Selective medium for Bacillus anthracis von Knisely, R F

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Differential Media for the Identification of Bacillus anthracis von Knisely, R F

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SELECTIVE MEDIA FOR THE ISOLATION OF PASTEURELLA PESTIS von KNISELY, R F, SWANEY, L M, FRIEDLANDER, H

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EFFECT OF HEMATIN ON THE RECOVERY OF BACILLUS ANTHRACIS AND RELATED ORGANISMS von KNISELY, R F

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A comprehensive review of MR imaging changes following radiosurgery to 500 brain metastases von Patel, T R, McHugh, B J, Bi, W L, Minja, F J, Knisely, J P S, Chiang, V L

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Differences in presentation and progression between severe FIC1 and BSEP deficiencies von Pawlikowska, Ludmila, Strautnieks, Sandra, Jankowska, Irena, Czubkowski, Piotr, Emerick, Karan, Antoniou, Anthony, Wanty, Catherine, Fischler, Bjorn, Jacquemin, Emmanuel, Wali, Sami, Blanchard, Samra, Nielsen, Inge-Merete, Bourke, Billy, McQuaid, Shirley, Lacaille, Florence, Byrne, Jane A, van Eerde, Albertien M, Kolho, Kaija-Leena, Klomp, Leo, Houwen, Roderick, Bacchetti, Peter, Lobritto, Steven, Hupertz, Vera, McClean, Patricia, Mieli-Vergani, Giorgina, Shneider, Benjamin, Nemeth, Antal, Sokal, Etienne, Freimer, Nelson B, Knisely, A.S, Rosenthal, Philip, Whitington, Peter F, Pawlowska, Joanna, Thompson, Richard J, Bull, Laura N

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Biallelic IARS Mutations Cause Growth Retardation with Prenatal Onset, Intellectual Disability, Muscular Hypotonia, and Infantile Hepatopathy von Kopajtich, Robert, Murayama, Kei, Janecke, Andreas R., Haack, Tobias B., Breuer, Maximilian, Knisely, A.S., Harting, Inga, Ohashi, Toya, Okazaki, Yasushi, Watanabe, Daisaku, Tokuzawa, Yoshimi, Kotzaeridou, Urania, Kölker, Stefan, Sauer, Sven, Carl, Matthias, Straub, Simon, Entenmann, Andreas, Gizewski, Elke, Feichtinger, René G., Mayr, Johannes A., Lackner, Karoline, Strom, Tim M., Meitinger, Thomas, Müller, Thomas, Ohtake, Akira, Hoffmann, Georg F., Prokisch, Holger, Staufner, Christian

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Mutations in VPS33B , encoding a regulator of SNARE-dependent membrane fusion, cause arthrogryposis-renal dysfunction-cholestasis (ARC) syndrome von Stapelbroek, Janneke M, Morgan, Neil V, Johnson, Colin A, Lo, Bryan, Karet, Fiona E, McKiernan, Patrick J, Knisely, A S, Forshew, Tim, Morris, Andrew A M, Trembath, Richard C, Houwen, Roderick H J, Wraith, James E, Quarrell, Oliver W, Cooper, Wendy N, Maher, Eamonn R, Klomp, Leo W J, Thompson, Richard J, Wali, S, Gissen, Paul, Kelly, Deirdre A, McClean, Patricia, Di Rocco, Maja, Mandel, Hanna, Lynch, Sally A

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Genetic Defects in Bile Acid Conjugation Cause Fat-Soluble Vitamin Deficiency von Setchell, Kenneth D.R, Heubi, James E, Shah, Sohela, Lavine, Joel E, Suskind, David, Al–Edreesi, Mohammed, Potter, Carol, Russell, David W, O'Connell, Nancy C, Wolfe, Brian, Jha, Pinky, Zhang, Wujuan, Bove, Kevin E, Knisely, Alex S, Hofmann, Alan F, Rosenthal, Philip, Bull, Laura N

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A gene encoding a liver-specific ABC transporter is mutated in progressive familial intrahepatic cholestasis von Tanner, M. Stuart, Sokal, Etienne, Strautnieks, Sandra S, Dahan, Karine, Pawlowska, Joanna, Dahl, Niklas, Freimer, Nelson B, Gardiner, R. Mark, Childs, Sarah, Kagalwalla, Amir F, Knisely, Alexander S, Thompson, Richard J, Ling, Victor, Németh, Antal, Baker, Alastair, Arnell, Henrik, Kocoshis, Samuel A, Mieli-Vergani, Giorgina, Bull, Laura N

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Hepatocellular carcinoma in ten children under five years of age with bile salt export pump deficiency von Knisely, A. S., Strautnieks, Sandra S., Meier, Yvonne, Stieger, Bruno, Byrne, Jane A., Portmann, Bernard C., Bull, Laura N., Pawlikowska, Ludmila, Bilezikçi, Banu, Özçay, Figen, László, Aranka, Tiszlavicz, László, Moore, Lynette, Raftos, Jeremy, Arnell, Henrik, Fischler, Björn, Németh, Antal, Papadogiannakis, Nikos, Cielecka‐Kuszyk, Joanna, Jankowska, Irena, Pawłowska, Joanna, Melín‐Aldana, Hector, Emerick, Karan M., Whitington, Peter F., Mieli‐Vergani, Giorgina, Thompson, Richard J.

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Dosimetric and Clinical Data from Linac-Based Stereotactic Arrhythmia Radioablation von Gregucci, F., Ng, J., Knisely, J.P.S., Cheung, J.W., Thomas, G., Liu, C.F., Muller, L., Pennell, R., Formenti, S.C.

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Acquisition and Processing Considerations for Infrared Images of Rotating Turbine Blades von Knisely, Brian F, Berdanier, Reid A, Thole, Karen A, Haldeman, Charles W, Markham, James R, Cosgrove, Joseph E, Carlson, Andrew E, Scire, James J

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Progressive familial intrahepatic cholestasis, type 1, is associated with decreased farnesoid X receptor activity von Chen, Frank, Ananthanarayanan, M., Emre, Sukru, Neimark, Ezequiel, Bull, Laura N., Knisely, A.S., Strautnieks, Sandra S., Thompson, Richard J., Magid, Margret S., Gordon, Ronald, Balasubramanian, N., Suchy, Frederick J., Shneider, Benjamin L.

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Black Americans With Sickle Cell Disease (SCD) Demonstrate Accelerated Epigenetic Pace of Aging Compared to Black Americans Without SCD von Garrett, Melanie E, Le, Brandon, Bourassa, Kyle J, Dennis, Michelle F, Hatch, Daniel, Yang, Qing, Tanabe, Paula, Shah, Nirmish, Luyster, Faith S, Oyedeji, Charity, Strouse, John J, Cohen, Harvey J, Kimbrel, Nathan A, Beckham, Jean C, Knisely, Mitchell R, Telen, Marilyn J, Ashley-Koch, Allison E

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Phase II Evaluation of Preoperative Chemoradiation and Postoperative Adjuvant Chemotherapy for Squamous Cell and Adenocarcinoma of the Esophagus von HEATH, E. I, BURTNESS, B. A, TOPAZIAN, M, WU, T.-T, OLUKAYODE, K, FORASTIERE, A. A, HEITMILLER, R. F, SALEM, R, KLEINBERG, L, KNISELY, J. P. S, YANG, S. C, TALAMINI, M. A, KAUFMAN, H. S, CANTO, M. I

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Mutations in ENPP1 are associated with 'idiopathic' infantile arterial calcification von Rutsch, Frank, Suk, Anita, Ferre, Merry, Höhne, Wolfgang, Knisely, Alex, Hinrichs, Bernd, Lehmann, Mandy, Epplen, Jörg T, Ruf, Nico, Vallance, Hillary, Terkeltaub, Robert, Schnabel, Dirk, Schauer, Galen, Smith, Wendy, Sinaiko, Alan R, Roscioli, Tony, Filippone, Marco, Vaingankar, Sucheta, McGill, James, Toliat, Mohammad R, Superti-Furga, Andrea, Nürnberg, Peter

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Genetic and morphological findings in progressive familial intrahepatic cholestasis (Byler disease [PFIC‐1] and Byler syndrome): Evidence for heterogeneity von Bull, L N, Carlton, V E, Stricker, N L, Baharloo, S, DeYoung, J A, Freimer, N B, Magid, M S, Kahn, E, Markowitz, J, DiCarlo, F J, McLoughlin, L, Boyle, J T, Dahms, B B, Faught, P R, Fitzgerald, J F, Piccoli, D A, Witzleben, C L, O'Connell, N C, Setchell, K D, Agostini, R M, Kocoshis, S A, Reyes, J, Knisely, A S

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Antibacterial Resistance Leadership Group: Open for Business von Chambers, Henry F., Bartlett, John G., Bonomo, Robert A., Chiou, Christine, Cosgrove, Sara E., Cross, Heather R., Daum, Robert S., Downing, Michele, Evans, Scott R., Knisely, Jane, Kreiswirth, Barry N., Lautenbach, Ebbing, Mickley, Brenda S., Patel, Robin, Pettigrew, Melinda M., Rodvold, Keith A., Spellberg, Brad, Fowler, Vance G.

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A gene encoding a P-type ATPase mutated in two forms of hereditary cholestasis von Bull, Laura N., van Eijk, Michiel J.T., Pawlikowska, Ludmila, DeYoung, Joseph A., Juijn, Jenneke A., Liao, Mira, Klomp, Leo W.J., Lomri, Noureddine, Berger, Ruud, Scharschmidt, Bruce R., Knisely, Alexander S., Houwen, Roderick H.J., Freimer, Nelson B.

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