These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
178 related articles for article (PubMed ID: 6777461)
1. Cherry-red spot myoclonus syndrome and alpha-neuraminidase deficiency: neurophysiological, pharmacological and biochemical study in an adult. Franceschetti S; Uziel G; Di Donato S; Caimi L; Avanzini G J Neurol Neurosurg Psychiatry; 1980 Oct; 43(10):934-40. PubMed ID: 6777461 [TBL] [Abstract][Full Text] [Related]
2. Sialidase (alpha-n-acetyl neuraminidase) deficiency: the enzyme defect in an adult with macular cherry-red spots and myoclonus without dementia. Thomas GH; Tipton RE; Ch'ien LT; Reynolds LW; Miller CS Clin Genet; 1978 Apr; 13(4):369-79. PubMed ID: 657577 [TBL] [Abstract][Full Text] [Related]
3. 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]
6. Macular cherry-red spots and myoclonus with dementia: coexistent neuraminidase and beta-galactosidase deficiencies. Wenger DA; Tarby TJ; Wharton C Biochem Biophys Res Commun; 1978 May; 82(2):589-95. PubMed ID: 96839 [No Abstract] [Full Text] [Related]
7. Electrophysiological studies of myoclonus in sialidosis type 2. Tobimatsu S; Fukui R; Shibasaki H; Kato M; Kuroiwa Y Electroencephalogr Clin Neurophysiol; 1985 Jan; 60(1):16-22. PubMed ID: 2578348 [TBL] [Abstract][Full Text] [Related]
8. Multimodality evoked potentials and EEG in a case of cherry red spot-myoclonus syndrome and alpha-neuraminidase deficiency (sialidosis type 1). Louboutin JP; Nogues B; Caillaud C; Elie B Eur Neurol; 1995; 35(3):175-7. PubMed ID: 7628501 [No Abstract] [Full Text] [Related]
10. The cherry red spot-myoclonus syndrome: a newly recognized inherited lysosomal storage disease due to acid neuraminidase deficiency. O'Brien JS Clin Genet; 1978 Jul; 14(1):55-60. PubMed ID: 679523 [TBL] [Abstract][Full Text] [Related]
11. Sialidosis: the cherry-red spot--myoclonus syndrome. Kirkham TH; Coupland SG; Guitton D Can J Ophthalmol; 1980 Jan; 15(1):35-9. PubMed ID: 7378886 [TBL] [Abstract][Full Text] [Related]
12. To jerk or not to jerk: A clinical pathophysiology of myoclonus. Apartis E; Vercueil L Rev Neurol (Paris); 2016; 172(8-9):465-476. PubMed ID: 27568397 [TBL] [Abstract][Full Text] [Related]
13. Neuraminidase deficiency in the cherry red spot-myoclonus syndrome. O'Brien JS Biochem Biophys Res Commun; 1977 Dec; 79(4):1136-41. PubMed ID: 603649 [No Abstract] [Full Text] [Related]
14. 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]
15. Successful treatment of cherry red spot-myoclonus syndrome with 5-hydroxytryptophan. Gascon G; Wallenberg B; Daif AK; Ozand P Ann Neurol; 1988 Sep; 24(3):453-5. PubMed ID: 3265864 [TBL] [Abstract][Full Text] [Related]
16. 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]