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Ritsuo Nishiuchi

Okayama University

33

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334

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A deep intronic mutation of c.1166-285 T > G in SLC46A1 is shared by four unrelated Japanese patients with hereditary folate malabsorption (HFM)

2019 Clinical Immunology
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Pediatric intestinal Behçet disease complicated by myeloid malignancies.

2017 International Journal of Hematology
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Barth Syndrome: Different Approaches to Diagnosis

2017 The Journal of Pediatrics
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Two cases of late-onset epileptic spasms after encephalitis/encephalopathy

2017 European Journal of Paediatric Neurology
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Barth Syndrome: Different Approaches to Diagnosis

2017 The Journal of Pediatrics
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Verification of risk scores to predict i.v. immunoglobulin resistance in incomplete Kawasaki disease

2016 Pediatrics International
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Persistent clonal chromosomal abnormalities in a chronic myeloid leukemia patient

2016 Pediatrics International
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Ventriculoperitoneal shunt outcomes among infants.

2015 Acta Medica Okayama
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Changes in the features of invasive pneumococcal disease after introduction of the seven-valent pneumococcal conjugate vaccine in a regional core hospital of Kochi, Japan.

2015 Acta Medica Okayama
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192 FIVE CASES OF PEDIATRIC-ONSET BEHCET DISEASE COMPLICATED WITH MYELODYSPLASTIC SYNDROME

2015 Leukemia Research
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