Výsledky vyhledávání - Charles, Adrian
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Phylogeny of Wilms tumor? Autor Charles, Adrian, Greer, Ian A.
Vydáno 2016Text -
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Incidence of NUT carcinoma in Western Australia from 1989 to 2014: a review of pediatric and adolescent cases from Perth Children’s Hospital Autor Carter, Tina, Crook, Maxine, Murch, Ashleigh, Beesley, Alex H., de Klerk, Nick, Charles, Adrian, Kees, Ursula R.
Vydáno 2021Text -
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Inflammatory and Haematological Markers in the Maternal, Umbilical Cord and Infant Circulation in Histological Chorioamnionitis Autor Howman, Rebecca A., Charles, Adrian K., Jacques, Angela, Doherty, Dorota A., Simmer, Karen, Strunk, Tobias, Richmond, Peter C., Cole, Catherine H., Burgner, David P.
Vydáno 2012Text -
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Methods to decrease variability in histological scoring in placentas from a cohort of preterm infants Autor Straughen, Jennifer K, Misra, Dawn P, Ernst, Linda M, Charles, Adrian K, VanHorn, Samantha, Ghosh, Samiran, Buhimschi, Irina, Buhimschi, Catalin, Divine, George, Salafia, Carolyn M
Vydáno 2017Text -
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Thymic Indoleamine 2,3-Dioxygenase-Positive Eosinophils in Young Children: Potential Role In Maturation of the Naive Immune System Autor Tulic, Meri K., Sly, Peter D., Andrews, David, Crook, Maxine, Davoine, Francis, Odemuyiwa, Solomon O., Charles, Adrian, Hodder, Megan L., Prescott, Susan L., Holt, Patrick G., Moqbel, Redwan
Vydáno 2009Text -
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Connective tissue growth factor is expressed in bone marrow stromal cells and promotes interleukin-7-dependent B lymphopoiesis Autor Cheung, Laurence C., Strickland, Deborah H., Howlett, Meegan, Ford, Jette, Charles, Adrian K., Lyons, Karen M., Brigstock, David R., Goldschmeding, Roel, Cole, Catherine H., Alexander, Warren S., Kees, Ursula R.
Vydáno 2014Text -
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An evaluation of classification systems for stillbirth Autor Flenady, Vicki, Frøen, J Frederik, Pinar, Halit, Torabi, Rozbeh, Saastad, Eli, Guyon, Grace, Russell, Laurie, Charles, Adrian, Harrison, Catherine, Chauke, Lawrence, Pattinson, Robert, Koshy, Rachel, Bahrin, Safiah, Gardener, Glenn, Day, Katie, Petersson, Karin, Gordon, Adrienne, Gilshenan, Kristen
Vydáno 2009Text -
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Human AGR2 Deficiency Causes Mucus Barrier Dysfunction and Infantile Inflammatory Bowel Disease Autor Al-Shaibi, Ahmad A., Abdel-Motal, Ussama M., Hubrack, Satanay Z., Bullock, Alex N., Al-Marri, Amna A., Agrebi, Nourhen, Al-Subaiey, Abdulrahman A., Ibrahim, Nazira A., Charles, Adrian K., Elawad, Mamoun, Uhlig, Holm H., Lo, Bernice
Vydáno 2021Text -
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Causes of death and associated conditions (Codac) – a utilitarian approach to the classification of perinatal deaths Autor Frøen, J Frederik, Pinar, Halit, Flenady, Vicki, Bahrin, Safiah, Charles, Adrian, Chauke, Lawrence, Day, Katie, Duke, Charles W, Facchinetti, Fabio, Fretts, Ruth C, Gardener, Glenn, Gilshenan, Kristen, Gordijn, Sanne J, Gordon, Adrienne, Guyon, Grace, Harrison, Catherine, Koshy, Rachel, Pattinson, Robert C, Petersson, Karin, Russell, Laurie, Saastad, Eli, Smith, Gordon CS, Torabi, Rozbeh
Vydáno 2009Text -
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Evaluation of an international educational programme for health care professionals on best practice in the management of a perinatal death: IMproving Perinatal mortality Review and... Autor Gardiner, Paul A., Kent, Alison L., Rodriguez, Viviana, Wojcieszek, Aleena M., Ellwood, David, Gordon, Adrienne, Wilson, Patricia A., Bond, Diana M., Charles, Adrian, Arbuckle, Susan, Gardener, Glenn J., Oats, Jeremy J., Erwich, Jan Jaap, Korteweg, Fleurisca J., Duc, T. H. Nguyen, Leisher, Susannah Hopkins, Kishore, Kamal, Silver, Robert M., Heazell, Alexander E., Storey, Claire, Flenady, Vicki
Vydáno 2016Text -
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BCG vaccination–induced emergency granulopoiesis provides rapid protection from neonatal sepsis Autor Brook, Byron, Harbeson, Danny J., Shannon, Casey P., Cai, Bing, He, Daniel, Ben-Othman, Rym, Francis, Freddy, Huang, Joe, Varankovich, Natallia, Liu, Aaron, Bao, Winnie, Bjerregaard-Andersen, Morten, Schaltz-Buchholzer, Frederik, Sanca, Lilica, Golding, Christian N., Larsen, Kristina Lindberg, Levy, Ofer, Kampmann, Beate, Tan, Rusung, Charles, Adrian, Wynn, James L., Shann, Frank, Aaby, Peter, Benn, Christine S., Tebbutt, Scott J., Kollmann, Tobias R., Amenyogbe, Nelly
Vydáno 2020Text -
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Mutations in KLHL40 Are a Frequent Cause of Severe Autosomal-Recessive Nemaline Myopathy Autor Ravenscroft, Gianina, Miyatake, Satoko, Lehtokari, Vilma-Lotta, Todd, Emily J., Vornanen, Pauliina, Yau, Kyle S., Hayashi, Yukiko K., Miyake, Noriko, Tsurusaki, Yoshinori, Doi, Hiroshi, Saitsu, Hirotomo, Osaka, Hitoshi, Yamashita, Sumimasa, Ohya, Takashi, Sakamoto, Yuko, Koshimizu, Eriko, Imamura, Shintaro, Yamashita, Michiaki, Ogata, Kazuhiro, Shiina, Masaaki, Bryson-Richardson, Robert J., Vaz, Raquel, Ceyhan, Ozge, Brownstein, Catherine A., Swanson, Lindsay C., Monnot, Sophie, Romero, Norma B., Amthor, Helge, Kresoje, Nina, Sivadorai, Padma, Kiraly-Borri, Cathy, Haliloglu, Goknur, Talim, Beril, Orhan, Diclehan, Kale, Gulsev, Charles, Adrian K., Fabian, Victoria A., Davis, Mark R., Lammens, Martin, Sewry, Caroline A., Manzur, Adnan, Muntoni, Francesco, Clarke, Nigel F., North, Kathryn N., Bertini, Enrico, Nevo, Yoram, Willichowski, Ekkhard, Silberg, Inger E., Topaloglu, Haluk, Beggs, Alan H., Allcock, Richard J.N., Nishino, Ichizo, Wallgren-Pettersson, Carina, Matsumoto, Naomichi, Laing, Nigel G.
Vydáno 2013Text