Výsledky vyhledávání - Edmondson, Andrew
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Overgrowth Syndromes Autor Edmondson, Andrew C., Kalish, Jennifer M.
Vydáno 2015Text -
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A rare cause of infantile achalasia: GMPPA‐congenital disorder of glycosylation with two novel compound heterozygous variants Autor Geiculescu, Irina, Dranove, Jason, Cosper, Graham, Edmondson, Andrew C., Morava‐Kozicz, Eva, Carter, Lauren B.
Vydáno 2022Text -
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X-linked cellular mosaicism underlies age-dependent occurrence of seizure-like events in mouse models of CDKL5 deficiency disorder Autor Terzic, Barbara, Cui, Yue, Edmondson, Andrew C., Tang, Sheng, Sarmiento, Nicolas, Zaitseva, Daria, Marsh, Eric D., Coulter, Douglas A., Zhou, Zhaolan
Vydáno 2020Text -
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Spontaneous improvement of carbohydrate-deficient transferrin in PMM2-CDG without mannose observed in CDG natural history study Autor Witters, Peter, Edmondson, Andrew C., Lam, Christina, Johnsen, Christin, Patterson, Marc C., Raymond, Kimiyo M., He, Miao, Freeze, Hudson H., Morava, Eva
Vydáno 2021Text -
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Increased Clinical Sensitivity and Specificity of Plasma Protein N-Glycan Profiling for Diagnosing Congenital Disorders of Glycosylation by Use of Flow Injection–Electrospray Ioniz... Autor Chen, Jie, Li, Xueli, Edmondson, Andrew, Meyers, Gail Ditewig, Izumi, Kosuke, Ackermann, Amanda M., Morava, Eva, Ficicioglu, Can, Bennett, Michael J., He, Miao
Vydáno 2019Text -
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The NLRP3 Inflammasome Mediates Inflammation Produced by Bladder Outlet Obstruction Autor Hughes, Francis M., Hill, Hayden M., Wood, Case M., Edmondson, Andrew T., Dumas, Aliya, Foo, Wen-Chi, Oelsen, James M., Rac, Goran, Purves, J. Todd
Vydáno 2015Text -
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A Community-Led Approach as a Guide to Overcome Challenges for Therapy Research in Congenital Disorders of Glycosylation Autor Francisco, Rita, Brasil, Sandra, Pascoal, Carlota, Edmondson, Andrew C., Jaeken, Jaak, Videira, Paula A., de Freitas, Cláudia, Ferreira, Vanessa dos Reis, Marques-da-Silva, Dorinda
Vydáno 2022Text -
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Liver manifestations in a cohort of 39 patients with congenital disorders of glycosylation: pin-pointing the characteristics of liver injury and proposing recommendations for follo... Autor Starosta, Rodrigo Tzovenos, Boyer, Suzanne, Tahata, Shawn, Raymond, Kimiyo, Lee, Hee Eun, Wolfe, Lynne A., Lam, Christina, Edmondson, Andrew C., Schwartz, Ida Vanessa Doederlein, Morava, Eva
Vydáno 2021Text -
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A naturally occurring variant of endothelial lipase associated with elevated HDL exhibits impaired synthesis Autor Brown, Robert J., Edmondson, Andrew C., Griffon, Nathalie, Hill, Theophelus B., Fuki, Ilia V., Badellino, Karen O., Li, Mingyao, Wolfe, Megan L., Reilly, Muredach P., Rader, Daniel J.
Vydáno 2009Text -
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The T111I variant in the endothelial lipase gene and risk of coronary heart disease in three independent populations Autor Jensen, Majken K., Rimm, Eric B., Mukamal, Kenneth J., Edmondson, Andrew C., Rader, Daniel J., Vogel, Ulla, Tjønneland, Anne, Sørensen, Thorkild I.A., Schmidt, Erik B., Overvad, Kim
Vydáno 2009Text -
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Clinical and biochemical improvement with galactose supplementation in SLC35A2-CDG Autor Witters, Peter, Tahata, Shawn, Barone, Rita, Õunap, Katrin, Salvarinova, Ramona, Grønborg, Sabine, Hoganson, George, Scaglia, Fernando, Lewis, Andrea Margaret, Mori, Mari, Sykut-Cegielska, Jolanta, Edmondson, Andrew, He, Miao, Morava, Eva
Vydáno 2020Text -
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Mining the LIPG Allelic Spectrum Reveals the Contribution of Rare and Common Regulatory Variants to HDL Cholesterol Autor Khetarpal, Sumeet A., Edmondson, Andrew C., Raghavan, Avanthi, Neeli, Hemanth, Jin, Weijun, Badellino, Karen O., Demissie, Serkalem, Manning, Alisa K., DerOhannessian, Stephanie L., Wolfe, Megan L., Cupples, L. Adrienne, Li, Mingyao, Kathiresan, Sekar, Rader, Daniel J.
Vydáno 2011Text -
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Pathway-Wide Association Study Implicates Multiple Sterol Transport and Metabolism Genes in HDL Cholesterol Regulation Autor Wang, Kai, Edmondson, Andrew C., Li, Mingyao, Gao, Fan, Qasim, Atif N., Devaney, Joseph M., Burnett, Mary Susan, Waterworth, Dawn M., Mooser, Vincent, Grant, Struan F. A., Epstein, Stephen E., Reilly, Muredach P., Hakonarson, Hakon, Rader, Daniel J.
Vydáno 2011Text -
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Newborn Screening for X-Linked Adrenoleukodystrophy: Review of Data and Outcomes in Pennsylvania Autor Priestley, Jessica R. C., Adang, Laura A., Drewes Williams, Sarah, Lichter-Konecki, Uta, Menello, Caitlin, Engelhardt, Nicole M., DiPerna, James C., DiBoscio, Brenda, Ahrens-Nicklas, Rebecca C., Edmondson, Andrew C., Reynoso Santos, Francis Jeshira, Ficicioglu, Can
Vydáno 2022Text