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Results 1 - 10 of 606 > >>
EC Number Disease PubMed ID Title of Publication Category Confidence Level
Display the word mapDisplay the reaction diagram Show all sequences 3.1.6.13Anaphylaxis 23621439 IgE-mediated anaphylaxis and allergic reactions to idursulfase in patients with Hunter syndrome. causal interaction
diagnostic usage
ongoing research
therapeutic application
3
2
3
4
Display the word mapDisplay the reaction diagram Show all sequences 3.1.6.13Anaphylaxis 33458989 [Idursulfase desensitization in a child with Hunter syndrome (mucopolysaccharidosis II)]. causal interaction
therapeutic application
unassigned
1
4
0
Display the word mapDisplay the reaction diagram Show all sequences 3.1.6.13arylsulfatase (type i) deficiency 2863138 Synthesis and stability of arylsulfatase A and B in fibroblasts from multiple sulfatase deficiency. causal interaction
diagnostic usage
ongoing research
therapeutic application
4
2
2
2
Display the word mapDisplay the reaction diagram Show all sequences 3.1.6.13arylsulfatase (type i) deficiency 9880143 Pathologic findings of multiple sulfatase deficiency reflect the pattern of enzyme deficiencies. causal interaction
unassigned
4
0
Display the word mapDisplay the reaction diagram Show all sequences 3.1.6.13Contracture 27351199 Clinical and Genetic Characteristics of Romanian Patients with Mucopolysaccharidosis Type II. causal interaction
unassigned
4
0
Display the word mapDisplay the reaction diagram Show all sequences 3.1.6.13Drug-Related Side Effects and Adverse Reactions 23497636 Phase I/II clinical trial of enzyme replacement therapy with idursulfase beta in patients with mucopolysaccharidosis II (Hunter Syndrome). causal interaction
diagnostic usage
ongoing research
therapeutic application
4
2
3
4
Display the word mapDisplay the reaction diagram Show all sequences 3.1.6.13Dysostoses 23375472 Effects of idursulfase enzyme replacement therapy for Mucopolysaccharidosis type II when started in early infancy: comparison in two siblings. causal interaction
therapeutic application
unassigned
3
4
0
Display the word mapDisplay the reaction diagram Show all sequences 3.1.6.13Fabry Disease 29152458 Lysosomal storage diseases. causal interaction
diagnostic usage
therapeutic application
unassigned
1
2
2
0
Display the word mapDisplay the reaction diagram Show all sequences 3.1.6.13Fragile X Syndrome 23634718 Deletion Xq27.3q28 in female patient with global developmental delays and skewed X-inactivation. unassigned 0
Display the word mapDisplay the reaction diagram Show all sequences 3.1.6.13Gaucher Disease 29152458 Lysosomal storage diseases. causal interaction
diagnostic usage
therapeutic application
unassigned
1
2
2
0
Results 1 - 10 of 606 > >>