Search Results - Trittmann, JK

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    Using clinical and genetic data to predict pulmonary hypertension in bronchopulmonary dysplasia

    Using clinical and genetic data to predict pulmonary hypertension in bronchopulmonary dysplasia by Trittmann, J K, Bartenschlag, A, Zmuda, E J, Frick, J, Stewart, W C L, Nelin, L D

    Published in Acta Paediatrica
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  2. 2
    A single nucleotide polymorphism in the dimethylarginine dimethylaminohydrolase gene is associated with lower risk of pulmonary hypertension in bronchopulmonary dysplasia

    A single nucleotide polymorphism in the dimethylarginine dimethylaminohydrolase gene is associated with lower risk of pulmonary hypertension in bronchopulmonary dysplasia by Trittmann, Jennifer K., Gastier-Foster, Julie M., Zmuda, Erik J., Frick, Jessica, Rogers, Lynette K., Vieland, Veronica J., Chicoine, Louis G., Nelin, Leif D.

    Published in Acta Paediatrica
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    Arginase I gene single-nucleotide polymorphism is associated with decreased risk of pulmonary hypertension in bronchopulmonary dysplasia

    Arginase I gene single-nucleotide polymorphism is associated with decreased risk of pulmonary hypertension in bronchopulmonary dysplasia by Trittmann, JK, Nelin, LD, Zmuda, EJ, Gastier-Foster, JM, Chen, B, Backes, CH, Frick, J, Vaynshtok, P, Vieland, VJ, Klebanoff, MA

    Published in Acta Paediatrica
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