Methods of plugging a permeable porous cellular body von Daugherty, Julie Marie, Cecce, Anthony Joseph, Tepesch, Patrick David, Bubb, Keith Norman, Drury, Kenneth Joseph

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METHODS OF PLUGGING A PERMEABLE POROUS CELLULAR BODY von TEPESCH, PATRICK DAVID, CECCE, ANTHONY JOSEPH, BUBB, KEITH NORMAN, DRURY, KENNETH JOSEPH, DAUGHERTY, JULIE MARIE

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METHODS OF PLUGGING A PERMEABLE POROUS CELLULAR BODY von TEPESCH, Patrick David, DAUGHERTY, Julie Marie, CECCE, Anthony Joseph, BUBB, Keith Norman, DRURY, Kenneth Joseph

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HONEYCOMB PLUGGING APPARATUS AND METHODS PROVIDING REDUCED SLUMP von Daugherty, Julie Marie, Cecce, Anthony Joseph, Tepesch, Patrick David, Bubb, Keith Norman, Bergman, Richard

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Imaging and inspection of plugged honeycomb body von Daugherty, Julie Marie, Zou, Xiaotian, Jamison, Joshua Adam, Treacy, Eric Daniel, Madara, Russel Wayne, Sellers, Duane Otis

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METHODS OF PLUGGING A PERMEABLE POROUS CELLULAR BODY von Daugherty, Julie Marie, Cecce, Anthony Joseph, Tepesch, Patrick David, Bubb, Keith Norman, Drury, Kenneth Joseph

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METHODS OF PLUGGING A PERMEABLE POROUS CELLULAR BODY von TEPESCH, Patrick David, DAUGHERTY, Julie Marie, CECCE, Anthony Joseph, BUBB, Keith Norman, DRURY, Kenneth Joseph

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IMAGING AND INSPECTION OF PLUGGED HONEYCOMB BODY von Daugherty, Julie Marie, Zou, Xiaotian, Jamison, Joshua Adam, Treacy, Eric Daniel, Madara, Russel Wayne, Sellers, Duane Otis

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METHODS OF PLUGGING A PERMEABLE POROUS CELLULAR BODY von TEPESCH, Patrick David, DAUGHERTY, Julie Marie, CECCE, Anthony Joseph, BUBB, Keith Norman, DRURY, Kenneth Joseph

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IMAGING AND INSPECTION OF PLUGGED HONEYCOMB BODY von JAMISON, Joshua Adam, ZOU, Xiaotian, SELLERS, Duane Otis, TREACY, Eric Daniel, DAUGHERTY, Julie Marie, MADARA, Russell Wayne

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METHODS OF PLUGGING A PERMEABLE POROUS CELLULAR BODY von DAUGHERTY JULIE MARIE, TEPESCH PATRICK DAVID, BUBB KEVIN NORMAN, DRURY KENNETH JOSEPH, CECCE ANTHONY JOSEPH

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Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease von Stephens, Jonathan, Dewhurst, Eleanor, Malka, Samantha, Plagnol, Vincent, Rizzo, Roberta, Scott, Richard H., Henderson, Robert H.H., MacLaren, Robert E., Paterson, Joan, Aitman, Timothy, Ali, Sonia, Ambegaonkar, Gautum, Arno, Gavin, Astle, William, Attwood, Antony, Bennett, David, Bitner-Glindzicz, Maria, Bleda, Marta, Boggard, Harm, Carss, Keren, Clements-Brod, Naomi, DaCosta, Rosa, De Vries, Minka, Dewhurst, Eleanor, Drewe, Elizabeth, Egner, William, Erber, Wendy N., Everington, Tamara, Fletcher, Debra, Freson, Kathleen, Gale, Daniel, Ghali, Neeti, Ghurye, Rohit, Gräf, Stefan, Greene, Daniel, Grigoriadou, Sofia, Grozeva, Detelina, Hackett, Scott, Hadinnapola, Charaka, Hague, Rosie, Hammerton, Tracey, Heemskerk, Johan W.M., Holder, Muriel, Holder, Susan, Huissoon, Aarnoud, Hurst, Jane, Jolles, Stephen, Keeling, David, Kennedy, Fiona, Kiely, David, Lawrie, Allan, Lear, Sara, Lees, Melissa, Lentaigne, Claire, Lorenzo, Lorena, Mangles, Sarah, Mapeta, Rutendo, Masati, Larahmie, Mathias, Mary, Michaelides, Michel, Millar, Carolyn M., Moledina, Shahin, Moore, Anthony, Murng, Sai, Oksenhendler, Eric, Park, Soo-Mi, Patch, Chris, Paterson, Joan, Penkett, Christopher J., Pepke-Zaba, Joanna, Pollock, Val, Qasim, Waseem, Quinti, Isabella, Reid, Evan, Rondina, Matthew, Rosser, Elisabeth, Santra, Saikat, Sargur, Ravishankar, Savic, Sinisa, Scully, Marie, Sewell, Carrock, Smith, Kenneth, Southgate, Laura, Stauss, Hans, Stein, Penelope, Talks, Kate, Thomas, Ellen, Thrasher, Adrian, Tischkowitz, Marc, Titterton, Catherine, Turro, Ernest, von Ziegenweldt, Julie, Vonk Noordegraaf, Anton, Wakeling, Emma, Wanjiku, Ivy, Welch, Steve, Westbury, Sarah, Woods, Geoffrey, Yong, Patrick, Webster, Andrew R.

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Genome sequencing and comprehensive rare-variant analysis of 465 families with neurodevelopmental disorders von Sanchis-Juan, Alba, Megy, Karyn, Stephens, Jonathan, Armirola Ricaurte, Camila, Dewhurst, Eleanor, Low, Kayyi, French, Courtney E., Grozeva, Detelina, Stirrups, Kathleen, Erwood, Marie, McTague, Amy, Penkett, Christopher J., Shamardina, Olga, Tuna, Salih, Daugherty, Louise C., Gleadall, Nicholas, Duarte, Sofia T., Hedrera-Fernández, Antonio, Vogt, Julie, Ambegaonkar, Gautam, Chitre, Manali, Josifova, Dragana, Kurian, Manju A., Parker, Alasdair, Rankin, Julia, Reid, Evan, Wakeling, Emma, Wassmer, Evangeline, Woods, C. Geoffrey, Raymond, F. Lucy, Carss, Keren J.

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ACC/AHA/ASE/HRS/ISACHD/SCAI/SCCT/SCMR/SOPE 2020 Appropriate Use Criteria for Multimodality Imaging During the Follow-Up Care of Patients With Congenital Heart Disease von Sachdeva, Ritu, Valente, Anne Marie, Armstrong, Aimee K., Cook, Stephen C., Han, B. Kelly, Lopez, Leo, Lui, George K., Pickard, Sarah S., Powell, Andrew J., Bhave, Nicole M., Sachdeva, Ritu, Valente, Anne Marie, Pickard, Sarah S., Baffa, Jeanne M., Banka, Puja, Cohen, Scott B., Glickstein, Julie S., Kanter, Joshua P., Kanter, Ronald J., Kim, Yuli Y., Kipps, Alaina K., Latson, Larry A., Lin, Jeannette P., Parra, David A., Rodriguez, Fred H., Saarel, Elizabeth V., Srivastava, Shubhika, Stephenson, Elizabeth A., Stout, Karen K., Zaidi, Ali N.

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Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations von Lorenzini, Tiziana, Fliegauf, Manfred, Klammer, Nils, Proietti, Michele, Bulashevska, Alla, Schejter, Yael D., Atschekzei, Faranaz, Stepensky, Polina, Pedroza, Luis A., van der Flier, Michiel, Martínez-Gallo, Mónica, Svec, Peter, Fischer, Ute, Ip, Winnie, Geha, Raif, Chou, Janet, Alosaimi, Mohammed, Weintraub, Lauren, Dos Santos Vilela, Maria Marluce, Holzinger, Dirk, Seidl, Maximilian, Lougaris, Vassilios, Plebani, Alessandro, Abolhassani, Hassan, Thaventhiran, James E., Warnatz, Klaus, Grimbacher, Bodo, Ashford, Sofie, Bacchelli, Chiara, Batista, Joana, Bibi, Shahnaz, Boardman, Barbara, Booth, Claire, Breen, Gerome, Burns, Siobhan O., Burren, Oliver S., Carss, Keren, Chambers, John, Cooper, Nichola, Davies, E.G., Dempster, John, Dewhurst, Eleanor F., Drewe, Elizabeth, Duarte, Daniel, Edgar, J. David M., Egner, William, El-Shanawany, Tariq, Erwood, Marie, Fox, James, Frontini, Mattia, Furnell, Abigail, Gaspar, H. Bobby, Gleadall, Nicholas S., Grigoriadou, Sofia, Hackett, Scott, Hague, Rosie, Haimel, Matthias, Hayman, Grant, Hu, Fengyuan, Huissoon, Aarnoud P., Jolles, Stephen, Kasanicki, Mary A., Kelleher, Peter, Klein, Nigel, Kreuzhuber, Roman, Kuijpers, Taco W., Kumararatne, Dinakantha, Allen, Hana Lango, Linger, Rachel, Lorenzo, Lorena E., Maimaris, Jesmeen, Martin, Jennifer, McDermott, Elizabeth M., Meacham, Stuart, Morrisson, Valerie, Nasir, Iman, Nejentsev, Sergey, Papadia, Sofia, Ponsford, Mark J., Quinn, Ellen, Quinti, Isabella, Rayner-Matthews, Paula J., Samani, Nilesh, Sanchis-Juan, Alba, Savic, Sinisa, Simpson, Michael A., Smith, Kenneth G.C., Thaventhiran, James E., Tilly, Tobias, Titterton, Catherine, Tuna, Salih, Urniaz, Rafal, von Ziegenweidt, Julie, Watt, Christopher, Welch, Steven B., Whitehorn, Deborah, Wood, Yvette, Workman, Sarita, Worth, Austen, Young, Timothy

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GWAS meta-analysis of intrahepatic cholestasis of pregnancy implicates multiple hepatic genes and regulatory elements von Dixon, Peter H., Levine, Adam P., Cebola, Inês, Chan, Melanie M. Y., Amin, Aliya S., Aich, Anshul, Mozere, Monika, Maude, Hannah, Mitchell, Alice L., Zhang, Jun, Chambers, Jenny, Syngelaki, Argyro, Donnelly, Jennifer, Cooley, Sharon, Geary, Michael, Nicolaides, Kypros, Thorsell, Malin, Hague, William M., Estiu, Maria Cecilia, Marschall, Hanns-Ulrich, Gale, Daniel P., Williamson, Catherine

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ACC/AHA/ASE/HRS/ISACHD/SCAI/SCCT/SCMR/SOPE 2020 Appropriate Use Criteria for Multimodality Imaging During the Follow-Up Care of Patients With Congenital Heart Disease: A Report of... von Sachdeva, Ritu, Valente, Anne Marie, Armstrong, Aimee K, Cook, Stephen C, Han, B Kelly, Lopez, Leo, Lui, George K, Pickard, Sarah S, Powell, Andrew J, Bhave, Nicole M, Baffa, Jeanne M, Banka, Puja, Cohen, Scott B, Glickstein, Julie S, Kanter, Joshua P, Kanter, Ronald J, Kim, Yuli Y, Kipps, Alaina K, Latson, Larry A, Lin, Jeannette P, Parra, David A, Rodriguez, 3rd, Fred H, Saarel, Elizabeth V, Srivastava, Shubhika, Stephenson, Elizabeth A, Stout, Karen K, Zaidi, Ali N, Gluckman, Ty J, Aggarwal, Niti R, Dehmer, Gregory J, Gilbert, Olivia N, Kumbhani, Dharam J, Price, Andrea L, Winchester, David E, Gulati, Martha, Doherty, John U, Daugherty, Stacie L, Dean, Larry S, Desai, Milind Y, Gillam, Linda D, Mehrotra, Praveen

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Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes von West, Hannah, Carss, Keren, Shakeel, Hassan, Adlard, Julian, Cole, Trevor, Kwong, Ava, Paterson, Joan, Searle, Claire, Skytte, Anne-Bine, Aitman, Timothy, Ambegaonkar, Gautum, Antrobus, Richard, Arno, Gavin, Astle, William, Attwood, Antony, Austin, Steve, Bakchoul, Tamam, Bennett, David, Bitner-Glindzicz, Maria, Bleda, Marta, Bolton-Maggs, Paula, Booth, Claire, Clements-Brod, Naomi, Clowes, Virginia, Collins, Peter, Cookson, Victoria, Creaser-Myers, Amanda, DaCosta, Rosa, Davies, Sophie, Deegan, Patrick, Dewhurst, Eleanor, Doffinger, Rainer, Drewe, Elizabeth, Favier, Remi, Firth, Helen, Furie, Bruce, Furnell, Abigail, Gardham, Alice, Gissen, Paul, Gomez, Keith, Graf, Stefan, Gräf, Stefan, Greenhalgh, Alan, Hackett, Scott, Haimel, Matthias, Herwadkar, Archana, Holder, Muriel, Huissoon, Aarnoud, James, Roger, Kennedy, Fiona, Kingston, Nathalie, Kuijpers, Taco, Lawrie, Allan, Lentaigne, Claire, Machado, Rajiv, Maher, Eamonn, Mangles, Sarah, Manson, Ania, Matser, Vera, McDermott, Elizabeth, Megy, Karyn, Millar, Carolyn M., Morrell, Nicholas, Ouwehand, Willem H., Papadia, Sofia, Payne, Jeanette, Peacock, Andrew, Pollock, Val, Quinti, Isabella, Rayner-Matthews, Paula, Rehnstrom, Karola, Rhodes, Christopher J., Richardson, Sylvia, Richter, Alex, Rondina, Matthew, Rosser, Elisabeth, Rue-Albrecht, Kevin, Sargur, Ravishankar, Savic, Sinisa, Schotte, Gwen, Schulze, Harald, Seneviratne, Suranjith, Shamardina, Olga, Simeoni, Ilenia, Staines, Simon, Stark, Hannah, Stock, Sophie, Thaventhiran, James, Thompson, Dorothy, Toh, Cheng-Hock, Turek, Wojciech, Wassmer, Evangeline, Watt, Christopher, Wharton, John, Williamson, Catherine, Woods, Geoff, Wort, John, Yeatman, Nigel, Tischkowitz, Marc D., Maher, Eamonn R.

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Specific Alleles of CLN7/MFSD8, a Protein That Localizes to Photoreceptor Synaptic Terminals, Cause a Spectrum of Nonsyndromic Retinal Dystrophy von Khan, Kamron N, El-Asrag, Mohammed E, Ku, Cristy A, Holder, Graham E, McKibbin, Martin, Arno, Gavin, Poulter, James A, Carss, Keren, Bommireddy, Tejaswi, Bagheri, Saghar, Bakall, Benjamin, Scholl, Hendrik P, Raymond, F Lucy, Toomes, Carmel, Inglehearn, Chris F, Pennesi, Mark E, Moore, Anthony T, Michaelides, Michel, Webster, Andrew R, Ali, Manir

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ACC/AHA/ASE/HRS/ISACHD/SCAI/SCCT/SCMR/SOPE 2020 Appropriate Use Criteria for Multimodality Imaging During the Follow-Up Care of Patients With Congenital Heart Disease von Sachdeva, Ritu, Valente, Anne Marie, Armstrong, Aimee K., Cook, Stephen C., Han, B. Kelly, Lopez, Leo, Lui, George K., Pickard, Sarah S., Powell, Andrew J., Bhave, Nicole M., Baffa, Jeanne M., Banka, Puja, Cohen, Scott B., Glickstein, Julie S., Kanter, Joshua P., Kanter, Ronald J., Kim, Yuli Y., Kipps, Alaina K., Latson, Larry A., Lin, Jeannette P., Parra, David A., Rodriguez, Fred H., Saarel, Elizabeth, Srivastava, Shubhika, Stephenson, Elizabeth A., Stout, Karen K., Zaidi, Ali N., Gluckman, Ty J., Aggarwal, Niti R., Dehmer, Gregory J., Gilbert, Olivia N., Kumbhani, Dharam J., Price, Andrea L., Winchester, David E., Gulati, Martha, Doherty, John U., Daugherty, Stacie L., Dean, Larry S., Desai, Milind Y., Gillam, Linda D., Mehrotra, Praveen

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