Paediatrics (Lund)
1961 – 1970 of 2743
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- 2008
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N1421K mutation in the glycoprotein Ib binding domain impairs ristocetin- and botrocetin-mediated binding of von Willebrand factor to platelets.
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- Contribution to journal › Article
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Haemophilia in the first years of life.
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- Contribution to journal › Article
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Cord blood islet autoantibodies and seasonal association with the type 1 diabetes high-risk genotype.
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- Contribution to journal › Article
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Wireless Esophageal pH Monitoring in Children.
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- Contribution to journal › Article
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TLR- and CXCR1-dependent innate immunity: insights into the genetics of urinary tract infections.
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- Contribution to journal › Scientific review
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Mark
Deletion of the SCN gene cluster on 2q24.4 is associated with severe epilepsy: An array-based genotype-phenotype correlation and a comprehensive review of previously published cases.
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- Contribution to journal › Article
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Mark
Coronary artery stenosis in asymptomatic child after arterial switch operation: detection by transthoracic colour-flow doppler echocardiography.
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- Contribution to journal › Article
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Laparoscopic aided cholecystostomy as a treatment of inspissated bile syndrome.
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- Contribution to journal › Article
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Restricted immunoglobulin constant heavy G chain genes in primary immunodeficiencies.
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- Contribution to journal › Article
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Factor H dysfunction in patients with atypical hemolytic uremic syndrome contributes to complement deposition on platelets and their activation.
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- Contribution to journal › Article