Benign fibrous histiocytoma occurred in the alveolar mucosa accompanying with sialidosis type 2 in Japanese infant

Author:

Hidaka Miyoko,Yamashita Akihiro,Sakamoto Kouzou,Mukaisho Ken-ichi,Hattori Takanori,Yamamoto Gaku

Publisher

Elsevier BV

Subject

Oncology,Otorhinolaryngology,Pathology and Forensic Medicine,Oral Surgery

Reference28 articles.

1. Molecular heterogeneity in human beta-galactosidase and neuraminidase deficiency;Galjaard;Enzyme,1987

2. The genetic mucolipidoses. Diagnosis and differential diagnosis;Spranger;Humangenetik,1970

3. Mucolipidosis I: Increased sialic acid content and deficiency of an alpha-N-acetylneuraminidase in cultured fibroblasts;Cantz;Biochem Biophys Res Commun,1977

4. Sialidosis (mucolipidosis I);Durand;Helv Paediatr Acta,1977

5. Neuraminidase deficiency in the cherry red spot-myoclonus syndrome;O’Brien;Biochem Biophys Res Commun,1977

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