The challenge of implementing interoperable electronic medical records von Dechene, James C

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Crises

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QMHC interview with James C. Dechene, JD von Dechene, J C

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Multiple solvent crystal structures of RNAse A von Dechene, Michelle C, Wink, Glenna, Cholewa, Crystal, Swartz, Paul, Mattos, Carla

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Preferred provider organization structures and agreements von Dechene, J C

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Myelination of the Mouse Vestibular Ganglion von Dechesne, Claude J., Desmadryl, Gilles, Dememes, Danielle

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Reactivity of human anti-α-galactosyl IgG antibody with α(1→3)-linked galactosyl epitopes exposed on basement membranes and on glomerular epithelial cells: an in vitro and in vivo... von LI VECCHI, M, DAVIN, J. C, CASTRONOVO, V, FOIDART, J. M, MALAISE, M, FOIDART, J. B, DECHENE, C, BARBAGALLO SANGIORGI, G, MAHIEU, P

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MURRAY AND CHURCH AND STATE von Dechene, Arthur C.

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PROTESTANTS ON THE COUNCIL von Dechene, Arthur C.

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Lab discounts. How deep is too deep? von Dechene, J C, Howton, T

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QMHC interview with James C. Dechene, JD von Dechene, J C

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Recessive truncating titin gene, TTN, mutations presenting as centronuclear myopathy von Ceyhan-Birsoy, Ozge, Agrawal, Pankaj B., Hidalgo, Carlos, Schmitz-Abe, Klaus, DeChene, Elizabeth T., Swanson, Lindsay C., Soemedi, Rachel, Vasli, Nasim, Iannaccone, Susan T., Shieh, Perry B., Shur, Natasha, Dennison, Jane M., Lawlor, Michael W., Laporte, Jocelyn, Markianos, Kyriacos, Fairbrother, William G., Granzier, Henk, Beggs, Alan H.

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Automated Clinical Exome Reanalysis Reveals Novel Diagnoses von Baker, Samuel W., Murrell, Jill R., Nesbitt, Addie I., Pechter, Kieran B., Balciuniene, Jorune, Zhao, Xiaonan, Yu, Zhenming, Denenberg, Elizabeth H., DeChene, Elizabeth T., Wilkens, Alisha B., Bhoj, Elizabeth J., Guan, Qiaoning, Dulik, Matthew C., Conlin, Laura K., Abou Tayoun, Ahmad N., Luo, Minjie, Wu, Chao, Cao, Kajia, Sarmady, Mahdi, Bedoukian, Emma C., Tarpinian, Jennifer, Medne, Livija, Skraban, Cara M., Deardorff, Matthew A., Krantz, Ian D., Krock, Bryan L., Santani, Avni B.

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Clinical phenotype-based gene prioritization: an initial study using semantic similarity and the human phenotype ontology von Masino, Aaron J, Dechene, Elizabeth T, Dulik, Matthew C, Wilkens, Alisha, Spinner, Nancy B, Krantz, Ian D, Pennington, Jeffrey W, Robinson, Peter N, White, Peter S

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Processes and preliminary outputs for identification of actionable genes as incidental findings in genomic sequence data in the Clinical Sequencing Exploratory Research Consortium von Berg, Jonathan S., Amendola, Laura M., Eng, Christine, Van Allen, Eliezer, Gray, Stacy W., Wagle, Nikhil, Rehm, Heidi L., DeChene, Elizabeth T., Dulik, Matthew C., Hisama, Fuki M., Burke, Wylie, Spinner, Nancy B., Garraway, Levi, Green, Robert C., Plon, Sharon, Evans, James P., Jarvik, Gail P.

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Gonadal Function Recovery in Patients With Advanced Hodgkin Lymphoma Treated With a PET-Adapted Regimen: Prospective Analysis of a Randomized Phase III Trial (AHL2011) von Demeestere, Isabelle, Racape, Judith, Dechene, Julie, Dupuis, Jehan, Morschhauser, Franck, De Wilde, Virginie, Lazarovici, Julien, Ghesquieres, Hervé, Touati, Mohamed, Sibon, David, Alexis, Magda, Gac, Anne-Claire, Moatti, Hannah, Virelizier, Emmanuelle, Maisonneuve, Hervé, Pranger, Delphine, Houot, Roch, Fornecker, Luc-Matthieu, Tempescul, Adrian, André, Marc, Casasnovas, René-Olivier

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O-088 Effect of low, medium and high risk chemotherapy on the ovarian reserve in children: results of the interim analysis of a prospective multicentric trial (CHANCE) von Demeestere, I, Racape, J, Dechene, J, Sudour-Bonnange, H, Labarque, V, Grysole, C, Bruno, B, Decanter, C, Devalck, C

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Mo1406 BIOPSY AND IMAGING OF THE BILIARY TREE USING A CRYOGENIC BIOPSY DEVICE von Dechene, Nicholas M., Otuya, David O., Jacobson, Brian C., Tearney, Guillermo

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Utility and limitations of exome sequencing as a genetic diagnostic tool for children with hearing loss von Sheppard, Sarah, Biswas, Sawona, Li, Mindy H., Jayaraman, Vijayakumar, Slack, Ian, Romasko, Edward J., Sasson, Ariella, Brunton, Joshua, Rajagopalan, Ramakrishnan, Sarmady, Mahdi, Abrudan, Jenica L., Jairam, Sowmya, DeChene, Elizabeth T., Ying, Xiahoan, Choi, Jiwon, Wilkens, Alisha, Raible, Sarah E., Scarano, Maria I., Santani, Avni, Pennington, Jeffrey W., Luo, Minjie, Conlin, Laura K., Devkota, Batsal, Dulik, Matthew C., Spinner, Nancy B., Krantz, Ian D.

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Novel Mutations Widen the Phenotypic Spectrum of Slow Skeletal/β-Cardiac Myosin (MYH7) Distal Myopathy von Lamont, Phillipa J., Wallefeld, William, Hilton-Jones, David, Udd, Bjarne, Argov, Zohar, Barboi, Alexandru C., Bonneman, Carsten, Boycott, Kym M., Bushby, Kate, Connolly, Anne M., Davies, Nicholas, Beggs, Alan H., Cox, Gerald F., Dastgir, Jahannaz, DeChene, Elizabeth T., Gooding, Rebecca, Jungbluth, Heinz, Muelas, Nuria, Palmio, Johanna, Penttilä, Sini, Schmedding, Eric, Suominen, Tiina, Straub, Volker, Staples, Christopher, Van den Bergh, Peter Y.K., Vilchez, Juan J., Wagner, Kathryn R., Wheeler, Patricia G., Wraige, Elizabeth, Laing, Nigel G.

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