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Article title matches
- Category:Metachromatic leukodystrophy (59 bytes)
1: List of pages with the keyword Metachromatic leukodystrophy - Category:Leukodystrophy (45 bytes)
1: List of pages with the keyword Leukodystrophy - Category:Infantile leukodystrophy (55 bytes)
1: List of pages with the keyword Infantile leukodystrophy
Page text matches
- 1e7z (5,860 bytes)
11: ...00]. A severe autosomal recessive hypomyelinating leukodystrophy characterized by early infantile onset of global ... - 1fsu (4,212 bytes)
11: ...dual sulfatase deficiencies such as metachromatic leukodystrophy, mucopolysaccharidosis, chondrodysplasia punctata... - 1auk (5,161 bytes)
11: ...dual sulfatase deficiencies such as metachromatic leukodystrophy, mucopolysaccharidosis, chondrodysplasia punctata... - 1e1z (7,624 bytes)
11: ...dual sulfatase deficiencies such as metachromatic leukodystrophy, mucopolysaccharidosis, chondrodysplasia punctata... - 1e2s (7,712 bytes)
11: ...dual sulfatase deficiencies such as metachromatic leukodystrophy, mucopolysaccharidosis, chondrodysplasia punctata... - 1e33 (7,192 bytes)
11: ...dual sulfatase deficiencies such as metachromatic leukodystrophy, mucopolysaccharidosis, chondrodysplasia punctata...
26: ...f the most common mutations causing metachromatic leukodystrophy, the P426L-allele of arylsulfatase A (ASA), the d...
28: ...of its instability in lysosomes and metachromatic leukodystrophy.,von Bulow R, Schmidt B, Dierks T, Schwabauer N, ... - 1e3c (7,655 bytes)
11: ...dual sulfatase deficiencies such as metachromatic leukodystrophy, mucopolysaccharidosis, chondrodysplasia punctata... - 1euj (3,801 bytes)
10: ...00]. A severe autosomal recessive hypomyelinating leukodystrophy characterized by early infantile onset of global ... - 1fl0 (3,970 bytes)
10: ...00]. A severe autosomal recessive hypomyelinating leukodystrophy characterized by early infantile onset of global ... - 1m12 (4,870 bytes)
10: ...0]. MLD-SAPB is an atypical form of metachromatic leukodystrophy. It is characterized by tissue accumulation of ce... - 1n2k (5,243 bytes)
11: ...dual sulfatase deficiencies such as metachromatic leukodystrophy, mucopolysaccharidosis, chondrodysplasia punctata... - 1n2l (6,815 bytes)
11: ...dual sulfatase deficiencies such as metachromatic leukodystrophy, mucopolysaccharidosis, chondrodysplasia punctata... - 1n69 (5,201 bytes)
11: ...0]. MLD-SAPB is an atypical form of metachromatic leukodystrophy. It is characterized by tissue accumulation of ce... - 1sn6 (4,888 bytes)
10: ...0]. MLD-SAPB is an atypical form of metachromatic leukodystrophy. It is characterized by tissue accumulation of ce... - 1y1e (3,548 bytes)
11: ...dual sulfatase deficiencies such as metachromatic leukodystrophy, mucopolysaccharidosis, chondrodysplasia punctata... - 1y1f (5,157 bytes)
11: ...dual sulfatase deficiencies such as metachromatic leukodystrophy, mucopolysaccharidosis, chondrodysplasia punctata... - 1y1g (5,161 bytes)
11: ...dual sulfatase deficiencies such as metachromatic leukodystrophy, mucopolysaccharidosis, chondrodysplasia punctata... - 1y1h (5,171 bytes)
11: ...dual sulfatase deficiencies such as metachromatic leukodystrophy, mucopolysaccharidosis, chondrodysplasia punctata... - 1y1i (5,086 bytes)
11: ...dual sulfatase deficiencies such as metachromatic leukodystrophy, mucopolysaccharidosis, chondrodysplasia punctata... - 1y1j (5,243 bytes)
11: ...dual sulfatase deficiencies such as metachromatic leukodystrophy, mucopolysaccharidosis, chondrodysplasia punctata...
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