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mannose-binding lectin
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Mannose-binding Lectin Deficiency
2005 |
Second Faculty of Medicine
publication
Mannose-binding lectin deficiency
1999 |
Second Faculty of Medicine
publication
Churg-Strauss syndrome and mannose-binding lectin deficiency in adult patient
2004 |
Second Faculty of Medicine
publication
Serum mannose-binding lectin (MBL) concentrations are reduced in non-pregnant women with previous adverse pregnancy outcomes
2020 |
First Faculty of Medicine
publication
Plasma mannose-binding lectin is stimulated by PPAR alpha in humans
2012 |
First Faculty of Medicine
publication
Gene polymorphisms and serum levels of mannose-binding lectin in Czech patients with recurrent aphthous stomatitis: A case-control study
2023 |
First Faculty of Medicine
publication
Polymorphisms in the mannose binding lectin gene affect the cystic fibrosis pulmonary phenotype
2004 |
Second Faculty of Medicine
publication
Low maternal serum concentrations of mannose-binding lectin are associated with the risk of shorter duration of pregnancy and lower birthweight
2018 |
First Faculty of Medicine
publication
Churg-Strauss syndrome (CSS) with mannose-binding lectin (MBL) deficiency in an adult patient, case report
2004 |
Publication without faculty affiliation
publication
Churg-Strauss syndrome (CSS) with mannose-binding lectin (MBL) deficiency in an adult patient, case report.
2004 |
First Faculty of Medicine, Faculty of Physical Education and Sport
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Cost-effective genotyping of human MBL2 gene mutations using multiplex PCR
2004 |
Second Faculty of Medicine
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No Evidence for Linkage between the Hereditary Angiooedema Clinical Phenotype and the BDKR1, BDKR2, ACE or MBL2 gene
2011 |
Second Faculty of Medicine
publication
Diagnostic relevance of Langerin detection in cells from bronchoalveolar lavage of patients with pulmonary Langerhans cell histiocytosis, sarcoidosis and idiopathic pulmonary fibrosis
2004 |
Publication without faculty affiliation
publication
Spectrum and Management of Complement Immunodeficiencies (Excluding Hereditary Angioedema) Across Europe
2015 |
Publication without faculty affiliation
publication
Complement System Deficiencies in Elite Athletes
2024 |
First Faculty of Medicine
publication
Genetic Modifiers of Liver Disease in Cystic Fibrosis
2009 |
Second Faculty of Medicine
publication
Label-free proteomic analysis reveals differentially expressed Wolbachia proteins in Tyrophagus putrescentiae: Mite allergens and markers reflecting population-related proteome differences
2021 |
Faculty of Science, Central Library of Charles University