Masashi
0000-0001-5863-9315
6 papers found
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Patients with keratinization disorders due to ABCA12 variants showing pityriasis rubra pilaris phenotypes
Classical Vohwinkel syndrome with heterozygous p.Asp66His mutation in GJB2 gene: Second Asian case
Indeterminate dendritic cell neoplasm accompanied by eosinophilic pneumonia successfully treated by systemic steroid therapy: Report of the first case with muscular and parotid involvement and review of published work
Urticarial vasculitis and subcutaneous nodules in the extremities seen in a patient with mucopolysaccharidosis II after hematopoietic stem cell therapy
Chromosomal inversions as a hidden disease-modifying factor for somatic recombination phenotypes
CD1a-positive cutaneous mastocytosis: Electron microscopic evidence of pleomorphic mast cell proliferation
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