tooth disease--comparison between Southern blot and polymerase chain reaction analysis in the detection of PMP-22 gene duplication

Restriction fragment length polymorphisms among Japanese detected with a dihydropteridine reductase cDNA gene probe

Treatment and prognostic factors of stage I and II non-Hodgkin's lymphoma

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