Anwar M, Ibrahim Laila I
BMC Complement Med Ther. 2024; 24(1):153.
PMID: 38581023
PMC: 10996088.
DOI: 10.1186/s12906-024-04447-9.
Pedersen J, Duno M, Wibrand F, Hammer C, Krag T, Vissing J
JIMD Rep. 2022; 63(6):540-545.
PMID: 36341176
PMC: 9626661.
DOI: 10.1002/jmd2.12324.
Ahsan F, Mahmood T, Wani T, Zargar S, Siddiqui M, Usmani S
Life (Basel). 2022; 12(7).
PMID: 35888151
PMC: 9317748.
DOI: 10.3390/life12071063.
Singh R, Chopra S, Graham C, Langer M, Ng R, Ullal A
Diagnostics (Basel). 2020; 10(5).
PMID: 32403245
PMC: 7277946.
DOI: 10.3390/diagnostics10050294.
Kelainy E, Ibrahim Laila I, Ibrahim S
Environ Sci Pollut Res Int. 2019; 26(31):31675-31684.
PMID: 31482528
DOI: 10.1007/s11356-019-06099-6.
Acid ceramidase deficiency: Farber disease and SMA-PME.
Yu F, Amintas S, Levade T, Medin J
Orphanet J Rare Dis. 2018; 13(1):121.
PMID: 30029679
PMC: 6053731.
DOI: 10.1186/s13023-018-0845-z.
Diagnostic value of alpha-L-fucosidase for hepatocellular carcinoma: a meta-analysis.
Gan Y, Liang Q, Song X
Tumour Biol. 2014; 35(5):3953-60.
PMID: 24395655
DOI: 10.1007/s13277-013-1563-8.
Improved behavior and neuropathology in the mouse model of Sanfilippo type IIIB disease after adeno-associated virus-mediated gene transfer in the striatum.
Cressant A, Desmaris N, Verot L, Brejot T, Froissart R, Vanier M
J Neurosci. 2004; 24(45):10229-39.
PMID: 15537895
PMC: 6730192.
DOI: 10.1523/JNEUROSCI.3558-04.2004.
A model of mucopolysaccharidosis IIIB (Sanfilippo syndrome type IIIB): N-acetyl-alpha-D-glucosaminidase deficiency in Schipperke dogs.
Ellinwood N, Wang P, Skeen T, Sharp N, Cesta M, Decker S
J Inherit Metab Dis. 2003; 26(5):489-504.
PMID: 14518829
DOI: 10.1023/a:1025177411938.
Mouse model of Sanfilippo syndrome type B produced by targeted disruption of the gene encoding alpha-N-acetylglucosaminidase.
Li H, Yu W, Rozengurt N, Zhao H, Lyons K, Anagnostaras S
Proc Natl Acad Sci U S A. 1999; 96(25):14505-10.
PMID: 10588735
PMC: 24466.
DOI: 10.1073/pnas.96.25.14505.
Tay-Sachs disease with atypical chronic course and limited brain storage: alpha-locus hexosaminidase genetic compound.
Philippart M, Carrel R, LANDING B
Neurochem Res. 1995; 20(11):1323-8.
PMID: 8786818
DOI: 10.1007/BF00992507.
Alterations in certain lysosomal glycohydrolases and cathepsins in rats on dexamethasone administration.
Rajashree S, Puvanakrishnan R
Mol Cell Biochem. 1996; 154(2):165-70.
PMID: 8717430
DOI: 10.1007/BF00226784.
In vivo inhibition of beta-glucosidase and beta-mannosidase activity in rats by 2-deoxy-2-fluoro-beta-glycosyl fluorides and recovery of activity in vivo and in vitro.
McCarter J, Adam M, Hartman N, Withers S
Biochem J. 1994; 301 ( Pt 2):343-8.
PMID: 8042975
PMC: 1137085.
DOI: 10.1042/bj3010343.
Investigation of tissue organelles by a combination of analytical subcellular fractionation and enzymic microanalysis: a new approach to pathology.
Peters T
J Clin Pathol. 1981; 34(1):1-12.
PMID: 7462432
PMC: 1146399.
DOI: 10.1136/jcp.34.1.1.
The effect of chloroquine on lysosomal function and cell-coat glycoprotein transport in the absorptive cells of cultured human small-intestinal tissue.
Blok J, Ginsel L, DAEMS W
Cell Tissue Res. 1981; 218(2):227-51.
PMID: 7261028
DOI: 10.1007/BF00210340.
Hereditary neurovisceral mannosidosis associated with alpha-mannosidase deficiency in a family of Persian cats.
Vandevelde M, FANKHAUSER R, Bichsel P, Wiesmann U, HERSCHKOWITZ N
Acta Neuropathol. 1982; 58(1):64-8.
PMID: 7136518
DOI: 10.1007/BF00692699.
Rapid detection of yeast enzymes by using 4-methylumbelliferyl substrates.
Bobey D, EDERER G
J Clin Microbiol. 1981; 13(2):393-4.
PMID: 7009643
PMC: 273796.
DOI: 10.1128/jcm.13.2.393-394.1981.
Sanfilippo A syndrome (mucopolysaccharidosis III A): a neurochemical study.
Federico A, Robert J, Zanetta J, GUAZZI G
Ital J Neurol Sci. 1981; 2(2):119-27.
PMID: 6800974
DOI: 10.1007/BF02335431.
Prenatal diagnosis of Hurler's syndrome--biochemical studies on the affected fetus.
Ikeno T, Minami R, Wagatsuma K, Fujibayashi S, Nakao T, Abo K
Hum Genet. 1981; 59(4):353-9.
PMID: 6800929
DOI: 10.1007/BF00295471.
Beta-glucuronidase deficiency: enzyme studies in an affected family and prenatal diagnosis.
Maire I, Mandon G, Zabot M, Mathieu M, GUIBAUD P
J Inherit Metab Dis. 1980; 2(2):29-34.
PMID: 6796758
DOI: 10.1007/BF01799071.
