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5. The prevalence and diagnosis of lysosomal storage diseases in Poland. Tylki-Szymańska A; Czartoryska B; Ługowska A; Górska D Eur J Pediatr; 2001 Apr; 160(4):261-2. PubMed ID: 11317653 [No Abstract] [Full Text] [Related]
6. Exocytosis of storage material in a lysosomal disorder. Klein D; Büssow H; Fewou SN; Gieselmann V Biochem Biophys Res Commun; 2005 Feb; 327(3):663-7. PubMed ID: 15649398 [TBL] [Abstract][Full Text] [Related]
7. Epidemiology of lysosomal storage diseases in Sweden. Hult M; Darin N; von Döbeln U; Månsson JE Acta Paediatr; 2014 Dec; 103(12):1258-63. PubMed ID: 25274184 [TBL] [Abstract][Full Text] [Related]
8. [Recent advances in the diagnosis and treatment of lysosomal storage diseases]. Wu XR; Bao XH Beijing Da Xue Xue Bao Yi Xue Ban; 2005 Aug; 37(4):440-4. PubMed ID: 16086072 [TBL] [Abstract][Full Text] [Related]
9. Juvenile metachromatic leukodystrophy: understanding the disease and implications for nursing care. Barrell C J Pediatr Oncol Nurs; 2007; 24(2):64-9. PubMed ID: 17332420 [TBL] [Abstract][Full Text] [Related]
11. Problems in the application of cell culture to human genetics. Davidson RG Birth Defects Orig Artic Ser; 1974; 10(10):14-8. PubMed ID: 4618130 [No Abstract] [Full Text] [Related]
12. The incidence rate of hospitalized lysosomal storage diseases in Poland in 2013-2015 based on data from the National Health Fund. Grzeszczak W; Franek E; Szypowska A; Filipow W; Zięba M; Kabicz P; Więckowska B Pediatr Endocrinol Diabetes Metab; 2021; 27(3):191-198. PubMed ID: 34498441 [TBL] [Abstract][Full Text] [Related]
13. Brain hexosaminidase and arylsulfatase isoenzymes in normal and vitamin E-deficient rats: an hypothesis for isoenzyme patterns in GM2 gangliosidoses and MLD. Koenig H; Patel A Trans Am Neurol Assoc; 1974; 99():140-3. PubMed ID: 4463525 [No Abstract] [Full Text] [Related]
14. [Adult metachromatic leukodystrophy]. Wang L Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1990 Dec; 23(6):354-5, 385. PubMed ID: 2098247 [TBL] [Abstract][Full Text] [Related]
15. Molecular and phenotypic characteristics of metachromatic leukodystrophy patients from Poland. Ługowska A; Berger J; Tylki-Szymańska A; Löschl B; Molzer B; Zobel M; Czartoryska B Clin Genet; 2005 Jul; 68(1):48-54. PubMed ID: 15952986 [TBL] [Abstract][Full Text] [Related]
17. The frequency of lysosomal storage diseases in The Netherlands. Poorthuis BJ; Wevers RA; Kleijer WJ; Groener JE; de Jong JG; van Weely S; Niezen-Koning KE; van Diggelen OP Hum Genet; 1999; 105(1-2):151-6. PubMed ID: 10480370 [TBL] [Abstract][Full Text] [Related]
18. Arylsulfatases isoenzymes in metachromatic leucodystrophy/detection of a new variant by electrophoresis improvement of quantitative assay. Dubois G; Turpin JC; Baumann N Biomedicine; 1975 Apr; 23(3):116-9. PubMed ID: 4167 [TBL] [Abstract][Full Text] [Related]
20. [An exceptional case of a family suffering from metachromatic leukocystrophy. Very low level of arylsulfatase A and cerebroside sulfate sulfatase in healthy subjects]. Turpin JC; Bergondi C; Haidar H; Dubois G Nouv Presse Med; 1977 Apr; 6(16):1373, 1379. PubMed ID: 16245 [No Abstract] [Full Text] [Related] [Next] [New Search]