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Neuronal Ceroid Lipofuscinoses (Batten Disease)
2018 Neuronal ceroid lipofuscinoses (NCL) are a group of autosomal recessive genetic disorders which represent the most common form of childhood neurodegenerative disease. Classically the disease was described according to the age of diagnosis resulting in four common phenotypes: (i) infantile or Santavuori-Haltia, (ii) late infantile or Jansky-Bielschowsky,openaire +1 more sourceBatten Disease
2009 Alexander K. C. Leung, Marcus Schmitt, Christie P. Thomas, Cord Sunderkötter, Meinhard Schiller, Thomas Schwarz, Mark Berneburg, Alfried Kohlschütter, Lorenzo Cerroni, Haner Direskeneli, Kenneth Calamia, Gloria L. David, Darryl C. Zeldin, Bärbel Schütte, Lee A. Denson, Andreas Erhardt, Ralf Kubitz, Dieter Häussinger, Wendy M. Sealey, Donald M. Mock, Barry Wolf, Johannes Schumacher, Peter Propping, Dieter Metze, Alexander K. C. Leung, Andrew L. Wong, Mark Berneburg, Thomas Schwarz, Markus Hengstschläger, Whitney A. High, Kenneth R. Shroyer, M. Elizabeth McCready, Dennis E. Bulman, Ali R. Afzal, David B. Everman, Claude Stoll, Sukran Darcan, Yu Ru Kou, You Shuei Lin, Yoichi Suzuki, Keiya Tada, Alexander K. C. Leung, Susan Kupka, Wolfgang Dietmaier, Arndt Hartmann, Raoul C. M. Hennekam, John A. Belperio, Michael P. Keane, M. Iain Smith, Robert M. Strieter, Nestor A. Molfino, Francesca Sciandra, Tom Rossenbacker, Silvia G. Priori, Marco Senzolo, Christos Triantos, Dimitrios Samonakis, Evangelos Cholongitas, Andrew K. Burroughs, Marco Mura, Markus Braun-Falco, Silke Hofmann, Leena Bruckner-Tuderman +62 moreopenaire +1 more source
