Paroxysmal Cranial Dyskinesia and Nail‐Patella Syndrome Caused by a Novel Variant in the LMX1B Gene von Bech, Sara, Løkkegaard, Annemette, Nielsen, Troels T., Nørremølle, Anne, Grønborg, Sabine, Hasholt, Lis, Steffensen, Gudrun K., Graehn, Gabor, Olesen, Jess H., Tommerup, Niels, Mang, Yuan, Bak, Mads, Nielsen, Jørgen E., Eiberg, Hans, Hjermind, Lena E.

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Anxiety- and depression-like phenotype of hph-1 mice deficient in tetrahydrobiopterin von Nasser, Arafat, Møller, Lisbeth B., Olesen, Jess H., Konradsen, Louise S., Andreasen, Jesper T.

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Paroxysmal Cranial Dyskinesia and Nail-Patella Syndrome Caused by a Novel Variant in theLMX1BGene von Bech, Sara, Lokkegaard, Annemette, Nielsen, Troels T., Norremolle, Anne, Gronborg, Sabine, Hasholt, Lis, Steffensen, Gudrun K., Graehn, Gabor, Olesen, Jess H., Tommerup, Niels, Mang, Yuan, Bak, Mads, Nielsen, Jorgen E., Eiberg, Hans, Hjermind, Lena E.

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Abnormal Newborn Screening in a Healthy Infant of a Mother with Undiagnosed Medium-Chain Acyl-CoA Dehydrogenase Deficiency von Aksglaede, Lise, Christensen, Mette, Olesen, Jess H., Duno, Morten, Olsen, Rikke K. J., Andresen, Brage S., Hougaard, David M., Lund, Allan M.

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Corrigendum to “Anxiety- and depression-like phenotype of the hph-1 mice deficient in tetrahydrobiopterin” [Neurosci. Res. 89 (2014) 44–53] von Nasser, Arafat, Møller, Lisbeth B., Olesen, Jess H., Refsgaard, Louise K., Andreasen, Jesper T.

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Novel ASIC architecture and synthesis methodologies for future multiplexed datapath designs von Catthoor, F., Wehn, N., Courtois, B., De Man, H., van Eijndhoven, J., Glesner, M., Goutis, C., Jess, J., Madsen, J., O'Brien, K., Olesen, O., Philipson, L., Pochmuller, P.

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