Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Bronchopulmonary Dysplasia and MBL2[original query] |
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Association of polymorphisms in the mannose-binding lectin gene and pulmonary morbidity in preterm infants. Genes and immunity 2007 Dec 8 (8): 671-7. Hilgendorff A, Heidinger K, Pfeiffer A, Bohnert A, König I R, Ziegler A, Merz C, Frey G, Chakraborty T, Gortner L, Bein |
Mannose-binding lectin polymorphisms and pulmonary outcome in premature neonates: a pilot study. Intensive care medicine 2007 Oct 33 (10): 1787-94. Capoluongo Ettore, Vento Giovanni, Rocchetti Sandro, Giardina Emiliano, Concolino Paola, Sinibaldi Cecilia, Santonocito Concetta, Vendettuoli Valentina, Tana Milena, Tirone Chiara, Zuppi Cecilia, Romagnoli Costantino, Novelli Giuseppe, Giardina Bruno, Ameglio Fran |
Mannose-binding lectin gene polymorphism and early neonatal outcome in preterm infants. Neonatology 2010 98 (4): 305-12. Koroglu Ozge Altun, Onay Huseyin, Erdemir Gulin, Yalaz Mehmet, Cakmak Bilin, Akisu Mete, Ozkinay Ferda, Kultursay Nilg |
Association between bronchopulmonary dysplasia and MBL2 and IL1-RN polymorphisms. Pediatrics international : official journal of the Japan Pediatric Society 2012 Dec 54 (6): 863-8. Cakmak Bilin Cetinkaya, Calkavur Sebnem, Ozkinay Ferda, Koroglu Ozge Altun, Onay Huseyin, Itirli Gulcin, Karaca Emin, Yalaz Mehmet, Akisu Mete, Kultursay Nilg |
Bronchopulmonary dysplasia and wnt pathway-associated single nucleotide polymorphisms. Pediatric research 2021 Dec . Akat Ayberk, Yilmaz Semerci Seda, Ugurel Osman Mutluhan, Erdemir Aysegul, Danhaive Olivier, Cetinkaya Merih, Turgut-Balik Dil |
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