Histochemical and ultrastructural studies of inclusion bodies found in tissues from three siblings with 1-cell disease
Author:
Publisher
Wiley
Subject
General Medicine,Pathology and Forensic Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1440-1827.1994.tb02596.x/fullpdf
Reference12 articles.
1. Enzymatic phosphorylation of lysosomal enzymes in the presence of UDP-N-t acetylglucosamine: Absence of the activity in l-cell fibroblasts;Hasilik;I Biochem. Biophys. Res. Commun.,1981
2. Fibroblasts from patients with l-cell disease and pseudo-Hurler polydystrophy are deficient in uridine 5-diphosphate-N-acetylglucosamine: Glycoprotein N-acetyl-glucosaminylphosphotransferase activity;Reitman;J. Clin. Invest.,1981
3. Prenatal diagnosis and fetal pathology of l-cell disease (mucolipidosis II);Aula;J. Pediatr.,1975
4. l-cell disease (mucolipidosis II): A report on its pathology;Martin;Acta Neuropathol.,1975
5. Ultrastructural studies in 1 fetal l-cell disease;Abe;Pediatr. Res.,1976
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1. Placental pathology in an unsuspected case of mucolipidosis type II with secondary hyperparathyroidism in a premature infant;Molecular Genetics and Metabolism Reports;2021-06
2. B-cell-specific accumulation of inclusion bodies loaded with HLA class II molecules in patients with mucolipidosis II (I-cell disease);Pediatric Research;2018-11-21
3. I-Cell Disease (Mucolipidosis II);Diagnostic Pathology: Kidney Diseases;2016
4. Peripheral blood lymphocyte appearance in a case of I cell disease;Journal of Clinical Pathology;2001-09-01
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