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Chemistry (Weinheim an Der Bergstrasse, Germany)
|
November 7, 2001
Synthesis of Streptococcus pneumoniae type 3 neoglycoproteins varying in oligosaccharide chain length, loading and carrier protein
D J Lefeber, J P Kamerling, J F Vliegenthart
Acta Neurologica Scandinavica
|
March 5, 2010
Chitotriosidase activity in controls and multiple sclerosis
M M Verbeek, D J Lefeber, P J H Jongen
Clinical and Diagnostic Laboratory Immunology
|
May 8, 2000
Towards a synthetic pneumococcal vaccine: synthetic oligosaccharides as tools for improving the specificity of enzyme-linked immunosorbent assays
H Snippe, W T Jansen, J P Kamerling, et al.
Molecular Genetics and Metabolism
|
March 19, 2013
Thrombotic complications in patients with PMM2-CDG
M Linssen, M Mohamed, R A Wevers, et al.
Pediatric Hematology and Oncology
|
December 10, 2008
Recurrent thrombo-embolism in a child with a congenital disorder of glycosylation (CDG) type Ib and treatment with mannose
R Y J Tamminga, D J Lefeber, W A Kamps, et al.
Carbohydrate Research
|
August 26, 1998
Synthesis of the spacer-containing beta-D-GalpNAc-(1-->4)-beta-D- GlcpNAc-(1-->3)-alpha-D-Galp moiety, representing the non-fucosylated backbone trisaccharide of the glycocalyx glycan of the parasite Schistosoma mansoni
K M Halkes, D J Lefeber, C T Fransen, et al.
Infection and Immunity
|
June 13, 2001
Synthetic polysaccharide type 3-related di-, tri-, and tetrasaccharide-CRM(197) conjugates induce protection against Streptococcus pneumoniae type 3 in mice
B Benaissa-Trouw, D J Lefeber, J P Kamerling, et al.
Journal of Inherited Metabolic Disease
|
November 10, 2009
Substrate deprivation therapy in juvenile Sandhoff disease
S B Wortmann, D J Lefeber, G Dekomien, et al.
Acta Psychiatrica Scandinavica
|
December 31, 2009
Sanfilippo B in an elderly female psychiatric patient: a rare but relevant diagnosis in presenile dementia
W M A Verhoeven, R Csepán, C L M Marcelis, et al.
Journal of Inherited Metabolic Disease
|
May 27, 2008
Congenital disorder of glycosylation type Ix: review of clinical spectrum and diagnostic steps
E Morava, H Wosik, J Kárteszi, et al.
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Search research articles
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Showing results (1-10 of 29) with videos related to
Sort By:
Page
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Chemistry (Weinheim an Der Bergstrasse, Germany)
|
November 7, 2001
Synthesis of Streptococcus pneumoniae type 3 neoglycoproteins varying in oligosaccharide chain length, loading and carrier protein
D J Lefeber, J P Kamerling, J F Vliegenthart
Acta Neurologica Scandinavica
|
March 5, 2010
Chitotriosidase activity in controls and multiple sclerosis
M M Verbeek, D J Lefeber, P J H Jongen
Clinical and Diagnostic Laboratory Immunology
|
May 8, 2000
Towards a synthetic pneumococcal vaccine: synthetic oligosaccharides as tools for improving the specificity of enzyme-linked immunosorbent assays
H Snippe, W T Jansen, J P Kamerling, et al.
Molecular Genetics and Metabolism
|
March 19, 2013
Thrombotic complications in patients with PMM2-CDG
M Linssen, M Mohamed, R A Wevers, et al.
Pediatric Hematology and Oncology
|
December 10, 2008
Recurrent thrombo-embolism in a child with a congenital disorder of glycosylation (CDG) type Ib and treatment with mannose
R Y J Tamminga, D J Lefeber, W A Kamps, et al.
Carbohydrate Research
|
August 26, 1998
Synthesis of the spacer-containing beta-D-GalpNAc-(1-->4)-beta-D- GlcpNAc-(1-->3)-alpha-D-Galp moiety, representing the non-fucosylated backbone trisaccharide of the glycocalyx glycan of the parasite Schistosoma mansoni
K M Halkes, D J Lefeber, C T Fransen, et al.
Infection and Immunity
|
June 13, 2001
Synthetic polysaccharide type 3-related di-, tri-, and tetrasaccharide-CRM(197) conjugates induce protection against Streptococcus pneumoniae type 3 in mice
B Benaissa-Trouw, D J Lefeber, J P Kamerling, et al.
Journal of Inherited Metabolic Disease
|
November 10, 2009
Substrate deprivation therapy in juvenile Sandhoff disease
S B Wortmann, D J Lefeber, G Dekomien, et al.
Acta Psychiatrica Scandinavica
|
December 31, 2009
Sanfilippo B in an elderly female psychiatric patient: a rare but relevant diagnosis in presenile dementia
W M A Verhoeven, R Csepán, C L M Marcelis, et al.
Journal of Inherited Metabolic Disease
|
May 27, 2008
Congenital disorder of glycosylation type Ix: review of clinical spectrum and diagnostic steps
E Morava, H Wosik, J Kárteszi, et al.
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of 3