Abnormal First Trimester Serum Interleukin 18 Levels are Associated with a Poor Outcome in Women with a History of Recurrent Miscarriage von Wilson, Rhoda, Moor, Judith, Jenkins, Carol, Miller, Helen, Walker, James J., McLean, Marjorie A., Norman, J., McInnes, I. B.

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Maternal environmental risk factors and the development of internalizing and externalizing problems in childhood: The complex role of genetic factors von Ensink, Judith B. M., Moor, Marleen H. M., Zafarmand, Mohammad Hadi, Laat, Sanne, Uitterlinden, André, Vrijkotte, Tanja G. M., Lindauer, Ramón, Middeldorp, Christel M.

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Exhaled breath analysis by use of eNose technology: a novel diagnostic tool for interstitial lung disease von Moor, Catharina C, Oppenheimer, Judith C, Nakshbandi, Gizal, Aerts, Joachim G J V, Brinkman, Paul, Maitland-van der Zee, Anke-Hilse, Wijsenbeek, Marlies S

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Diagnostic Performance of Electronic Nose Technology in Sarcoidosis von van der Sar, Iris G., Moor, Catharina C., Oppenheimer, Judith C., Luijendijk, Megan L., van Daele, Paul L.A., Maitland-van der Zee, Anke H., Brinkman, Paul, Wijsenbeek, Marlies S.

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Changing characteristics, treatment approaches and survival of patients with brain metastasis: data from six thousand and thirty-one individuals over an observation period of 30 ye... von Steindl, Ariane, Brunner, Tabea J., Heimbach, Kira, Schweighart, Katharina, Moser, Georg M., Niziolek, Helena M., Moor, Elisabeth, Kreminger, Judith, Starzer, Angelika M., Dieckmann, Karin, Gatterbauer, Brigitte, Widhalm, Georg, Preusser, Matthias, Berghoff, Anna S.

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Beyond Animal Testing Index: Benchmarking Tool for a World beyond Animal Testing von Krul, Cyrille, De Moor, Annick, Stegmeijer, Koen, Stoop, Reinout, Van Luijk, Judith, Prins, Jan-Bas

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A variant in FTO shows association with melanoma risk not due to BMI von Iles, Mark M, Law, Matthew H, Stacey, Simon N, Han, Jiali, Fang, Shenying, Pfeiffer, Ruth, Harland, Mark, Macgregor, Stuart, Taylor, John C, Aben, Katja K, Akslen, Lars A, Avril, Marie-Françoise, Azizi, Esther, Bakker, Bert, Benediktsdottir, Kristrun R, Bergman, Wilma, Scarrà, Giovanna Bianchi, Brown, Kevin M, Calista, Donato, Chaudru, Valérie, Fargnoli, Maria Concetta, Cust, Anne E, Demenais, Florence, de Waal, Anne C, Dębniak, Tadeusz, Elder, David E, Friedman, Eitan, Galan, Pilar, Ghiorzo, Paola, Gillanders, Elizabeth M, Goldstein, Alisa M, Gruis, Nelleke A, Hansson, Johan, Helsing, Per, Hočevar, Marko, Höiom, Veronica, Hopper, John L, Ingvar, Christian, Janssen, Marjolein, Jenkins, Mark A, Kanetsky, Peter A, Kiemeney, Lambertus A, Lang, Julie, Lathrop, G Mark, Leachman, Sancy, Lee, Jeffrey E, Lubiński, Jan, Mackie, Rona M, Mann, Graham J, Martin, Nicholas G, Mayordomo, Jose I, Molven, Anders, Mulder, Suzanne, Nagore, Eduardo, Novaković, Srdjan, Okamoto, Ichiro, Olafsson, Jon H, Olsson, Håkan, Pehamberger, Hubert, Peris, Ketty, Grasa, Maria Pilar, Planelles, Dolores, Puig, Susana, Puig-Butille, Joan Anton, Randerson-Moor, Juliette, Requena, Celia, Rivoltini, Licia, Rodolfo, Monica, Santinami, Mario, Sigurgeirsson, Bardur, Snowden, Helen, Song, Fengju, Sulem, Patrick, Thorisdottir, Kristin, Tuominen, Rainer, Van Belle, Patricia, van der Stoep, Nienke, van Rossum, Michelle M, Wei, Qingyi, Wendt, Judith, Zelenika, Diana, Zhang, Mingfeng, Landi, Maria Teresa, Thorleifsson, Gudmar, Bishop, D Timothy, Amos, Christopher I, Hayward, Nicholas K, Stefansson, Kari, Bishop, Julia A Newton, Barrett, Jennifer H

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Inherited variants in the MC1R gene and survival from cutaneous melanoma: a BioGenoMEL study von Davies, John R., Randerson-Moor, Juliette, Kukalizch, Kairen, Harland, Mark, Kumar, Rajiv, Madhusudan, Srinivasan, Nagore, Eduardo, Hansson, Johan, Höiom, Veronica, Ghiorzo, Paola, Gruis, Nelleke A., Kanetsky, Peter A., Wendt, Judith, Pjanova, Dace, Puig, Susana, Saiag, Philippe, Schadendorf, Dirk, Soufir, Nadem, Okamoto, Ichiro, Affleck, Paul, García-Casado, Zaida, Ogbah, Zighereda, Ozola, Aija, Queirolo, Paola, Sucker, Antje, Barrett, Jennifer H., van Doorn, Remco, Bishop, D. Timothy, Newton-Bishop, Julia

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Inherited variation in the PARP1 gene and survival from melanoma von Davies, John R., Jewell, Rosalyn, Affleck, Paul, Anic, Gabriella M., Randerson‐Moor, Juliette, Ozola, Aija, Egan, Kathleen M., Elliott, Faye, García‐Casado, Zaida, Hansson, Johan, Harland, Mark, Höiom, Veronica, Jian, Guan, Jönsson, Göran, Kumar, Rajiv, Nagore, Eduardo, Wendt, Judith, Olsson, Håkan, Park, Jong Y., Patel, Poulam, Pjanova, Dace, Puig, Susana, Schadendorf, Dirk, Sivaramakrishna Rachakonda, P., Snowden, Helen, Stratigos, Alexander J., Bafaloukos, Dimitrios, Ogbah, Zighereda, Sucker, Antje, den Oord, Joost J., Doorn, Remco, Walker, Christy, Okamoto, Ichiro, Wolter, Pascal, Barrett, Jennifer H., Timothy Bishop, D., Newton‐Bishop, Julia

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The NIH MRI study of normal brain development: Performance of a population based sample of healthy children aged 6 to 18 years on a neuropsychological battery von WABER, DEBORAH P., DE MOOR, CARL, FORBES, PETER W., ALMLI, C. ROBERT, BOTTERON, KELLY N., LEONARD, GABRIEL, MILOVAN, DENISE, PAUS, TOMAS, RUMSEY, JUDITH

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The effect of 3% and 6% hypertonic saline in viral bronchiolitis: a randomised controlled trial von TEUNISSEN, Jasmijn, HOCHS, Anne H. J, ROSIAS, Philippe P. R, POTGIETER, Steph, FABER, Marianne R, HENDRIKS, Han J. E, JANSSEN-HEIJNEN, Maryska L. G, LOZA, Bettina F, VAESSEN-VERBERNE, Anja, BOEHMER, Annemie L. M, SMEETS, Carien C. J. M, BRACKEL, Hein, VAN GENT, René, WESSELING, Judith, LOGTENS-STEVENS, Danielle, DE MOOR, Ronald

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Depression, Anxiety, and Quality of Life in Patients with Epithelial Ovarian Cancer von Bodurka-Bevers, Diane, Basen-Engquist, Karen, Carmack, Cindy L., Fitzgerald, Mary A., Wolf, Judith K., de Moor, Carl, Gershenson, David M.

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Decreased Anemia Prevalence Among Women and Children in Rural Baja California, Mexico: A 6-Year Comparative Study von Moor, Molly A., Fraga, Miguel A., Garfein, Richard S., Harbertson, Judith, Rodriguez-Lainz, Alfonso, Rashidi, Hooman H., Elder, John P., Brodine, Stephanie K.

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An inherited variant in the gene coding for vitamin D-binding protein and survival from cutaneous melanoma: a BioGenoMEL study von Davies, John R., Field, Sinead, Randerson-Moor, Juliette, Harland, Mark, Kumar, Rajiv, Anic, Gabriella M., Nagore, Eduardo, Hansson, Johan, Höiom, Veronica, Jönsson, Göran, Gruis, Nelleke A., Park, Jong Y., Guan, Jian, Sivaramakrishna Rachakonda, P., Wendt, Judith, Pjanova, Dace, Puig, Susana, Schadendorf, Dirk, Okamoto, Ichiro, Olsson, Håkan, Affleck, Paul, García-Casado, Zaida, Puig-Butille, Joan Anton, Stratigos, Alexander J., Kodela, Elizabeth, Donina, Simona, Sucker, Antje, Hosen, Ismail, Egan, Kathleen M., Barrett, Jennifer H., van Doorn, Remco, Bishop, D. Timothy, Newton-Bishop, Julia

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Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing von Sifrim, Alejandro, Hitz, Marc-Phillip, Wilsdon, Anna, Breckpot, Jeroen, Turki, Saeed H. Al, Thienpont, Bernard, McRae, Jeremy, Fitzgerald, Tomas W, Singh, Tarjinder, Swaminathan, Ganesh Jawahar, Prigmore, Elena, Rajan, Diana, Abdul-Khaliq, Hashim, Banka, Siddharth, Bauer, Ulrike M.M, Bentham, Jamie, Berger, Felix, Bhattacharya, Shoumo, Bu'Lock, Frances, Canham, Natalie, Colgiu, Irina-Gabriela, Cosgrove, Catherine, Cox, Helen, Daehnert, Ingo, Daly, Allan, Danesh, John, Fryer, Alan, Gewillig, Marc, Hobson, Emma, Hoff, Kirstin, Homfray, Tessa, the INTERVAL Study, Kahlert, Anne-Karin, Ketley, Ami, Kramer, Hans-Heiner, Lachlan, Katherine, Lampe, Anne Katrin, Louw, Jacoba J, Manickara, Ashok Kumar, Manase, Dorin, McCarthy, Karen P, Metcalfe, Kay, Moore, Carmel, Newbury-Ecob, Ruth, Omer, Seham Osman, Ouwehand, Willem H, Park, Soo-Mi, Parker, Michael J, Pickardt, Thomas, Pollard, Martin O, Robert, Leema, Roberts, David J, Sambrook, Jennifer, Setchfield, Kerry, Stiller, Brigitte, Thornborough, Chris, Toka, Okan, Watkins, Hugh, Williams, Denise, Wright, Michael, Mital, Seema, Daubeney, Piers E.F, Keavney, Bernard, Goodship, Judith, the UK10K Consortium, Abu-Sulaiman, Riyadh Mahdi, Klaassen, Sabine, Wright, Caroline F, Firth, Helen V, Barrett, Jeffrey C, Devriendt, Koenraad, FitzPatrick, David R, Brook, J. David, the Deciphering Developmental Disorders Study, Hurles, Matthew E

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An inherited variant in the gene coding for vitamin D ‐binding protein and survival from cutaneous melanoma: a B io G eno MEL study von Davies, John R., Field, Sinead, Randerson‐Moor, Juliette, Harland, Mark, Kumar, Rajiv, Anic, Gabriella M., Nagore, Eduardo, Hansson, Johan, Höiom, Veronica, Jönsson, Göran, Gruis, Nelleke A., Park, Jong Y., Guan, Jian, Sivaramakrishna Rachakonda, P., Wendt, Judith, Pjanova, Dace, Puig, Susana, Schadendorf, Dirk, Okamoto, Ichiro, Olsson, Håkan, Affleck, Paul, García‐Casado, Zaida, Puig‐Butille, Joan Anton, Stratigos, Alexander J., Kodela, Elizabeth, Donina, Simona, Sucker, Antje, Hosen, Ismail, Egan, Kathleen M., Barrett, Jennifer H., van Doorn, Remco, Bishop, D. Timothy, Newton‐Bishop, Julia

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Determination of selenium in sediments by inductively coupled plasma-mass spectrometry: high resolution versus hydride generation von Moor, Christoph, Kobler, Judith

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AS01 How salty may it be? Effect of inhaled hypertonic saline solution to treat infants hospitalized with viral bronchiolitis von Teunissen, Jasmijn, Hochs, Anne, Vaessen-Verberne, Anja, Boehmer, Annemie, Smeets, Carien, Brackel, Hein, van Gent, Rene, Wesseling, Judith, de Moor, Ronald, Rosias, Philippe, Potgieter, Steven, Droog, Richard, Hendriks, Han, Logtens-Stevens, Danielle, Janssen-Heijnen, Mariska, Loza, Bettina

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ENCAPSULATED VOLATILE LIQUID SOURCE FOR AN AEROSOL-GENERATING SYSTEM von WALLER, Judith, MOOR, Philippe

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Pays nordiques von Arwill-Nordbladh, Elisabeth, Birk Jørgensen, Morten, Bogh, Mikkel, Delfiner, Judith, Demoule, Jean-Paul, De Moor, Hannah, Doe Stone, Elizabeth, Eriksen, Stefka G, Escach, Nicolas, Frisch, Sidsel, García-Antón, Katya, Glørstad, Håkon, Gullickson, Charis, Høegh Stigsen, Bilo, Högkvist, Stina, Kervanto Nevanlinna, Anja, Kristensen, Jens Tang, Kristianson, Kristian, Krysa, Joasia, Larsen, Lars Bang, Lindstrand, Tor, Ljøgodt, Knut, Nilsson, Håkan, Nilsson Stutz, Liv, Ólafsdóttir, Ásdís, Olsson, Carl-Johan, Opsvik, Peter, Pekonen, Osmo, Perrin Khelissa, Anne, Persen, Synnøve, Ravn, Mads, Roffidal, Émilie, Schnapp, Alain, Sigurjónsdóttir, Æsa, Sjåstad, Øystein, Svenbro, Jesper, Tanninen-Mattila, Maija, Topp, Leslie

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