Susceptibility of Chickens to Low Pathogenic Avian Influenza (LPAI) Viruses of Wild Bird- and Poultry-Associated Subtypes von Bergervoet, Saskia A, Germeraad, Evelien A, Alders, Marc, Roose, Marit M, Engelsma, Marc Y, Heutink, Rene, Bouwstra, Ruth, Fouchier, Ron A M, Beerens, Nancy

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Guidelines for diagnostic next-generation sequencing von Matthijs, Gert, Souche, Erika, Alders, Mariëlle, Corveleyn, Anniek, Eck, Sebastian, Feenstra, Ilse, Race, Valérie, Sistermans, Erik, Sturm, Marc, Weiss, Marjan, Yntema, Helger, Bakker, Egbert, Scheffer, Hans, Bauer, Peter

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Mutations in PCYT2 disrupt etherlipid biosynthesis and cause a complex hereditary spastic paraplegia von Vaz, Frédéric M, McDermott, John H, Alders, Mariëlle, Wortmann, Saskia B, Kölker, Stefan, Pras-Raves, Mia L, Vervaart, Martin A T, van Lenthe, Henk, Luyf, Angela C M, Elfrink, Hyung L, Metcalfe, Kay, Cuvertino, Sara, Clayton, Peter E, Yarwood, Rebecca, Lowe, Martin P, Lovell, Simon, Rogers, Richard C, van Kampen, Antoine H C, Ruiter, Jos P N, Wanders, Ronald J A, Ferdinandusse, Sacha, van Weeghel, Michel, Engelen, Marc, Banka, Siddharth

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Guidelines for diagnostic next-generation sequencing von Matthijs, Gert, Souche, Erika, Alders, Mariëlle, Corveleyn, Anniek, Eck, Sebastian, Feenstra, Ilse, Race, Valérie, Sistermans, Erik, Sturm, Marc, Weiss, Marjan, Yntema, Helger, Bakker, Egbert, Scheffer, Hans, Bauer, Peter

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Sex‐specific newborn screening for X‐linked adrenoleukodystrophy von Albersen, Monique, Beek, Samantha L., Dijkstra, Inge M. E., Alders, Mariëlle, Barendsen, Rinse W., Bliek, Jet, Boelen, Anita, Ebberink, Merel S., Ferdinandusse, Sacha, Goorden, Susan M. I., Heijboer, Annemieke C., Jansen, Mandy, Jaspers, Yorrick R. J., Metgod, Ingrid, Salomons, Gajja S., Vaz, Frédéric M., Verschoof‐Puite, Rendelien K., Visser, Wouter F., Dekkers, Eugènie, Engelen, Marc, Kemp, Stephan

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Recurrent GNAO1 Mutations Associated With Developmental Delay and a Movement Disorder von Menke, Leonie A., Engelen, Marc, Alders, Mariel, Odekerken, Vincent J. J., Baas, Frank, Cobben, Jan M.

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Adrenoleukodystrophy Newborn Screening in the Netherlands (SCAN Study): The X-Factor von Barendsen, Rinse W, Dijkstra, Inge M E, Visser, Wouter F, Alders, Mariëlle, Bliek, Jet, Boelen, Anita, Bouva, Marelle J, van der Crabben, Saskia N, Elsinghorst, Ellen, van Gorp, Ankie G M, Heijboer, Annemieke C, Jansen, Mandy, Jaspers, Yorrick R J, van Lenthe, Henk, Metgod, Ingrid, Mooij, Christiaan F, van der Sluijs, Elise H C, van Trotsenburg, A S Paul, Verschoof-Puite, Rendelien K, Vaz, Frédéric M, Waterham, Hans R, Wijburg, Frits A, Engelen, Marc, Dekkers, Eugènie, Kemp, Stephan

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Biallelic variants in LIG3 cause a novel mitochondrial neurogastrointestinal encephalomyopathy von Bonora, Elena, Chakrabarty, Sanjiban, Kellaris, Georgios, Tsutsumi, Makiko, Bianco, Francesca, Bergamini, Christian, Ullah, Farid, Isidori, Federica, Liparulo, Irene, Diquigiovanni, Chiara, Masin, Luca, Rizzardi, Nicola, Cratere, Mariapia Giuditta, Boschetti, Elisa, Papa, Valentina, Maresca, Alessandra, Cenacchi, Giovanna, Casadio, Rita, Martelli, Pierluigi, Matera, Ivana, Ceccherini, Isabella, Fato, Romana, Raiola, Giuseppe, Arrigo, Serena, Signa, Sara, Sementa, Angela Rita, Severino, Mariasavina, Striano, Pasquale, Fiorillo, Chiara, Goto, Tsuyoshi, Uchino, Shumpei, Oyazato, Yoshinobu, Nakamura, Hisayoshi, Mishra, Sushil K, Yeh, Yu-Sheng, Kato, Takema, Nozu, Kandai, Tanboon, Jantima, Morioka, Ichiro, Nishino, Ichizo, Toda, Tatsushi, Goto, Yu-ichi, Ohtake, Akira, Kosaki, Kenjiro, Yamaguchi, Yoshiki, Nonaka, Ikuya, Iijima, Kazumoto, Mimaki, Masakazu, Kurahashi, Hiroki, Raams, Anja, MacInnes, Alyson, Alders, Mariel, Engelen, Marc, Linthorst, Gabor, de Koning, Tom, den Dunnen, Wilfred, Dijkstra, Gerard, van Spaendonck, Karin, van Gent, Dik C, Aronica, Eleonora M, Picco, Paolo, Carelli, Valerio, Seri, Marco, Katsanis, Nicholas, Duijkers, Floor A.M, Taniguchi-Ikeda, Mariko, De Giorgio, Roberto

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CUL3-related neurodevelopmental disorder: Clinical phenotype of 20 new individuals and identification of a potential phenotype-associated episignature von van der Laan, Liselot, Silva, Ananília, Kleinendorst, Lotte, Rooney, Kathleen, Haghshenas, Sadegheh, Lauffer, Peter, Alanay, Yasemin, Bhai, Pratibha, Brusco, Alfredo, de Munnik, Sonja, de Vries, Bert B.A., Vega, Angelica Delgado, Engelen, Marc, Herkert, Johanna C., Hochstenbach, Ron, Hopman, Saskia, Kant, Sarina G., Kira, Ryutaro, Kato, Mitsuhiro, Keren, Boris, Kroes, Hester Y., Levy, Michael A., Lock-Hock, Ngu, Maas, Saskia M., Mancini, Grazia M.S., Marcelis, Carlo, Matsumoto, Naomichi, Mizuguchi, Takeshi, Mussa, Alessandro, Mignot, Cyril, Närhi, Anu, Nordgren, Ann, Pfundt, Rolph, Polstra, Abeltje M., Trajkova, Slavica, van Bever, Yolande, José van den Boogaard, Marie, van der Smagt, Jasper J., Barakat, Tahsin Stefan, Alders, Mariëlle, Mannens, Marcel M.A.M., Sadikovic, Bekim, van Haelst, Mieke M., Henneman, Peter

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Erratum: Guidelines for diagnostic next-generation sequencing von Matthijs, Gert, Souche, Erika, Alders, Mariëlle, Corveleyn, Anniek, Eck, Sebastian, Feenstra, Ilse, Race, Valérie, Sistermans, Erik, Sturm, Marc, Weiss, Marjan, Yntema, Helger, Bakker, Egbert, Scheffer, Hans, Bauer, Peter

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Developing Outcomes Assessments as Endpoints for Registrational Clinical Trials of Antibacterial Drugs: 2015 Update From the Biomarkers Consortium of the Foundation for the Nationa... von Talbot, George H., Powers, John H., Hoffmann, Steven C.

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Guidelines for diagnostic next-generation sequencing von Matthijs, Gert, Souche, Erika, Alders, Mariëlle, Corveleyn, Anniek, Eck, Sebastian, Feenstra, Ilse, Race, Valérie, Sistermans, Erik, Sturm, Marc, Weiss, Marjan, Yntema, Helger, Bakker, Egbert, Scheffer, Hans, Bauer, Peter

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Dihydropyrimidine Dehydrogenase Deficiency: Homozygosity for an Extremely Rare Variant in DPYD due to Uniparental Isodisomy of Chromosome 1 von van Kuilenburg, André B. P., Meijer, Judith, Meinsma, Rutger, Pérez-Dueñas, Belén, Alders, Marielle, Bhuiyan, Zahurul A., Artuch, Rafael, Hennekam, Raoul C. M.

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The Role of the Epinephrine Test in the Diagnosis and Management of Children Suspected of Having Congenital Long QT Syndrome von Clur, Sally-Ann B., Chockalingam, Priya, Filippini, Luc H., Widyanti, Ari P., Van Cruijsen, Marc, Blom, Nico A., Alders, Mariel, Hofman, Nynke, Wilde, Arthur A. M.

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Corrigendum: Adrenoleukodystrophy Newborn Screening in the Netherlands (SCAN Study): The X-Factor von Barendsen, Rinse W, Dijkstra, Inge M E, Visser, Wouter F, Alders, Mariëlle, Bliek, Jet, Boelen, Anita, Bouva, Marelle J, van der Crabben, Saskia N, Elsinghorst, Ellen, van Gorp, Ankie G M, Heijboer, Annemieke C, Jansen, Mandy, Jaspers, Yorrick R J, van Lenthe, Henk, Metgod, Ingrid, Mooij, Christiaan F, van der Sluijs, Elise H C, van Trotsenburg, A S Paul, Verschoof-Puite, Rendelien K, Vaz, Frédéric M, Waterham, Hans R, Wijburg, Frits A, Engelen, Marc, Dekkers, Eugènie, Kemp, Stephan

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Dihydropyrimidine Dehydrogenase Deficiency: Metabolic Disease or Biochemical Phenotype? von Fleger, M., Willomitzer, J., Meinsma, R., Alders, M., Meijer, J., Hennekam, R. C. M., Huemer, M., van Kuilenburg, A. B. P.

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The Social Maze: A Collaborative Game to Motivate MS Patients for Upper Limb Training von De Weyer, Tom, Robert, Karel, Renny Octavia Hariandja, Johanna, Alders, Geert, Coninx, Karin

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Heat shield element von DEISS, OLGA, KLEINFELD, JENS, TERTILT, MARC, ALDERS, CLAUDIA, VONNEMANN, BERND

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Guidelines for diagnostic next-generation sequencing (vol 24, pg 2, 2016) von Matthijs, Gert, Souche, Erika, Alders, Mariëlle, Corveleyn, Anniek, Eck, Sebastian, Feenstra, Ilse, Race, Valerie, Sistermans, Erik, Sturm, Marc, Weiss, Marjan, Yntema, Helger, Bakker, Egbert, Scheffer, Hans, Bauer, Peter

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Heat shield element von DEISS, OLGA, KLEINFELD, JENS, TERTILT, MARC, ALDERS, CLAUDIA, VONNEMANN, BERND

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