Results 91 to 100 of about 796 (126)

Mucopolysaccharidoses, glycoproteinoses and mucolipidoses

, 2011
Wraith, JE
core   +12 more sources

Keratan sulphate levels in mucopolysaccharidoses and mucolipidoses

Journal of Inherited Metabolic Disease, 2004
SummaryThe mucopolysaccharidoses (MPS) is characterized by accumulation of glycosaminoglycans (GAGs), and mucolipidosis (ML) by accumulation of GAGs and sphingolipids. Each type of MPS accumulates specific GAGs. The lysosomal enzymes N‐acetylgalactosamine‐6‐sulphate sulphatase and β‐galactosidase involve the stepwise degradation of keratan sulphate (KS)
S, Tomatsu, K, Okamura, H, Maeda, T, Taketani, S V, Castrillon, M A, Gutierrez, T, Nishioka, A A, Fachel, K O, Orii, J H, Grubb, A, Cooper, M, Thornley, E, Wraith, L A, Barrera, L S, Laybauer, R, Giugliani, I V, Schwartz, G Schulze, Frenking, M, Beck, S G, Kircher, E, Paschke, S, Yamaguchi, K, Ullrich, M, Haskins, K, Isogai, Y, Suzuki, T, Orii, N, Kondo, M, Creer, T, Okuyama, A, Tanaka, A, Noguchi   +31 more
openaire   +3 more sources

Mucolipidoses

, 1985
Hans Georg Hansen, Elisabeth Graucob
openaire   +2 more sources

Mucolipidoses

, 2011
core   +3 more sources

Mucolipidoses

, 1995
Jorge Cervós-Navarro, Henry Urich
openaire   +2 more sources

Mucolipidoses

, 2017
openaire   +2 more sources

Mucolipidoses

, 2007
openaire   +2 more sources

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The mucolipidoses

Seminars in Roentgenology, 1973
John P Dorst
exaly   +2 more sources

Mucolipidoses

, 2008
openaire   +2 more sources

Mucolipidoses

, 2013
N Mazumder
openaire   +2 more sources