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4. Sialidosis type I: first report in the Czech population of two siblings with cherry-red spot myoclonus syndrome but without sialyloligosacchariduria. Ledvinová J; Poupĕtová H; Elleder M; Tichý J; Pĕnicková V; Harzer K J Inherit Metab Dis; 1994; 17(1):118-9. PubMed ID: 8051919 [No Abstract] [Full Text] [Related]
6. Neuraminidase activities in sialidosis and mucolipidosis. Kuriyama M; Miyatake T; Owada M; Kitagawa T J Neurol Sci; 1982 May; 54(2):181-7. PubMed ID: 7097297 [TBL] [Abstract][Full Text] [Related]
7. Sialidosis type 1: cherry red spot-myoclonus syndrome with sialidase deficiency and altered electrophoretic mobility of some enzymes known to be glycoproteins. II. Enzymes studies. Swallow DM; Evans L; Stewart G; Thomas PK; Abrams JD Ann Hum Genet; 1979 Jul; 43(1):27-35. PubMed ID: 496393 [TBL] [Abstract][Full Text] [Related]
8. Sialidosis type 1: cherry red spot-myoclonus syndrome with sialidase deficiency and altered electrophoretic mobilities of some enzymes known to be glycoproteins. 1. Clinical findings. Thomas PK; Abrams JD; Swallow D; Stewart G J Neurol Neurosurg Psychiatry; 1979 Oct; 42(10):873-80. PubMed ID: 512662 [TBL] [Abstract][Full Text] [Related]